Results 141 to 150 of about 4,926,805 (180)

A case of mixed histiocytosis (Erdheim-Chester disease and Langerhans cell histiocytosis) with STEAP3-associated anemia and type 4 hemochromatosis. [PDF]

Orphanet J Rare Dis
Buianova AA, Gaydina TA, Reznik EV, Iarovoi MD, Kuznetsova AA, Belova VA, Ignatyuk MA, Shatalov PA, Repinskaia ZA, Shinkarina AP, Volodkin AV, Atiakshin DA, Korostin DO.   +12 more
europepmc   +1 more source

Erdheim-Chester disease with predominant cerebellar manifestations: a case report with literature review. [PDF]

Oxf Med Case Reports
Al-Badri SG, Duhan A, Al-Taie RH, Al Gehadi MYH, Afridi A.   +4 more
europepmc   +1 more source

Case Report: Relapsing pleural effusions and coated aorta revealing Erdheim-Chester disease. [PDF]

Front Immunol
Ouattara TR, Pezel T, Lorillon G, Kante A, Reiner P, Le Gal A, Lefèvre M, Vieira T, Mouly S, Tazi A, Haroche J, Goncalves T, Sène D, Emile JF, Comarmond C.   +14 more
europepmc   +1 more source

Case Report: The rare pancreatic involvement in Erdheim-Chester disease. [PDF]

Front Immunol
Li J, Zhang M, Zou Y, Zhang J, Song J, Li T, Li SG.   +6 more
europepmc   +1 more source

Erdheim-Chester Disease

Journal of Cutaneous Medicine and Surgery: Incorporating Medical and Surgical Dermatology, 2003
Background: Erdheim–Chester disease is a rare non-Langerhans' cell histiocytosis. Objective: This case report is presented to familiarize clinicians with Erdheim–Chester disease and its differential diagnosis.
Susan E, Lenahan, Klaus F, Helm, Kenneth D, Hopper   +2 more
core   +7 more sources

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Erdheim–Chester Disease

Clinical Radiology, 2001
Erdheim-Chester disease (ECD) is a rare histiocytic infiltrative disease, characterized by long bone sclerosis. We describe two confirmed cases of ECD, both of which demonstrate non-malignant retroperitoneal and peri-renal infiltration causing dilatation of the upper renal tracts. The cases are illustrated with contrast studies, computed tomography (CT)
D, Murray, M, Marshall, E, England, J, Mander, T M, Chakera   +4 more
exaly   +3 more sources

Gastrointestinal Erdheim-Chester disease.

Irish medical journal, 2014
Leinster
Tevlin, R, Cahalane, AM, Larkin, JO, Treacy, A, Connaghan, D, Winter, DC   +5 more
openaire   +3 more sources

Erdheim-Chester Disease

American Journal of Neuroradiology, 2023
Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis. The disease is widely variable in its severity, ranging from incidental findings in asymptomatic patients to a fatal multisystem illness. CNS involvement occurs in up to one-half of patients, most often leading to diabetes insipidus and cerebellar dysfunction.
J.C. Benson, R. Vaubel, B.A. Ebne, I.T. Mark, M. Peris Celda, C.C. Hook, W.O. Tobin, C. Giannini   +7 more
openaire   +4 more sources

Erdheim-Chester Disease

Archives of Neurology, 2012
Erdheim-Chester disease is a rare systemic non-Langerhans cell histiocytosis requiring clinical, radiographic, and pathologic findings to confirmthediagnosis.Bonepain,the most common presenting symptom, occurs in 50% of cases, and there is near-universal symmetric sclerosis of the metaphyses and diaphyses of the long bones.
Eric M, Liotta, Miral D, Jhaveri, John C, Fox, Venugopal, Parameswaran, Steven L, Lewis   +4 more
openaire   +4 more sources