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儿童同时出现肾母细胞瘤和对侧神经节细胞瘤:病例报告及文献综述

Simultaneous Presentation of Wilms' Tumor and Contralateral Ganglioneuroma in a Child: Case Report and Literature Review.

作者信息

Bayramoglu Zuhal, Adaletli Ibrahim, Caliskan Emine, Kilicaslan Isin, Karaoglan Cagla S, Celik Alaattin, Gun Soysal Feryal, Bay Sema B, Zulfikar Bulent

机构信息

Departments of Radiology.

Pathology.

出版信息

J Pediatr Hematol Oncol. 2018 Aug;40(6):e400-e404. doi: 10.1097/MPH.0000000000001081.

Abstract

We demonstrate a 4-year-old girl who presented with progressive, asymmetrical, firm abdominal distention and was diagnosed with synchronous Wilms' tumor and left para-aortic ganglioneuroma (GN). Although synchronous tumors in the pediatric population are commonly associated with malignancy-predisposing syndromes, the patient in question was found to be otherwise healthy and had no clinical evidence nor family history of a syndrome. This case is the second one in the literature diagnosed with synchronous presentation of Wilms' tumor and GN in a previously healthy child. In addition, a GN foci presumed to be a previous metastasis of a neurogenic tumor that subsequently matured to GN was depicted within a left para-aortic lymph node. We aimed to emphasize an extremely rare synchronous occurrence of these embryonal tumors, increase the awareness of physicians, and discuss the radiologic differential diagnosis and management.

摘要

我们展示了一名4岁女孩,她出现进行性、不对称、坚实的腹部膨隆,被诊断为同时患有肾母细胞瘤和左主动脉旁神经节瘤(GN)。尽管儿科人群中的同步肿瘤通常与易患恶性肿瘤的综合征相关,但该患者在其他方面健康,没有该综合征的临床证据或家族史。该病例是文献中第二例诊断为先前健康儿童同时出现肾母细胞瘤和GN的病例。此外,在左主动脉旁淋巴结内发现了一个GN病灶,推测是神经源性肿瘤先前的转移灶,随后成熟为GN。我们旨在强调这些胚胎性肿瘤极其罕见的同步发生情况,提高医生的认识,并讨论放射学鉴别诊断和管理。

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