Results 81 to 90 of about 4,926,805 (180)
Spinal dural involvement in Erdheim-Chester disease: MRI findings
, 2002 There are very few reported cases of Erdheim-Chester disease that document involvement of dura at the level of the spinal cord. Among these reports, we know of no publication that includes detailed MRI findings.
Zulfikar, Z +4 more
core +1 more source
A 50‐year‐old man with a 12‐year history of extensive pachymeningeal thickening
Brain Pathology, Volume 36, Issue 4, July 2026.
Alyssa M. Lee +3 more
wiley +1 more source
Case Reports in Hematology, 2018 Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocyte disorder most commonly characterized by multifocal osteosclerotic lesions of the long bones demonstrating sheets of foamy histiocyte infiltrates on biopsy with or without histiocytic ...
Hamza Hashmi +5 more
doaj +1 more source
Cardiac involvement in Erdheim-Chester disease : a case report [PDF]
, 2014 Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis of unknown etiology characterized by proliferation of lipid-containing foamy histiocytes affecting bones and potentially every organ.
Torres, Felipe Soares +2 more
core +2 more sources
Cardiovascular Manifestations of Erdheim-Chester's Disease: A Case Series
Arquivos Brasileiros de CardiologiaErdheim-Chester Disease is a rare entity, classified as an inflammatory myeloid neoplasm, with an unknown incidence, occurring preferentially in men after 50 years of age.
Isabela Bispo Santos da Silva Costa +7 more
doaj +1 more source
Unravelling a hidden case of Erdheim-Chester disease in persistent pericardial effusion
Romanian Journal of CardiologyErdheim-Chester disease (ECD) is a rare non-Langerhans cell, non-familial multisystemic histiocytosis, with widespread manifestations and of highly variable severity.
Alexandru Trenchea +6 more
doaj +1 more source
Erdheim-Chester disease : a case report [PDF]
, 2020 We report the case of a 47-year-old woman with unexplained inflammatory syndrome and asthenia. Imaging findings show bilateral abnormalities of femurs and tibias, suggesting an Erdheim-Chester disease, which is confirmed by a bone marrow biopsy of the ...
KOOPMANSCH, Benjamin +7 more
core +1 more source
Erdheim-Chester Disease With Renal Involvement: A Case Report
The Turkish Journal of Gastroenterology, 2017 Erdheim-Chester disease is a type of non-Langerhans cell histiocytosis. It is a rare, multisystem disorder with unknown etiology. Heterogeneity of the clinical symptoms makes the diagnosis challenging.
Ali Kürşat GANİYUSUFOĞLU +3 more
doaj
Erdheim-Chester disease associated with a novel, complex BRAF p.Thr599_Val600delinsArgGlu mutation
, 2017 BRAF mutation testing to determine eligibility for treatment with vemurafenib was performed on archival skin lesions of a 54-year-old patient diagnosed with Erdheim-Chester disease (ECD) in 1999. Sanger sequencing of DNA extracted from a 2008 skin lesion
R. Mancera (23441674) +9 more
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