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Complete androgen insensitivity syndrome: a case report and literature review

Complete androgen insensitivity syndrome (CAIS) is a rare disease that can be easily misdiagnosed. Before puberty, this condition is easily misdiagnosed as an inguinal hernia. This case report describes a 31-year-old phenotypically female patient with CAIS who was misdiagnosed twice previously with...

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Autores principales: Guo, Min, Huang, Jin-Cheng, Li, Cui-Fen, Liu, Yan-Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983103/
https://www.ncbi.nlm.nih.gov/pubmed/36851849
http://dx.doi.org/10.1177/03000605231154413
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author Guo, Min
Huang, Jin-Cheng
Li, Cui-Fen
Liu, Yan-Yan
author_facet Guo, Min
Huang, Jin-Cheng
Li, Cui-Fen
Liu, Yan-Yan
author_sort Guo, Min
collection PubMed
description Complete androgen insensitivity syndrome (CAIS) is a rare disease that can be easily misdiagnosed. Before puberty, this condition is easily misdiagnosed as an inguinal hernia. This case report describes a 31-year-old phenotypically female patient with CAIS who was misdiagnosed twice previously with an inguinal hernia. Her karyotype analysis showed that she was 46, XY. She underwent a bilateral gonadectomy and long-term hormone replacement therapy. A Leydig cell tumour of the right testis was diagnosed postoperatively. This report also reviews the current understanding of the diagnosis and treatment of CAIS.
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spelling pubmed-99831032023-03-04 Complete androgen insensitivity syndrome: a case report and literature review Guo, Min Huang, Jin-Cheng Li, Cui-Fen Liu, Yan-Yan J Int Med Res Case Report and Case Series Complete androgen insensitivity syndrome (CAIS) is a rare disease that can be easily misdiagnosed. Before puberty, this condition is easily misdiagnosed as an inguinal hernia. This case report describes a 31-year-old phenotypically female patient with CAIS who was misdiagnosed twice previously with an inguinal hernia. Her karyotype analysis showed that she was 46, XY. She underwent a bilateral gonadectomy and long-term hormone replacement therapy. A Leydig cell tumour of the right testis was diagnosed postoperatively. This report also reviews the current understanding of the diagnosis and treatment of CAIS. SAGE Publications 2023-02-27 /pmc/articles/PMC9983103/ /pubmed/36851849 http://dx.doi.org/10.1177/03000605231154413 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report and Case Series
Guo, Min
Huang, Jin-Cheng
Li, Cui-Fen
Liu, Yan-Yan
Complete androgen insensitivity syndrome: a case report and literature review
title Complete androgen insensitivity syndrome: a case report and literature review
title_full Complete androgen insensitivity syndrome: a case report and literature review
title_fullStr Complete androgen insensitivity syndrome: a case report and literature review
title_full_unstemmed Complete androgen insensitivity syndrome: a case report and literature review
title_short Complete androgen insensitivity syndrome: a case report and literature review
title_sort complete androgen insensitivity syndrome: a case report and literature review
topic Case Report and Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983103/
https://www.ncbi.nlm.nih.gov/pubmed/36851849
http://dx.doi.org/10.1177/03000605231154413
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