Paranasal Rosai-Dorfman Disease with Osseous Destruction [PDF]
, 2017 Rosai-Dorfman disease is a rare histiocytic proliferative disorder of unknown etiology typically characterized by cervical lymphadenopathy. Extranodal involvement often manifests in the head and neck region. We present a 10-year-old male who presented to
Changxing Liu +2 more
core +2 more sources
Sinus histiocytosis with massive lymphadenopathy : is the lymph node enlargement always massive? [PDF]
, 2007 Sinus histiocytosis with massive lymphadenopathy (SHML) is a benign proliferating histiocytic disorder, predominantly of lymph nodes with extra-nodal involvement in some cases.
Jain, Shyama +2 more
core
Increased and pathologic emperipolesis of neutrophils within megakaryocytes associated with marrow fibrosis in GATA-1low mice [PDF]
, 2004 Lucia Centurione +9 more
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Emperipolesis of erythroblasts within Kupffer cells during hepatic hemopoiesis in human fetus [PDF]
, 1999 Won Bok Lee +3 more
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Rosai-Dorfman Disease Presenting as Recurrent Nasal Polyposis
Philippine Journal of Otolaryngology Head and Neck Surgery, 2014 Objective: To present a case of Rosai-Dorfman disease in an individual with a 14-year history of recurrent nasal polyposis, and discuss its clinical presentation, physical examination, radiologic findings, histopathologic characteristics, and available ...
Neil Louis L. Apale +2 more
doaj +1 more source
Extranodal Rosai-Dorfman disease involving soft tissue associated with increased IgG4 plasma cells
Human Pathology: Case Reports, 2021 Background: Rosai-Dorfman disease (RDD) is a rare entity characterized by lymphadenopathy with dilated lymph node sinuses containing lymphocytes, plasma cells, and histiocytes exhibiting emperipolesis.
Karen D. Thomas +4 more
doaj
Emperipolesis, Apoptosis and Hemophagocytosis during Acute Epstein-Barr Virus (EBV) infection: A Case Report [PDF]
, 2023 Bandana Mehrotra
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Rosai-Dorfman disease in a 12-year-old Nigerian male
South African Journal of Child Health, 2016 Rosai-Dorfman disease is a rare disorder of systemic histioproliferation, first described in 1969 by Juan Rosai and Ronald Dorfman. It is characterised by massive lymphadenopathy, particularly of the head and neck region, and it is sometimes associated ...
Jacintha Chinyere Elo-Ilo +2 more
doaj
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