| Literature DB >> 22106034 |
Ines Rego1, Mariasavina Severino, Concetta Micalizzi, Maura Faraci, Daniela Pende, Carlo Dufour, Maurizio Aricò, Andrea Rossi.
Abstract
Haemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome caused by deficient down-regulation of the immune response. Presence of central nervous system (CNS) involvement at diagnosis is a poor prognostic sign, and should be carefully investigated. Herein, we describe the neuroradiological findings, clinical data, and treatment outcome in 12 patients with genetic HLH and CNS complications. Neuroimaging was important in identifying CNS involvement, monitoring treatment responses, and detecting treatment complications.Entities:
Mesh:
Year: 2011 PMID: 22106034 DOI: 10.1002/pbc.23405
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167