Erdheim-chester disease

Edward F McCarthy

doi:10.1007/978-1-4471-6578-1_72

Erdheim-chester disease

Edward F McCarthy

School of Medicine

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Abstract

Erdheim-Chester disease, or lipid granulomatosis, is a rare disorder characterized by the proliferation of histiocytes in bone and in extraosseous locations. It is thought perhaps to be a lipid storage disease, in which foamy lipid-laden histiocytes accumulate in the bone marrow. Extravasated lipid results in cholesterol granulomas and a fi broinfl ammatory reaction.

Original language	English (US)
Title of host publication	Tumors and Tumor-Like Lesions of Bone: For Surgical Pathologists, Orthopedic Surgeons and Radiologists
Publisher	Springer-Verlag London Ltd
Pages	951-955
Number of pages	5
ISBN (Print)	9781447165781, 9781447165774
DOIs	https://doi.org/10.1007/978-1-4471-6578-1_72
State	Published - Jan 1 2015

ASJC Scopus subject areas

Medicine(all)
Biochemistry, Genetics and Molecular Biology(all)

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10.1007/978-1-4471-6578-1_72

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McCarthy, E. F. (2015). Erdheim-chester disease. In Tumors and Tumor-Like Lesions of Bone: For Surgical Pathologists, Orthopedic Surgeons and Radiologists (pp. 951-955). Springer-Verlag London Ltd. https://doi.org/10.1007/978-1-4471-6578-1_72

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