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巨大囊性嗜铬细胞瘤。

Giant cystic pheochromocytoma.

作者信息

Cajipe Kris Miguel, Gonzalez Gabriela, Kaushik Dharam

机构信息

Department of Urology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.

Department of Pathology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.

出版信息

BMJ Case Rep. 2017 Nov 8;2017:bcr-2017-222264. doi: 10.1136/bcr-2017-222264.

Abstract

A 56-year-old healthy woman presents with 2-year history of symptoms classic for pheochromocytoma. Evaluation revealed one of the largest cystic pheochromocytomas reported but without any metastatic disease. After achieving medical management of her symptoms, surgical removal was performed successfully and without any complications intraoperatively. Pathology of the mass confirmed the diagnosis. The patient had complete resolution of her symptoms thereafter.

摘要

一名56岁的健康女性出现了有2年嗜铬细胞瘤典型症状的病史。评估发现这是所报道的最大的囊性嗜铬细胞瘤之一,但没有任何转移性疾病。在对其症状进行药物治疗后,成功进行了手术切除,术中无任何并发症。肿块的病理检查确诊了病情。此后患者的症状完全缓解。

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Giant cystic pheochromocytoma.巨大囊性嗜铬细胞瘤。
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本文引用的文献

9
Preoperative management of the pheochromocytoma patient.嗜铬细胞瘤患者的术前管理。
J Clin Endocrinol Metab. 2007 Nov;92(11):4069-79. doi: 10.1210/jc.2007-1720.
10
Phaeochromocytoma.嗜铬细胞瘤
Lancet. 2005;366(9486):665-75. doi: 10.1016/S0140-6736(05)67139-5.

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