Results 31 to 40 of about 4,926,805 (180)

Erdheim-Chester disease: misdiagnosed as multiple sclerosis

, 2023
Erdheim-Chester disease is a rare histiocytic neoplasm with a wide range of clinical manifestations. Due to its rarity and protean characteristics, this condition often presents a diagnostic challenge.
Yang, Jason, Khoo, Tien Kheng, Imlay-Gillespie, Louise, Dierkes, Judith Gerarda   +3 more
core   +1 more source

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

Radiology Case Reports, 2022
Erdheim–Chester disease is a rare multisystemic non-Langerhans histiocytosis characterized by histiocytes that stain positive for CD68 and negative for CD1a.
Rene Epunza Kanza, MD, PhD, Olivier Houle, MS, Pierre-Luc Simard, MD, Jonathan St-Gelais, MD, Catherine Raymond, MD   +4 more
doaj   +1 more source

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, Cynthia Gunsteen, Sima Patel, Ted Clevy-Schneller, Sucha Nand, Divya Jain, Raquel Garcia-Roca, Amishi Desai, Sanjeev Akkina   +8 more
doaj   +1 more source

Intracranial mass lesions and skin discoloration in the armpits as unusual clues to Erdheim-Chester disease: a case report

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, Isabelle de Sousa Pereira, Valter Barbalho Lima Filho, Daniel Aguiar Dias, Paulo Ribeiro Nóbrega, Pedro Braga-Neto   +5 more
doaj   +1 more source

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), Adem Tellioglu (15138849), Muhittin Taskapili (5764466), Kubra Serefoglu Cabuk (5761196), Korhan Fazil (15138852), Tuğrul Elverdi (15138855), Senay Asik Nacaroglu (5862134), Gamze Ozturk Karabulut (12652536)   +7 more
core   +1 more source

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, Cușnir, Valeriu, Pavlovschi, Tavifa, Groppa, Stanislav, Dumbrăveanu, Lilia   +4 more
core   +1 more source

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, Pereira, Bruno Alberto Falcão, Guimarães, Vivianne de Paula Reis, Cavalcante, Alan Rodrigues, Ramos, Amanda luiza Silva de Aguiar, Rogério, Ricardo Mendes, da Silva, Luciana Gabriela de Souza, de Souza, Soane Cristina Silveira   +7 more
core   +1 more source

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, Kyung Ah Kim, Seong Su Hwang, Soo Youn Park, Hyun A Kim   +4 more
doaj   +1 more source

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*
core   +1 more source

Case of Erdheim–Chester presenting with xanthelasma-like eruption and osteolytic bone lesions: A case report

SAGE Open Medical Case Reports, 2019
Erdheim–Chester disease is a rare multisystemic non-Langerhans cell histiocytosis presenting 95% with skeletal lesions. Erdheim–Chester disease is due to mutations in the RAS-MEK-ERK pathway where 50% are due to BRAF-V600E mutations.
Evelyn Alarcon Chinchilla, Marie-Pascale Gourde, Karine Turcotte, Steve Mathieu, Mohamed Amin-Hashem   +4 more
doaj   +1 more source