Dhawan Shashi, Chopra Prem, Dhawan Sanjay
Department of Pathology, Sir Ganga Ram Hospital, New Delhi, India.
Urol Ann. 2012 Jan;4(1):48-50. doi: 10.4103/0974-7796.91623.
Primary leiomyosarcoma is an extremely rare entity constituting only 0.5-1% of all invasive renal tumors. It is frequently diagnosed on histological examination because it does not have any specific diagnostic features clinically and radiologically. At times, it is difficult to differentiate leiomyosarcoma from the sarcomatoid renal cell carcinoma even in histopathology as both the tumors have spindle-shaped atypical cells. Moreover, some epithelial markers can be present in pure smooth muscle sarcomas, while some smooth muscle markers are positive in carcinomas. Hence, a diagnosis of primary renal leiomyosarcoma should be made with caution. Since the prognosis for a renal sarcoma is particularly poor, differentiation from sarcomatoid renal cell carcinoma is necessary. The diagnostic challenge of one such tumor is discussed.
原发性平滑肌肉瘤是一种极其罕见的疾病,仅占所有侵袭性肾肿瘤的0.5%-1%。由于其在临床和放射学上没有任何特异性诊断特征,故常在组织学检查时被诊断出来。有时,即使在组织病理学上,平滑肌肉瘤与肉瘤样肾细胞癌也很难区分,因为这两种肿瘤都有梭形的非典型细胞。此外,一些上皮标志物可能出现在纯平滑肌肉瘤中,而一些平滑肌标志物在癌中呈阳性。因此,原发性肾平滑肌肉瘤的诊断应谨慎进行。由于肾肉瘤的预后特别差,因此有必要与肉瘤样肾细胞癌进行鉴别。本文讨论了一种此类肿瘤的诊断挑战。