A case of adrenocortical adenoma following long-term
treatment in a patient with congenital adrenal hyperplasia |
Seung Rim Lho, So Hyun Park, Min Ho Jung, Byung Churl Lee |
Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea |
장기간 치료받은 부신 피질 과형성증 환아에서 발생한 부신 피질 종양 1례 |
노승림, 박소현, 정민호, 이병철 |
가톨릭대학교 의과대학 소아과학교실 |
Correspondence:
Byung Churl Lee, Email: byungcl@catholic.ac.kr |
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Abstract |
As a result of the widespread use and enhanced quality of high-resolution radiological techniques, a recent report has revealed a relatively high prevalence of small adrenal tumors in patients with untreated congenital adrenal hyperplasia due to 21-hydroxylase deficiency. However, there are scarcely any pediatric cases of adrenocortical tumor following long-term treatment in patients suffering with congenital adrenal hyperplasia. We report here on a pediatric female case of adrenocortical adenoma despite adequate long-term treatment for the salt-losing type of congenital adrenal hyperplasia. |
Key Words:
Congenital adrenal hyperplasia , Adrenocortical tumor |
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