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A case of acute Sheehan’s syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage
BACKGROUND: 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....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471854/ https://www.ncbi.nlm.nih.gov/pubmed/28615049 http://dx.doi.org/10.1186/s12884-017-1380-y |
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author | Matsuzaki, Shinya Endo, Masayuki Ueda, Yutaka Mimura, Kazuya Kakigano, Aiko Egawa-Takata, Tomomi Kumasawa, Keiichi Yoshino, Kiyoshi Kimura, Tadashi |
author_facet | Matsuzaki, Shinya Endo, Masayuki Ueda, Yutaka Mimura, Kazuya Kakigano, Aiko Egawa-Takata, Tomomi Kumasawa, Keiichi Yoshino, Kiyoshi Kimura, Tadashi |
author_sort | Matsuzaki, Shinya |
collection | PubMed |
description | BACKGROUND: 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. CASE PRESENTATION: 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. CONCLUSION: 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. |
format | Online Article Text |
id | pubmed-5471854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54718542017-06-19 A case of acute Sheehan’s syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage Matsuzaki, Shinya Endo, Masayuki Ueda, Yutaka Mimura, Kazuya Kakigano, Aiko Egawa-Takata, Tomomi Kumasawa, Keiichi Yoshino, Kiyoshi Kimura, Tadashi BMC Pregnancy Childbirth Case Report BACKGROUND: 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. CASE PRESENTATION: 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. CONCLUSION: 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. BioMed Central 2017-06-14 /pmc/articles/PMC5471854/ /pubmed/28615049 http://dx.doi.org/10.1186/s12884-017-1380-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Matsuzaki, Shinya Endo, Masayuki Ueda, Yutaka Mimura, Kazuya Kakigano, Aiko Egawa-Takata, Tomomi Kumasawa, Keiichi Yoshino, Kiyoshi Kimura, Tadashi A case of acute Sheehan’s syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage |
title | A case of acute Sheehan’s syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage |
title_full | A case of acute Sheehan’s syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage |
title_fullStr | A case of acute Sheehan’s syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage |
title_full_unstemmed | A case of acute Sheehan’s syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage |
title_short | A case of acute Sheehan’s syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage |
title_sort | case of acute sheehan’s syndrome and literature review: a rare but life-threatening complication of postpartum hemorrhage |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471854/ https://www.ncbi.nlm.nih.gov/pubmed/28615049 http://dx.doi.org/10.1186/s12884-017-1380-y |
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