Case Report: An Unusual Case of Pheochromocytoma

被引：0

作者：

Liao, Ying ^{[1
]}

Shi, Shanshan ^{[1
,2
]}

Liao, Lihua ^{[1
,2
]}

Zhao, Yukun ^{[1
,2
]}

Lin, Rongwen ^{[1
]}

Chen, Kaihong ^{[1
]}

机构：

[1] Fujian Med Univ, Longyan Affiliated Hosp 1, Longyan, Peoples R China

[2] Fujian Med Univ, Clin Med Coll 3, Fuzhou, Peoples R China

来源：

FRONTIERS IN CARDIOVASCULAR MEDICINE | 2022年 / 9卷

关键词：

syncope; pheochromocytoma; long QT syndrome; malignant arrhythmias; torsade de pointes; MANIFESTATIONS;

D O I：

10.3389/fcvm.2022.919500

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

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.

引用

页数：7

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