Erdheim-Chester disease: Challenges in diagnosing and treating a rare multisystemic disease in Malaysia

Erdheim-Chester disease: Challenges in diagnosing and treating a rare multisystemic disease in Malaysia

Erdheim-Chester disease (ECD) or lipoid granulomatosis is a rare non-langerhan cell histiocytosis disease characterised by infiltration of foamy histocytes into the affected organs of different systems. ECD lesions are recognised to cause progressive scarring and fibrosis that pervade multiple organ...

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Bibliographic Details
Main Authors: Qinglin Lau, De Yee Gan, Soon Ching Gan, Nor Haisyah Binti Noor Kasim, Ahmad Zakiyy Bin Mohamed
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Rare
Subjects:
Erdheim-chester disease
Retroperitoneal fibrosis
Histiocytosis
Multisystemic
Rare disease
Online Access:http://www.sciencedirect.com/science/article/pii/S2950008724000103
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