Neuroimaging manifestations of paediatric histiocytoses
- PMID: 37964685
- DOI: 10.1111/1754-9485.13602
Neuroimaging manifestations of paediatric histiocytoses
Abstract
Histiocytoses are rare multi-system disorders marked by abnormal histiocyte cell proliferation, affecting children with diverse clinical presentations. Classified into five groups in 2016, including Langerhans-related (L), cutaneous (C), malignant (M), Rosai-Dorfman disease (R) and haemophagocytic lymphohistiocytosis (H), newer entities such as ALK-positive histiocytosis have also emerged, heralding the era of molecular (sub)classification. Common entities include Langerhans cell histiocytosis (LCH), Erdheim-Chester disease (ECD), Rosai-Dorfman disease (RDD) and haemophagocytic lymphohistiocytosis (HLH). This pictorial essay aids radiologists in recognising and differentiating paediatric histiocytoses based on unique neuroimaging features.
Keywords: head and neck imaging; magnetic resonance imaging; neuroradiology; oncologic imaging; paediatric imaging.
© 2023 The Royal Australian and New Zealand College of Radiologists.
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