Small renal masses: observation, surgery and image-guided ablation

An unexpected spot on a kidney scan can be alarming. A small renal mass usually means a solid, enhancing growth measuring 4 cm or less and confined to the kidney. It is not automatically cancer: some are benign, and many small kidney cancers grow slowly. The right approach depends on the scan, any biopsy result, kidney function, other health conditions and what matters to you. [1,2]

How do we investigate it?

I review the original imaging and usually arrange a dedicated, multiphase contrast CT or MRI to establish whether the lesion enhances, its size and position, and whether it looks like a simple cyst or another benign condition. Blood tests assess kidney function. The need for chest imaging depends on the findings and clinical circumstances. If contrast is unsuitable because of impaired kidney function, we plan an alternative with the radiologist. [1,2]

A needle biopsy can help when knowing whether a mass is benign or what type of cancer it contains would change the decision. A biopsy can occasionally be inconclusive. If ablation is planned, the European Association of Urology (EAU) recommends biopsy before a separate ablation session to avoid treating benign lesions unnecessarily. [1]

What are the choices?

Approach When it may suit Main consideration
Active surveillance A very small mass, particularly under 2 cm; slow growth; or a patient who prefers to defer treatment Planned scans and a clear trigger to reconsider treatment
Partial nephrectomy A mass requiring treatment when kidney-sparing surgery is technically suitable Removes the tumour and supplies a complete specimen, but requires an operation
Percutaneous ablation A selected small mass when treatment is indicated, especially if surgery carries greater risk or preserving kidney tissue is important Less invasive, but imaging follow-up is essential and repeat treatment may be needed
Radical nephrectomy A tumour that cannot reasonably be treated with a kidney-sparing approach Removes the whole kidney and may have a greater effect on kidney function

For masses under 2 cm, surveillance is often a sensible first option. For masses 2–4 cm, surveillance, partial nephrectomy and ablation may all deserve discussion. If surgery is appropriate, guidelines generally favour partial nephrectomy for a treatable small cancer. Frailty or limited life expectancy may make symptom-focused observation preferable. [1,2]

Surveillance is an active plan, not neglect. Scans are often repeated every 3–6 months initially and then every 6–12 months if stable, with timing adapted to the individual. Growth beyond 4 cm, repeated growth above approximately 5 mm a year, new concerning features or patient preference can prompt reconsideration; growth rate alone does not prove that a mass is dangerous. [2]

What is radiofrequency ablation (RFA)?

RFA destroys tissue by passing an electrical current through a thin probe, generating heat inside the mass. An interventional radiologist usually places the probe through the skin using CT or ultrasound guidance. Anaesthesia or sedation, patient positioning and sometimes fluid injected to protect nearby bowel are planned around the tumour’s location. The radiologist treats the mass and a small surrounding margin, then checks for immediate complications. Many patients have a short hospital stay, but arrangements vary. [1–3]

RFA is most established for small, accessible masses, particularly those up to 3 cm. A mass deep in the kidney, next to the urine-drainage system or bowel, or near major vessels can be harder to treat safely or completely. EAU guidance advises against routinely offering RFA for masses over 3 cm, because control becomes less reliable. A mass between 3 and 4 cm needs an individual discussion rather than an automatic exclusion. [1]

What other ablation methods are available?

  • Cryoablation uses probes to freeze the tumour. The visible ice ball can help the operator plan the treatment margin. It is an established alternative to RFA; the EAU advises against its routine use for tumours over 4 cm. [1,2]
  • Microwave ablation uses microwave energy to heat tissue. Experience is growing and the EAU describes encouraging results, though long-term comparative evidence remains less certain than for surgery. Availability and expertise vary. [1]
  • Irreversible electroporation delivers electrical pulses to disrupt cell membranes. Evidence for routine treatment of small renal cancers remains limited. [2]
  • Stereotactic ablative radiotherapy (SABR/SBRT) directs highly focused radiation without inserting a probe. It can be discussed for selected patients who need treatment but are unsuitable for surgery; long-term comparisons remain limited. [1]

The choice depends on tumour size and position, prior treatment, kidney function, local expertise and the patient’s preferences. No technique is right for every lesion.

Benefits, limitations and risks

Percutaneous ablation can avoid a surgical incision, usually involves less immediate recovery than surgery and can preserve functioning kidney tissue. Risks include bleeding, infection, pain, injury to the urine-collecting system or nearby organs, and incomplete treatment or local recurrence. Risks depend strongly on where the tumour sits. A second ablation or surgery may be possible if follow-up imaging shows persistent disease. [1,2]

Evidence comparing ablation with partial nephrectomy largely comes from observational studies involving patients with different health risks. Ablation offers good local control for carefully selected small tumours, but its long-term cancer control relative to surgery is less certain; it should not be described as a guaranteed equivalent. [1,2]

What happens after ablation?

Treatment destroys the lesion in place, so there is no whole-tumour surgical specimen. Contrast-enhanced CT or MRI checks for remaining enhancing tissue and later recurrence. One published guideline suggests imaging at 3, 6 and 12 months, then annually after ablation, adjusted to biopsy findings, renal function and the treating team’s protocol. We also monitor kidney function. A new enhancing focus requires specialist review and may lead to repeat biopsy or treatment. [1,2]

My role in your care

I can review the findings and discuss surveillance, biopsy and the treatment choices with you. I no longer perform nephrectomies. If an operation is the best option, I will refer you to a colleague who performs kidney surgery. If ablation appears suitable, I will arrange assessment by an experienced interventional radiology team; the final decision follows review of the images and your overall health.

Seek urgent medical attention for heavy visible bleeding, inability to pass urine, fever with flank pain, or severe worsening pain after a procedure.

This article provides general information. Individual advice requires assessment of your imaging, biopsy findings where relevant, kidney function and medical history.

Dr Jo Schoeman | Patient information | September 2026

References

  1. European Association of Urology. EAU Guidelines on Renal Cell Carcinoma: Disease Management, current online edition, accessed September 2026.
  2. Richard PO, et al. Canadian Urological Association guideline: Management of small renal masses. Canadian Urological Association Journal. 2022;16(2)–E75.
  3. Park BK, et al. Asian Conference on Tumor Ablation guidelines for renal cell carcinoma. Investigative and Clinical Urology. 2021.
  4. European Association of Urology. EAU Guidelines on Renal Cell Carcinoma: Follow-up, current online edition, accessed September 2026.

A kidney tumour larger than 3 cm: what does it mean?

By Dr Jo Schoeman | Patient information | September 2026

Finding a kidney mass can be frightening. The first question is whether it is cancer; the next is whether it is confined to the kidney. A mass measuring 3.1 cm is not automatically advanced cancer. If a renal cell carcinoma (RCC) is no more than 4 cm and remains within the kidney, it is classified as T1a. A tumour over 4 cm but no more than 7 cm, still confined to the kidney, is T1b. Lymph-node and distant spread are assessed separately. Some kidney masses are benign, and imaging alone cannot always tell us which. [1–3]

How might it present?

Many tumours are discovered by chance during an ultrasound or CT scan for another problem. Others cause blood in the urine, persistent pain in the side or back, or occasionally a palpable lump. Unexplained weight loss, fatigue, anaemia or fever warrant assessment, although they have many possible causes. The combination of blood in the urine, pain and a palpable mass is uncommon. Visible blood in the urine should always be investigated; a kidney mass does not rule out another source of bleeding. [2]

What investigations are needed?

