Adrenocortical tumors (ACT) include both adrenocortical adenomas (ACA) and adrenocortical carcinomas (ACC). Carcinomas are rare in children and adolescents. In the United States, Surveillance Epidemiology and End Results (SEER) data from the National Cancer Institute show that the proportion of adrenocortical tumors (ACT) in childhood carcinoma is only about 1.3%, and the proportion of ACT in childhood malignancies is only about 0.2%. With childhood ACC being less common, there were only 36 cases of adrenocortical carcinomas younger than age 20 years reported to SEER during 20 years period of 1975-1995, 18 of them occurred in children younger than 5 years of age. Herein, we report our experience of a 9 monthes old female infant ACC case presenting with huge abdomen mass as the main clinical manifestation. The patient has a favorable outcome combined with surgical and chemotherapy treatments.
基金：
Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding Support [ZY201404]
通讯机构：[1]Capital Med Univ, Beijing Childrens Hosp, Hematol Oncol Ctr,Minist Educ, Beijing Key Lab Pediat Hematol Oncol,Natl Key Dis, Beijing, Peoples R China;[3]Capital Med Univ, Beijing Childrens Hosp, Hematol Oncol Ctr, Nan Li Shi Rd, Beijing 100045, Peoples R China
推荐引用方式(GB/T 7714)：
Duan Yanlong,He Lejian,Zhang Wei,et al.An infant with rare adrenocortical carcinoma[J].INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY.2016,9(5):5777-5779.
APA：
Duan, Yanlong,He, Lejian,Zhang, Wei,Huang, Cheng,Zhang, Dawei...&Ma, Xiaoli.(2016).An infant with rare adrenocortical carcinoma.INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY,9,(5)
MLA：
Duan, Yanlong,et al."An infant with rare adrenocortical carcinoma".INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY 9..5(2016):5777-5779
