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A Case of Congenital Adrenal Hyperlasia Misdiagnosed as Leydig Cell Tumor / 대한소아내분비학회지
Journal of Korean Society of Pediatric Endocrinology ; : 182-186, 2001.
Article in Korean | WPRIM | ID: wpr-190203
ABSTRACT
We experienced a boy manifesting sexual precocity with unilateral testicular tumor, who was finally diagnosed as CAH with 21-hydroxylase deficiency. Initial laboratory findings were compatible with peripheral precocious puberty. Ultrasonogram for testes showed heterogenous high echoic mass in the right testicle. Radical orchiectomy was performed and its pathology revealed benign Leydig cell tumor without Reinke crystal. But, testosterone was not decreased after 1 month of surgery. Second laboratory exam revealed increased DHEA-S and 17-hydroxyprogesterone. Finally, this case was recognized as CAH(simple virilizing type) with unilateral testicular adrenal rest tumor. In conclusion, CAH should always be considered during etiologic study for the male sexulal precocity even with unilateral testicular tumor.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Puberty, Precocious / Testis / Testosterone / Steroid 21-Hydroxylase / Orchiectomy / Ultrasonography / Adrenal Hyperplasia, Congenital / Adrenal Rest Tumor / 17-alpha-Hydroxyprogesterone Type of study: Diagnostic study Limits: Humans / Male Language: Korean Journal: Journal of Korean Society of Pediatric Endocrinology Year: 2001 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Puberty, Precocious / Testis / Testosterone / Steroid 21-Hydroxylase / Orchiectomy / Ultrasonography / Adrenal Hyperplasia, Congenital / Adrenal Rest Tumor / 17-alpha-Hydroxyprogesterone Type of study: Diagnostic study Limits: Humans / Male Language: Korean Journal: Journal of Korean Society of Pediatric Endocrinology Year: 2001 Type: Article