Results 41 to 50 of about 40,642 (271)

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

Mycobacterial Spindle Cell Pseudotumor Presenting as a Pancreatic Head Mass: A Case Report

open access: yesPathogens
Mycobacterial spindle cell pseudotumors (MSCPs) are rare lesions characterized by the proliferation of spindle-shaped histiocytes caused by mycobacterial infections.
Frank A Cusimano   +5 more
doaj   +1 more source

Indeterminate cell tumor (Histiocytosis)

open access: yesSaudi Journal of Medicine and Medical Sciences, 2013
Indeterminate cell tumor (ICT; histiocytosis) is a rare disorder characterized by accumulation of histiocytes that do not fulfill the phenotypic criteria designated for Langerhans cells (LC).
Ayesha Ahmed   +6 more
doaj   +1 more source

Benign Fibrous Histiocytoma: An Uncommon Presentation [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2017
Intracranial fibrous histiocytomas are rare; Benign Fibrous Histiocytoma (BFH) being uncommon than its malignant counterpart. BFH comprises fibroblasts and histiocytes without any nuclear pleomorphism or atypia.
SAGARIKA SARKAR   +3 more
doaj   +1 more source

Malakoplakia of the appendix, an uncommon entity at an unusual site: a case report [PDF]

open access: yes, 2008
Introduction Malakoplakia is an uncommon inflammatory condition usually affecting the genitourinary tract, which has been associated with infections, tumours and immunocompromised states. Case presentation We report a case of malakoplakia in the appendix
Sameer S. Shaktawat, Mark C. J. Sissons
core   +2 more sources

Intraosseous sarcoidosis imitating peri‐implantitis: A case study

open access: yesClinical Advances in Periodontics, EarlyView.
Abstract Background Sarcoidosis is a multisystem granulomatous disorder of unknown cause, typically affecting the lungs and lymph nodes, but it can also involve the eyes, skin, heart, bones, and other organs. The exact cause is unclear, but genetic factors and environmental triggers like infections, chemicals, or dust may play a role.
Magdalena Orlowska   +2 more
wiley   +1 more source

A Rare Xanthogranulomatous Oophoritis Presenting as Ovarian Cancer [PDF]

open access: yes, 2012
Xanthogranulomatous inflammation is an uncommon form of chronic inflammation that is destructive to affected organs; it is characterized by the presence of lipid-filled macrophages with admixed lymphocytes, plasma cells, and neutrophils. Only a few cases
Bafna, UD   +5 more
core  

Involvement of metal particles in loosening of metal-plastic total hip prostheses. [PDF]

open access: yes, 1985
Four loosened metal-on-plastic total hip prostheses and associated tissues were examined. Each implant showed an uncommonly high formation of metal particles produced by wear or corrosion of the femoral stem.
Ceciliani L   +3 more
core   +1 more source

Quantitative Analysis of Cytologic Features: Application to Mucoepidermoid Carcinoma

open access: yesDiagnostic Cytopathology, EarlyView.
ABSTRACT Introduction Cytologic diagnosis relies on recognition of morphologic features, yet the diagnostic value of individual cytologic features or their combinations is rarely quantified. In this study, we apply a quantitative cytologic feature analysis (QCFA) approach that treats each cytologic feature as a diagnostic test with measurable ...
John Effat Bacilious Diks   +3 more
wiley   +1 more source

A macrophage model of osseointegration

open access: yesCurrent Directions in Biomedical Engineering, 2016
The mechanisms of peri-implant de novo bone formation and contact osteogenesis are still largely unknown. In 1984 Donath et al. showed that macrophages were the first cells to colonize a titanium implant.
Jennissen Herbert P.
doaj   +1 more source

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