Journal
JOURNAL OF PEDIATRIC RESEARCH
Volume 9, Issue 3, Pages 307-313Publisher
GALENOS PUBL HOUSE
DOI: 10.4274/jpr.galenos.2022.05579
Keywords
Oncocytic variant adrenocortical cancer; peripheral precocious puberty; clitoromegaly
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Androgen-secreting adrenal tumors are aggressive cancers in childhood but rare in clinical practice. This article reports a case of pure androgen-secreting adrenal carcinoma, emphasizing the possibility of adrenal tumors in patients presenting with virilization.
Androgen-secreting adrenal tumors are aggressive cancers in childhood; however, they are rare in clinical practice. Children with adrenal carcinoma usually present with peripheral precocious puberty, premature pubarche, signs of virilization and clitoromegaly. We present a case of 4 year-old girl with premature pubarche, clitoromegaly and bone age advancement, who was subsequently diagnosed with pure androgen-secreting oncocytic adrenal carcinoma. After the removal of the adrenal tumor, our patient developed precocious puberty. In patients with functioning adrenocortical carcinoma who have had surgical removal, clinical follow-up and hormonal marker examination for the secondary effects of excessive hormone secretion at least every 2 or 3 months may be a useful option after surgery. The aim of this article is to emphasize that adrenal tumors can be seen in patients presenting with virilization findings. We also present a literature review of these tumors, which are very rare in childhood.
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