Cardiac and pleuropulmonary involvement in Erdheim-Chester disease without bone lesions: A case report.

Autor: Kanza RE; Department of Radiology, Chicoutimi Hospital, 305 Rue Saint-Vallier, Saguenay, QC G7H5H6, Canada.; Faculty of Medicine, University of Sherbrooke, Saguenay, QC, Canada., Houle O; Faculty of Medicine, University of Sherbrooke, Saguenay, QC, Canada., Simard PL; Department of Medicine, Division of Cardiology, Chicoutimi Hospital, Saguenay, QC, Canada., St-Gelais J; Department of Medicine, Division of Hemato-Oncology, Chicoutimi Hospital, Saguenay, QC, Canada., Raymond C; Department of Pathology, Chicoutimi Hospital, Saguenay, QC, Canada.
Jazyk: angličtina
Zdroj: Radiology case reports [Radiol Case Rep] 2021 Dec 16; Vol. 17 (3), pp. 525-530. Date of Electronic Publication: 2021 Dec 16 (Print Publication: 2022).
DOI: 10.1016/j.radcr.2021.11.056
Abstrakt: Erdheim-Chester disease is a rare multisystemic non-Langerhans histiocytosis characterized by histiocytes that stain positive for CD68 and negative for CD1a. Skeletal involvement is reported to be present in up to 96% cases and BRAF mutation in about half of the cases. Here, we report a patient with an unusual longstanding BRAF-negative Erdheim-Chester disease without bone lesions who developed pleuropulmonary and cardiac involvement.
(© 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington.)
Databáze: MEDLINE