  • Dedicated imaging: A multiphase contrast CT of the kidneys and abdomen shows whether the lesion enhances, its exact position, its relationship to major blood vessels and the collecting system, and whether there are enlarged nodes or signs of spread. Chest imaging completes staging; its extent is tailored to the tumour and clinical circumstances. MRI may clarify an uncertain lesion or suspected tumour extension into a vein, or be useful when CT contrast is unsuitable. A complex kidney cyst needs its own imaging assessment. [2]
  • Blood and urine tests: Kidney function (creatinine and eGFR), a full blood count and other tests guided by the clinical picture help assess fitness for treatment and preserve kidney function. Urine testing may identify infection or another cause of bleeding. [2]
  • Biopsy: A needle biopsy can be useful if its result will change management, particularly before ablation or drug treatment without prior tissue diagnosis. A typical surgically removable solid mass does not always need a biopsy beforehand. A biopsy can occasionally be inconclusive. [2]
  • Further staging: Bone or brain scans are generally reserved for relevant symptoms or suspected advanced disease. Routine PET scans and bone scans are not recommended for initial RCC staging. [2]

The team should review the images, kidney function, other medical conditions and the patient’s priorities together. An indeterminate mass should not be labelled definitively as RCC before appropriate assessment.

A note about my practice: I no longer perform nephrectomies. I can assess your kidney mass, discuss the findings and treatment options with you, and, if an operation is appropriate, refer you to a colleague who performs kidney surgery. We can also arrange input from a multidisciplinary team where needed.

Treatment when the tumour is confined to the kidney

Partial nephrectomy removes the tumour while preserving the rest of the kidney. This is generally preferred for T1 cancers when technically feasible, particularly if kidney function is reduced or there is only one functioning kidney. It can be performed by robotic, laparoscopic or open surgery according to tumour complexity and surgical expertise. Risks include bleeding, urine leak, infection, reduced kidney function and, occasionally, the need to remove the whole kidney. [1]

Radical nephrectomy removes the kidney and may be appropriate when a safe partial nephrectomy is not feasible, particularly with a larger or more complex tumour. Robotic or laparoscopic surgery offers an approach to the operation; it does not change the underlying choice between partial and radical removal. [1]

Active surveillance may suit selected people with a small, slow-growing mass, competing health risks or a strong preference to defer treatment. It involves planned scans and a clear trigger to reconsider treatment. A tumour just above 3 cm needs a particularly careful discussion because the room for further growth before 4 cm is limited. Thermal ablation, such as cryoablation or radiofrequency or microwave ablation, may suit selected small tumours, especially when surgery is unsuitable; a biopsy is recommended before ablation. Local recurrence and the possible need for repeat treatment should be discussed. [1, 2]

Stereotactic ablative radiotherapy (SABR) is also being used in specialist centres for selected patients with localised RCC who cannot undergo surgery. It is a distinct option from routine radiation after an operation, and its long-term comparative evidence continues to mature. [1]

What if lymph nodes look enlarged?

An enlarged node on a scan is suspicious, not proof of cancer; inflammation can also enlarge nodes. The team considers the appearance and site of the nodes, whether there is disease elsewhere and whether tissue confirmation will change treatment. If nephrectomy is planned, visibly enlarged regional nodes may be removed for diagnosis and staging. Removing normal-looking nodes routinely has not been shown to improve survival for organ-confined RCC. The survival benefit of removing involved nodes is uncertain. [1]

Confirmed regional node involvement is a substantial change in risk even if the kidney tumour is small. It calls for multidisciplinary discussion about whether all visible disease can be removed, whether postoperative drug treatment is appropriate, and how closely to monitor. Nodes beyond the regional area, or spread to organs such as the lung or bone, may represent metastatic disease and require a different plan. Surgery on the kidney is not automatically the best first step when cancer is widespread. [1, 3]

When does immunotherapy help?

For selected patients with clear-cell RCC at higher risk of recurrence after complete surgery, a course of pembrolizumab may lower recurrence risk and has shown an overall survival benefit in the KEYNOTE-564 study. The eligible groups include some patients with confirmed regional node involvement and no distant metastases. A 3–4 cm node-negative tumour confined to the kidney would not usually qualify based on size alone. The final pathology, stage and overall health matter. [1, 4]

If cancer has spread and cannot all be removed, initial treatment for clear-cell RCC often combines immune checkpoint drugs with each other (nivolumab plus ipilimumab) or combines immunotherapy with an oral targeted drug (for example, pembrolizumab plus axitinib, pembrolizumab plus lenvatinib, or nivolumab plus cabozantinib). The best regimen depends on risk group, other illnesses, kidney function, previous treatment and the specific cancer subtype. Papillary and other non-clear-cell cancers may need different approaches. Availability and subsidy in Australia should be checked for the individual indication. [1]

Immunotherapy can cause serious inflammation of the bowel, lungs, liver, kidneys or hormone-producing glands; targeted drugs can cause high blood pressure, diarrhoea, fatigue and other adverse effects. Some immune effects can persist after treatment ends. Benefits and risks need an individual discussion with a medical oncologist. [1, 4]

Is chemotherapy useful?

Conventional cytotoxic chemotherapy is generally ineffective for the common types of RCC and is not standard treatment for ordinary clear-cell RCC. Rare subtypes, including collecting duct and renal medullary carcinoma, are exceptions in which chemotherapy may have a role. A cancer arising from the lining of the renal pelvis (upper-tract urothelial carcinoma) is a different disease with different chemotherapy options; establishing the diagnosis matters. [1]

Does radiation offer a benefit?

Radiotherapy is not routinely given after nephrectomy to prevent recurrence of localised RCC. Its clearest established role is treating specific problems from spread, such as painful bone lesions, brain metastases or symptoms from another site. Precisely targeted radiation may also control selected limited metastases or treat a primary tumour in someone unsuitable for surgery. Whether it adds benefit to systemic therapy or surgery in an individual case depends on the site, number and behaviour of lesions and is best decided with radiation oncology input. It should not be presented as a standard substitute for an operable partial nephrectomy. [1, 5]

Questions worth asking at your consultation

  1. Is this definitely a solid enhancing kidney tumour, and what is its exact size and location?
  2. Is the disease confined to the kidney? Are any nodes merely enlarged, or proven to contain cancer?
  3. Can we safely preserve part of the kidney? What is my current kidney function?
  4. Would a biopsy change the plan?
  5. If the cancer is clear-cell and higher risk, would adjuvant pembrolizumab be suitable?
  6. Would drug treatment or targeted radiation offer a benefit in my particular situation?

Seek prompt medical attention for heavy bleeding with clots, inability to pass urine, severe persistent pain, or sudden neurological symptoms. This article is general information and cannot replace review of your scans and pathology at a multidisciplinary meeting.

References

  1. European Association of Urology. EAU Guidelines on Renal Cell Carcinoma: Disease Management. 2026.
  2. European Association of Urology. EAU Guidelines on Renal Cell Carcinoma: Diagnostic Evaluation. 2026.
  3. European Association of Urology. EAU Guidelines on Renal Cell Carcinoma: Staging and Classification Systems. 2026.
  4. National Cancer Institute. Adjuvant Keytruda improves kidney cancer survival, reporting updated KEYNOTE-564 outcomes. 2024.
  5. National Cancer Institute. Renal Cell Cancer Treatment (PDQ), Health Professional Version. Accessed September 2026.

