Gender reversal in 46XX congenital virilizing adrenal hyperplasia

Autor: S. Ahmed, V. Sripathi, A. Al-Ashwal, N. Sakati
Rok vydání: 1997
Předmět:
Zdroj: BJU International. 79:785-789
ISSN: 1464-410X
1464-4096
DOI: 10.1046/j.1464-410x.1997.00127.x
Popis: Objective To review the results of gender reversal in six patients with 46XX congenital virilizing adrenal hyperplasia (CVAH). Patients and methods Fifty-one patients with 46XX CVAH were seen in an 8 year period; 45 were managed by conventional feminizing genitoplasty, but six underwent gender reversal and were managed as males. The clinical decision for gender reversal was made after appropriate counselling and was based primarily on parental choice, this being influenced significantly by a delayed diagnosis in four patients. Surgical management consisted of gonadectomy, excision of Mullerian structures and staged hypospadias repair/chordee correction in four patients, and circumcision in two completely masculinized children. Results All six boys are well adjusted to their gender of rearing, with ages ranging from 3 years to 16.5 years (mean 8.5) at the time of review. Two children have normal penises and four have a satisfactory result after two-stage repair of hypospadias/chordee. Conclusion Most patients with 46XX CVAH are preferably raised as females and require a feminizing genitoplasty. However, the clinical decision may be influenced by many factors, including delay in diagnosis, social bias and the premium on male rearing in certain communities. When male rearing is chosen, early gonadectomy and excision of Mullerian structures, together with staged hypospadias repair, gives satisfactory results.
Databáze: OpenAIRE