Results 41 to 50 of about 4,675 (181)
Kidney Transplantation for Erdheim-Chester Disease
Case Reports in Transplantation, 2020 Erdheim-Chester disease is a rare inflammatory disease that infiltrates skeletal and extra-skeletal tissue. Chronic kidney disease (CKD) in Erdheim-Chester disease is usually attributed to retroperitoneal lesions that lead to urologic obstruction and ...
Jongwon Yoo +8 more
doaj +1 more source
BMC Neurology, 2021 Background Erdheim–Chester disease (ECD) is a non-Langerhans histiocytosis that results in multi-organ disease involving the skin, bones, lungs and kidneys. Central nervous system (CNS) involvement occurs in about 50 % of patients, and diabetes insipidus,
Pedro Gustavo Barros Rodrigues +5 more
doaj +1 more source
Klinicka onkologie, 2021 Erdheim-Chester disease is a rare inflammatory myeloid clonal disease which is classified into histiocytoses. It is characterized by excessive production and accumulation of foamy histiocytes and Touton giant cells in various tissues and organs. Foamy histiocytes and Touton giant cells produce proinflammatory cytokines and chemokines and contain ...
M, Brychtová +5 more
openaire +2 more sources
Enfermedad de Erdheim-Chester: primer caso pediátrico reportado en Colombia
, 2021 The Erdheim-Chester’s disease is extremely rare in children. We present the case of a 12-year-old girl with histological and radiological diagnosis of this disease and mutation of the BRAF gene, who developed multisystemic compromise requiring treatment ...
Salazar, Luis Carlos +3 more
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Erdheim-Chester Disease Presenting with Bradycardia [PDF]
Turk J HaematolTufanoğlu FH, Hunutlu FÇ.
europepmc +3 more sources
Erdheim-Chester disease with chorioretinal and orbital involvement: a case report
, 2023 A 42-year-old woman presented with bilateral proptosis, chemosis, leg pain, and vision loss. Orbital, chorioretinal, and multi-organ involvement of Erdheim-Chester disease, a rare non-Langerhans histiocytosis, with a negative BRAF mutation was diagnosed ...
Safak Karslioglu (15138858) +7 more
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Erdheim-Chester Disease with Perirenal Masses Containing Macroscopic Fat Tissue
대한영상의학회지, 2015 Erdheim-Chester disease is a rare non-Langerhans-cell histiocytosis involving multiple organs. On histological evaluation, lipid-laden histiocyte aggregates in Erdheim-Chester disease is detected, but fat tissue in affected organs is not noted grossly on
Jonghyun Byeon +4 more
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A case study on Erdheim ‐ Chester Disease
, 2020 A case study on Jakob Erdheim-Chester disease. Jakob Erdheim, pathologist, collector, scientist and educator was born in 1874 in Galicia and received his medical degree from the University of Vienna in 1900.
Jakob Erdheim, Harald Koeck*
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Erdheim-Chester disease. Clinical case [PDF]
, 2022 Summary. Erdheim–Chester disease (ECD) is an extremely rare disease characterized by the abnormal multiplication of a specific type of white blood cells called histiocytes, or tissue macrophages (technically, this disease is termed a non-Langerhans-cell
Mindruţa-Stratan, Rodica +4 more
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Doença de Erdheim-Chester: relato de caso / Erdheim-Chester disease: a case report Erdheim-Chester disease: a case report [PDF]
, 2022 A doença de Erdheim-Chester é uma rara histiocitose de células não-Langerhans, primeiramente descrita por Jakob Erdheim e William Chester em 1930 de etiologia desconhecida.
de Almeida, Rafaela Veras +7 more
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