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DOI 10.5830/cvja-2022-043

Медицинская библиотека · Cardiovascular journal of Africa · 2022

A rare endocrine cause of ventricular tachycardia: a case series of two patients and a literature review.

Yu Ming, Sun Lin, Yang Hong-Liang, Sun Huan, Wang Chang, Yao Shuai, Yang Ping

ОбзорКлинический случайСтатьяПеревод в очереди

Аннотация

Sheehan's syndrome is a type of hypopituitarism caused by massive uterine bleeding and hypovolaemic shock after or during delivery. Heart involvement has been documented sporadically among the various clinical manifestations of Sheehan's syndrome but life-threatening arrhythmias are infrequent. Here, we report on two rare cases of ventricular tachycardia caused by Sheehan's syndrome. Both female patients were diagnosed with Sheehan's syndrome 30 years previously, due to massive postpartum bleeding. Both of them terminated hormone replacement therapy recently. Both patients presented with torsade de pointes. The electrocardiogram showed prolonged QT interval. In addition to potassium supplementation and anti-arrhythmia therapy, steroids and thyroid hormone replacement therapy were employed, QT-interval prolongation and T-wave inversion were normalised, and implantable cardioverter defibrillator implantation was avoided. One of the patients was recovering well at the one-year follow up and the other patient was in a coma at the time of this report. We also review the literature for cases of Sheehan's syndrome presenting with ventricular tachycardia.

Для цитирования: Yu Ming, Sun Lin, Yang Hong-Liang, Sun Huan, Wang Chang, Yao Shuai, Yang Ping. A rare endocrine cause of ventricular tachycardia: a case series of two patients and a literature review.. Cardiovascular journal of Africa. 2022. DOI: 10.5830/cvja-2022-043.

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