Posterior Reversible Encephalopathy Syndrome in a Patient With Macrophage Activation Syndrome and Herpes Simplex Virus 2.

anakinra hemophagocytic lymphohistiocytosis (hlh) herpes simplex virus 2 macrophage activation syndrome posterior reversible encephalopathy syndrome (pres)

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
Aug 2021
Historique:
accepted: 17 08 2021
entrez: 20 9 2021
pubmed: 21 9 2021
medline: 21 9 2021
Statut: epublish

Résumé

Posterior reversible encephalopathy syndrome (PRES) is a symptomatic and radiographic syndrome characterized by neurologic changes and concomitant neuroimaging findings typically involving posterior cerebral white matter edema. While there are many competing views on the pathophysiology of PRES, inflammatory conditions, particularly autoimmune diseases, tend to have some degree of correlation. Most cases where patients who have PRES and autoimmune diseases typically involve systemic lupus erythematosus. There is relatively little information in the literature on PRES occurring in adult patients with hemophagocytic lymphohistiocytosis (HLH)/macrophage activation syndrome or of concomitant herpes simplex virus 2 (HSV2) infection. Here, we present the case of a patient with PRES in the setting of adult-onset Still's disease and HLH with concomitant HSV2 infection.

Identifiants

pubmed: 34540494
doi: 10.7759/cureus.17273
pmc: PMC8448276
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e17273

Informations de copyright

Copyright © 2021, Luster et al.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Joshua D Luster (JD)

Medicine, Brooke Army Medical Center, San Antonio, USA.

Ricardo Galindo (R)

Medicine, Brooke Army Medical Center, San Antonio, USA.

Classifications MeSH