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完全型雄激素不敏感综合征合并无性细胞瘤一例

尹雨鑫 王长河

国际妇产科学杂志2024,Vol.51Issue(4):392-394,3.
国际妇产科学杂志2024,Vol.51Issue(4):392-394,3.DOI:10.12280/gjfckx.20240083

完全型雄激素不敏感综合征合并无性细胞瘤一例

A Case Report of Complete Androgen Insensitivity Syndrome Complicated with Dysgerminoma

尹雨鑫 1王长河2

作者信息

  • 1. 272013 山东省济宁市,济宁医学院临床医学院
  • 2. 济宁市第一人民医院
  • 折叠

摘要

Abstract

Androgen insensitivity syndrome(AIS)is rare and difficult to diagnose at an early stage.This paper reports the diagnosis and treatment of a patient with complete androgen insensitivity syndrome(CAIS)complicated with dysgerminoma.The patient was admitted to the hospital due to abdominal distension for 2 days and received color ultrasound in the outpatient department indicating pelvic tumor.After admission,pelvic tumor resection was performed.Since the cause of hyperandrogenemia was unknown before surgery,it was diagnosed as CAIS complicated with dysgerminoma by chromosome analysis and genetic testing,finally underwent radical resection of gonadal malignant tumor.At present,the patient is still under close follow-up and his condition is stable.Through retrospective analysis of the clinical characteristics and diagnosis and treatment of this case,in order to improve the clinical understanding of the disease.

关键词

雄激素迟钝综合征/性发育障碍/无性细胞瘤/雄激素增多症/病例报告

Key words

Androgen-insensitivity syndrome/Disorders of sex development/Dysgerminoma/Hyperandrogenism/Case reports

引用本文复制引用

尹雨鑫,王长河..完全型雄激素不敏感综合征合并无性细胞瘤一例[J].国际妇产科学杂志,2024,51(4):392-394,3.

国际妇产科学杂志

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1674-1870

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