Complete androgen insensitivity syndrome

Introduction. Androgen insensitivity syndrome (AIS) belongs to disorders of sex development, resulting from complete or partial resistance to the biological actions of androgens in persons who are genetically males (XY) with normally developed testes and age-appropriate for males of serum...

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Main Authors: Tančić-Gajić Milina, Vujović Svetlana, Ivović Miomira, Marina Ljiljana V., Arizanović Zorana, Raković Dragana, Micić Dragan
Format: Article
Language:English
Published: Serbian Medical Society 2015-01-01
Series:Srpski Arhiv za Celokupno Lekarstvo
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0370-8179/2015/0370-81791504214T.pdf
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spelling doaj-9dda092b065d464580d3516f0db09f792021-01-02T00:41:43ZengSerbian Medical SocietySrpski Arhiv za Celokupno Lekarstvo0370-81792015-01-011433-421421810.2298/SARH1504214T0370-81791504214TComplete androgen insensitivity syndromeTančić-Gajić Milina0Vujović Svetlana1Ivović Miomira2Marina Ljiljana V.3Arizanović Zorana4Raković Dragana5Micić Dragan6School of medicine, Belgrade + Clinical Center of Serbia, Clinic for Endocrinology, Diabetes and Metabolism Diseases, BelgradeSchool of medicine, Belgrade + Clinical Center of Serbia, Clinic for Endocrinology, Diabetes and Metabolism Diseases, BelgradeSchool of medicine, Belgrade + Clinical Center of Serbia, Clinic for Endocrinology, Diabetes and Metabolism Diseases, BelgradeSchool of medicine, Belgrade + Clinical Center of Serbia, Clinic for Endocrinology, Diabetes and Metabolism Diseases, BelgradeSchool of medicine, Belgrade + Clinical Center of Serbia, Clinic for Endocrinology, Diabetes and Metabolism Diseases, BelgradeSchool of medicine, Belgrade + Clinical Center of Serbia, Clinic for Endocrinology, Diabetes and Metabolism Diseases, BelgradeSchool of medicine, Belgrade + Clinical Center of Serbia, Clinic for Endocrinology, Diabetes and Metabolism Diseases, BelgradeIntroduction. Androgen insensitivity syndrome (AIS) belongs to disorders of sex development, resulting from complete or partial resistance to the biological actions of androgens in persons who are genetically males (XY) with normally developed testes and age-appropriate for males of serum testosterone concentration. Case Outline. A 21-year-old female patient was admitted at our Clinic further evaluation and treatment of testicular feminization syndrome, which was diagnosed at the age of 16 years. The patient had never menstruated. On physical examination, her external genitalia and breast development appeared as completely normal feminine structures but pubic and axillary hair was absent. Cytogenetic analysis showed a 46 XY karyotype. The values of sex hormones were as in adult males. The multisliced computed tomography (MSCT) showed structures on both sides of the pelvic region, suggestive of testes. Bilateral orchiectomy was performed. Hormone replacement therapy was prescribed after gonadectomy. Vaginal dilatation was advised to avoid dyspareunia. Conclusion. The diagnosis of complete androgen insensitivity is based on clinical findigs, hormonal analysis karyotype, visualization methods and genetic analysis. Bilateral gonadectomy is generally recommended in early adulthood to avoid the risk of testicular malignancy. Vaginal length may be short requiring dilatation in an effort to avoid dyspareunia. Vaginal surgery is rarely indicated for the creation of a functional vagina. [Projekat Ministarstva nauke Republike Srbije, br. 175067]http://www.doiserbia.nb.rs/img/doi/0370-8179/2015/0370-81791504214T.pdfandrogen insensitivity syndrome46 XYandrogen receptorprimary amenorrhea
collection DOAJ
language English
format Article
sources DOAJ
author Tančić-Gajić Milina
Vujović Svetlana
Ivović Miomira
Marina Ljiljana V.
Arizanović Zorana
Raković Dragana
Micić Dragan
spellingShingle Tančić-Gajić Milina
Vujović Svetlana
Ivović Miomira
Marina Ljiljana V.
Arizanović Zorana
Raković Dragana
Micić Dragan
Complete androgen insensitivity syndrome
Srpski Arhiv za Celokupno Lekarstvo
androgen insensitivity syndrome
46 XY
androgen receptor
primary amenorrhea
author_facet Tančić-Gajić Milina
Vujović Svetlana
Ivović Miomira
Marina Ljiljana V.
Arizanović Zorana
Raković Dragana
Micić Dragan
author_sort Tančić-Gajić Milina
title Complete androgen insensitivity syndrome
title_short Complete androgen insensitivity syndrome
title_full Complete androgen insensitivity syndrome
title_fullStr Complete androgen insensitivity syndrome
title_full_unstemmed Complete androgen insensitivity syndrome
title_sort complete androgen insensitivity syndrome
publisher Serbian Medical Society
series Srpski Arhiv za Celokupno Lekarstvo
issn 0370-8179
publishDate 2015-01-01
description Introduction. Androgen insensitivity syndrome (AIS) belongs to disorders of sex development, resulting from complete or partial resistance to the biological actions of androgens in persons who are genetically males (XY) with normally developed testes and age-appropriate for males of serum testosterone concentration. Case Outline. A 21-year-old female patient was admitted at our Clinic further evaluation and treatment of testicular feminization syndrome, which was diagnosed at the age of 16 years. The patient had never menstruated. On physical examination, her external genitalia and breast development appeared as completely normal feminine structures but pubic and axillary hair was absent. Cytogenetic analysis showed a 46 XY karyotype. The values of sex hormones were as in adult males. The multisliced computed tomography (MSCT) showed structures on both sides of the pelvic region, suggestive of testes. Bilateral orchiectomy was performed. Hormone replacement therapy was prescribed after gonadectomy. Vaginal dilatation was advised to avoid dyspareunia. Conclusion. The diagnosis of complete androgen insensitivity is based on clinical findigs, hormonal analysis karyotype, visualization methods and genetic analysis. Bilateral gonadectomy is generally recommended in early adulthood to avoid the risk of testicular malignancy. Vaginal length may be short requiring dilatation in an effort to avoid dyspareunia. Vaginal surgery is rarely indicated for the creation of a functional vagina. [Projekat Ministarstva nauke Republike Srbije, br. 175067]
topic androgen insensitivity syndrome
46 XY
androgen receptor
primary amenorrhea
url http://www.doiserbia.nb.rs/img/doi/0370-8179/2015/0370-81791504214T.pdf
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