Rare malignant kidney (renal) tumor – leiomyosarcoma of the renal vein (clinical case)-Reference-Cited by-同舟云学术

Rare malignant kidney (renal) tumor – leiomyosarcoma of the renal vein (clinical case)

Published:2022-05-06 Issue:1 Volume:18 Page:143-150
ISSN:1996-1812
Container-title:Cancer Urology
language:
Short-container-title:Onkourologiâ

Author:

Dementyev I. O.¹^ORCID,Chaykov V. S.¹^ORCID,Troyanov A. V.¹^ORCID,Parkov D. A.¹^ORCID,Shchukina E. O.¹^ORCID,Anurova O. A.¹,Fedenko A. A.¹^ORCID,Kaprin A. D.¹^ORCID,Ivanov S. A.²

Affiliation:

1. P.A. Hertzen Moscow Oncology Research Institute – branch of the National Medical Research Radiological Center, Ministry of Health of Russia

2. A.F. Tsyb Medical Radiological Research Center – branch of the National Medical Research Radiological Center, Ministry of Health of Russia

Abstract

Soft tissue sarcomas are a rare group of malignant tumors that develop from different types of connective tissue. One of the histological variants of primary renal sarcoma is renal leiomyosarcoma. Leiomyosarcoma of kidneys can develop from the renal vasculature, renal veins, pelvic muscles, smooth muscle components of the renal capsule. Clinical and radiologic signs of leiomyosarcoma are nonspecific. Diagnosis is based on histological and immunohistochemical studies after surgical intervention. This article presents a clinical case of diagnosis and treatment of leiomyosarcoma of the renal vein.

Publisher

Publishing House ABV Press

Subject

Urology,Nephrology,Radiology, Nuclear Medicine and imaging,Oncology,Surgery

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