Results 91 to 100 of about 4,926,805 (180)

Erdheim-Chester Disease Presented with Bilateral Carotid Artery Occlusion: Case Report

, 2010
Erdheim-Chester disease is a rare, non-Langerhans form of systemic histiocytosis of unknown etiology. The disease affects multiple organ systems, including musculoskeletal, cardiac, pulmonary, gastrointestinal, and central nervous systems, producing ...
Albayram, Sait, Balci, Kemal, Asil, Talip, Temizoz, Osman, Celik, Yahya, Hamamcioglu, Mustafa Kemal, Tuzun, Erdem   +6 more
core   +2 more sources

A rare case of Erdheim Chester disease

Radiology Case Reports
Erdheim-Chester disease (ECD) is a rare form of non-Langerhans cell histiocytosis. There are few documented cases in the medical literature. Here, we present an infrequent case of a 53-year-old patient who presented with cutaneous xanthelasma and a ...
Feryal El Oualladi, MD, Mohamed Labied, MD, Rabab Hassani, MD, Chorouk Mountassir, MD, Ghizlane Lembarki, MD, Mouna Sabiri, PhD, Samira Lezar, PhD   +6 more
doaj   +1 more source

Multidetector Computed Tomographic Imaging of Erdheim-Chester Disease

, 2014
Erdheim-Chester disease is a rarely reported disease that can affect nearly every organ and chiefly infiltrates the connective, perivascular, and adipose tissue.
BAYRAKTUTAN, Ümmügülsüm, Yuceler, Zeyneb, Kantarci, M., Akman, C., Ogul, H., Yuceler, Z., Akman, Canan, KARABULUT, NEVZAT, Kantarci, Mecit, OĞUL, Hayri, Bayraktutan, U.   +10 more
core   +1 more source

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Choroidal and Optic Nerve Involvement in Erdheim-Chester Disease

, 2011
Erdheim-Chester disease is a rare, systemic histiocytosis that involves multiple organ ...
Elvira Naftaliev; Igal Leibovitch; Michaela Goldstein; Anat Kesler
core  

Bilateral orbital involvement in Erdheim-Chester disease

, 1998
Erdheim-Chester disease is an idiopathic condition characterized by a xanthogranulomatous process infiltrating the bones, lungs, heart, retroperitoneum and other tissues. This condition is often fatal. Ocular findings are rare.
RAVALLI L., GRISANTI F., DE PALMA, Paolo, NIELSEN I., MARZOLA, Andrea, ROSSI, Antonio   +5 more
core   +1 more source

Erdheim-Chester Disease

Internal Medicine, 2008
Vanichaniramol, Narong, Kingpetch, Kanaungnit, Buranasupkajorn, Patinut, Sunthornyothin, Sarat, Snabboon, Thiti   +4 more
openaire   +3 more sources

Malattia di Erdheim-Chester

, 2018
La malattia di Erdheim-Chester è una malattia molto rara, descritta per la prima volta, nel 1930, da William Chester e Jakob Erdheim come granulomatosi lipoide.
santopietro michelina, giona fiorina
core  

Clinical Images: Erdheim‐Chester disease

ACR Open Rheumatology, 2022
Rohan Mehta, Robert Silvers, Bob Sun
doaj   +1 more source

Imaging of Erdheim-Chester Disease [PDF]

Journal of Bone and Mineral Research, 2002
José M, Olmos, Ana, Canga, Carmen, Velero, Jesús, González-Macías   +3 more
openaire   +2 more sources