The Rare Case of Anti-VGKC Limbic Encephalitis Secondary to High-Grade Glioma

被引：0

作者：

Johnson, DeJarra Caprii ^{[1
,2
]}

Feldman, David Edward Kline ^{[3
]}

Marri, Preethi ^{[2
,4
]}

机构：

[1] Univ S Alabama, Coll Med, Mobile, AL USA

[2] Childrens & Womens Hosp, Dept Pediat, Mobile, AL USA

[3] USA Hlth Univ Hosp, Dept Radiol, Mobile, AL USA

[4] Childrens & Womens Hosp, Div Hematol Oncol, Mobile, AL USA

来源：

JOURNAL OF PEDIATRIC NEUROLOGY | 2020年 / 18卷 / 02期

关键词：

glioma; limbic encephalitis; paraneoplastic syndrome;

D O I：

10.1055/s-0039-1678662

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Paraneoplastic limbic encephalitis secondary to a glial tumor is rare, and limited reports on this occurrence have been made in the pediatric population. This case involves a 13-year-old female patient with anti-voltage gated potassium channel (anti-VGKC) limbic encephalitis secondary to a high-grade glioma (HGG) in the suprasellar region. HHGs, associated with anti-VGKC antibodies, are a rare occurrence. This case highlights the need for the inclusion of glial neoplasms in the differential diagnosis for patients presenting with symptoms associated with paraneoplastic encephalitis.

引用

页码：95 / 97

页数：3

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