Results 111 to 120 of about 24,507 (317)
Treatment of Xanthoma disseminatum – a systematic literature review
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.Summary Xanthoma disseminatum is a rare disease from the spectrum of non‐Langerhans cell histiocytoses, which can be categorized into three types and is sometimes associated with systemic involvement. Due to the its rarity, there are no standardized treatment guidelines for this disease, making treatment in everyday clinical practice more difficult ...
Inga Hansen‐Abeck +4 more
wiley +1 more source
Histiocitosis de células de Langerhans en el raquis infantil [PDF]
, 2006 Introducción: la Histiocitosis de células de Langerhans incluye un amplio espectro de enfermedades de etiología desconocida, observada preponderantemente en niños.
Fernández, Claudio A. +2 more
core
The foreign body reaction in total hip arthroplasties. A correlated light-microscopy, SEM, and TEM study. [PDF]
, 1987 An in vivo histological and ultrastructural study of the cellular reaction to particulate material currently used in orthopaedic surgery produced evidence that, on a strictly cellular level, the main damage is done by the smallest particles produced by ...
Dell'Orbo C, Pazzaglia UE, Wilkinson MJ.
core +1 more source
The Clinicopathologic Spectrum of Rosai–Dorfman–Destombes Disease in Adults: An Analysis of 16 Cases
European Journal of Haematology, EarlyView.ABSTRACT Rosai–Dorfman–Destombes disease (RDD) is a rare histiocytic proliferation with protean clinical manifestations, resulting from the accumulation of activated histiocytes within nodal and extra‐nodal tissues. The diagnosis can be missed, particularly when biopsies are obtained from extra‐nodal sites, where histological features may be less ...
Mark Trinder +8 more
wiley +1 more source
Case report: Primary sarcoma of the mandible with a novel SLMAP-BRAF fusion
Frontiers in OncologyPrimary sarcomas of the jaw are very rare tumor with unclear mechanism of tumorigenesis. Identification of genetic alterations contributes to better understanding of tumorigenesis and extension of tumor spectrum, as well as potential therapeutic targets ...
Peng Zhou +7 more
doaj +1 more source
Extranodal Rosai-Dorfman disease of the bone treated with surgery and radiotherapy
Rare Tumors, 2014 Rosai-Dorfman disease (RDD) is a rare, benign histiocyte disorder originally described by Rosai and Dorfman in 1969 as sinus histiocytosis with massive lymphadenopathy.
Nitesh N. Paryani +3 more
doaj +1 more source
Visceral leishmaniasis, hypertriglyceridemia and secondary hemophagocytic lymphohistiocytosis [PDF]
, 2016 Visceral leishmaniasis (VL), a protozoan disease, is 100 % fatal if left untreated. Anemia is common in VL which plays a role in expression of clinically overt VL disease.
Barberi, G. +7 more
core +2 more sources
International Journal of Laboratory Hematology, EarlyView.This study investigates myeloperoxidase (MPO) in Kikuchi's disease, analyzing protein expression and mRNA levels in 43 patients. Results reveal 100% MPO protein positivity, elevated mRNA expression, and a positive correlation between mRNA and protein levels.
Chen Chang +4 more
wiley +1 more source
Langerhans cell histiocytosis: unusual bone marrow infiltration—report of 2 cases in Ecuador
Frontiers in MedicineLangerhans cell histiocytosis (LCH) is a histiocytic neoplasm characterized by the abnormal proliferation of Langerhans cells. Bone marrow (BM) involvement is associated with high-risk disease and poor survival.
Paulina Santana +3 more
doaj +1 more source
Erdheim-Chester Disease with Perirenal Masses Containing Macroscopic Fat Tissue
대한영상의학회지, 2015 Erdheim-Chester disease is a rare non-Langerhans-cell histiocytosis involving multiple organs. On histological evaluation, lipid-laden histiocyte aggregates in Erdheim-Chester disease is detected, but fat tissue in affected organs is not noted grossly on
Jonghyun Byeon +4 more
doaj +1 more source