Journal of Kidney Cancer and VHL (Mar 2022)

Renal Leiomyosarcoma, a Rare Presentation

  • Toukilnan Djiwa,
  • Kossi Akomola Sabi,
  • Panakinao Simgban,
  • Mayi Bombonne,
  • Bagassam Mézéwè Sama,
  • Mazamaesso Tchaou,
  • Tchin Darré

Journal volume & issue
Vol. 9, no. 1

Abstract

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Renal sarcomas are very rare malignant tumours with a very poor prognosis. Renal leiomyosarcoma, a malignant tumour of smooth muscle origin, is the most common histological type. The article reports a case of leiomyosarcoma of renal location, with a review of the literature. A 38-year-old female patient, with no previous pathological history, consulted the nephrology department of the Teaching Hospital of Lomé for abdominal pain that had been present for 4 years. Histology showed a tumour proliferation of fasciculated architecture, made of spindle cells arranged in long bundles, with cytonuclear atypia and cytoarchitectural abnormalities. Immunohistochemical examination showed positive staining for smooth muscle actin, h-caldesmone, desmin and CD34 and negative for pancytokeratin (AE1/AE3), myogenin and PS100. Renal leiomyosarcoma is an exceptional malignancy. It remains the most common renal sarcoma, the differential diagnosis of which is based on immunohistochemical findings.

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