Literature DB >> 29141820

Fulminant intramedullary spinal cord sarcoidosis.

Jonas Graf1, Marius Ringelstein1, Orhan Aktas1, Mike P Wattjes2, Hans-Peter Hartung3.   

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.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Intramedullary; MRI; Neurosarcoidosis; Spinal cord

Mesh:

Year:  2017        PMID: 29141820     DOI: 10.1016/j.msard.2017.09.010

Source DB:  PubMed          Journal:  Mult Scler Relat Disord        ISSN: 2211-0348            Impact factor:   4.339


  1 in total

1.  Syringomyelia-like syndrome in neuromyelitis optica spectrum disorder complicated with Sjogren's syndrome: a case report.

Authors:  Xiangling Li; Zhengqi Lu; Yanqiang Wang
Journal:  BMC Neurol       Date:  2018-10-09       Impact factor: 2.474

  1 in total

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