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Renal tumors-1

Renal tumors-1. Dr. Abdelaty Shawky Assistant professor of pathology. * Classification of Renal tumors:. I. Benign tumors: Cortical adenoma. Oncocytoma . II. Malignant tumors: Renal cell carcinoma. Wilms tumor.

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Renal tumors-1

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  1. Renal tumors-1 Dr. Abdelaty Shawky Assistant professor of pathology

  2. * Classification of Renal tumors: I. Benign tumors: • Cortical adenoma. • Oncocytoma. II. Malignant tumors: • Renal cell carcinoma. • Wilms tumor.

  3. With the exception of oncocytoma, benign tumors rarely cause clinical problems. • Malignant tumors, on the other hand, are of great importance clinically and deserve considerable emphasis. • By far the most common of these malignant tumors is renal cell carcinoma that affects adults, followed by Wilms tumor, which is found in children

  4. Renal cortical adenoma * Clinical Features: • Usually an incidental finding. • Often seen in patients receiving long-term hemodialysis, also more common in kidneys scarred from chronic pyelonephritis.

  5. * Gross examination: • The tumor is smaller than 5 mm. • Soft, well-circumscribed mass with yellow to gray cut surface surrounded by compressed adjacent kidney parenchyma

  6. * Microscopic examination: • They are composed of complex, branching, papillomatous structures. The cells may also grow as tubules, glands, and cords. • The cells are cuboidal to polygonal in shape and have regular, small central nuclei, scanty cytoplasm, and no atypia.

  7. Renal adenoma

  8. Renal oncocytoma * Clinical Features: • Most are asymptomatic, although flank pain may be a presenting complaint; hematuria may be seen. • CT or MRI may identify a central scar.

  9. * Gross Pathology: • Well-circumscribed, homogeneous cortical tumor • Mahogany-brown cut surface. • Often shows a central, irregular fibrous scar (in about 40% of cases). • Bilateral or multicentric in 2% to 3% of cases

  10. Renal oncocytoma

  11. On microscopic examination: the tumor consists of large, eosinophilic cells having small, round, benign-appearing nuclei that have large nucleoli. The cells are arranged in nests separated by edematous and hyalinized fibrous stroma.

  12. Renal oncocytoma

  13. Renal cell carcinoma

  14. * Epidemiology: • Renal cell carcinomas represent about 1% to 3% of all visceral cancers and account for 85% of renal malignancy in adults. • The tumors occur most often in older individuals, usually in the sixth and seventh decades of life, showing a male preponderance in the ratio of 3:1.

  15. Because of their gross yellow color and the resemblance of the tumor cells to clear cells of the adrenal cortex, they were at one time called hypernephroma. It is now clear that all these tumors arise from tubular epithelium and are therefore renal adenocarcinomas. • Most renal cancer is sporadic, but unusual forms of autosomal-dominant familial cancers occur, usually in younger individuals.

  16. * Risk factors for RCC: • Cigarette smoking is the most significant risk factor. • Obesity (particularly in women). • Hypertension. • Unopposed estrogen therapy. • Exposure to asbestos, petroleum products, and heavy metals. • Acquired polycystic kidney disease secondary to dialysis

  17. * Clinical presentation of RCC: • Hematuria. • Flank pain. • Flank lump. • This triad is seen in only 10% of cases. The most reliable of the three is hematuria, but it is usually intermittent and may be microscopic; thus, the tumor may remain silent until it attains a large size.

  18. Renal cell carcinoma tends to produce a diversity of systemic symptoms not related to the kidney termed paraneoplastic syndromes, ascribed to abnormal hormone production including; • Polycythemia. • Hypercalcemia. • Hypertension.

  19. Hepatic dysfunction. • Feminization or masculinization. • Cushing syndrome. • Leukemoid reactions. • Amyloidosis.

  20. One of the common characteristics of this tumor is its tendency to metastasize widely before giving rise to any local symptoms or signs. • In 25% of patients with renal cell carcinoma, there is radiologic evidence of metastases at the time of presentation. • The most common locations of metastasis are the lungs (more than 50%) and bones (33%), followed in order by the regional lymph nodes, liver and adrenals, and brain.

  21. * Classification of Renal Cell Carcinoma: 1. Clear cell RCC. 2. Papillary RCC. 3. Chromophobe RCC. 4. Collecting duct carcinoma.

  22. 1. Clear cell RCC. • This is the most common type, accounting for 70% to 80% of RCC. * Gross Pathology: • Solitary renal cortical mass • Bilateralityand multifocality more common in familial cases. • Well-circumscribed, lobulated with golden-yellow cut surface. • Cystic change, hemorrhage, necrosis, and calcification often present

  23. * Histopathology: • Nests of clear cells interspersed by delicate vascular network.

  24. References: Robbins and Cotran’s: Pathologic Basis of Disease. Seventh edition.

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