Non-RCC Renal Malignancies

Sarcomas of the Kidney

Background

• Renal sarcoma is less common but more lethal than sarcoma of any other genitourinary site

Epidemiology

• Represent 1-2% of all malignant renal tumors in adults
• Peak incidence in the 5th decade of life

Pathology

• Leiomyosarcoma is the most common histologic subtype of renal sarcoma

Natural History

• High-grade sarcomas often metastasize, with the lungs being a primary site of spread, and prognosis is poor; many patients die of disease progression in a matter of months.
  • Sarcomas are derived from mesenchymal components and are thus free of many of the natural barriers to dissemination that confine other tumor types.
• Low-grade sarcomas tend to pursue a more indolent course

Diagnosis and Evaluation

• Signs and Symptoms (similar to those seen with large, rapidly growing RCCs)
  1. Palpable mass
  2. Abdominal or flank pain
  3. Hematuria
• Differentiation of renal sarcoma from sarcomatoid RCC is often difficult on the basis of clinical presentation, radiographic findings, and, in some cases, pathologic analysis

Management

• Primarily a surgical disease
  • Wide excision is the goal with intraoperative monitoring of margin status
    • The initial resection is the key event because this is the best chance for a long-term cure.
    • This often mandates RN along with en bloc excision of adjacent organs.
• Chemotherapy
  • Has demonstrated some activity against metastatic sarcomas
  • Response rates are disappointing
• Combined radiation therapy and chemotherapy
  • Has proved effective in an adjuvant setting for the management of sarcomas of the extremity, has not provided much benefit for renal or retroperitoneal sarcomas.
• A multimodal approach is often pursued if performance status allows, given the poor prognosis.

Prognosis

• Most important prognostic factors for sarcomas (2)
  1. Margin status
  2. Tumor grade

Renal lymphoma and leukemia

• Renal involvement with hematologic malignancies, which include the lymphomas and leukemias, is common
  • The most common hematologic malignancy to involve the kidney is lymphoma
• Renal lymphoma should be suspected in patients with (4):
  1. Infiltrative renal lesions
  2. Splenomegaly
  3. Lymphadenopathy that is out of proportion to the renal primary
  4. Lymphadenopathy in other regions of the body or atypical regions within the retroperitoneum
     • Lymphadenopathy centered outside of the main landing zones (see above) should raise suspicion for lymphoma
• The radiographic patterns manifested by renal lymphoma are diverse and can be difficult to differentiate from RCC
• Any patient with a prior history of lymphoma and a renal mass should also be evaluated for renal recurrence rather than for RCC.

• Renal involvement related to leukemia is more common in children
• Renal lymphoma and leukemia are commonly silent but can be associated with hematuria, flank pain, or progressive renal failure. Fever, weight loss, and fatigue, the so-called B symptoms of lymphoma, are much more common
• If lymphoma or leukemic renal involvement is suspected, consideration should be given to percutaneous biopsy or aspiration to obtain a pathologic diagnosis
• Extirpative surgery should be avoided if renal lymphoma and leukemia are suspected because the primary treatment of these processes is systemic chemotherapy with or without radiation therapy
  • Nephrectomy is seldom indicated except in patients with severe symptoms, such as uncontrollable hemorrhage.
  • The other notable exception is the extremely rare patient with primary renal lymphoma in whom a combination of nephrectomy and systemic chemotherapy may represent optimal therapy

Metastatic tumours

• Metastatic tumors are the most common malignant neoplasms in the kidney, outnumbering primary renal tumors by a wide margin. Autopsy studies have shown that 12% of patients dying of cancer have renal metastases, making the kidney one of the most common sites for metastatic dissemination. The profuse vascularity of the kidney makes it hot spot for the deposition and growth of cancer cells.
• The most frequent sources of renal metastases include lung, breast, and gastrointestinal cancers, malignant melanoma, and the hematologic malignant neoplasms
• Metastases to the kidney are often multifocal, poorly enhancing, and infiltrative rather than well demarcated, although there are exceptions to these rules.
• Renal metastases should be suspected in any patient with multiple renal lesions and widespread systemic metastases or a history of nonrenal primary cancer. If there is any uncertainty about the diagnosis, percutaneous renal biopsy usually provides pathologic confirmation

Other malignant tumours of the kidney

• Carcinoid tumors
  • Arise from neuroendocrine cells, which are not normally present in the kidney.
  • An association with horseshoe kidneys has been reported.
  • Measurement of urinary or plasma serotonin or its metabolites can be diagnostic.
  • Only a minority of patients will present with the carcinoid syndrome—episodic flushing, wheezing, and diarrhea.
  • Surgical excision is the mainstay of treatment
  • Generally good prognosis
• Multimodal therapy should be considered for renal small cell carcinoma, round cell or Ewing’s family of tumours, or adult Wilm’s tumours.

References

• Wein AJ, Kavoussi LR, Partin AW, Peters CA (eds): CAMPBELL-WALSH UROLOGY, ed 11. Philadelphia, Elsevier, 2015, chap 57