[Rare Differential Diagnosis in Bilateral Gonalgia]
Overview
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We report on a 47-year-old patient suffering from bilateral gonalgia, weight loss and night sweats without fever of several months' duration. Diagnostic work-up for infectious and autoimmune diseases showed no abnormal results. A CT scan showed extensive foci of sclerosis throughout the axial skeleton. In the trephine biopsy, foamy cell infiltrates were found with expression of histiocytic markers without expression of Langerhans cell markers. Molecular analysis revealed a low allelic BRAF V600E and BCOR mutation. The diagnosis of Erdheim-Chester disease (ECD) was made. The histologic findings and molecular findings, the clinical and radiologic presentation before and 6 months after therapy as well as possible differential diagnoses of this very rare disease are discussed.
[Mutation pedigree and treatment selection of Erdheim-Chester disease].
Lang M, Zhou D, Cao X Zhonghua Xue Ye Xue Za Zhi. 2023; 44(10):876-880.
PMID: 38049347 PMC: 10694082. DOI: 10.3760/cma.j.issn.0253-2727.2023.10.019.