Information Sheet: Renal Cancers

Upper Tract Urothelial Carcinoma

Cancer of the Renal Pelvis and Ureter

Urothelial carcinoma is most commonly associated with the bladder, but the same specialised lining extends all the way from the bladder up the ureters and into the collecting system of each kidney.

When a urothelial cancer develops in the renal pelvis or ureter, it is called upper tract urothelial carcinoma (UTUC).

UTUC is considerably less common than bladder cancer. Importantly, its behaviour varies enormously. Some tumours are small, superficial and relatively slow growing, while others are aggressive cancers capable of invading the kidney, surrounding tissues, lymph nodes and distant organs.

The key to successful management is therefore not simply finding the tumour, but determining how aggressive it is and how likely it is to spread.


What Is the Upper Urinary Tract?

Urine produced by the kidney drains through:

Kidney → renal calyces → renal pelvis → ureter → bladder → urethra

The inner surface of the renal pelvis, ureter and bladder is covered by urothelium, previously called transitional epithelium.

Cancer arising from these cells is called urothelial carcinoma.

UTUC can therefore occur in:

  • the renal pelvis;
  • one or more renal calyces;
  • the upper, middle or lower ureter;
  • multiple areas of the same urinary tract; or
  • occasionally both upper urinary tracts.

Patients with UTUC may also develop urothelial tumours within the bladder, either at the same time or later.


What Causes Upper Tract Urothelial Cancer?

Cancer develops when genetic damage accumulates within urothelial cells, allowing them to grow and divide abnormally.

Frequently there is no single identifiable cause, but several important risk factors are recognised.

Smoking

Cigarette smoking is one of the most important preventable risk factors for urothelial carcinoma.

Carcinogenic chemicals absorbed through the lungs enter the bloodstream, are filtered by the kidneys and become concentrated in the urine. The urothelium may therefore be exposed to these substances for many years.

Stopping smoking remains important even after diagnosis because of its wider health benefits and potential relevance to future urothelial cancer risk.

Previous bladder cancer

Patients who have previously had urothelial carcinoma of the bladder have an increased risk of developing urothelial carcinoma elsewhere within the urinary tract.

Similarly, patients treated for UTUC remain at risk of subsequently developing bladder cancer.

Occupational chemical exposure

Long-term exposure to certain industrial chemicals, particularly some aromatic amines historically associated with dye, rubber, textile, leather and chemical industries, has been associated with urothelial cancer.

Lynch syndrome

A small but important proportion of UTUC occurs in people with Lynch syndrome, an inherited disorder caused by abnormalities in DNA mismatch-repair genes.

UTUC, particularly in a younger patient or someone with a strong family history of bowel, endometrial or other Lynch-associated cancers, may prompt consideration of genetic assessment.

Chronic inflammation

Long-standing urinary tract inflammation and some chronic infections may contribute to malignant change. Chronic stone disease has particularly been associated with squamous carcinoma of the renal pelvis, which is a different and much less common tumour type.

Previous analgesic exposure

Heavy historical exposure to certain analgesics, particularly phenacetin-containing preparations that are no longer routinely used in many countries, has been associated with upper tract urothelial malignancy.


What Are the Symptoms?

Blood in the urine

The most common warning sign is:

Haematuria: blood in the urine

This may be obvious, turning the urine pink, red or occasionally dark brown.

Importantly, haematuria may:

  • occur only once;
  • disappear for weeks or months;
  • be completely painless; or
  • only be detected microscopically on a urine test.

Visible blood in the urine should always be appropriately investigated, particularly in adults.

Do not assume that painless bleeding is simply due to infection, prostate enlargement or a blood-thinning medication without appropriate assessment.


Flank or loin pain

A tumour can obstruct drainage of urine from the kidney.

This may produce:

  • persistent flank discomfort;
  • loin pain;
  • renal colic;
  • hydronephrosis, where the kidney becomes dilated because urine cannot drain normally.

Blood clots passing down the ureter can occasionally produce severe colicky pain resembling a kidney stone.


Recurrent urinary symptoms

Some patients experience:

  • urinary frequency;
  • urgency;
  • burning when passing urine;
  • recurrent apparent urinary tract infections.

These symptoms are much more commonly caused by benign conditions, but persistent or unexplained symptoms may warrant further investigation.


General symptoms

More advanced disease can occasionally cause:

  • unexplained weight loss;
  • loss of appetite;
  • fatigue;
  • persistent pain;
  • anaemia.

Fortunately, many tumours are detected before these symptoms develop.


How Is UTUC Diagnosed?

Investigation usually involves several complementary tests.

1. Urine testing

Urine is assessed for:

  • microscopic blood;
  • infection;
  • renal abnormalities; and
  • sometimes malignant cells.

Urine cytology

Urine cytology examines shed urinary cells under a microscope.

It is particularly useful for detecting high-grade urothelial carcinoma, although a negative cytology result does not completely exclude cancer.

Selective urine samples may sometimes be collected directly from the affected upper urinary tract.


2. CT Urography

CT urography is one of the most important imaging investigations for suspected UTUC.

Contrast-enhanced CT imaging allows assessment of:

  • the kidneys;
  • renal collecting systems;
  • ureters;
  • bladder;
  • lymph nodes; and
  • surrounding organs.

A tumour may appear as a filling defect, thickening of the ureter or renal pelvis, or an infiltrating mass.

CT can also identify obstruction and hydronephrosis.


3. Cystoscopy

Because urothelial cancer can occur at more than one location, the bladder should generally also be examined.

A flexible cystoscope is passed through the urethra into the bladder to look for associated bladder tumours.


Ureteroscopy and Biopsy

Sometimes imaging alone cannot provide enough information about the tumour.

A ureteroscope is a very fine telescope passed through the urethra and bladder and then into the ureter and renal collecting system.

This allows the urologist to directly inspect the tumour.

During ureteroscopy it may be possible to:

  • identify the location of the tumour;
  • assess whether there is one tumour or several;
  • estimate its size;
  • obtain selective urine cytology;
  • take a biopsy; and
  • in selected low-risk tumours, treat the lesion with a laser.

Biopsy is particularly helpful in determining whether the tumour is low-grade or high-grade.

An important limitation is that ureteroscopic biopsy samples are small, so determining the exact depth of invasion before definitive surgery can sometimes be difficult.


Low-Risk Versus High-Risk Disease

Modern management increasingly divides UTUC according to its risk of invasion and progression.

Factors considered include:

  • tumour grade;
  • appearance on CT;
  • tumour size;
  • number of tumours;
  • presence of hydronephrosis;
  • urine cytology;
  • ureteroscopic appearance;
  • biopsy findings;
  • evidence of invasion; and
  • previous urothelial cancer.

This distinction is extremely important because treatment can range from relatively conservative endoscopic therapy to removal of the entire kidney and ureter.


Treatment of Low-Risk UTUC

Selected patients with low-risk disease may be suitable for kidney-sparing treatment.

The objective is to control the cancer while preserving as much functioning kidney tissue as possible.

