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Sheehan syndrome: a current approach to a dormant disease
Zuleyha Karaca1, Fahrettin Kelestimur2
1Department of Endocrinology and Metabolism, Faculty of Medicine, Erciyes University, Kayseri, Türkiye.
Pituitary
|January 25, 2025
Summary
Sheehan syndrome (SS) is postpartum pituitary necrosis causing hypopituitarism due to severe blood loss. Early recognition and treatment are vital to prevent severe health consequences in affected women.
Area of Science:
- Endocrinology
- Obstetrics
- Reproductive Medicine
Background:
- Sheehan syndrome (SS) is a rare but serious condition of postpartum pituitary necrosis.
- It results from ischemic necrosis of the pituitary gland, often triggered by severe postpartum hemorrhage.
- While improved obstetric care has reduced its incidence, SS remains a critical consideration in hypopituitarism etiologies.
Purpose of the Study:
- To review the epidemiology, pathophysiology, clinical manifestations, and treatment of Sheehan syndrome.
- To emphasize the importance of physician awareness for timely diagnosis and management.
- To highlight the impact of diagnostic delays on patient morbidity and mortality.
Main Methods:
- Literature review of recent studies on Sheehan syndrome.
- Analysis of epidemiological data, pathophysiological mechanisms, and clinical presentations.
- Synthesis of current treatment strategies and management guidelines.
Main Results:
- Sheehan syndrome leads to severe hypopituitarism with nonspecific symptoms, often causing diagnostic delays.
- Delayed diagnosis exposes patients to risks of increased morbidity and mortality due to untreated hypopituitarism.
- Physician awareness is crucial for prompt recognition and intervention.
Conclusions:
- Sheehan syndrome, though less common, requires continued vigilance in clinical practice.
- Early diagnosis and appropriate hormone replacement therapy are essential for improving patient outcomes.
- Further research and education are needed to enhance the management of this condition.

