Results 71 to 80 of about 4,675 (181)

Orbital mass and hairy kidney as characteristics of Erdheim‐Chester disease

open access: yesClinical Case Reports, 2021
Erdheim‐Chester disease (ECD) is a rare non‐Langerhans cell histiocytosis, involving multiple organs. We report a case of ECD with typical features of an orbital mass and "hairy kidneys," whose recognition can lead to early diagnosis and treatment.
Koichiro Yamamoto   +3 more
doaj   +1 more source

Circulating Tumour DNA and Extracellular Vesicle‐Associated DNA as Biomarkers for Cancer Detection: A Systematic Review and Meta‐Analysis

open access: yesJournal of Extracellular Biology, Volume 5, Issue 4, April 2026.
ABSTRACT Liquid biopsy is an emerging tool that allows the detection and monitoring of tumours through the analysis of various analytes in biofluids like blood. An important component of liquid biopsy is circulating tumour (ct) DNA, small fragments of DNA that are released by cancer cells, which have been shown to be a robust biomarker and are already ...
Tad Wu   +8 more
wiley   +1 more source

Erdheim-chester disease: A case report

open access: yes, 2015
Objective: Rare disease Background: The diagnosis of Erdheim-Chester disease, a rare illness, is difficult and requires increased awareness. Case Report: We report the case of a 56-year-old woman who initially presented with a mesenteric panniculitis and
Klastersky, Jean, Alexiou, Jean
core   +1 more source

Pericarditis heralding Erdheim-Chester disease

open access: yes, 2008
Images in Cardiovascular Medicine: Pericarditis Heralding Erdheim-Chester ...
Corradi, Domenico   +5 more
core   +1 more source

Neurological manifestations of Erdheim–Chester Disease

open access: yesAnnals of Clinical and Translational Neurology, 2020
Objective To characterize the spectrum of neurologic involvement in Erdheim–Chester Disease (ECD), a treatable inflammatory neoplasm of histiocytes.
Louisa C. Boyd   +11 more
doaj   +1 more source

A case of Erdheim-Chester disease initially mistaken for retroperitoneal lymphoma

open access: yesRadiology Case Reports, 2020
Erdheim-Chester disease (ECD) is an infrequent, autoimmune disorder that is not Langerhans histiocytosis and is characterized by bilateral sclerosis of the diametaphyseal medullary regions of the long bones and possible multiorgan involvement.
Sharifa K. Alduraibi, MD
doaj   +1 more source

ALK‐Positive Histiocytosis With Unilateral Breast Involvement: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT APH is a rare disorder characterized by the proliferation of ALK‐expressing histiocytes with variable anatomical involvement; however, mammary involvement is exceptionally rare. A 32‐year‐old woman presented with a painless right breast mass. Ultrasound identified a 9 × 8 mm hypoechoic nodule, categorized as BI‐RADS 4A.
Xuechun Liu, Dong Ren, Yanfang Liang
wiley   +1 more source

Anakinra-responsive lichen planus in a woman with Erdheim-Chester disease: a therapeutic enigma [PDF]

open access: yes, 2014
Background:  Anakinra is a recombinant form of interleukin-1 receptor antagonist.  It is the drug of choice for Schnitzler syndrome and cryopyrin-associated periodic syndromes.  It has also recently been demonstrated to have activity in ...
Cohen, Philip R, Kurzrock, Razelle
core   +1 more source

Erdheim‐Chester disease: A multisystem disease case illustration with rare manifestations and treatment challenges

open access: yesClinical Case Reports, 2023
Erdheim‐Chester disease is a rare multisystemic disease. A 50‐year‐old woman, presented with a recurrent pain and swelling of the left knee. Bone scintigraphy showed increased tracer uptake of peripheral skeleton.
Maysam Jridi   +7 more
doaj   +1 more source

Novel BRAF fusion in Erdheim–Chester disease with pulmonary manifestations: Importance of RNA‐based testing and response to MEK inhibition

open access: yes
Histopathology, EarlyView.
Igor Odintsov   +5 more
wiley   +1 more source

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