Ureteroscopic Laser Treatment

A ureteroscope is passed to the tumour and the lesion is treated using laser energy.

Laser treatment can:

  • vaporise;
  • coagulate; or
  • fragment the tumour.

Modern flexible ureteroscopes allow access to much of the renal collecting system.

Advantages

Kidney-sparing treatment may:

  • preserve kidney function;
  • avoid major abdominal surgery;
  • reduce recovery time;
  • be particularly valuable in patients with impaired kidney function or a solitary kidney.

Disadvantages

The trade-off is the need for very careful surveillance.

UTUC has a tendency to recur, so patients may require repeated:

  • ureteroscopy;
  • urine cytology;
  • CT imaging; and
  • occasionally further laser treatments or biopsies.

Kidney preservation therefore does not mean that the tumour can simply be treated once and forgotten.


Segmental Ureterectomy

Some tumours confined to a relatively short section of ureter can be treated by removing only the affected portion.

This is known as segmental ureterectomy.

It is particularly useful for appropriately selected tumours of the distal ureter.

The affected segment is removed and the remaining ureter is either reconnected or reimplanted into the bladder.

This can preserve the kidney while providing a complete surgical specimen for pathological examination.


Treatment of High-Risk UTUC

For patients with high-risk localised disease, the standard definitive operation is generally:

Radical Nephroureterectomy

This involves removal of:

the kidney + entire ureter + a cuff of bladder surrounding the ureteric opening

Removing the complete ureter is important because leaving part of the affected ureter behind may allow cancer to recur within the remaining urothelium.

The procedure can often be performed using:

  • robotic surgery;
  • laparoscopic surgery; or
  • occasionally open surgery.

The choice depends upon tumour characteristics, anatomy, previous surgery and individual circumstances.


What About the Lymph Nodes?

For selected high-risk tumours, lymph nodes draining the affected area may also be removed.

A lymph-node dissection can provide important staging information and may be incorporated into the surgical management of appropriately selected high-risk disease.


Chemotherapy

Systemic chemotherapy plays an important role in selected patients with higher-risk UTUC.

Platinum-based chemotherapy, particularly cisplatin-containing treatment, has traditionally formed an important part of systemic treatment.

Chemotherapy may be given:

Before surgery: neoadjuvant chemotherapy

One potential advantage is that both kidneys are still present, and renal function may therefore be better able to tolerate cisplatin.

After surgery: adjuvant chemotherapy

Chemotherapy may be recommended after nephroureterectomy when the final pathology demonstrates sufficiently high-risk disease.

An important consideration is that removing a kidney can reduce renal function, potentially affecting the patient’s ability to receive certain chemotherapy drugs.

Treatment decisions are therefore ideally made by a multidisciplinary uro-oncology team.


Immunotherapy and Newer Treatments

The treatment of advanced urothelial carcinoma has changed considerably in recent years.

Depending upon the stage, previous treatment and molecular characteristics of the cancer, systemic therapy may include combinations of:

  • platinum-based chemotherapy;
  • immune checkpoint inhibitors;
  • antibody-drug conjugates; and
  • targeted treatments for selected molecular abnormalities such as FGFR alterations.

These treatments are particularly relevant to patients with locally advanced, recurrent or metastatic disease.

Treatment is increasingly individualised according to the biological characteristics of the tumour and the patient’s kidney function and overall health.


Treatment Placed Directly Into the Upper Urinary Tract

For carefully selected non-invasive disease, medication may sometimes be delivered directly into the renal pelvis and ureter.

Options can include topical chemotherapy or immunotherapy in selected circumstances.

A chemoablative gel formulation of mitomycin has also been developed for selected low-grade UTUC, allowing prolonged contact between chemotherapy and the tumour.

These treatments are specialised and are not suitable for every patient.


What Happens After Treatment?

Follow-up is particularly important because urothelial carcinoma has a characteristic ability to develop at another point along the urinary tract.

After treatment, surveillance may include:

  • cystoscopy;
  • urine cytology;
  • CT urography or other upper-tract imaging;
  • blood tests to assess kidney function;
  • ureteroscopy following kidney-sparing treatment.

The exact surveillance schedule depends upon whether the original tumour was low or high risk and what treatment was performed.


Can the Cancer Return in the Bladder?

Yes.

One of the distinctive features of UTUC is the significant risk of subsequently developing urothelial carcinoma within the bladder.

Published data have reported subsequent bladder tumours in a substantial proportion of patients following treatment of UTUC.

For this reason, regular cystoscopic surveillance remains important even when the original kidney or ureteric tumour has been completely removed.


What Is the Prognosis?

The outlook for UTUC depends predominantly upon:

  • tumour stage;
  • tumour grade;
  • lymph-node involvement;
  • metastatic spread;
  • tumour multifocality;
  • response to treatment; and
  • certain pathological and molecular characteristics.

The most important question is whether the cancer remains superficial or has invaded deeply through the wall of the renal pelvis or ureter.

Superficial, localised disease

The outlook can be excellent when a tumour is identified while still superficial and confined to the upper urinary tract. The National Cancer Institute reports that more than 90% of superficial cancers confined to the renal pelvis or ureter may be curable.

Invasive disease

Once a tumour has invaded deeply into the wall or surrounding tissues, the risk of lymph-node involvement and distant spread increases substantially.

High-grade and invasive tumours therefore usually require more aggressive treatment and closer surveillance.

Metastatic disease

When UTUC has spread to distant organs, treatment is generally systemic rather than surgical alone.

Although metastatic UTUC remains a serious disease, modern systemic treatments have expanded considerably and can provide meaningful cancer control for selected patients.


UTUC and Kidney Function

Preserving kidney function is an important part of treatment planning.

Removing one kidney is usually well tolerated when the opposite kidney is healthy, but kidney function can become particularly important in patients with:

  • pre-existing chronic kidney disease;
  • diabetes;
  • hypertension;
  • a solitary kidney;
  • bilateral upper-tract tumours; or
  • conditions likely to affect future kidney function.

The decision between kidney-sparing treatment and radical nephroureterectomy therefore involves balancing two priorities:

adequate cancer control and preservation of renal function.

Cancer safety remains the priority, but in appropriately selected low-risk disease these objectives can often coexist.


When Should You See a Urologist?

Seek medical assessment if you develop:

  • visible blood in the urine;
  • persistent microscopic haematuria;
  • unexplained flank or loin pain;
  • recurrent unexplained urinary symptoms;
  • abnormal findings on kidney imaging; or
  • haematuria with a previous history of urothelial cancer.

Blood in the urine should not automatically be attributed to prostate enlargement, infection, kidney stones or blood-thinning medication without appropriate investigation.


The Bottom Line

Upper tract urothelial carcinoma is an uncommon cancer arising from the lining of the renal pelvis or ureter.

Blood in the urine is its most important warning sign.

Investigation commonly involves CT urography, cystoscopy, urine cytology and, when required, ureteroscopy with biopsy.

Treatment is increasingly tailored to the biological risk of the tumour.

Small, low-grade tumours may sometimes be managed with kidney-sparing ureteroscopic laser treatment or segmental surgery, while high-risk invasive cancers generally require radical nephroureterectomy with removal of the bladder cuff, sometimes combined with lymph-node surgery and systemic treatment.

Long-term surveillance is essential because urothelial cancer can recur elsewhere within the urinary tract, particularly the bladder.

