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肾门嗜铬细胞瘤:一例报告

Renal hilar pheochromocytoma: a case report.

作者信息

Ahallal Youness, Tazi Mohammed Fadl, Elfatemi Hind, Znati Kaoutar, Tazi Elmehdi, Amarti Afaf, El Fassi Mohammed Jamal, Moulay Hassan Farih M H

机构信息

Department of Urology, Hassan II Teaching Hospital, Fez, Morocco.

出版信息

Cases J. 2009 Jun 29;2:6416. doi: 10.4076/1757-1626-2-6416.

Abstract

Paraganglioma is a rare tumor arising from undifferentiated cells of the primitive neural crest. These tumors are most commonly found in the adrenal gland, other localisations are also possible. A 58-year-old woman who presented with history of left lumbar pain, headache, hypertension, palpitation and sweating was found to have a secreting left renal hilar pheochromocytoma. Radical excision of the tumor was therefore undertaken and her hypertension was controlled. From the case report and literature review, the authors suggest a diagnostic and therapeutic strategy for the management of ectopic localization of pheochromocytoma.

摘要

副神经节瘤是一种起源于原始神经嵴未分化细胞的罕见肿瘤。这些肿瘤最常见于肾上腺,也可能出现在其他部位。一名58岁女性,有左腰痛、头痛、高血压、心悸和出汗病史,被发现患有分泌性左肾门嗜铬细胞瘤。因此对该肿瘤进行了根治性切除,其高血压得到了控制。通过该病例报告和文献复习,作者提出了嗜铬细胞瘤异位定位的诊断和治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be57/2740209/02356451dc39/1757-1626-0002-0000006416-001.jpg

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