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Case Report: The first familial hCG syndrome in a Chinese family
Familial hCG syndrome is a rare and benign cause of elevated serum beta human chorionic gonadotropin (hCG). We present here a case of familial hCG syndrome diagnosed in a Hong Kong Chinese family, which we believe to be the first reported in Chinese. A 38-year-old woman presented with incidental fin...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8240598/ https://www.ncbi.nlm.nih.gov/pubmed/34249343 http://dx.doi.org/10.12688/f1000research.53636.1 |
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author | Hung, Ling-Yin Leung, Mei-Tik Chan, Toby Chun-Hei Cheung, Hoi-Ning Li, Wai-Hon Cheung, Yui-Shing Wong, Assumpta Sze-Man Shek, Chi-Chung Chen, Sammy Pak-Lam |
author_facet | Hung, Ling-Yin Leung, Mei-Tik Chan, Toby Chun-Hei Cheung, Hoi-Ning Li, Wai-Hon Cheung, Yui-Shing Wong, Assumpta Sze-Man Shek, Chi-Chung Chen, Sammy Pak-Lam |
author_sort | Hung, Ling-Yin |
collection | PubMed |
description | Familial hCG syndrome is a rare and benign cause of elevated serum beta human chorionic gonadotropin (hCG). We present here a case of familial hCG syndrome diagnosed in a Hong Kong Chinese family, which we believe to be the first reported in Chinese. A 38-year-old woman presented with incidental finding of persistently elevated hCG, analytically confirmed both in urine and blood. Extensive radiological and biochemical work-up were performed but were negative for pregnancy and malignancy. Testing of another asymptomatic family member revealed unexplained elevation of serum hCG, confirming the diagnosis of familial hCG syndrome. Knowledge and awareness of this entity among clinicians are important to avoid unnecessary investigations and treatment in affected families. |
format | Online Article Text |
id | pubmed-8240598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-82405982021-07-09 Case Report: The first familial hCG syndrome in a Chinese family Hung, Ling-Yin Leung, Mei-Tik Chan, Toby Chun-Hei Cheung, Hoi-Ning Li, Wai-Hon Cheung, Yui-Shing Wong, Assumpta Sze-Man Shek, Chi-Chung Chen, Sammy Pak-Lam F1000Res Case Report Familial hCG syndrome is a rare and benign cause of elevated serum beta human chorionic gonadotropin (hCG). We present here a case of familial hCG syndrome diagnosed in a Hong Kong Chinese family, which we believe to be the first reported in Chinese. A 38-year-old woman presented with incidental finding of persistently elevated hCG, analytically confirmed both in urine and blood. Extensive radiological and biochemical work-up were performed but were negative for pregnancy and malignancy. Testing of another asymptomatic family member revealed unexplained elevation of serum hCG, confirming the diagnosis of familial hCG syndrome. Knowledge and awareness of this entity among clinicians are important to avoid unnecessary investigations and treatment in affected families. F1000 Research Limited 2021-06-08 /pmc/articles/PMC8240598/ /pubmed/34249343 http://dx.doi.org/10.12688/f1000research.53636.1 Text en Copyright: © 2021 Hung LY et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Hung, Ling-Yin Leung, Mei-Tik Chan, Toby Chun-Hei Cheung, Hoi-Ning Li, Wai-Hon Cheung, Yui-Shing Wong, Assumpta Sze-Man Shek, Chi-Chung Chen, Sammy Pak-Lam Case Report: The first familial hCG syndrome in a Chinese family |
title | Case Report: The first familial hCG syndrome in a Chinese family |
title_full | Case Report: The first familial hCG syndrome in a Chinese family |
title_fullStr | Case Report: The first familial hCG syndrome in a Chinese family |
title_full_unstemmed | Case Report: The first familial hCG syndrome in a Chinese family |
title_short | Case Report: The first familial hCG syndrome in a Chinese family |
title_sort | case report: the first familial hcg syndrome in a chinese family |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8240598/ https://www.ncbi.nlm.nih.gov/pubmed/34249343 http://dx.doi.org/10.12688/f1000research.53636.1 |
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