Guandalini Michael, Butler Andrew, Mandelstam Simone
Department of Medical Imaging, Royal Children's Hospital Melbourne, Flemington Road, Parkville, VIC 3052, Australia.
Department of Medical Imaging, Royal Children's Hospital Brisbane, Herston, QLD, Australia.
J Clin Neurosci. 2014 Feb;21(2):305-10. doi: 10.1016/j.jocn.2013.03.032. Epub 2013 Oct 9.
Hemophagocytic lymphohistiocytosis (HLH) is a rare multisystem disorder characterised by the proliferation and infiltration of lymphocytes and histiocytes. Central nervous system (CNS) infiltration is particularly devastating. Neuroradiological findings have been reported predominantly as individual case reports due to the rarity of the condition. To our knowledge there have been no published studies of imaging in Australian patients. This study aimed to retrospectively describe and illustrate the MRI appearances of CNS involvement by HLH in a cohort of seven Australian children from two paediatric centres between 2000 and 2011. MRI appearances demonstrate intersubject and intrasubject variability over time, likely reflecting the severity of CNS infiltration and associated demyelination. Familiarity with MRI patterns is important for assessing and monitoring disease activity.
噬血细胞性淋巴组织细胞增生症(HLH)是一种罕见的多系统疾病,其特征为淋巴细胞和组织细胞的增殖与浸润。中枢神经系统(CNS)浸润尤其具有破坏性。由于该病罕见,神经放射学检查结果主要以个案报告形式呈现。据我们所知,尚无关于澳大利亚患者影像学表现的已发表研究。本研究旨在回顾性描述并展示2000年至2011年间来自两个儿科中心的七名澳大利亚儿童HLH累及中枢神经系统的MRI表现。MRI表现显示,随着时间推移,不同个体之间以及同一个体内均存在差异,这可能反映了中枢神经系统浸润及相关脱髓鞘的严重程度。熟悉MRI表现模式对于评估和监测疾病活动很重要。