Rare Case of Complete Androgen Insensitivity Syndrome
Copyright © 2024, Fava Spessoto et al..
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.
| Medienart: |
E-Artikel |
|---|
| Erscheinungsjahr: |
2024 |
|---|---|
| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:16 |
|---|---|
| Enthalten in: |
Cureus - 16(2024), 2 vom: 04. Feb., Seite e54550 |
| Sprache: |
Englisch |
|---|
| Beteiligte Personen: |
Fava Spessoto, Luís Cesar [VerfasserIn] |
|---|
| Links: |
|---|
| Themen: |
Androgen insensitivity |
|---|
| Anmerkungen: |
Date Revised 23.03.2024 published: Electronic-eCollection Citation Status PubMed-not-MEDLINE |
|---|
| doi: |
10.7759/cureus.54550 |
|---|
| funding: |
|
|---|---|
| Förderinstitution / Projekttitel: |
|
| PPN (Katalog-ID): |
NLM370060679 |
|---|
| LEADER | 01000naa a22002652 4500 | ||
|---|---|---|---|
| 001 | NLM370060679 | ||
| 003 | DE-627 | ||
| 005 | 20240323235838.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 240323s2024 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.7759/cureus.54550 |2 doi | |
| 028 | 5 | 2 | |a pubmed24n1343.xml |
| 035 | |a (DE-627)NLM370060679 | ||
| 035 | |a (NLM)38516495 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 100 | 1 | |a Fava Spessoto, Luís Cesar |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Rare Case of Complete Androgen Insensitivity Syndrome |
| 264 | 1 | |c 2024 | |
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a ƒaComputermedien |b c |2 rdamedia | ||
| 338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
| 500 | |a Date Revised 23.03.2024 | ||
| 500 | |a published: Electronic-eCollection | ||
| 500 | |a Citation Status PubMed-not-MEDLINE | ||
| 520 | |a Copyright © 2024, Fava Spessoto et al. | ||
| 520 | |a 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 | ||
| 650 | 4 | |a Case Reports | |
| 650 | 4 | |a androgen insensitivity | |
| 650 | 4 | |a androgen receptor | |
| 650 | 4 | |a male pseudohermaphroditism | |
| 650 | 4 | |a treatment | |
| 650 | 4 | |a urology | |
| 700 | 1 | |a Avelino Silveira, Júlia Saraiva |e verfasserin |4 aut | |
| 700 | 1 | |a Abularach, Andres Menacho |e verfasserin |4 aut | |
| 700 | 1 | |a Santana Garcia, Gustavo |e verfasserin |4 aut | |
| 700 | 1 | |a Almeida, Matheus Castro |e verfasserin |4 aut | |
| 700 | 1 | |a Gonzales, Guilherme Cerqueira |e verfasserin |4 aut | |
| 700 | 1 | |a Nagle Spessoto, Ana Clara |e verfasserin |4 aut | |
| 700 | 1 | |a Facio, Fernando Nestor |c Jr |e verfasserin |4 aut | |
| 700 | 1 | |a Silva Faria, Mateus Henrique |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Cureus |d 2013 |g 16(2024), 2 vom: 04. Feb., Seite e54550 |w (DE-627)NLM24118083X |x 2168-8184 |7 nnns |
| 773 | 1 | 8 | |g volume:16 |g year:2024 |g number:2 |g day:04 |g month:02 |g pages:e54550 |
| 856 | 4 | 0 | |u http://dx.doi.org/10.7759/cureus.54550 |3 Volltext |
| 912 | |a GBV_USEFLAG_A | ||
| 912 | |a GBV_NLM | ||
| 951 | |a AR | ||
| 952 | |d 16 |j 2024 |e 2 |b 04 |c 02 |h e54550 | ||