Neuroimaging manifestations of paediatric histiocytoses

Author:

Tan Hsern Ern Ivan12ORCID,Lakshmanan Rahul13,Warne Richard1,Walwyn Thomas34,Roebuck Derek13

Affiliation:

1. Department of Medical Imaging Perth Children's Hospital Perth Western Australia Australia

2. Department of Medical Imaging Fiona Stanley Hospital Perth Western Australia Australia

3. University of Western Australia Perth Western Australia Australia

4. Department of Oncology Perth Children's Hospital Perth Western Australia Australia

Abstract

SummaryHistiocytoses 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.

Publisher

Wiley

Subject

Radiology, Nuclear Medicine and imaging,Oncology

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