Grade II Pilocytic Astrocytoma in a 3-Month-Old Patient with Encephalocraniocutaneous Lipomatosis (ECCL): Case Report and Literature Review of Low Grade Gliomas in ECCL

被引：16

作者：

Bieser, Sarah ^{[1
]}

Reis, Martin ^{[1
]}

Guzman, Miguel ^{[1
]}

Gauvain, Karen ^{[2
]}

Elbabaa, Samer ^{[1
]}

Braddock, Stephen R. ^{[1
]}

Abdel-Baki, Mohamed S. ^{[1
]}

机构：

[1] St Louis Univ, Sch Med, St Louis, MO USA

[2] Washington Univ, Sch Med, St Louis, MO USA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2015年 / 167卷 / 04期

关键词：

encephalocraniocutaneous; lipomatosis; glioma; CHILDREN;

D O I：

10.1002/ajmg.a.37017

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Encephalocraniocutaneous lipomatosis (ECCL) is a rare congenital syndrome with an unknown etiology. Since 1970, around 60 cases have been reported in English literature. ECCL is usually classified by cutaneous lesions and non-progressive intracranial or spinal lipomas; however three cases of ECCL associated with low grade glioma (LGG) have been described. We report on the fourth case of LGG in a patient with ECCL; a grade II pilocytic astrocytoma with pilomyxoid features in a 3-month-old male, the youngest in literature. (c) 2015 Wiley Periodicals, Inc.

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收藏

页码：878 / 881

页数：4

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