The reassuring part is that when UTUC is detected while still superficial and localised, the likelihood of successful treatment can be very high.


A Note for Patients

Every upper tract urothelial tumour is different. Treatment depends upon the tumour’s location, size, grade, stage, number of lesions, kidney function and your general health.

Management should therefore be individualised following discussion with your urologist and, for higher-risk disease, a multidisciplinary uro-oncology team.

This information is intended for general patient education and should not replace individual medical advice, examination or treatment recommendations from your treating specialist.

The current 2026 EAU guideline specifically incorporates updated risk stratification, kidney-sparing management, bladder-cuff and lymph-node considerations, systemic therapy, and follow-up recommendations.

Small Renal Masses: When a Small Kidney Tumour Needs Watching, Treating or Removing

Finding a small mass on the kidney can be unsettling, particularly when it appears unexpectedly on an ultrasound or CT scan performed for something completely unrelated.

The reassuring news is that small does not automatically mean dangerous, and a renal mass does not automatically mean kidney cancer. Even when a small renal mass is malignant, many grow slowly and have a low risk of spreading. This means that immediate surgery is not always necessary.

Modern management has therefore moved away from a simple philosophy of “there is a lump, so it must come out”. Instead, treatment is tailored to the size and appearance of the mass, its growth rate, kidney function, the patient’s age and general health, and individual preferences.

Options range from:

  • Active surveillance
  • Percutaneous biopsy
  • Minimally invasive ablation, including cryoablation and thermal techniques
  • Robotic partial nephrectomy
  • Occasionally, radical nephrectomy

The aim is straightforward: control the cancer when treatment is necessary while preserving as much normal kidney function as possible.


What Is a Small Renal Mass?

A small renal mass (SRM) generally refers to a kidney tumour measuring 4 cm or less, corresponding to a clinical T1a renal tumour when confined to the kidney.

Many are discovered incidentally during imaging performed for abdominal pain, gallstones, bowel problems, back pain or another unrelated condition. The kidney lesion is often an unexpected passenger on the scan.

Importantly, not every small renal mass is cancer.

Benign lesions include:

  • Oncocytoma
  • Angiomyolipoma
  • Some complex renal cysts
  • Other uncommon benign tumours

Among malignant masses, renal cell carcinoma is the most important diagnosis. However, many small renal cancers demonstrate relatively indolent behaviour. Published guideline data suggest that more than 20% of small renal masses may ultimately prove benign, while many malignant lesions within this size range have relatively favourable biology.

This creates an important clinical dilemma: we want to treat a potentially dangerous cancer, but we also want to avoid unnecessary treatment of a tumour that may never have caused harm.


Step One: Properly Characterising the Mass

An incidental renal mass generally requires appropriate imaging before deciding what to do.

This usually involves a:

  • Multiphasic contrast CT scan, or
  • MRI scan

These scans help determine:

  • Exact tumour size
  • Whether the lesion is solid or cystic
  • Whether it enhances with contrast
  • Its position within the kidney
  • Relationship to blood vessels and the collecting system
  • Whether there are concerning features suggesting malignancy
  • Whether there is any evidence of disease outside the kidney

High-quality contrast CT or MRI is recommended for the characterisation of a newly discovered small renal mass.

Blood tests will usually include kidney function, particularly serum creatinine and estimated glomerular filtration rate (eGFR).


What About Complex Kidney Cysts?

Not every suspicious renal lesion is a solid tumour.

Complex renal cysts are usually classified according to the Bosniak classification, which estimates the likelihood that a cystic lesion represents malignancy.

Some Bosniak III and selected predominantly cystic lesions can also be considered for surveillance, particularly when they are small or when the risks of treatment outweigh the anticipated benefits. Larger or increasingly complex lesions are more likely to require intervention.


Do We Need a Kidney Biopsy?

Sometimes.

A renal mass biopsy involves passing a needle through the skin into the tumour, usually under ultrasound or CT guidance, and obtaining small samples for examination by a pathologist.

Biopsy can be particularly useful when:

  • The diagnosis is uncertain
  • Active surveillance is being considered
  • The biopsy result could change management
  • Ablation is planned
  • Imaging suggests a tumour that may not require surgery
  • There is a possibility of metastatic disease or another unusual diagnosis

A biopsy is not automatically necessary for every small renal mass.

Possible complications include:

  • Pain
  • Bruising
  • Bleeding around the kidney
  • Rare significant haemorrhage
  • Non-diagnostic biopsy
  • Sampling error

The important question is not simply “Can we biopsy it?” but rather:

“Will knowing the biopsy result change what we do?”


Option 1: Active Surveillance

Active surveillance is increasingly recognised as a legitimate management strategy rather than simply “doing nothing.”

There is an important difference.

Doing nothing means ignoring the tumour.

Active surveillance means deliberately monitoring it and treating it if its behaviour changes.

For appropriately selected small renal masses, particularly those less than 2 cm, active surveillance can be an excellent initial strategy. The AUA notes very favourable cancer-specific and metastasis-free outcomes in published surveillance series of these very small tumours.

The overall risk of metastatic progression among carefully selected patients undergoing surveillance for small renal masses has been reported at approximately 1–2% or less in early follow-up series, although risk varies according to tumour and patient characteristics and increases with more aggressive biological behaviour.

Who May Be Suitable for Active Surveillance?

Surveillance may be particularly attractive for:

  • Tumours less than 2 cm
  • Small tumours with favourable imaging characteristics
  • Slowly growing lesions
  • Older patients
  • Patients with significant medical problems
  • Patients with impaired kidney function
  • Patients with a solitary kidney
  • Patients at increased anaesthetic or surgical risk
  • Patients who wish to avoid or delay intervention

For renal masses measuring 2–4 cm, both surveillance and definitive treatment may be reasonable depending upon individual circumstances.


What Does an Active Surveillance Protocol Look Like?

There is no single surveillance schedule suitable for every patient.

A commonly used approach is:

Baseline

Obtain good-quality CT or MRI imaging to accurately document:

  • Tumour size
  • Tumour characteristics
  • Location
  • Complexity

A renal mass biopsy may be considered when the result would influence management.

First follow-up

Repeat cross-sectional imaging is commonly performed approximately 3–6 months after entering surveillance to determine whether there is meaningful interval growth. This approach is specifically supported by AUA guidance.

Ongoing surveillance

If the lesion remains stable, imaging may then be performed approximately:

Every 6–12 months, depending upon the patient’s age, tumour characteristics, previous growth rate and overall health.

Ultrasound can sometimes reduce the number of CT scans required, provided that the lesion can be reliably visualised and measured. CT or MRI is preferred if there is uncertainty regarding growth or tumour characteristics.

The Canadian guideline notes that commonly used protocols involve abdominal imaging every 3–6 months during the first year and every 6–12 months thereafter if stable, although there is no universally agreed schedule.


When Do We Stop Watching and Start Treating?

This is perhaps the most important aspect of active surveillance.

Treatment may be recommended if there is:

  • Significant tumour growth
  • Increasing radiological complexity
  • Growth towards or beyond 4 cm
  • A consistent growth rate greater than approximately 5 mm per year
  • Concerning biopsy findings
  • Evidence of spread
  • Development of symptoms
  • A change in the patient’s health or treatment preference

Commonly recognised triggers include tumour growth beyond 4 cm or consecutive growth exceeding approximately 0.5 cm per year, although no single measurement should be considered in isolation.

