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病例报告:一例罕见的嗜铬细胞瘤病例。

Case Report: An Unusual Case of Pheochromocytoma.

作者信息

Liao Ying, Shi Shanshan, Liao Lihua, Zhao Yukun, Lin Rongwen, Chen Kaihong

机构信息

Longyan First Affiliated Hospital of Fujian Medical University, Longyan, China.

The Third Clinical Medicine College, Fujian Medical University, Fuzhou, China.

出版信息

Front Cardiovasc Med. 2022 Jun 10;9:919500. doi: 10.3389/fcvm.2022.919500. eCollection 2022.

Abstract

Pheochromocytoma is a benign catecholamine secreting tumor, which is rare and originates from the adrenal gland. It has been known for a wide range of clinical manifestations and can mimic other difficult-to-diagnose diseases. Here, we report a female patient with acquired long QT syndrome, which is a rare complication of pheochromocytoma. Although relatively rare, the presence of pheochromocytoma should be considered in the case of malignant arrhythmias and electrocardiographic changes in patients.

摘要

嗜铬细胞瘤是一种分泌儿茶酚胺的良性肿瘤,较为罕见,起源于肾上腺。它具有广泛的临床表现,可酷似其他难以诊断的疾病。在此,我们报告一名患有获得性长QT综合征的女性患者,这是嗜铬细胞瘤的一种罕见并发症。尽管相对罕见,但对于出现恶性心律失常和心电图改变的患者,应考虑嗜铬细胞瘤的存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8723/9226414/2649b23fe1dc/fcvm-09-919500-g0001.jpg

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