Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor in the Adrenal Gland of an Adolescent: A Case Report and Review of the Literature

被引:8
|
作者
Yoon, Jong Hyung [1 ,3 ]
Kim, Hyery [1 ]
Lee, Ji Won [1 ]
Kang, Hyoung Jin [1 ]
Park, Hyeon Jin [3 ]
Park, Kyung Duk [1 ]
Park, Byung-Kiu [3 ]
Shin, Hee Young [1 ]
Park, June Dong [1 ]
Park, Sung-Hye [2 ]
Ahn, Hyo Seop [1 ]
机构
[1] Seoul Natl Univ, Coll Med, Canc Res Inst, Dept Pediat,Div Hematol Oncol, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 110744, South Korea
[3] Natl Canc Ctr, Ctr Pediat Oncol, Goyang, South Korea
关键词
Ewing sarcoma/peripheral primitive neuroectodermal tumors; adrenal gland; adolescent; SARCOMA FAMILY; ONCOLOGY-GROUP; MANAGEMENT; CHILDREN; BIOLOGY;
D O I
10.1097/MPH.0000000000000058
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ewing sarcoma/peripheral primitive neuroectodermal tumors (ES/pPNETs) typically occur in the long or flat bones, the chest wall, extraskeletal soft tissue, or less frequently, in solid organs. They can arise from anywhere in the body; however, ES/pPNETs arising from the adrenal gland are very rare, especially in children and adolescents. Herein, the authors report a case of an ES/pPNET in the adrenal gland of a 17-year-old girl, who was successfully treated with a multimodal treatment, with a brief review of the pertinent literature.
引用
收藏
页码:E456 / E459
页数:4
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