A tumour that grows by a millimetre on one scan has not necessarily sounded the alarm bell. Small differences can occur simply because of how the scan or measurement was performed.

The trend matters more than a single measurement.


Risks and Disadvantages of Active Surveillance

The main advantages are avoiding or delaying unnecessary treatment and preserving kidney function.

Potential disadvantages include:

  • Anxiety associated with living with an untreated renal mass
  • Repeated scans
  • Radiation exposure from repeated CT imaging
  • Contrast exposure
  • Possibility of tumour growth
  • Small risk of metastatic progression
  • Possibility that treatment becomes technically more difficult if the tumour grows substantially

Active surveillance therefore works best when there is a clear follow-up plan rather than a vague agreement to “scan it again sometime.”


Option 2: Minimally Invasive Tumour Ablation

For selected small renal masses, it may be possible to destroy the tumour without surgically removing it.

This is known as renal tumour ablation.

The principal techniques include:

Cryoablation

Cryoablation uses extremely low temperatures to freeze and destroy tumour cells.

Radiofrequency Ablation

Radiofrequency ablation uses thermal energy to heat and destroy tumour tissue.

Microwave Ablation

Microwave energy can similarly produce controlled heating and destruction of tumour tissue.

These treatments can often be performed percutaneously, meaning probes are inserted through the skin under CT or ultrasound guidance without requiring conventional surgery.


Who Is Suitable for Renal Ablation?

Ablation may be considered for patients with:

  • A small renal tumour
  • A tumour in a technically accessible location
  • Significant medical comorbidities
  • Increased surgical or anaesthetic risk
  • Reduced kidney function
  • A solitary kidney
  • Previous kidney surgery
  • A strong preference for a less invasive treatment

Current European guidance particularly supports tumour ablation as an alternative for patients with small cT1 renal tumours who require treatment but are unfit for surgery, while emphasising that long-term comparative evidence against partial nephrectomy remains less robust.

Renal mass biopsy is generally recommended before percutaneous ablation.


Advantages of Ablation

Potential benefits include:

  • No large surgical incision
  • Shorter hospital stay
  • Faster recovery
  • Less postoperative discomfort
  • Preservation of kidney tissue
  • Potential suitability for patients who are poor surgical candidates
  • Ability to repeat treatment in selected cases

Risks and Complications of Ablation

Possible complications include:

  • Bleeding
  • Haematoma
  • Infection
  • Pain
  • Damage to nearby organs
  • Injury to the collecting system
  • Urine leakage
  • Thermal injury to surrounding structures
  • Incomplete treatment
  • Persistent viable tumour
  • Local tumour recurrence
  • Need for repeat ablation
  • Need for subsequent surgery

Tumour size matters. European guidance advises against routinely using radiofrequency ablation for tumours larger than approximately 3 cm and cryoablation for tumours larger than approximately 4 cm, because recurrence becomes more concerning as tumour size increases.

Long-term oncological evidence for ablation is also less mature than the evidence supporting surgical excision, and local recurrence appears somewhat more frequent than following partial nephrectomy.


Option 3: Robotic Partial Nephrectomy

When definitive surgical treatment is appropriate, the modern objective is usually:

Remove the tumour, not the entire kidney.

A partial nephrectomy removes the renal tumour together with an appropriate margin while leaving the remaining healthy kidney intact.

For suitable T1a renal masses, partial nephrectomy is generally preferred over removing the whole kidney because it provides excellent cancer control while preserving more functioning renal tissue.

Increasingly, this operation is performed using robotic-assisted laparoscopic surgery.


What Happens During Robotic Partial Nephrectomy?

Several small incisions are made in the abdomen.

Using robotic instruments, the surgeon:

  1. Identifies the kidney and renal tumour.
  2. Carefully defines the tumour margins.
  3. May temporarily control blood flow to the kidney.
  4. Removes the tumour while preserving as much healthy kidney as possible.
  5. Repairs any opening into the collecting system if necessary.
  6. Controls bleeding.
  7. Reconstructs the remaining kidney.

The removed tumour is then sent to pathology, providing definitive information regarding:

  • Whether the tumour is benign or malignant
  • Type of renal tumour
  • Tumour grade
  • Exact size
  • Surgical margin status

This pathological information is one of the major advantages of surgical excision.


Who Should Consider Robotic Partial Nephrectomy?

Surgery may be preferred for:

  • Young and otherwise healthy patients
  • Enlarging tumours
  • Tumours approaching or exceeding 4 cm
  • Tumours with concerning imaging characteristics
  • Aggressive findings on biopsy
  • Patients with a long life expectancy
  • Tumours unsuitable for ablation
  • Patients who prefer definitive removal

Partial nephrectomy is particularly valuable when preserving kidney function is important, including patients with:

  • Chronic kidney disease
  • A solitary functioning kidney
  • Bilateral renal tumours
  • Conditions that may threaten future kidney function

Complications of Robotic Partial Nephrectomy

Although robotic surgery is minimally invasive, it remains a significant operation.

Potential complications include:

  • Bleeding
  • Blood transfusion
  • Infection
  • Urinary tract infection
  • Injury to surrounding organs
  • Urine leakage from the kidney
  • Damage to the renal collecting system
  • Temporary reduction in kidney function
  • Permanent loss of some kidney function
  • Blood clots
  • Anaesthetic complications
  • Hernia
  • Positive surgical margin
  • Conversion to open surgery
  • Conversion to radical nephrectomy
  • Rare loss of the kidney
  • Rare cardiovascular or other serious complications

One particular delayed complication is a renal artery pseudoaneurysm, which may cause bleeding several days or even weeks after surgery and occasionally requires radiological embolisation.

Fortunately, most patients undergoing uncomplicated robotic partial nephrectomy recover relatively quickly and retain excellent kidney function.


Does the Whole Kidney Ever Need to Be Removed?

Yes, but for a straightforward small renal mass this is increasingly avoided when partial nephrectomy is technically and oncologically appropriate.

A radical nephrectomy removes the entire kidney.

It may still be necessary when:

  • The tumour is very large
  • The tumour occupies much of the kidney
  • Tumour location makes partial nephrectomy unsafe
  • There is extensive involvement of major renal blood vessels
  • The remaining kidney tissue would provide little useful function
  • Cancer control would be compromised by attempting partial nephrectomy

The decision is therefore not simply based upon tumour diameter. Tumour anatomy matters enormously.


What Happens After Treatment?

Treating the tumour does not mean that follow-up disappears.

Continued surveillance is important following both ablation and surgery.

The intensity of follow-up depends upon:

  • Final pathology
  • Tumour stage
  • Tumour grade
  • Surgical margins
  • Treatment performed
  • Kidney function
  • Patient age and general health
  • Risk of recurrence

Follow-Up After Partial Nephrectomy

Patients will generally undergo periodic assessment including:

  • Blood pressure
  • Kidney function
  • Serum creatinine and eGFR
  • Urinalysis when indicated
  • Abdominal imaging
  • Chest imaging when clinically appropriate

CT, MRI or ultrasound may be used depending upon the patient’s recurrence risk and kidney function.

