Ewing Sarcoma of the Kidney, a Rare Entity: Case Report.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
Case Reports in Medicine Pub Date : 2025-07-26 eCollection Date: 2025-01-01 DOI:10.1155/carm/2598222
Alina Baral, C B Pun, Binita Goyal, Subha Lamichhane
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引用次数: 0

Abstract

Ewing sarcoma is a small round cell tumor of uncertain differentiation, primarily originating in bone in children and adolescents. Ewing sarcoma of the kidney is a rare occurrence and follows an aggressive course with early metastasis. Herein, we present a case of a 16-year-old male presenting with abdominal pain and lump. He underwent nephrectomy and histopathological diagnosis of small round cell tumor with differential diagnosis of Ewing sarcoma was made which was further confirmed by immunohistochemistry. Thus, Ewing sarcoma must also be taken into consideration while dealing with tumors of the kidney in young age group.

Abstract Image

Abstract Image

罕见的肾脏尤因肉瘤:1例报告。
尤文氏肉瘤是一种分化不明确的小圆细胞肿瘤,主要起源于儿童和青少年的骨骼。肾脏尤文氏肉瘤是一种罕见的肿瘤,具有早期转移的侵袭性病程。在此,我们提出一个16岁的男性表现为腹痛和肿块。行肾切除术,组织病理诊断为小圆细胞瘤,鉴别诊断为尤因肉瘤,免疫组化进一步证实。因此,在处理年轻年龄组肾脏肿瘤时,也必须考虑尤因肉瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Case Reports in Medicine
Case Reports in Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
0.00%
发文量
53
审稿时长
13 weeks
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