Results 81 to 90 of about 10,310,741 (229)
Adhesion and transcellular migration of neutrophils and B lymphocytes on fibroblasts [PDF]
During tissue inflammation, infiltrated leukocytes may have physical contacts with fibroblasts. We observed that neutrophils and B lymphocytes adhered in a larger proportion than T cells on cultured fibroblasts.
Couture, Patrick +3 more
core +2 more sources
Tissue‐Resident Myeloid and Histiocytic Cells in Health and Disease: Novel Emerging Concepts
ABSTRACT Although all myeloid cells are considered to derive from hematopoietic stem cells, the cells in each myeloid lineage are heterogeneous populations, and their distribution and functions vary, depending on underlying physiologic and pathologic processes, age, sex, and genetic and epigenetic signatures.
Peter Valent +27 more
wiley +1 more source
Rosai Dorfman Disease: A Rare Cause of Cervical Lymphadenopathy [PDF]
Rosai Dorfman disease, a sinus histiocytosis, is rare to find and difficult to diagnose. It may masquerade as commoner diseases including infections and malignancies.
Sreenath Sreenivasan +4 more
doaj +1 more source
Functional neurological disorders (FNDs) can present acutely at any stage of a brain tumor illness and may result in inappropriate investigations and treatment. Improved awareness of this issue will facilitate earlier diagnosis of FND, encourage development of multidisciplinary pathways to treat FND, and prevent delays to tumor treatment.
Stuart C. Innes +7 more
wiley +1 more source
Rosai-Dorfman disease manifesting as a solitary mass with fat in the thymus a case report
Background Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease, is a rare, self-limiting disease that predominantly affects children and young adults. Moreover, the disease is characterized by painless bilateral cervical
Dan Liu +3 more
doaj +1 more source
Spinal Rosai–Dorfman disease: Case report of a rare disorde
Background: Rosai–Dorfman disease (sinus histiocytosis with massive lymphadenopathy (SHML)) is a rare, histiocytic, lymphoproliferative disease of unknown etiology affecting young people with male predominance.
A. Elsotouhy +4 more
doaj +1 more source
IgG4-related disease: A systematic review of this unrecognized disease in pediatrics [PDF]
Background: Immunoglobulin G4-related disease (IgG4-RD) is a systemic fibro-inflammatory condition with an unclear pathophysiological mechanism affecting different parts of the body.
Bramer, W.M. (Wichor) +6 more
core +4 more sources
The Clinicopathologic Spectrum of Rosai–Dorfman–Destombes Disease in Adults: An Analysis of 16 Cases
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
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a rare benign disease of unknown etiology presenting with massive lymphadenopathy. These cases can often be misdiagnosed as lymphoma.
Kushwaha Rashmi +2 more
doaj
Orbital Rosai–Dorfman disease: a case report and literature review
We report a case of orbital Rosai–Dorfman disease in a 45-year-old man who presented with exophthalmos as the first symptom for 6 months. He did not have any itching, photophobia, tears, headache, dizziness, nausea, vomiting, or other symptoms of ...
Xin Su, Liqing Zhang
doaj +1 more source