Higher-grade or higher-stage cancers generally require more intensive surveillance than a small, completely excised low-grade tumour.

Long-term follow-up is important because renal cell carcinoma can occasionally recur many years after apparently successful treatment.


Follow-Up After Ablation

Imaging is particularly important after tumour ablation because the tumour remains physically present even though the tissue has been destroyed.

Follow-up CT or MRI is therefore used to assess whether there is any persistent or recurrent contrast enhancement, which may indicate viable tumour.

Patients commonly require imaging relatively early after treatment followed by continued surveillance over subsequent years.

If residual tumour is identified, options may include:

  • Repeat ablation
  • Partial nephrectomy
  • Other surgical treatment
  • Continued surveillance in selected circumstances

And What About the Other Kidney?

Follow-up is not only about looking for recurrence.

Kidney health matters.

Patients who have undergone treatment for a renal tumour should pay attention to:

  • Blood pressure
  • Diabetes control
  • Smoking cessation
  • Healthy body weight
  • Kidney function
  • Avoidance of unnecessary kidney-toxic medications
  • Cardiovascular health

Preserving functioning kidney tissue is one reason partial nephrectomy and appropriately selected minimally invasive approaches have become so important.


The Bottom Line

A small renal mass is not automatically an emergency and not automatically a cancer requiring immediate surgery.

Modern management is increasingly personalised.

For one patient, the safest option may be:

Watch it carefully.

For another:

Biopsy it first.

For another:

Ablate it.

And for another:

Remove the tumour robotically while preserving the kidney.

The decision depends upon the tumour’s size, location, appearance, growth and biology, balanced against the patient’s age, kidney function, general health and personal preferences.

Perhaps the most important message is this:

Small renal masses deserve respect, but not necessarily panic.

Active surveillance can be an active treatment strategy in itself. Minimally invasive ablation can provide an alternative for selected patients, particularly those who are less suitable for surgery. And when definitive surgery is appropriate, robotic partial nephrectomy allows many tumours to be removed while preserving the majority of the kidney.

Whichever strategy is chosen, the story does not finish on treatment day. Continued imaging and kidney-function surveillance remain an important part of long-term care.


This information is intended for general patient education and should not replace individual assessment by a urologist. Management of a renal mass should be personalised according to imaging findings, kidney function, medical history, tumour characteristics and patient preferences.

Please note, I no longer do surgery for renal cancer but will continue with your surveillance as long as it does not require surgery. I will then refer you to a Urologist interested in doing these procedures. I can however manage this for you where focal therapy is done by the intervention radiologist.

Renal angiomyolipoma (AML): when to watch, when to treat and when to seek urgent help

An angiomyolipoma, usually shortened to AML, is a growth in the kidney made up of blood vessels, muscle-like tissue and fat. Most are found by chance on a scan and never cause trouble. The main concern is that some AMLs can bleed, occasionally quite severely. The right plan depends on the diagnosis, the growth’s features and your circumstances, not its diameter alone. [1,2]

In this article, “AML” means angiomyolipoma, not acute myeloid leukaemia.

Is an AML cancer?

A classic renal AML is generally a benign tumour. Most occur on their own (sporadic AML). Some occur with tuberous sclerosis complex (TSC) or, less commonly, lymphangioleiomyomatosis (LAM); these can be multiple, affect both kidneys and require a different surveillance and treatment approach. A rare epithelioid AML can behave aggressively and needs specialist assessment. Not every solid renal mass presumed to be an AML can be confidently identified on a scan, particularly when little visible fat is present. [1,3,4]

What symptoms can it cause?

Many AMLs have no symptoms. Possible symptoms include aching or pain in the side, visible blood in the urine, or, less commonly, a palpable swelling. A sudden bleed into or around the kidney may cause abrupt, severe flank or abdominal pain, sometimes with dizziness, fainting, weakness or a racing heart. Blood in the urine and flank pain can also have other causes, including stones or cancer, so they should be assessed rather than attributed automatically to a known AML. [1–3]

Emergency warning: If you develop sudden severe side or abdominal pain, especially with faintness, collapse, a racing heart or visible bleeding, call 000 in Australia or attend an emergency department immediately. A bleeding AML can cause major blood loss even when blood is not visible in the urine. Do not wait for a routine appointment. [1,3]

How is it diagnosed?

An AML may first appear on an ultrasound performed for another reason. CT or MRI helps confirm whether it contains fat and assess its size, location, blood vessels and any evidence of bleeding. Contrast-enhanced imaging may be needed for an indeterminate lesion or procedural planning, with the choice adapted to kidney function, pregnancy and other factors. A classic fat-rich AML is often diagnosed on imaging alone. A fat-poor AML may resemble kidney cancer; specialist review, further imaging or a biopsy may be appropriate if the result would change management. Biopsy has limitations and is chosen case by case. [1,3,4]

The assessment may also include blood pressure, kidney function and a blood count if bleeding is suspected. Multiple or bilateral AMLs, especially in a younger person, should prompt consideration of TSC or LAM and appropriate specialist input. [3,5]

Is there a critical size that must be treated?

There is no single diameter at which every AML must be removed. The traditional rule to treat an AML once it reaches 4 cm is no longer considered an automatic trigger. The European Association of Urology (EAU) states that the relationship between size and bleeding risk is uncertain and that no universal intervention threshold exists. Some larger AMLs can still be watched safely; a smaller one may need treatment if it bleeds or causes persistent symptoms. [1,2]

Size remains one part of the discussion. The team may also consider growth, vascular features or aneurysms seen on imaging, prior bleeding, pain, kidney function, pregnancy plans, blood-thinning medicines and access to urgent care. An aneurysm measurement such as 5 mm has been proposed as a risk marker, but recent evidence questions how reliably it predicts bleeding on its own. These findings guide an individual discussion; they do not supply a stand-alone rule. [1,3,6]

Management options

Active surveillance

For a confidently diagnosed, symptom-free AML, monitoring is often appropriate. It avoids exposing people with stable lesions to procedure risks. A surveillance plan records the starting size and imaging characteristics, checks for new symptoms and uses ultrasound, MRI or CT when appropriate to look for change. There is no single imaging interval suitable for all sporadic AMLs. A small, stable lesion may need little or no ongoing imaging after specialist review; a larger or changing lesion usually needs closer follow-up. Agree on the next scan, who will review it and what changes should prompt earlier contact. [1–3]

Selective arterial embolisation

An interventional radiologist passes a catheter into the blood vessels feeding the AML and blocks selected branches. Embolisation can control active bleeding and can be considered in advance for selected higher-risk or symptomatic tumours, while preserving kidney tissue. Pain, fever and nausea can occur afterwards; infection, non-target embolisation and repeat treatment are possible. In the EAU systematic review, around 30% of embolised cases required a further intervention, although individual outcomes vary. [1,2]

Kidney-sparing surgery

A partial nephrectomy removes the AML while aiming to preserve the rest of the kidney. Open, laparoscopic or robotic approaches may be considered depending on anatomy and surgical expertise. Surgery may be useful when imaging is uncertain, symptoms persist, embolisation is unsuitable or a definitive removal is preferred. It carries anaesthetic, bleeding, urine leak and kidney-function risks. Removal of the whole kidney is generally reserved for situations where kidney-sparing care is not feasible, especially in an emergency. [1–3]

Ablation and medicines

Thermal ablation is used less often for AML, and the evidence is more limited than for surveillance, embolisation and surgery. For TSC-associated AML, specialist teams may use an mTOR inhibitor such as everolimus for an asymptomatic but growing lesion over 3 cm when treatment is appropriate. This TSC recommendation should not be applied automatically to an isolated sporadic AML. Medicines require monitoring for adverse effects and interactions. [1,2,5]

What happens if an AML bleeds?

