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

来源：

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | 2014年 / 36卷 / 07期

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

页码：E456 / E459

页数：4

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