True Hermaphroditism in a phenotypic male without ambiguous genitalia: An unusual presentation at puberty

被引:10
|
作者
Alonso, Guillermo
Pasqualini, Titania
Busaniche, Julio
Ruiz, Eduardo
Chemes, Hector
机构
[1] Hosp Italiano Buenos Aires, Dept Pediat, Secc Crecimiento Desarrollo & Endocrinol, Buenos Aires, DF, Argentina
[2] Hosp Italiano Buenos Aires, Dept Pediat, Div Cirugia, Buenos Aires, DF, Argentina
[3] Hosp Ninos Dr Ricardo Gutierrez, Ctr Invest Endocrinol, Buenos Aires, DF, Argentina
关键词
true hermaphroditism; ambiguous genitalia; mosaicism; chimerism;
D O I
10.1159/000102693
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
True hermaphroditism usually appears with ambiguous genitalia requiring extensive evaluation during the neonatal period. There have been occasional cases with better differ-entiation of external genitalia, leading to delays in diagnosis. We report the case of an adolescent boy with true hermaphroditism who presented with normal external genitalia and no sexual ambiguity. He was referred due to progressive gynecomastia and arrest of puberty. He presented at the age of 16 years for gynecomastia of rapid progression with normal penile development and both gonads in scrotum and normal testosterone and increased gonadotropin levels. Gonadal ultrasound scan was compatible with testicular and ovarian tissues in scrotum, and the karyotype showed two cellular lines ( 46, XX/ 46, XY). Gonadal histology revealed bilateral ovotestes. A genotype polymerase chain reaction mediated analysis using seven microsatellite markers did not confirm chimerism. Clinical findings and mechanism of generation are discussed. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:261 / 264
页数:4
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