In hospital, the immediate priorities are resuscitation, blood tests and imaging to locate the bleed. Treatment may include intravenous fluids, blood transfusion and urgent selective arterial embolisation to stop the bleeding. Surgery is considered if embolisation is unavailable, unsuccessful or otherwise unsuitable. After recovery, follow-up checks the AML, remaining kidney function and whether further treatment is needed. [1,3]

How is surveillance different with tuberous sclerosis?

TSC-related AMLs require a coordinated long-term plan because lesions may occur in both kidneys and kidney function needs protection over a lifetime. The 2021 international TSC recommendations advise abdominal MRI every 1–3 years, with blood pressure, kidney function and urine protein checked at least yearly; the interval is tailored to individual risk. Growing AMLs greater than 3 cm may merit first-line mTOR treatment when intervention is indicated, while acute bleeding is generally managed with embolisation. A TSC specialist team can help balance treatment against the need to preserve kidney tissue. [5]

Questions to bring to your appointment

  • Is the imaging diagnosis of a classic AML secure, or is more investigation needed?
  • What are its size, growth pattern and vascular features?
  • What is my personal risk of bleeding, and how does kidney function affect my options?
  • If we monitor it, when is my next scan and what result would change the plan?
  • If treatment is recommended, why is embolisation, surgery or another option best for me?

This article provides general information and does not replace individual assessment or advice.

References

  1. European Association of Urology. EAU Guidelines on Renal Cell Carcinoma, section on other renal tumours and AML. Accessed September 2026.
  2. Fernández-Pello S, et al. Management of sporadic renal angiomyolipomas: a systematic review to guide EAU recommendations. European Urology Oncology. 2020;3:57–72. doi:10.1016/j.euo.2019.04.005.
  3. Guo Y, et al. Canadian Urological Association best practice report: Diagnosis and management of sporadic angiomyolipomas. Canadian Urological Association Journal. 2020;14–E536. doi:10.5489/cuaj.6942.
  4. Wilson MP, et al. Diagnostic performance of MRI in detection of renal lipid-poor angiomyolipomas: systematic review and meta-analysis. Radiology. 2020;296:511–520.
  5. Northrup H, et al. Updated international TSC diagnostic criteria and surveillance and management recommendations. Pediatric Neurology. 2021;123:50–66. See also Tuberous Sclerosis Australia: Kidneys.
  6. Swärd J, et al. Renal angiomyolipoma: investigating radiological signs indicative of bleeding risk. Insights into Imaging. 2025.

Robotic Assisted Partial Nephrectomy

Indications:

  • Small renal cancers
  • Exophytic
  • Not involving the collecting system
  • Single kidney
  • Fit for surgery
  • Nephron-sparing

No longer offered in my practice and will be referred a Urologist who does.

Robotic Assisted Radical Nephrectomy

Indications:

  • Renal Cancer meeting the criteria for surgery

Unfortunately, this procedure is no longer done in my practice, and you will be referred to a Urologist who does.

Drainage Renal Abscess

To drain a large abscess causing low grade to high temperatures. Percutaneous or open procedure for the drainage of abscess.

Why is it done?

  • Patients presenting with low grade persistent fevers, even high fevers requiring admission to High Dependency Unit for septicemia.
  • Usually immune compromised patients: Diabetics, Corticosteroid users, Viral immune-deficiency states etc.
  • This condition requires urgent drainage.
  • The patients’ need to be resuscitated first by an emergency team with appropriate fluids and antibiotics and placed in an area where all systems can be supported (HDU).
  • As soon as the patient is stable, this abscess needs to be drained, either with open surgery or percutaneous drain placement.
  • If it is a large pyonephrosis with a non-functioning kidney, a nephrectomy should be considered.

How is it done?

  • Patients will receive a general anesthesia.
  • Appropriate resuscitation would have been started.
  • Prophylactic anti-biotics is given.
  • An indwelling catheter is placed.
  • The correct kidney is identified and marked while you are awake.
  • If it is a small abscess, an ultrasound guided needle is placed through your back or side into the fluid collection. A guidewire will be placed through the cannula and a drain fed in over the guidewire. All the pus will be drained.
  • If it is a large loculated abscess, an incision will be made over the area closest to the skin. The cavity will be opened, drained and rinsed, after which a drain will be placed.
  • If you have a non-functioning kidney associated with this, your kidney may be removed at the same time.
  • A drain is left post-operatively.

What next?

  • You will spend up to 7 or more nights in hospital.
  • You may be on life support depending on the degree of sepsis.
  • You will have intravenous fluids, antibiotics and circulatory supporting drugs being administered. Either a central venous line for monitoring, an arterial line and a peripheral infusion line.
  • You will have a catheter for that time.
  • A drain for 2-3 days.
  • Your drain will be removed with minimal drainage present.
  • You will a trial without the catheter as soon as you are back in the ward.
  • You will be discharged as soon as your renal function has stabilized, and you have opened your bowels.
  • Allow for 6 weeks for stabilization of symptoms.
  • A follow-up appointment will be scheduled for 6 weeks.
  • DON’T SUFFER IN SILENCE, OR YOU WILL SUFFER ALONE!

Risks

  • This a potentially dangerous condition, which could result in death. It requires urgent management!
  • May lose your kidney in serious cases.
  • May risk dialysis when in septic shock.
  • Wound Infection.
  • Prolonged stay in HDU.
  • Post-operative hernia formations especially associated in the elderly with atrophic abdominal muscles.
  • NB! Each person is unique and for this reason symptoms vary

 

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Wes Drainage renal abcess

Nephropexy – Robotic Assisted

Why is it done?

  • Nephroptosis causing abdominal pain
  • Confirmed on standing Urogram with hydronephrosis caused by kinking of the ureter as the kidney falls down due to loss of supporting structures
  • Done with robotic assistance

Very Important!!

The correct side for surgery should be checked and confirmed with you,

Mark correct side,

CT scan present

How is it done?

  • GA
  • Prophylactic anti-biotics is given.
  • An indwelling catheter is placed.
  • The correct kidney is identified and marked while you are awake
  • Depending on the affected side of 5 incisions will be made.
  • Porst placed and attached to the Da Vinci robotic system
  • The colon is reflected to reveal the retro-peritoneal space
  • The ureter is identified and cleared up to the hilum
  • The upper pole of the kidney is mobilized with its surrounding fat.
  • A proximal spot on the psoas muscle is cleared
  • 2 non-dissolvable sutures are used to fix the upper pole of the kidney to the Psoas Muscle
  • A drain is placed

 

Complications

Side–effects

  • Minimal Blood loss
  • Wound Infection.
  • Post-operative hernia formations especially associated with the elderly with atrophic abdominal muscles
  • NB! Each person is unique and for this reason, symptoms vary

Repeat CT in 6 weeks

 

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Wes RA Nephropexy

Copyright 2019 Dr Jo Schoeman