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嗜铬细胞瘤——从内分泌科医生到外科医生

Pheochromocytoma--from endocrinologist to surgeon.

作者信息

Poiană C, Chiriţă C, Carşote M, Bulata R, Iosif C, Petrescu R, Verzea S, Stanescu B

机构信息

University of Medicine and Pharmacy Carol Davila, Bucharest, Romania.

出版信息

Chirurgia (Bucur). 2009 Nov-Dec;104(6):753-6.

Abstract

We report the case an asymptomatic patient who underwent left adrenalectomy for a incidentally discovered large, cystic adrenal tumor. The patient presented no hypertension before or during the intervention. The hystopatological exam revealed a pheochromocytoma, with signs suggesting malignancy. One year after the surgery, the patient is still asymptomatic, the metanephrine levels are normal, and the 1231-metaiodobenzylguanidine scintigraphy showed no metastases. The indications and limits of laparoscopic adrenalectomy are presented.

摘要

我们报告了一例无症状患者,该患者因偶然发现的巨大囊性肾上腺肿瘤接受了左肾上腺切除术。患者在干预前和干预期间均未出现高血压。组织病理学检查显示为嗜铬细胞瘤,有提示恶性的迹象。手术后一年,患者仍无症状,间甲肾上腺素水平正常,123I-间碘苄胍闪烁显像未显示转移。本文介绍了腹腔镜肾上腺切除术的适应证和局限性。

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