Erdheim-Chester disease (ECD) is a rare sporadic non-Langerhans cell histiocytic (LCH) proliferative disorder with systemic predilection. It usually affects adults in the 5th-7th decades of life and has non-specific clinical manifestations. Its suspicion is often heralded by the presence of characteristic radiological findings and subsequently confirmed by demonstration of CD68-positive xanthogranulomatous infiltrates on histopathology. Despite being a non-malignant entity, it might be fatal due to organ dysfunction. Imaging plays a key role in the diagnosis, management, and follow-up. Imaging findings are essential to establish the diagnosis, assess actual disease burden, and explore the aetiopathogenesis and therapeutic options to halt disease progression and associated morbidity.
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Univ Autonoma Barcelona, Vall dHebron Gen Hosp, Dept Internal Med, Barcelona 08035, SpainUniv Autonoma Barcelona, Vall dHebron Gen Hosp, Dept Internal Med, Barcelona 08035, Spain
Juanos-Iborra, Montserrat
Solanich-Moreno, Javier
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IDIBELL, Bellvitge Hosp, Dept Internal Med, Barcelona, SpainUniv Autonoma Barcelona, Vall dHebron Gen Hosp, Dept Internal Med, Barcelona 08035, Spain
Solanich-Moreno, Javier
Selva-O'Callaghan, Albert
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Univ Autonoma Barcelona, Vall dHebron Gen Hosp, Dept Internal Med, Barcelona 08035, SpainUniv Autonoma Barcelona, Vall dHebron Gen Hosp, Dept Internal Med, Barcelona 08035, Spain