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Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports

Development of ovarian hyperstimulation syndrome (OHSS) is very rare in a spontaneous ovulatory cycle and it is usually seen during pregnancy. In the etiology of OHSS, higher hCG (molar pregnancies or multiple pregnancies) and thyroid-stimulating hormone (TSH) levels have been accused. In recent yea...

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Autores principales: Topdagi Yilmaz, Emsal Pinar, Yapca, Omer Erkan, Topdagi, Yunus Emre, Kaya Topdagi, Seray, Kumtepe, Yakup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205315/
https://www.ncbi.nlm.nih.gov/pubmed/30410807
http://dx.doi.org/10.1155/2018/9294650
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author Topdagi Yilmaz, Emsal Pinar
Yapca, Omer Erkan
Topdagi, Yunus Emre
Kaya Topdagi, Seray
Kumtepe, Yakup
author_facet Topdagi Yilmaz, Emsal Pinar
Yapca, Omer Erkan
Topdagi, Yunus Emre
Kaya Topdagi, Seray
Kumtepe, Yakup
author_sort Topdagi Yilmaz, Emsal Pinar
collection PubMed
description Development of ovarian hyperstimulation syndrome (OHSS) is very rare in a spontaneous ovulatory cycle and it is usually seen during pregnancy. In the etiology of OHSS, higher hCG (molar pregnancies or multiple pregnancies) and thyroid-stimulating hormone (TSH) levels have been accused. In recent years, some follicle-stimulating hormone (FSH) receptor (FSHR) gene mutations have been described in patients with OHSS in the first trimester with normal hCG levels. Herein, we report two cases of FSHR gene mutation during the investigation of the etiology of spontaneous OHSS. Although OHSS is typically associated with ovulation induction, it should be kept in mind that this condition may also develop in spontaneous pregnancies.
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spelling pubmed-62053152018-11-08 Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports Topdagi Yilmaz, Emsal Pinar Yapca, Omer Erkan Topdagi, Yunus Emre Kaya Topdagi, Seray Kumtepe, Yakup Case Rep Obstet Gynecol Case Report Development of ovarian hyperstimulation syndrome (OHSS) is very rare in a spontaneous ovulatory cycle and it is usually seen during pregnancy. In the etiology of OHSS, higher hCG (molar pregnancies or multiple pregnancies) and thyroid-stimulating hormone (TSH) levels have been accused. In recent years, some follicle-stimulating hormone (FSH) receptor (FSHR) gene mutations have been described in patients with OHSS in the first trimester with normal hCG levels. Herein, we report two cases of FSHR gene mutation during the investigation of the etiology of spontaneous OHSS. Although OHSS is typically associated with ovulation induction, it should be kept in mind that this condition may also develop in spontaneous pregnancies. Hindawi 2018-10-15 /pmc/articles/PMC6205315/ /pubmed/30410807 http://dx.doi.org/10.1155/2018/9294650 Text en Copyright © 2018 Emsal Pinar Topdagi Yilmaz et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Topdagi Yilmaz, Emsal Pinar
Yapca, Omer Erkan
Topdagi, Yunus Emre
Kaya Topdagi, Seray
Kumtepe, Yakup
Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports
title Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports
title_full Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports
title_fullStr Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports
title_full_unstemmed Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports
title_short Spontaneous Ovarian Hyperstimulation Syndrome with FSH Receptor Gene Mutation: Two Rare Case Reports
title_sort spontaneous ovarian hyperstimulation syndrome with fsh receptor gene mutation: two rare case reports
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205315/
https://www.ncbi.nlm.nih.gov/pubmed/30410807
http://dx.doi.org/10.1155/2018/9294650
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