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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2021
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.
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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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