| Literature DB >> 27708931 |
Gülşen Özen1, Sibel Yılmaz-Öner1, Neşe Tuncer2, Türkay Akbaş3, Serhan Tuğlular4, Haner Direskeneli1.
Abstract
Normal/increased pressure hydrocephaly is an unusual manifestation of systemic lupus erythematosus (SLE), and the pathogenesis is still unclear. We report the case of an 18-year-old white female with severe refractory renal and pulmonary involvement who developed stupor during intensive immunosuppressive treatment. Enlarged ventricles on imaging and increased intracranial pressure with the exclusion of infectious and hemorrhagic/thrombotic processes suggested increased pressure communicating hydrocephalus associated with SLE. Few case reports are reviewed, and potential pathophysiologic mechanisms are discussed.Entities:
Keywords: Hydrocephalus; increased pressure communicating; systemic lupus erythematosus
Year: 2015 PMID: 27708931 PMCID: PMC5047267 DOI: 10.5152/eurjrheum.2015.0084
Source DB: PubMed Journal: Eur J Rheumatol ISSN: 2147-9720