Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor in the Adrenal Gland of an Adolescent: A Case Report and Review of the Literature
- Authors
- Yoon, Jong Hyung; Kim, Hyery; Lee, Ji Won; Kang, Hyoung Jin; Park, Hyeon Jin; Park, Kyung Duk; Park, Byung-Kiu; Shin, Hee Young; Park, June Dong; Park, Sung-Hye; Ahn, Hyo Seop
- Issue Date
- Oct-2014
- Publisher
- LIPPINCOTT WILLIAMS & WILKINS
- Keywords
- Ewing sarcoma/peripheral primitive neuroectodermal tumors; adrenal gland; adolescent
- Citation
- JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, v.36, no.7, pp E456 - E459
- Journal Title
- JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
- Volume
- 36
- Number
- 7
- Start Page
- E456
- End Page
- E459
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/74860
- DOI
- 10.1097/MPH.0000000000000058
- ISSN
- 1077-4114
1536-3678
- Abstract
- 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.
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