Results 21 to 30 of about 1,034 (137)

A Retrospective Histopathological Study of Cutaneous Granulomatous Diseases at A Tertiary Dermatology Center in Kuwait [PDF]

open access: yes, 2023
Background: Granulomatous inflammation is a common histological pattern observed in skin biopsy. Due to the overlapping histological features produced by different etiological agents, granulomatous inflammation poses a diagnostic problem for ...
Rawan Almutairi*, Humoud Al-Sabah
core   +1 more source

Characterization of multinucleated giant cells in synovium and subchondral bone in knee osteoarthritis and rheumatoid arthritis [PDF]

open access: yes, 2015
Background: Multinucleated giant cells have been noticed in diverse arthritic conditions since their first description in rheumatoid synovium. However, their role in the pathogenesis of osteoarthritis (OA) or rheumatoid arthritis (RA) still remains ...
A Consolaro   +61 more
core   +4 more sources

Erdheim-Chester Disease: a comprehensive review of the literature [PDF]

open access: yes, 2013
Erdheim-Chester Disease (ECD) is a rare form of non Langerhans' cell histiocytosis. Individuals affected by this disease are typically adults between their 5th and 7th decades of life. Males and females are almost equally affected.
Mirra Manevich-Mazor   +2 more
core   +1 more source

Thoracic, abdominal and musculoskeletal involvement in Erdheim-Chester disease: CT, MR and PET imaging findings. [PDF]

open access: yes, 2014
BACKGROUND: Erdheim-Chester disease (ECD) is a rare, non-Langerhans cell histiocytosis with characteristic radiological and histological features. This entity is defined by a mononuclear infiltrate consisting of lipid-laden, foamy histiocytes that stain
Antunes, C, Donato, P, Graça, B
core   +1 more source

A Case of Orbital Xanthogranuloma Treated by Surgical Excision [PDF]

open access: yes, 2010
Orbital xanthogranuloma is an uncommon tumor. It is usually associated with a systemic or hematological disease. This report presents a rare case of orbital xanthogranuloma associated with heart disease and thrombocytopenia.
Fujiwara, Sakuhei   +5 more
core   +6 more sources

Xanthogranuloma of the lacrimal sac as a manifestation of Wegener's granulomatosis [PDF]

open access: yes, 2007
McGill Univ, Ctr Hlth, Dept Ophthalmol & Pathol, Montreal, PQ H3A 2B4, CanadaHenry C Witelson Ocular Pathol Lab, Montreal, PQ, CanadaUniversidade Federal de São Paulo, Dept Ophthalmol, UNIFESP, EPM, São Paulo, BrazilMcGill Univ, Ctr Hlth, Dept Ophthalmol,
A Al-Kandari   +8 more
core   +1 more source

Lucio phenomenon in pregnancy: A histopathology review [PDF]

open access: yes, 2023
Background: Lucio phenomenon (LP) is a reaction occurring in lepromatous, non-nodular, diffuse leprosypatients who have not received multidrug therapy (MDT).
Fiqnasyani, Siti Efrida   +4 more
core   +2 more sources

Xanthogranulomatous hypophysitis: a rare and often mistaken pituitary lesion. [PDF]

open access: yes, 2015
Xanthogranulomatous hypophysitis (XGH) is a very rare form of pituitary hypophysitis that may present both clinically and radiologically as a neoplastic lesion. It may either be primary with an autoimmune aetiology and can occur in isolation or as a part
Bagga, V.   +5 more
core   +1 more source

A Rare Case of a Systemic Non-Langerhans Histiocytosis Presenting with Diabetes Insipidus and a Tentorial Mass [PDF]

open access: yes, 2015
Introduction The histiocytoses are a group of clinically diverse diseases distinguished from one another based on the specific immunophenotype of the lesional cells, implying derivation from the same precursor cell.
Barros, MS, Guilherme   +5 more
core   +2 more sources

Coordinate anatomy of the upper parts of urinary tract at ontogenesis stages: II mature age [PDF]

open access: yes, 2016
The research was aimed at study of the renal hilum normal anatomy with validation of system of morphometric indices of renal hilum morphotype at the stages of human postnatal ontogenesis.
Danylchenko, S.I., Shklar, A.S.
core   +2 more sources

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