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Hyperreactio luteinalis associated with fetal hyperandrogenism and cystic hygroma
A 23‐year‐old woman with a gestational age of 17 weeks presented with abdominal pain. The ultrasound showed maternal hyperreactio luteinalis with fetal cystic hygroma. After termination of pregnancy, the female fetus showed masculinization features with muscular hypertrophy. The hyperreactio luteina...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459097/ https://www.ncbi.nlm.nih.gov/pubmed/36101781 http://dx.doi.org/10.1002/ccr3.6310 |
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author | Ghassa, Ali Adwan, Dema Safadi, Mhd Firas |
author_facet | Ghassa, Ali Adwan, Dema Safadi, Mhd Firas |
author_sort | Ghassa, Ali |
collection | PubMed |
description | A 23‐year‐old woman with a gestational age of 17 weeks presented with abdominal pain. The ultrasound showed maternal hyperreactio luteinalis with fetal cystic hygroma. After termination of pregnancy, the female fetus showed masculinization features with muscular hypertrophy. The hyperreactio luteinalis regressed under hormonal suppression therapy. |
format | Online Article Text |
id | pubmed-9459097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94590972022-09-12 Hyperreactio luteinalis associated with fetal hyperandrogenism and cystic hygroma Ghassa, Ali Adwan, Dema Safadi, Mhd Firas Clin Case Rep Case Report A 23‐year‐old woman with a gestational age of 17 weeks presented with abdominal pain. The ultrasound showed maternal hyperreactio luteinalis with fetal cystic hygroma. After termination of pregnancy, the female fetus showed masculinization features with muscular hypertrophy. The hyperreactio luteinalis regressed under hormonal suppression therapy. John Wiley and Sons Inc. 2022-09-08 /pmc/articles/PMC9459097/ /pubmed/36101781 http://dx.doi.org/10.1002/ccr3.6310 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Ghassa, Ali Adwan, Dema Safadi, Mhd Firas Hyperreactio luteinalis associated with fetal hyperandrogenism and cystic hygroma |
title | Hyperreactio luteinalis associated with fetal hyperandrogenism and cystic hygroma |
title_full | Hyperreactio luteinalis associated with fetal hyperandrogenism and cystic hygroma |
title_fullStr | Hyperreactio luteinalis associated with fetal hyperandrogenism and cystic hygroma |
title_full_unstemmed | Hyperreactio luteinalis associated with fetal hyperandrogenism and cystic hygroma |
title_short | Hyperreactio luteinalis associated with fetal hyperandrogenism and cystic hygroma |
title_sort | hyperreactio luteinalis associated with fetal hyperandrogenism and cystic hygroma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459097/ https://www.ncbi.nlm.nih.gov/pubmed/36101781 http://dx.doi.org/10.1002/ccr3.6310 |
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