Bayramoglu Zuhal, Adaletli Ibrahim, Caliskan Emine, Kilicaslan Isin, Karaoglan Cagla S, Celik Alaattin, Gun Soysal Feryal, Bay Sema B, Zulfikar Bulent
Departments of Radiology.
Pathology.
J Pediatr Hematol Oncol. 2018 Aug;40(6):e400-e404. doi: 10.1097/MPH.0000000000001081.
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.
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。