首页 正文

Case Reports Radiology case reports. 2022 Apr 4;17(6):1866-1869. doi: 10.1016/j.radcr.2022.02.060 0.02025

Presacral ganglioneuroma in an 8-year-old child: case report, and literature review

八岁患儿骶前神经节细胞瘤一例并文献复习 翻译改进

Widad Abbou  1, Imane Guerrouj  1, Mahdi Tiabi  2, Yassine Derouich  3, Amal Bennani  2, Houssain Benhaddou  3, Imane Skiker  1, Imane Kamaoui  4

作者单位 +展开

作者单位

  • 1 Department of Radiology, Mohammed VI University hospital, faculty of Medicine, University Mohammed first, Oujda, Morocco.
  • 2 Department of anatomopathology, Mohammed VI University hospital, faculty of Medicine, University Mohammed first, Oujda, Morocco.
  • 3 Department of pediatric surgery Mohammed VI University hospital, faculty of Medicine, University Mohammed first, Oujda, Morocco.
  • 4 Vascular Anomalies Research Unit, Medical Science Research Laboratory Mohammed VI University hospital, faculty of Medicine, University Mohammed first, Oujda, Morocco.
  • DOI: 10.1016/j.radcr.2022.02.060 PMID: 35401895

    摘要 中英对照阅读

    Ganglioneuromas are benign tumors of the sympathetic nervous system, rarely found in the presacral region. In this study, we report the case of presacral ganglioneuroma in an 8-year-old girl, who complained of abdominal pain with diarrhea and abdominal distension. Ultrasound showed a large hypoechoic pelvic mass complicated by right ureter hydronephrosis. the CT and MRI confirm the presence of a presacral tissue mass with heterogeneous enhancement after contrast injection. The child underwent a complete surgical resection, and the anatomopathological study returned in favor of a ganglioneuroma. The presacral ganglioneuroma is an extremely rare tumor in that only twenty cases have been reported in the literature. 3 of which were less than 8-years-old. Through our case, we will review the epidemiological, clinical, radiological and therapeutic characteristics of this type of tumor.

    Keywords: Child; Ganglioneuroma; Presacral.

    Keywords:presacral ganglioneuroma; case report; literature review

    神经节神经瘤是副交感神经系统的一种良性肿瘤,很少出现在骶前区域。在这项研究中,我们报道了一名8岁女孩的骶前神经节神经瘤病例,她主诉腹痛、腹泻和腹部胀满。超声检查显示盆腔有一个大的低回声肿块,并伴有右侧输尿管积水。CT和MRI证实存在一个异质性增强的骶前组织肿块(注射对比剂后)。该患儿接受了完整的手术切除,病理学研究结果支持神经节神经瘤的诊断。骶前神经节神经瘤是一种极为罕见的肿瘤,文献中仅报道了20例,其中3例年龄小于8岁。通过我们的病例,我们将回顾这种类型肿瘤的流行病学、临床、放射学和治疗特征。

    关键词:儿童;神经节神经瘤;骶前。

    关键词:骶前神经节神经瘤; 病例报告; 文献回顾

    翻译效果不满意? 用Ai改进或 寻求AI助手帮助 ,对摘要进行重点提炼
    Copyright © Radiology case reports. 中文内容为AI机器翻译,仅供参考!

    相关内容

    期刊名:Radiology case reports

    缩写:

    ISSN:1930-0433

    e-ISSN:

    IF/分区:0.0/

    文章目录 更多期刊信息

    全文链接
    引文链接
    复制
    已复制!
    推荐内容
    Presacral ganglioneuroma in an 8-year-old child: case report, and literature review