Ewing Sarcoma/Primitive Neuroectodermal Tumor Arising From the Adrenal Gland in an Adolescent

被引：19

作者：

Stephenson, Jacob ^{[1
,2
]}

Gow, Kenneth W. ^{[1
,2
]}

Meehan, John ^{[1
,2
]}

Hawkins, Douglas S. ^{[3
]}

Avansino, Jeffrey ^{[1
,2
]}

机构：

[1] Seattle Childrens Hosp, Div Gen & Thorac Surg, Seattle, WA 98105 USA

[2] Univ Washington, Seattle, WA 98195 USA

[3] Seattle Childrens Hosp, Div Hematol Oncol, Seattle, WA 98105 USA

来源：

PEDIATRIC BLOOD & CANCER | 2011年 / 57卷 / 04期

关键词：

adrenal; Ewing tumors; Ewing/PNET; surgery; DIAGNOSIS; SARCOMA;

D O I：

10.1002/pbc.23034

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

We review the case of an adolescent who presented with flank pain, fatigue and a discrete nonfunctioning adrenal lesion which was found to be an adrenal Ewing sarcoma/primitive neuroectodermal tumor (ES/PNET). The patient was treated with a minimally invasive adrenalectomy as a component of multimodal therapy, including seven courses of chemotherapy and whole abdominal radiation. She is currently disease free 14 months after the operation and 3 months off therapy. Pediatr Blood Cancer 2011;57:691-692. (C) 2011 Wiley-Liss, Inc.

引用

页码：691 / 692

页数：2

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