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A case of acute Sheehan's syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage.

Authors :
Shinya Matsuzaki
Masayuki Endo
Yutaka Ueda
Kazuya Mimura
Aiko Kakigano
Tomomi Egawa-Takata
Keiichi Kumasawa
Kiyoshi Yoshino
Tadashi Kimura
Matsuzaki, Shinya
Endo, Masayuki
Ueda, Yutaka
Mimura, Kazuya
Kakigano, Aiko
Egawa-Takata, Tomomi
Kumasawa, Keiichi
Yoshino, Kiyoshi
Kimura, Tadashi
Source :
BMC Pregnancy & Childbirth. 6/14/2017, Vol. 17, p1-10. 10p.
Publication Year :
2017

Abstract

<bold>Background: </bold>Sheehan's syndrome occurs because of severe postpartum hemorrhage causing ischemic pituitary necrosis. Sheehan's syndrome is a well-known condition that is generally diagnosed several years postpartum. However, acute Sheehan's syndrome is rare, and clinicians have little exposure to it. It can be life-threatening. There have been no reviews of acute Sheehan's syndrome and no reports of successful pregnancies after acute Sheehan's syndrome. We present such a case, and to understand this rare condition, we have reviewed and discussed the literature pertaining to it. An electronic search for acute Sheehan's syndrome in the literature from January 1990 and May 2014 was performed.<bold>Case Presentation: </bold>A 27-year-old woman had massive postpartum hemorrhage (approximately 5000 mL) at her first delivery due to atonic bleeding. She was transfused and treated with uterine embolization, which successfully stopped the bleeding. The postpartum period was uncomplicated through day 7 following the hemorrhage. However, on day 8, the patient had sudden onset of seizures and subsequently became comatose. Laboratory results revealed hypothyroidism, hypoglycemia, hypoprolactinemia, and adrenal insufficiency. Thus, the patient was diagnosed with acute Sheehan's syndrome. Following treatment with thyroxine and hydrocortisone, her condition improved, and she was discharged on day 24. Her next pregnancy was established 2 years after her first delivery. She required induction of ovulation for the next conception. The pregnancy, delivery, and postpartum period were uneventful. An electronic search of the literature yielded 21 cases of acute Sheehan's syndrome. Presenting signs varied, including adrenal insufficiency (12 cases), diabetes insipidus (4 cases), hypothyroidism (2 cases), and panhypopituitarism (3 cases), with a median time of presentation after delivery for each of those conditions being 7.9, 4, 18, and 9 days, respectively. Serial changes in magnetic resonance imaging were reported in some cases of acute Sheehan's syndrome.<bold>Conclusion: </bold>Clinicians should be aware of the risk of acute Sheehan's syndrome after a massive postpartum hemorrhage in order to diagnose it accurately and treat it promptly. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712393
Volume :
17
Database :
Academic Search Index
Journal :
BMC Pregnancy & Childbirth
Publication Type :
Academic Journal
Accession number :
123641803
Full Text :
https://doi.org/10.1186/s12884-017-1380-y