Results 71 to 80 of about 2,806 (197)

Cutaneous sinus histiocytosis of face of the non-Langerhans cell histiocytoses type (cutaneous Rosai — Dorfman disease)

open access: yesVestnik Dermatologii i Venerologii, 2019
An extremely rare case of sinus histiocytosis of the non-Langerhans cell histiocytoses type is described in 55-year-old patient with isolated localization of cutanious lesion on the right cheek without involvement of nodular structures.
E. V. Sokolovsky   +4 more
doaj   +1 more source

Think highly of immunoglobulin G4‐related chronic rhinosinusitis as a clinical entity in immunoglobulin G4‐related disease

open access: yesEye &ENT Research, Volume 2, Issue 3, Page 151-163, September 2025.
Abstract IgG4‐related chronic rhinosinusitis (IgG4‐related CRS) is gaining recognition among various specialized physicians. As a systemic disease involving multiple organs, IgG4‐related CRS is still not widely recognized as an independent clinical entity. Given the complexity of diagnosing autoimmune‐related multisystem diseases, early recognition and
Lianqi Wan   +3 more
wiley   +1 more source

The Rosai Dorfman Syndrome–The Report of A Rare Case [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2013
Rosai Dorfman syndrome known as Sinus Histiocytosis with Massive Lymphadenopathy (SHML) is an uncommon benign systemic histio-proliferative disease which affects lymph nodes, most often those of the neck (cervical lymphadenopathy). The characteristic
Snehalatha R   +3 more
doaj   +1 more source

Analysis of Hyperexpanded T Cell Clones in SARS‐CoV‐2 Vaccine‐Associated Liver Injury by Spatial Proteomics and Transcriptomics

open access: yesLiver International, Volume 45, Issue 7, July 2025.
ABSTRACT Background and Aims SARS‐CoV‐2 vaccine‐associated liver injury (SVALI) is a rare event and its pathophysiology remains unclear. Previous studies have found an oligoclonal CD8+ T cell infiltrate and SARS‐CoV‐2 spike antigen‐specific T cells in the liver of patients with SVALI. Therefore, we aimed to characterise the immune infiltrate in a liver
Sarp Uzun   +11 more
wiley   +1 more source

Extranodal rosai dorfman disease: a case report of single soft tissue cystic lesion [PDF]

open access: yes, 2020
Rosai-Dorfman disease (RDD) is an uncommon benign histiocytic disorder. It is found worldwide and slightly more common among in men (1.4:1), affecting individuals are with an average age of 20.6 years. Extranodal tissue involvement is documented in 25-43%
Agrawal, Ruchi   +2 more
core   +2 more sources

Cell-in-Cell Phenomenon and Its Relationship With Tumor Microenvironment and Tumor Progression: A Review

open access: yesFrontiers in Cell and Developmental Biology, 2019
The term cell-in-cell, morphologically, refers to the presence of one cell within another. This phenomenon can occur in tumors but also among non-tumor cells.
Xinlong Wang   +20 more
doaj   +1 more source

Immune cell pathology in rabbit hemorrhagic disease [PDF]

open access: yesVeterinary World, 2019
Aim: The aim of this research was to study the effect of rabbit hemorrhagic disease virus (RHDV) on the host immune response by examining the cellular composition/pathology of lymphoid organs and serum levels of tumor necrosis factor-alpha (TNF-α) and ...
Anna Babken Semerjyan   +11 more
doaj   +1 more source

Characteristics of histiocytic neoplasms presenting as breast masses

open access: yes
British Journal of Haematology, Volume 208, Issue 1, Page 358-362, January 2026.
Theodore Vougiouklakis   +10 more
wiley   +1 more source

Rosai Dorfman disease- A rare entity: Case report in North Indian male

open access: yesAsian Journal of Medical Sciences, 2014
Rosai Dorfman disease is a rare disease characterized by histiocytic proliferation of lymph node in young adults. We present here the case of a 67 years old Indian male presenting with lymphadenopathy and pyrexia of unknown origin for 16 months duration.
Ankur Baruah
doaj   +1 more source

Management of Difficult Cases of Autoimmune Hepatitis [PDF]

open access: yes, 2016
Autoimmune hepatitis (AIH) is a complex autoimmune disease characterized by immune-mediated destruction of hepatic parenchyma which can result in cirrhosis, liver failure, and death.
Gawrieh, Samer   +3 more
core   +1 more source

Home - About - Disclaimer - Privacy