A Challenging Diagnosis of Sheehan’s Syndrome in Non-obstetric Critical Care and Emergency Settings: A Case Series of Five Patients with Varied Presentations
Categoria dell'articolo: Research Article
Pubblicato online: 12 ago 2022
Pagine: 214 - 222
Ricevuto: 21 gen 2022
Accettato: 14 giu 2022
DOI: https://doi.org/10.2478/jccm-2022-0018
Parole chiave
© 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.