Volume 7, Issue 3 (7-2017)                   Iran J Ped Hematol Oncol 2017, 7(3): 193-197 | Back to browse issues page

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Tabatabaei F, Sharif M R, Reisi N. Adrenocortical carcinoma in a 8 years old child: a Case Report. Iran J Ped Hematol Oncol. 2017; 7 (3) :193-197
URL: http://ijpho.ssu.ac.ir/article-1-325-en.html
. Isfahan Endocrine & Metabolism Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
Abstract:   (684 Views)

Background:Unilateral tumors or masses of the adrenal gland are common. They are categorized as either functional (hormone-secreting) or silent and as either benign or malignant. Adrenocortical tumors are rare in childhood, with an incidence of 0.3-0.5 cases per one million child-years. Almost half of childhood tumors are adrenocortical carcinomas (ACC). Most ACCs are sporadic, but specialy in children, some occur as a component of hereditary cancer syndromes. The most common presenting symptom occurring in 50-80% in children with ACC is virilization; overall, survival is poor for adrenocortical carcinoma (ACC). The prognosis in children who have adrenocortical carcinoma (ACC) appears to be better than that of adults, at least for early-stage disease. Residual or metastatic disease carries a poor prognosis. Complete resection is required for cure.

Case presentation: The patient is a 8 years old girl  presented progressive virilizing symptoms including  deepening of the voice, clitoromegaly , growth acceleration, acne and premature pubic and axillary hair development before 8 years old.

Conclusion: The clinical, biochemical, histological features along with differential diagnosis are discussed. This case is presented because of its rarity.This case study report a rare case and also to highlight the importance of differentiating ACC from an adenoma particularly in pediatric patients.

Full-Text [PDF 223 kb]   (337 Downloads)    
Type of Study: case report | Subject: Special
Received: 2015/04/27 | Accepted: 2016/02/17 | Published: 2017/07/16

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