Fulminant intramedullary spinal cord sarcoidosis

Jonas Graf, Marius Ringelstein, Orhan Aktas, Mike P. Wattjes, Hans Peter Hartung*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Neurosarcoidosis is a rare disease with various clinical phenotypes. Thus, case reports and series broaden the understanding of this entity (Ibitoye et al., 2017). We present a case of isolated intramedullary spinal cord sarcoidosis, an exceedingly rare phenotype, which needs to be distinguished especially from neuromyelitis optica spectrum disorders (NMOSD). This report exemplifies the need for a systematic approach to diagnosis and management of spinal cord sarcoidosis.

Original languageEnglish
Pages (from-to)47-48
Number of pages2
JournalMultiple Sclerosis and Related Disorders
Volume18
DOIs
Publication statusPublished - 1 Nov 2017

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