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[双侧肾上腺嗜铬细胞瘤]

[Bilateral adrenal pheochromocytoma].

作者信息

Segura Martín M, Lorenzo Romero J G, Santiago Salinas Sánchez A, Hernández Millán I, Martínez Martín M, Atienzar Tobarra M, Virseda Rodríguez J A

机构信息

Servicio de Urología, Hospital General de Albacete.

出版信息

Actas Urol Esp. 1998 Apr;22(4):355-8.

PMID:9658648
Abstract

Presentation of one case of bilateral suprarenal pheochromocytoma as early clinical evidence of a type 2 MEN, which at the time of diagnosis was a bilateral lesion. The presentation form was a picture of shock with HBP. Labetalol i.v. was used for initial control and phenoxybenzamine in the pre-operative. Diagnosis was achieved by biochemical (metanephrine) and radiological (CAT) testing. The patient was managed with bilateral suprarenalectomy through a single, anterior incision and abdominal cavity examination. The investigation of the remaining conditions that conform this syndrome was continued and a familial routine study implemented.

摘要

一例双侧肾上腺嗜铬细胞瘤作为2型多发性内分泌腺瘤病的早期临床证据的病例报告,诊断时为双侧病变。表现形式为伴有高血压的休克状态。静脉注射拉贝洛尔用于初始控制,术前使用酚苄明。通过生化(甲氧基肾上腺素)和放射学(计算机断层扫描)检查确诊。患者通过单一前入路切口行双侧肾上腺切除术及腹腔探查进行治疗。继续对符合该综合征的其他情况进行调查并开展家族常规研究。

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