Renal oncocytoma

Renal oncocytoma
Micrograph of a renal oncocytoma.
SpecialtyOncology

A renal oncocytoma is a tumour of the kidney made up of oncocytes, epithelial cells with an excess amount of mitochondria.[1][2]

Signs and symptoms

Renal oncocytomas are often asymptomatic and are frequently discovered by chance on a CT or ultrasound of the abdomen. Possible signs and symptoms of a renal oncocytoma include blood in the urine, flank pain, and an abdominal mass.

Pathophysiology

Renal oncocytoma is thought to arise from the intercalated cells of collecting ducts of the kidney. It represent 5% to 15% of surgically resected renal neoplasms. Ultrastructurally, the eosinophilic cells have numerous mitochondria.

Histologic appearance

An oncocytoma is an epithelial tumor composed of oncocytes, large eosinophilic cells having small, round, benign-appearing nuclei with large nucleoli and excessive amounts of mitochondria.

Diagnosis

In gross appearance, the tumors are tan or mahogany brown, well circumscribed and contain a central scar. They may achieve a large size (up to 12 cm in diameter).

The main differential diagnosis of renal oncocytoma is chromophobe renal cell carcinoma oncocytic variant, which like the renal oncocytoma has eosinophilic cytoplasm, but has perinuclear clearing and, typically, some degree of nuclear atypia.

Immunohistochemical profile

  • Cytokeratin AE1/AE3 +
  • Vimentin -
  • EMA +
  • CD10+/-
  • CK7 +/- parcellaire
  • CK20 -
  • CK19 -
  • AMACR (Racemase) -
  • S100 +
  • c-kit (CD117) +
  • Cadherin-E +
  • TFE3 -
  • CAM5.2 +

[3]

Treatment

Renal oncocytoma is considered benign, cured by nephrectomy. There are some familial cases in which these tumors are multicentric rather than solitary.[4] However, they may be resected to exclude a malignant tumor, e.g. renal cell carcinoma.

Prognosis

Histopathologic types of kidney tumor, with relative incidences and prognoses. Oncocytoma is seen at right in the pie chart.

The overall five-year survival rate has been estimated to be 63%, with 100% disease-specific survival.[5]

See also

References

  1. Coburn V, Radfar A, Snook D, Mahalingam M (2007). "Cutaneous oncocytoma - a report of three cases and review of the literature". J. Cutan. Pathol. 34 (4): 355–9. doi:10.1111/j.1600-0560.2006.00620.x. PMID 17381809. S2CID 19955625.
  2. "Atlas of Genetics and Cytogenetics in Oncology and Haematology - Thyroid:oncocytic tumors". Archived from the original on 2009-01-23. Retrieved 2009-02-01.
  3. [Renal Neoplasms: An Update on Immunohistochemical and Histochemical Features http://www.dako.com/08066_12may10_webchapter26.pdf Archived 2015-09-23 at the Wayback Machine]
  4. Robbins pathology, page 1015
  5. Gudbjartsson, Tomas; Hardarson, Sverrir; Petursdottir, Vigdis; Thoroddsen, Asgeir; Magnusson, Jonas; Einarsson, Gudmundur V. (2005). "Renal oncocytoma: a clinicopathological analysis of 45 consecutive cases". BJU International. 96 (9): 1275–1279. doi:10.1111/j.1464-410X.2005.05827.x. ISSN 1464-4096. PMID 16287444. S2CID 19390518.
Classification
This article is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.