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Acute Sheehan’s syndrome manifesting initially with diabetes insipidus postpartum: a case report and systematic literature review

PURPOSE: Acute Sheehan’s syndrome is a rare, but potentially life-threatening, obstetric event that can be complicated by diabetes insipidus. Little information on the diagnosis and treatment of Sheehan’s syndrome with diabetes insipidus is available. We report on a 28-year-old patient who developed...

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Autores principales: Olmes, Gregor Leonhard, Solomayer, Erich-Franz, Radosa, Julia Caroline, Sklavounos, Panagiotis, Agne, Philipp, Schunk, Stefan J., Haj Hamoud, Bashar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411080/
https://www.ncbi.nlm.nih.gov/pubmed/34779875
http://dx.doi.org/10.1007/s00404-021-06294-2
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author Olmes, Gregor Leonhard
Solomayer, Erich-Franz
Radosa, Julia Caroline
Sklavounos, Panagiotis
Agne, Philipp
Schunk, Stefan J.
Haj Hamoud, Bashar
author_facet Olmes, Gregor Leonhard
Solomayer, Erich-Franz
Radosa, Julia Caroline
Sklavounos, Panagiotis
Agne, Philipp
Schunk, Stefan J.
Haj Hamoud, Bashar
author_sort Olmes, Gregor Leonhard
collection PubMed
description PURPOSE: Acute Sheehan’s syndrome is a rare, but potentially life-threatening, obstetric event that can be complicated by diabetes insipidus. Little information on the diagnosis and treatment of Sheehan’s syndrome with diabetes insipidus is available. We report on a 28-year-old patient who developed acute Sheehan’s syndrome with diabetes insipidus after giving birth, and on a systematic review of similar cases. METHODS: We performed a systematic review of the literature cataloged in PubMed and Google Scholar using the keywords “Sheehan syndrome” OR “Sheehan's syndrome” AND “diabetes insipidus” to identify relevant case reports published between 1990 and 2021. Eight Reports met the inclusion criteria (English-language abstracts available, onset in the puerperium, information about the day of the onset). RESULTS: In the present case, postpartum curettage was necessary to remove the residual placenta. The total amount of blood loss was severe (2500 ml). On the second day postpartal, the patient developed polyuria. Laboratory analysis revealed hypernatremia with increased serum osmolality and decreased urinary osmolality. Hormone analysis showed partial hypopituitarism involving the thyroid, corticotropic, and gonadotropic axes. The prolactin level was elevated. Brain magnetic resonance imaging showed pituitary gland infarction. Desmopressin therapy was initiated and resolved the polyuria. Hormone replacement therapy was administered. Four months later, the patient was well, with partial diabetes insipidus. The literature review indicated that this case was typical in terms of symptoms and disease onset. Most reported cases involve hypotension and peripartum hemorrhage, but some patients without hemorrhage also develop Sheehan’s syndrome. Elevated prolactin levels are uncommon and associated with poor prognosis in patients with Sheehan’s syndrome. CONCLUSION: Acute Sheehan’s syndrome with diabetes insipidus involves nearly all pituitary hormone axes, indicating severe disease. Prolactin elevation could suggest that a case of Sheehan’s syndrome is severe.
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spelling pubmed-94110802022-08-27 Acute Sheehan’s syndrome manifesting initially with diabetes insipidus postpartum: a case report and systematic literature review Olmes, Gregor Leonhard Solomayer, Erich-Franz Radosa, Julia Caroline Sklavounos, Panagiotis Agne, Philipp Schunk, Stefan J. Haj Hamoud, Bashar Arch Gynecol Obstet Maternal-Fetal Medicine PURPOSE: Acute Sheehan’s syndrome is a rare, but potentially life-threatening, obstetric event that can be complicated by diabetes insipidus. Little information on the diagnosis and treatment of Sheehan’s syndrome with diabetes insipidus is available. We report on a 28-year-old patient who developed acute Sheehan’s syndrome with diabetes insipidus after giving birth, and on a systematic review of similar cases. METHODS: We performed a systematic review of the literature cataloged in PubMed and Google Scholar using the keywords “Sheehan syndrome” OR “Sheehan's syndrome” AND “diabetes insipidus” to identify relevant case reports published between 1990 and 2021. Eight Reports met the inclusion criteria (English-language abstracts available, onset in the puerperium, information about the day of the onset). RESULTS: In the present case, postpartum curettage was necessary to remove the residual placenta. The total amount of blood loss was severe (2500 ml). On the second day postpartal, the patient developed polyuria. Laboratory analysis revealed hypernatremia with increased serum osmolality and decreased urinary osmolality. Hormone analysis showed partial hypopituitarism involving the thyroid, corticotropic, and gonadotropic axes. The prolactin level was elevated. Brain magnetic resonance imaging showed pituitary gland infarction. Desmopressin therapy was initiated and resolved the polyuria. Hormone replacement therapy was administered. Four months later, the patient was well, with partial diabetes insipidus. The literature review indicated that this case was typical in terms of symptoms and disease onset. Most reported cases involve hypotension and peripartum hemorrhage, but some patients without hemorrhage also develop Sheehan’s syndrome. Elevated prolactin levels are uncommon and associated with poor prognosis in patients with Sheehan’s syndrome. CONCLUSION: Acute Sheehan’s syndrome with diabetes insipidus involves nearly all pituitary hormone axes, indicating severe disease. Prolactin elevation could suggest that a case of Sheehan’s syndrome is severe. Springer Berlin Heidelberg 2021-11-15 2022 /pmc/articles/PMC9411080/ /pubmed/34779875 http://dx.doi.org/10.1007/s00404-021-06294-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Maternal-Fetal Medicine
Olmes, Gregor Leonhard
Solomayer, Erich-Franz
Radosa, Julia Caroline
Sklavounos, Panagiotis
Agne, Philipp
Schunk, Stefan J.
Haj Hamoud, Bashar
Acute Sheehan’s syndrome manifesting initially with diabetes insipidus postpartum: a case report and systematic literature review
title Acute Sheehan’s syndrome manifesting initially with diabetes insipidus postpartum: a case report and systematic literature review
title_full Acute Sheehan’s syndrome manifesting initially with diabetes insipidus postpartum: a case report and systematic literature review
title_fullStr Acute Sheehan’s syndrome manifesting initially with diabetes insipidus postpartum: a case report and systematic literature review
title_full_unstemmed Acute Sheehan’s syndrome manifesting initially with diabetes insipidus postpartum: a case report and systematic literature review
title_short Acute Sheehan’s syndrome manifesting initially with diabetes insipidus postpartum: a case report and systematic literature review
title_sort acute sheehan’s syndrome manifesting initially with diabetes insipidus postpartum: a case report and systematic literature review
topic Maternal-Fetal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411080/
https://www.ncbi.nlm.nih.gov/pubmed/34779875
http://dx.doi.org/10.1007/s00404-021-06294-2
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