儿童散发性同步节细胞神经瘤——病例报告并文献复习

Sporadic synchronous ganglioneuromas in a child--case report and review.

机构信息

Department of Paediatric Surgery, St. John's Medical College Hospital, St. John's National Academy of Health Sciences, Johnnagara, Bangalore 560034, India.

出版信息

J Pediatr Surg. 2010 Apr;45(4):822-5. doi: 10.1016/j.jpedsurg.2010.01.027.

DOI:10.1016/j.jpedsurg.2010.01.027

PMID:20385294

Abstract

An 8-year-old girl presented with a relatively asymptomatic abdominopelvic mass that was detected in the neonatal period. She harbored a presacral mass with intraspinal extension and a right posterior mediastinal mass; all were excised completely and were ganglioneuromas. The report discusses the maturation of neuroblastoma-ganglioneuromas and details the staged management of sporadic synchronous ganglioneuromas in a child, probably the first in published English literature.

摘要

一位 8 岁女孩因新生儿期发现的无症状腹盆腔肿块就诊。她的骶前有一个肿块，向椎管内延伸，还有一个位于右后纵隔的肿块；所有肿块均被完全切除，病理结果均为神经节细胞瘤。该报告讨论了神经母细胞瘤-神经节细胞瘤的成熟过程，并详细介绍了儿童散发性同步神经节细胞瘤的分期管理，这可能是发表的英文文献中的首例。