A rare malignity observed in the appearance of angiomyolipoma; tubulocystic renal cell carcinoma after partial nephrectomy

Eser Ördek, İ. Albayrak, Muhammed Nur Karadeni̇z, B. Kati
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Abstract

Cystic neoplasms of the kidney are quite rare. Because they contain various differential diagnoses and their radiological features are not specific, their diagnosis is very difficult except for histopathological data. Usually, they can be confused radiologically with benign cysts of the kidney or angiomyolipoma. Radical or partial nephrectomy is the most commonly preferred curative treatment method when it shows features like rapidly growing or malignancy. Histopathological examination is required for definitive diagnosis. In this article, we aimed to present a rare case of tubulocystic renal cell carcinoma after partial nephrectomy in our clinic, who was followed up in another center for years with the pre-diagnosis of angiomyolipoma, in the light of the literature.
肾部分切除术后出现的一种罕见恶性肿瘤--血管脂肪瘤;肾管囊肿性肾细胞癌
肾脏囊性肿瘤非常罕见。由于囊性肿瘤有多种鉴别诊断方法,而且其放射学特征不具有特异性,因此除了组织病理学数据外,很难对其进行诊断。通常,它们在放射学上可与肾脏良性囊肿或血管肌脂肪瘤混淆。当出现快速生长或恶性等特征时,根治性或部分肾切除术是最常用的首选治疗方法。明确诊断需要进行组织病理学检查。在本文中,我们旨在根据文献资料,介绍本诊所一例罕见的肾部分切除术后肾小管囊肿性肾细胞癌病例,该病例曾在另一中心随访多年,前期诊断为血管肌脂肪瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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