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A case report of spontaneous ovarian hyperstimulation syndrome and the long-term management of the endocrine disorder

BACKGROUND: Spontaneous ovarian hyperstimulation syndrome (sOHSS) is a rarely reported clinical symptom of uncertain origin with the incidence of 0.2–1.2%. There is no report of the patients’ follow-up situation after the remission of the clinical symptom and this is the first one. The aim of this s...

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Autores principales: Liang, Xuefei, Yu, Xinting, Guo, Xiaoli, Wang, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011235/
https://www.ncbi.nlm.nih.gov/pubmed/35433987
http://dx.doi.org/10.21037/atm-22-827
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author Liang, Xuefei
Yu, Xinting
Guo, Xiaoli
Wang, Fang
author_facet Liang, Xuefei
Yu, Xinting
Guo, Xiaoli
Wang, Fang
author_sort Liang, Xuefei
collection PubMed
description BACKGROUND: Spontaneous ovarian hyperstimulation syndrome (sOHSS) is a rarely reported clinical symptom of uncertain origin with the incidence of 0.2–1.2%. There is no report of the patients’ follow-up situation after the remission of the clinical symptom and this is the first one. The aim of this study was to remind the medical staff of the necessity of long-term management. CASE DESCRIPTION: We report a case of severe sOHSS with a normal 15 week gestation twin pregnancy in a 21-year-old primigravida who presented in our emergency room result from the 1 week’s nausea and vomiting and progressively aggravated abdominal distension and pains for 3 days. The patient in our case had no significant precipitating factors and she had no previous outstanding medical history except that she had experienced acute glomerulonephritis when she was 9 years old. On ultrasound imaging, we found abnormally enlarged ovaries and massive ascites and moderate pleural fluid. A diagnosis of spontaneous ovarian hyperstimulation was made. The patient participated in followed-up visits for 1 year and experienced polycystic ovary syndrome (PCOS) and weight loss which up to 15kg after delivery. CONCLUSIONS: Typically, although sOHSS is potentially life-threatening, its clinical detection is often delayed. A proactive strategy should be encouraged in the management of high-risk patients. The therapeutic schedule of mild-to-moderate sOHSS can focus on symptomatic relief and supportive treatment. Our case report elucidates the possible long-term effects of sOHSS and reminds us of the need for long-term management of those affected.
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spelling pubmed-90112352022-04-16 A case report of spontaneous ovarian hyperstimulation syndrome and the long-term management of the endocrine disorder Liang, Xuefei Yu, Xinting Guo, Xiaoli Wang, Fang Ann Transl Med Case Report BACKGROUND: Spontaneous ovarian hyperstimulation syndrome (sOHSS) is a rarely reported clinical symptom of uncertain origin with the incidence of 0.2–1.2%. There is no report of the patients’ follow-up situation after the remission of the clinical symptom and this is the first one. The aim of this study was to remind the medical staff of the necessity of long-term management. CASE DESCRIPTION: We report a case of severe sOHSS with a normal 15 week gestation twin pregnancy in a 21-year-old primigravida who presented in our emergency room result from the 1 week’s nausea and vomiting and progressively aggravated abdominal distension and pains for 3 days. The patient in our case had no significant precipitating factors and she had no previous outstanding medical history except that she had experienced acute glomerulonephritis when she was 9 years old. On ultrasound imaging, we found abnormally enlarged ovaries and massive ascites and moderate pleural fluid. A diagnosis of spontaneous ovarian hyperstimulation was made. The patient participated in followed-up visits for 1 year and experienced polycystic ovary syndrome (PCOS) and weight loss which up to 15kg after delivery. CONCLUSIONS: Typically, although sOHSS is potentially life-threatening, its clinical detection is often delayed. A proactive strategy should be encouraged in the management of high-risk patients. The therapeutic schedule of mild-to-moderate sOHSS can focus on symptomatic relief and supportive treatment. Our case report elucidates the possible long-term effects of sOHSS and reminds us of the need for long-term management of those affected. AME Publishing Company 2022-03 /pmc/articles/PMC9011235/ /pubmed/35433987 http://dx.doi.org/10.21037/atm-22-827 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Case Report
Liang, Xuefei
Yu, Xinting
Guo, Xiaoli
Wang, Fang
A case report of spontaneous ovarian hyperstimulation syndrome and the long-term management of the endocrine disorder
title A case report of spontaneous ovarian hyperstimulation syndrome and the long-term management of the endocrine disorder
title_full A case report of spontaneous ovarian hyperstimulation syndrome and the long-term management of the endocrine disorder
title_fullStr A case report of spontaneous ovarian hyperstimulation syndrome and the long-term management of the endocrine disorder
title_full_unstemmed A case report of spontaneous ovarian hyperstimulation syndrome and the long-term management of the endocrine disorder
title_short A case report of spontaneous ovarian hyperstimulation syndrome and the long-term management of the endocrine disorder
title_sort case report of spontaneous ovarian hyperstimulation syndrome and the long-term management of the endocrine disorder
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011235/
https://www.ncbi.nlm.nih.gov/pubmed/35433987
http://dx.doi.org/10.21037/atm-22-827
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