Results 11 to 20 of about 212,365 (347)

Eosinophils in eosinophilic pneumonia [PDF]

open access: yesEuropean Respiratory Journal, 1996
Idiopathic eosinophilic pneumonia (IEP) is an uncom-mon disease of unknown aetiology characterized by theaccumulation of eosinophils in the lung, variable bloodeosinophilia and peripheral opacities on the chest radio-gram. The response to steroid treatment is dramatic butrelapses are frequent, requiring the use of long-termsteroid treatment [1 ...
ALBERA, Carlo, P. GHIO
openaire   +2 more sources

Dermatomyositis with Eosinophils [PDF]

open access: yesDermatopathology, 2023
Dermatomyositis is an idiopathic inflammatory myopathy that often presents with symmetric proximal skeletal muscle weakness and characteristic skin findings. Typical skin biopsy findings include vacuolar changes of the basal layer, increased dermal mucin, and a predominantly lymphocytic infiltrate.
Isabella I. Sanchez   +4 more
openaire   +4 more sources

Eosinophilic fasciitis [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2016
Eosinophilic fasciitis is a rare sclerodermiform syndrome of unknown etiology. It is characterized by the thickening of the muscular fascia and subcutaneous tissue, with a variable infiltration of eosinophils. Peripheral eosinophilia, poly or monoclonal hypergammaglobulinemia and increased erythrocyte sedimentation rate can be seen.
Lamback, Elisa Baranski   +2 more
openaire   +5 more sources

Eosinophilic angiocentric fibrosis of the orbit: A case report and review of literature

open access: yesIndian Journal of Pathology and Microbiology, 2015
Eosinophilic angiocentric fibrosis is a rare condition presenting with tumefactive lesions of the nasal cavity, paranasal sinuses, upper respiratory tract and rarely the orbit; and has characteristic histopathological features. We report the case of a 38-
Santhi Radhakrishnan   +2 more
doaj   +1 more source

Eosinophilic fasciitis (Shulman's disease): review and comparative evaluation of seven patients. [PDF]

open access: yes, 2019
OBJECTIVES: Eosinophilic fasciitis (EF) was described in 1974 by Shulman as a rare fibrosing connective tissue disease of unknown etiology. An undetermined trigger is thought to lead to the degranulation of eosinophils that interact with fibroblasts and
Cimbron, M   +3 more
core   +1 more source

Eosinophilic esophagitis [PDF]

open access: yesAllergy, Asthma & Clinical Immunology, 2018
Eosinophilic esophagitis (EoE) is an atopic condition of the esophagus that has become increasingly recognized over the last 15 years. Diagnosis of the disorder is dependent on the patient’s clinical manifestations, and must be confirmed by histologic findings on esophageal mucosal biopsies.
Carr, Stuart   +2 more
openaire   +4 more sources

Eosinophilic dermatosis of hematologic malignancy mimicking varicella zoster infection: report in a woman with chronic lymphocytic leukemia and review of the literature

open access: yesDermatology Practical & Conceptual, 2017
Eosinophilic dermatosis of hematologic malignancy is a rare papulovesicular eruption that presents in patients with hematoproliferative disorders, particularly chronic lymphocytic leukemia.
Omar Bari, Philip R. Cohen
doaj   +1 more source

A new formulation of oral viscous budesonide in treating of paediatric eosinophilic oesophagitis: a pilot study [PDF]

open access: yes, 2017
OBJECTIVES: Oral viscous budesonide is a recent therapeutic option for eosinophilic oesophagitis (EoE) compared with dietary restriction and inhaled steroids.
Amil, D. J.   +8 more
core   +1 more source

Eosinophilic Gastroenteritis with Eosinophilic Dermatitis

open access: yesYonsei Medical Journal, 2010
Eosinophilic gastroenteritis (EG) is characterized by eosinophilic infiltration of the bowel wall and variable gastrointestinal manifestations. Clinicians should have a high index of suspicion for EG when faced with gastrointestinal symptoms and peripheral eosinophilia to avoid incorrect diagnosis and inappropriate treatments.
Jae Myung Cha   +3 more
openaire   +3 more sources

Crystal-Storing Histiocytosis: The Iceberg of More Serious Conditions

open access: yesDiagnostics, 2023
Crystal-storing histiocytosis is a rare condition that is histologically characterized by intracellular cytoplasmic crystalline inclusions. It usually presents monoclonal immunoglobulins that deposit within histiocytes, which accumulate and affect ...
Mousa Mobarki   +8 more
doaj   +1 more source

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