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同时性盆腔神经鞘瘤和嫌色性肾细胞癌的诊断与开放性切除术

Diagnosis and open excision of concurrent pelvic schwannoma and chromophobe renal cell carcinoma.

作者信息

Klose Charles, Gibbs Mackenzie, Kahn Amanda, Baird Bryce, Farres Sam, Zganjar Andrew

机构信息

Mayo Clinic Department of Urology, 4500 San Pablo Rd S, Jacksonville, Florida, 32224, USA.

Mayo Clinic Department of Vascular and Endovascular Surgery, 4500 San Pablo Rd S, Jacksonville, Florida, 32224, USA.

出版信息

Urol Case Rep. 2024 Jul 22;56:102809. doi: 10.1016/j.eucr.2024.102809. eCollection 2024 Sep.

Abstract

Schwannomas are tumors that commonly affect the nerve sheath, typically involving peripheral and cranial nerves. These tumors are rarely found within the pelvis and retroperitoneum. To date, there have been no documented cases of concurrent chromophobe renal cell carcinoma and pelvic schwannoma. We present the case of a 57-year-old female with a right renal mass significant for chromophobe renal cell carcinoma and a left pelvic mass found to be a schwannoma. This case highlights the importance of adding schwannoma to the differential when considering a pelvic mass in the setting of renal cell carcinoma.

摘要

施万细胞瘤是一种通常影响神经鞘的肿瘤,典型地累及周围神经和颅神经。这些肿瘤很少见于盆腔和腹膜后。迄今为止,尚无关于同时存在嫌色性肾细胞癌和盆腔施万细胞瘤的病例报道。我们报告一例57岁女性患者,其右肾肿物经诊断为嫌色性肾细胞癌,左盆腔肿物经诊断为施万细胞瘤。该病例强调了在肾细胞癌背景下考虑盆腔肿物时,将施万细胞瘤纳入鉴别诊断的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72c0/11327479/ec1b44a541de/gr1.jpg

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