Case of Sheehan's Syndrome Misdiagnosed as Pituitary Apoplexy due to Pituitary Adenoma.
- Author:
Sun Hee PARK
1
;
Do Joon PARK
;
Kyoung Soo PARK
;
Seong Yeon KIM
;
Bo Youn CHO
;
Hong Kyu LEE
Author Information
1. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
- Publication Type:Case Report
- Keywords:
Sheehan's syndrome;
Pituitary adenoma;
Pituitary apoplexy
- MeSH:
Humans;
Hypopituitarism*;
Infarction;
Necrosis;
Pituitary Apoplexy*;
Pituitary Gland;
Pituitary Neoplasms*;
Postpartum Period
- From:Journal of Korean Society of Endocrinology
2000;15(1):107-112
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Postpartum ischemic necrosis of the pituitary gland, known as Sheehan's syndrome, is well-established clinical entity. The recent progress in radiological imaging allows an easy and noninvasive study of the pituitary area in the patients while still alive. An empty or partially empty sella is a constant feature of Sheehan's syndrome in the later phase. We report a case of nonhemorrhagic postpartum pituitary infarction documented in the acute phase with clinical, endocrine, and sequential magnetic resonance (MR) imaging studies.
