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Rosai-Dorfman Disease: A Clinico-pathological Presentation of Three Cases and Review of Literature [PDF]
Journal of Clinical and Diagnostic Research, 2018 Rosai-Dorfman Disease (RDD) or Sinus Histiocytosis with Massive Lymphadenopathy (SHML) is a rare histiocytic disorder of unknown aetiology which presents as a benign, self-limiting disease of phagocytic histiocytes occurring mainly in the first and ...
Francis Ikechukwu Ukekwe +4 more
doaj +1 more source
, 2022 Introduction and Importance. Rosai-Dorfman disease (RDD) is a rare, benign type II histiocytosis characterized by the infiltration of S100+ histiocytes and emperipolesis.
Dieter M. Lindskog +5 more
core +2 more sources
Extranodal Rosai-Dorfman disease involving paranasal sinuses, orbits and anterior cranial fossa
Indian Journal of Neurosurgery, 2014 Rosai-Dorfman disease (RDD) is a rare, benign pseudolymphatous condition, predominantly involving lymph nodes. Although several cases of extra-nodal involvement have been reported previously, central nervous system involvement, particularly in the ...
Sudhansu Sekhar Mishra +4 more
doaj +1 more source
Intensity of platelet staining and frequency of emperipolesis events in bone marrow megakaryocytes.
, 2016 Intensity of platelet staining and frequency of emperipolesis events in bone marrow megakaryocytes.
Rami Khoriaty (3181539) +8 more
core +1 more source
Megakaryocyte emperipolesis arms neutrophils via intracellular provisioning
Neutrophils are phenotypically heterogenous cells that mediate host defense and tissue homeostasis. Here, we identify emperipolesis – the evolutionarily conserved process by which neutrophils pass through megakaryocytes – as a phenotypically ...
Yoichiro Iwakura +22 more
core +1 more source
Emperipolesis of lymphoid cells by human follicular dendritic cells in vitro.
, 1992 peer reviewedIsolated follicular dendritic cells (FDCs) showed true and pseudoemperipolesis of fresh tonsillar lymphocytes, even after long-term (50-day) cultivation.
Mizu Kojima +15 more
core +1 more source
Clinical and Molecular Characteristics of Megakaryocytes in Myelodysplastic Syndrome
Global Medical GeneticsObjective Myelodysplastic syndrome (MDS) is a malignant clonal disorder of hematopoietic stem cells which is characterized by morphologic dysplasia.
Fangxiu Luo +6 more
doaj +1 more source
, 2017 Natural killer (NK) cells can induce liver fibrosis remission by killing hepatic stellate cells (HSCs) and producing interferon (IFN)-γ in a mouse model; however, their anti-fibrotic immune-characteristics and regulatory mechanisms by HSCs remain to be ...
Bo Tu +13 more
core +1 more source
Purely cutaneous rosai-dorfman disease with immunohistochemistry
Indian Journal of Dermatology, 2013 Background: The cutaneous form of Rosai-Dorfman disease (RDD) is a rare entity that manifests solely with skin papules or nodules and does not present with the usual myriad of symptoms of classical RDD.
Uzma Farooq +3 more
doaj +1 more source
Emperipolesis en síndrome mielodisplásic
, 2019 We report a 73 years old patient with diagnosis of myelodysplastic syndrome made in December 2018. Three months later he developed severe bi-cytopenia associated with febrile syndrome without infectious focus.
Lardo, Marta +6 more
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