Bilateral testicular tumors in congenital adrenal hyperplasia.

被引:4
|
作者
Dieckmann, K
Lecomte, P
Despert, F
Maurage, C
Sirinelli, D
Rolland, JC
机构
[1] CHU GATIEN CLOCKEVILLE,SERV PEDIAT ENDOCRINOL & CARDIOL A,F-37044 TOURS,FRANCE
[2] CHU GATIEN CLOCKEVILLE,SERV RADIOL PEDIAT,F-37044 TOURS,FRANCE
[3] HOP BRETONNEAU,SERV ENDOCRINOL & MED INTERNE,F-37044 TOURS,FRANCE
来源
ARCHIVES DE PEDIATRIE | 1995年 / 2卷 / 12期
关键词
adrenal hyperplasia; congenital; hydroxylases; testicular diseases;
D O I
10.1016/0929-693X(96)89917-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background. - Testicular tumors have been reported in boys and adolescents with congenital adrenal hyperplasia (CAH) inadequately controlled by hormonal therapy. Case reports. - Two adolescents were treated for CAH due to 21-hydroxylase deficiency. They developed hyperplastic nodular testes at the age of 16 and 17 years, respectively. CAH in both was inadequately controlled as confirmed by hormonal studies. The rumors regressed after adequate steroid therapy in the first patient but persisted in the second patient despite normalization of 17-OH progesterone and plasma renin activity. Conclusion. - Testicular ultrasonography should be systematic in all male patients with CAH since radiological findings are earlier than clinical manifestations. The ACTH-dependent tumors require intensification of hormonal therapy in order to obtain tumoral regression and to prevent infertility.
引用
收藏
页码:1167 / 1172
页数:6
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