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Rare Case of Complete Androgen Insensitivity Syndrome.

Authors :
Fava Spessoto LC
Avelino Silveira JS
Abularach AM
Santana Garcia G
Almeida MC
Gonzales GC
Nagle Spessoto AC
Facio FN Jr
Silva Faria MH
Source :
Cureus [Cureus] 2024 Feb 20; Vol. 16 (2), pp. e54550. Date of Electronic Publication: 2024 Feb 20 (Print Publication: 2024).
Publication Year :
2024

Abstract

Androgen insensitivity syndrome is a rare X-linked recessive condition in which patients present a female phenotype. After complete androgen insensitivity syndrome (CAIS) diagnosis, the timing of gonadectomy should be evaluated, considering the risks and benefits of this procedure. This paper reports an uncommon case of complete androgen insensitivity syndrome diagnosed belatedly in an adult patient. Surgical treatment was deemed necessary due to the elevated risk of gonadal malignancy.<br />Competing Interests: The authors have declared that no competing interests exist.<br /> (Copyright © 2024, Fava Spessoto et al.)

Details

Language :
English
ISSN :
2168-8184
Volume :
16
Issue :
2
Database :
MEDLINE
Journal :
Cureus
Publication Type :
Report
Accession number :
38516495
Full Text :
https://doi.org/10.7759/cureus.54550