Results 51 to 60 of about 1,868 (215)
Tissue‐Resident Myeloid and Histiocytic Cells in Health and Disease: Novel Emerging Concepts
American Journal of Hematology, Volume 100, Issue 12, Page 2305-2319, December 2025.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
Primary Rosai-Dorfman Disease of Bone: A Report of Two Cases
Case Reports in Radiology, 2019 Rosai-Dorfman disease (RDD), sometimes known as sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic disorder that most commonly presents as painless, massive cervical lymphadenopathy in young adults. Extranodal disease can occur in up
Andrew B. Ross +3 more
doaj +1 more source
Persistent Cutaneous Papules and Nodules in a Six-year-old Child: A Quiz
Acta Dermato-Venereologica, 2022 is missing (Quiz)
Jeanette Halskou Haugaard +3 more
doaj +1 more source
Diagnostic challenges in Rosai-Dorfman-Destombes disease (case description and literature review) [PDF]
, 2018 The described clinical case presents 39-year-old patient with no clinically significant accompanying diseases. Since the beginning of October 2015, the patient has complained of fever, abdominal pain and generalized enlarged lymph nodes.
Gercheva, Liana +3 more
core +2 more sources
Unmasking Rosai-Dorfman disease in a woman with cervical lymphadenopathy: a histopathological insight [PDF]
, 2023 Rosai-Dorfman disease (RDD) also called as sinus histiocytosis with massive lymphadenopathy is a rare benign proliferative self‐limiting disease of the macrophage‐histiocyte cell family.
Doshi, Anoushka A., Nelekar, Shruti B.
core +2 more sources
Sinus histiocytosis with massive lymphadenopathy. Multiple skull involvements [PDF]
Journal of Korean Medical Science, 1998 Sinus histiocytosis with massive lymphadenopathy is a non-neoplastic self-limiting disease of the bone marrow stem cell origin. It is characterized by painless, bilateral cervical lymphadenopathy accompanied by fever, leukocytosis, elevated erythrocyte sedimentation rate and hypergammaglobulinemia. Extranodal involvement including bone is rare.
Y K, Park, Y W, Kim, W S, Choi, Y J, Lim
openaire +2 more sources
SAGE Open Medical Case Reports, 2023 The Rosai-Dorfman disease (RDD) is a kind of sinus histiocytosis with massive lymphadenopathy and is remarkably rare. RDD is characterized by large histiocytes with emperipolesis.
Pingdan Liu +3 more
doaj +1 more source
European Journal of Case Reports in Internal Medicine, 2022 Rosai-Dorfman-Destombes disease (RDD) or sinus histiocytosis with massive lymphadenopathy is a rare non-Langerhans cell histiocytosis of unknown cause.
Kima López-Aldabe +11 more
doaj +1 more source
Rosai dorfman disease of the orbit [PDF]
, 2008 This is an Open Access article distributed under the terms of the Creative Commons Attribution ...
Honavar, Santosh G +2 more
core +4 more sources
Rosai-Dorfman disease of the oral cavity [PDF]
, 2023 First described by J Rosai and R F Dorfman in 1969, Rosai-Dorfman disease (RDD) is a benign, self-limiting histiocytosis of unknown etiology. It is usually seen in the first two decades of life.
Bellalah, Ahlem +5 more
core +2 more sources