Clinical Heterogeneity of Desmoplastic Infantile Ganglioglioma: A Case Series and Literature Review

被引:22
作者
Hummel, Trent R. [1 ]
Miles, Lili [2 ]
Mangano, Francesco T. [3 ]
Jones, Blaise V. [4 ]
Geller, James I. [1 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Div Oncol, Canc & Blood Dis Inst, Cincinnati, OH 45229 USA
[2] Cincinnati Childrens Hosp Med Ctr, Div Pathol & Lab Med, Cincinnati, OH 45229 USA
[3] Cincinnati Childrens Hosp Med Ctr, Dept Pediat Neurol Surg, Cincinnati, OH 45229 USA
[4] Cincinnati Childrens Hosp Med Ctr, Dept Radiol, Cincinnati, OH 45229 USA
关键词
desmoplastic infantile ganglioglioma; pediatric; brain tumor; cancer; SUPRATENTORIAL NEUROEPITHELIAL TUMORS; HISTOLOGICAL-FINDINGS; CEREBRAL ASTROCYTOMA; BRAIN-TUMORS; FEATURES; DIAGNOSIS; INFANCY; MRI; MANAGEMENT; SPECTRUM;
D O I
10.1097/MPH.0b013e3182580330
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Desmoplastic infantile gangliogliomas (DIG) are intracranial tumors described in 1987 as benign lesions of infancy. A literature review and the clinical course of 3 patients reported herein suggest that the initial description should be amended. Nearly 23% of DIG cases occur in children older than 24 months. Approximately 40% of DIG cases require additional medical, radiation, and/or further surgical intervention, and 15% of infants and children develop leptomeningeal spread or die from DIG. Such adverse outcomes, combined with the recognition that DIG represents a heterogeneous disease, underscore the need for an expanded biological and molecular investigation.
引用
收藏
页码:E232 / E236
页数:5
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