A Challenging Diagnosis of Sheehan’s Syndrome in Non-obstetric Critical Care and Emergency Settings: A Case Series of Five Patients with Varied Presentations
Artikel-Kategorie: Research Article
Online veröffentlicht: 12. Aug. 2022
Seitenbereich: 214 - 222
Eingereicht: 21. Jan. 2022
Akzeptiert: 14. Juni 2022
DOI: https://doi.org/10.2478/jccm-2022-0018
Schlüsselwörter
© 2022 Suhail Sarwar Siddiqui, Nibu Dominic, Sukriti Kumar, Kauser Usman, Sai Saran, Avinash Agrawal, Mohan Gurjar, Syed Nabeel Muzaffar, published by Sciendo
This work is licensed under the Creative Commons Attribution 4.0 International License.
Sheehan’s syndrome is a life-threatening endocrine emergency seen in postpartum females secondary to ischemic pituitary necrosis. It is a frequent cause of hypopituitarism in developing countries that occurs secondary to postpartum haemorrhage (PPH). Patients with Sheehan’s syndrome often present with organ dysfunctions in critical care settings, secondary to stressors precipitating the underlying hormonal deficiencies. The initial clinical picture of Sheehan’s syndrome may mimic some other disease, leading to misdiagnosis and diagnostic delay. Strict vigilance, timely diagnosis, and appropriate management are essential to avoid diagnostic delay and to improve the patient outcome. In this case series, we describe 5 cases of previously undiagnosed Sheehan’s syndrome (including young, middle aged and postmenopausal females) that presented to critical care and emergency settings with organ failures.