Long-standing undiagnosed sheehan syndrome presenting as polymorphic and monomorphic ventricular tachycardia: A case series of 2 patients

Muhammad Qamar Masood, Syed Ahsan Ali

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

Objective: To describe 2 cases of Sheehan syndrome presenting with ventricular tachycardia.

Methods: In this case series, we present 2 cases of Sheehan syndrome presenting with ventricular tachycardia, which is an extremely rare complication of Sheehan syndrome. We review the literature for cases of panhypopituitarism presenting with ventricular tachycardia and also review the pathophysiologic mechanisms underlying development of ventricular tachycardia in these patients.

Results: Two female patients presented with ventricular tachycardia. One patient had monomorphic and the other had polymorphic ventricular tachycardia. On further workup, both patients were found to have panhypopituitarism. Due to past history of postpartum hemorrhage, both patients were suspected of having Sheehan syndrome as the cause of panhypopituitarism. Electrocardiogram revealed prolonged QT interval. Both patients were started on hormone replacement therapy. Both patients responded well initially and were discharged home. One of the patients is alive and healthy at the time of this report. However, the other patient was readmitted with seizures a few days after discharge and unfortunately died of sudden cardiac arrest.

Conclusion: Untreated cases of Sheehan syndrome can present with fatal ventricular tachycardia. Hormone replacement in these patients can treat and prevent fatal arrhythmias.

Original languageEnglish
Pages (from-to)e211-e214
JournalEndocrine Practice
Volume20
Issue number11
DOIs
Publication statusPublished - 1 Nov 2014

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