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Journal of Pediatric Neurology 2020; 18(02): 095-097
DOI: 10.1055/s-0039-1678662
Case Report
Georg Thieme Verlag KG Stuttgart · New York

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

DeJarra Caprii Johnson
1   University of South Alabama College of Medicine, Mobile, Alabama, United States
2   Department of Pediatrics, Children's and Women's Hospital, Mobile, Alabama, United States
,
David Edward Kline Feldman
3   Department of Radiology, USA Health University Hospital, Mobile, Alabama, United States
,
Preethi Marri
2   Department of Pediatrics, Children's and Women's Hospital, Mobile, Alabama, United States
4   Division of Hematology-Oncology, Children's and Women's Hospital, Mobile, Alabama, United States
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Publikationsverlauf

30. August 2018

09. Januar 2019

Publikationsdatum:
21. Februar 2019 (online)

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Abstract

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.

Keywords

glioma - limbic encephalitis - paraneoplastic syndrome
 

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