Results 91 to 100 of about 4,675 (181)

Erdheim-Chester disease: a rare histiocytosis (case report and review of the literature)

The Pan African Medical Journal, 2018
We report a case of Erdheim-chester disease, a rare non-langerhans histiocytosis revealed by polydipsia-polyuria syndrome in a 26 years old woman, trated by interferon with a good response.
Mahtat El Mehdi, Safae Regragui, Hicham Eddou, Selim Jennane, Hicham El Maaroufi, Kamal Doghmi, Mohamed Mikdame   +6 more
doaj   +1 more source

Peculiar Distribution of Tumorous Xanthomas in an Adult Case of Erdheim-Chester Disease Complicated by Atopic Dermatitis

Case Reports in Dermatology, 2011
Erdheim-Chester disease is a rare non-Langerhans form of histiocytosis with multiple organ involvement. Approximately 20% of patients have xanthoma-like lesions, usually on the eyelids.
Yukako Murakami, Mari Wataya-Kaneda, Mika Terao, Hiroaki Azukizawa, Hiroyuki Murota, Yukiko Nakata, Ichiro Katayama   +6 more
doaj   +1 more source

Erdheim-Chester disease : diffusion-weighted imaging and dynamic contrast-enhanced MRI provide useful information

, 2023
This is, to our knowledge, the first case report with in-depth analysis of bone marrow and bone lesions with diffusion-weighted imaging and dynamic contrast-enhanced MRI in Erdheim-Chester disease to date. We present a case of a 70-year-old woman who was
Van Den Berghe, Thomas, Verstraete, Koenraad, Van Dorpe, Jo, Everaert, Nicolas, Candries, Esther, Saerens, Michael   +5 more
core   +1 more source

Risk of Second Cancer in Erdheim-Chester Disease.

JAMA Oncol
International audienceThis cohort study analyzes the risk of second cancers in a cohort of 515 patients with Erdheim-Chester disease followed up at 2 histiocytosis centers in France and ...
Pegoraro F, Peyronel F, Errahmani MY, Catamerò F, Papo M, Cohen-Aubart F, Tesi M, Razanamahery J, Charlotte F, Le Scornet T, Aouba A, Roos-Weil D, Tondo A, Sieni E, Amoura Z, Emile JF, Annesi-Maisano I, Vaglio A, Haroche J.   +18 more
europepmc   +2 more sources

A Rare Case of Erdheim-Chester Disease (Non-Langerhans Cell Histiocytosis) with Concurrent Langerhans Cell Histiocytosis: A Diagnostic and Therapeutic Challenge

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, Drew Murray, John Greenwell, Marwan Shaikh, Soumit Basu, Maxwell Krem   +5 more
doaj   +1 more source

Characteristics of histiocytic neoplasms presenting as breast masses

British Journal of Haematology, Volume 208, Issue 1, Page 358-362, January 2026.
Theodore Vougiouklakis, Marc K. Rosenblum, Matthew Cannavo, Kimberly Feigin, Andrew E. Rosenberg, Frederick Wittlin, Sonia Mahajan, Edi Brogi, Maria E. Arcila, Hannah Y. Wen, Eli L. Diamond   +10 more
wiley   +1 more source

Erdheim-Chester Disease

Internal Medicine, 2008
Vanichaniramol, Narong, Kingpetch, Kanaungnit, Buranasupkajorn, Patinut, Sunthornyothin, Sarat, Snabboon, Thiti   +4 more
  +6 more sources

Erdheim–Chester disease: description of two illustrative cases involving the lung

, 2018
Aim: Erdheim–Chester disease represents a clonal systemic proliferation of histiocytes. Bone is the most common site of involvement, although almost any organ, including the lungs, can be affected.
Lococo F.
core   +2 more sources

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, DELPORTE, Géraldine, RORIVE, Andrée, JEUGMANS, Anne-Marie, Delvenne, Philippe, MOONEN, Marie, Delcorde, I., Moonen, Gustave   +7 more
core  

Cardiac involvement in Erdheim-Chester disease: a case report.

Clinical and Biomedical Research, 2015
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.
Fernando Pivatto Júnior, Diogo Silva Piardi, Felipe Soares Torres   +2 more
doaj   +2 more sources