Results 71 to 80 of about 4,675 (181)
Orbital mass and hairy kidney as characteristics of Erdheim‐Chester disease
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
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
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
Images in Cardiovascular Medicine: Pericarditis Heralding Erdheim-Chester ...
Corradi, Domenico +5 more
core +1 more source
Neurological manifestations of Erdheim–Chester Disease
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
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
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]
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 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

