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A case of testicular adrenal rest tumor in a male child with congenital adrenal hyperplasia / 소아과
Korean Journal of Pediatrics ; : 1018-1022, 2008.
Article in English | WPRIM | ID: wpr-35042
ABSTRACT
Testicular adrenal rest tumors are a well-known complication in male patients with congenital adrenal hyperplasia. Corticosteroid suppressive therapy usually results in the regression of these tumors. We describe a patient with 21-hydroxylase deficiency who developed bilateral testicular masses. Despite steroid suppressive therapy, the tumors did not regress and hormonal control was poor. Consequently, bilateral partial orchiectomies were performed.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Testicular Neoplasms / Steroid 21-Hydroxylase / Orchiectomy / Adrenal Hyperplasia, Congenital / Adrenal Rest Tumor Limits: Child / Humans / Male Language: English Journal: Korean Journal of Pediatrics Year: 2008 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Testicular Neoplasms / Steroid 21-Hydroxylase / Orchiectomy / Adrenal Hyperplasia, Congenital / Adrenal Rest Tumor Limits: Child / Humans / Male Language: English Journal: Korean Journal of Pediatrics Year: 2008 Type: Article