年轻男性肾脏PEComa: 1例报告及文献见解

IF 0.5 Q4 UROLOGY & NEPHROLOGY
Rashad Sholan , Rufat Aliyev , Malahat Sultan , Anar Almazkhanli , Savalan Karim , Jalal Gasimov
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引用次数: 0

摘要

血管周围上皮样细胞瘤(PEComas)是一种罕见的间质肿瘤,常见于子宫和腹膜后。肾PEComas是非常罕见的,经常提出诊断挑战,由于其相似肾细胞癌(RCC)的影像学。我们提出的情况下,一个18岁的男性谁提出了发热,寒战和颤抖的非特异性症状。影像学显示肾脏肿块,最初怀疑为肾细胞癌。然而,在右侧根治性肾切除术后,组织病理学检查证实了恶性PEComa的诊断。本病例强调了肾PEComa的罕见性,并强调了早期诊断和适当的手术治疗以预防并发症的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Renal PEComa in a young male: A case report and insights from the literature
Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal neoplasms, commonly found in the uterus and retroperitoneum. Renal PEComas are exceedingly rare, often posing diagnostic challenges due to their resemblance to renal cell carcinoma (RCC) on imaging. We present the case of an 18-year-old male who presented with non-specific symptoms of fever, chills, and shivering. Imaging revealed a renal mass, initially suspected to be RCC. However, following a right radical nephrectomy, histopathological examination confirmed the diagnosis of malignant PEComa. This case highlights the rarity of renal PEComa and underscores the importance of early diagnosis and appropriate surgical management to prevent complications.
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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