Results 41 to 50 of about 1,911 (167)
A rare case of purely cutaneous Rosai–Dorfman’s disease: Xanthoma-like presentation
Indian Journal of Dermatopathology and Diagnostic Dermatology, 2022 Rosai–Dorfman’s disease (RDD) is sinus histiocytosis with massive lymphadenopathy. Cutaneous RDD is a rare entity that presents with isolated skin involvement without any systemic involvement. We report a 35-year-old man with an asymptomatic large nodule
Sushanti Jadhav +3 more
doaj +1 more source
Striking emperipolesis in megakaryocytes of gray platelet syndrome [PDF]
Blood, 2019 ![Figure][1] An 11-year-old girl was diagnosed with gray platelet syndrome (GPS) with compound heterozygous NBEAL2 mutations after presenting with recurrent epistaxis and thrombocytopenia. Bone marrow examination was performed to evaluate for myelofibrosis.
Eric McGinnis, Kate M. Chipperfield
openaire +2 more sources
Primary Tracheal Rosai‐Dorfman Disease Coexisting With Active Pulmonary Tuberculosis
Respirology Case Reports, Volume 14, Issue 8, August 2026.We report a rare case of primary tracheal Rosai‐Dorfman disease (RDD) with active pulmonary tuberculosis. Bronchoscopic resection immediately relieved > 90% airway obstruction, and anti‐tuberculosis therapy was given, resulting in no recurrence at one‐year follow‐up. ABSTRACT Rosai‐Dorfman disease (RDD) rarely involves the trachea, and active pulmonary
Shijie Yang +4 more
wiley +1 more source
Cell-in-Cell Structures in the Liver: A Tale of Four E’s
Frontiers in Immunology, 2020 The liver is our largest internal organ and it plays major roles in drug detoxification and immunity, where the ingestion of extracellular material through phagocytosis is a critical pathway. Phagocytosis is the deliberate endocytosis of large particles,
Scott P. Davies +4 more
doaj +1 more source
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
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
A Recurrent Indurated Plaque on the Thigh
JEADV Clinical Practice, EarlyView.
Tram T. Tran +3 more
wiley +1 more source
Chronic Pruritic Papular Eruption in an Elderly Man
JEADV Clinical Practice, EarlyView.
Filipe Monteiro +6 more
wiley +1 more source
Indonesian Biomedical JournalBACKGROUND: Ultraviolet B (UVB) radiation is commonly known to be related to skin inflammation. The inflammation process is orchestrated by many cell types, including immune cells.
Verda Farida +3 more
doaj +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