Results 21 to 30 of about 4,871,906 (165)
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 +1 more source
H Syndrome Associated With Pure Red Cell Aplasia, Rosai-Dorfman Disease, and Sensorineural Hearing Loss: Phenotypic Variability in Three Children With the Same SLC29A3 Mutation. [PDF]
Clin Case RepABSTRACT H syndrome is a rare autosomal recessive disorder caused by mutations in the SLC29A3 gene. We report three pediatric patients with a homozygous c.1309G>A (p.Gly437Arg) mutation presenting with distinct phenotypic variations. These cases expand the clinical spectrum and emphasize the importance of early genetic diagnosis and family counseling.
Najajrah M +5 more
europepmc +2 more sources
Intracranial Rosai-Dorfman Disease [PDF]
, 2014 Rosai-Dorfman disease (RDD) is a rare, benign pseudolymphomatous condition, predominantly involving lymph nodes. Rosai-Dorfman disease (RDD) (sinus histiocytes with massive lymphadenopathy) rarely affects the intracranial region without involvement of ...
Peng Yi Peng +2 more
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Journal of Medical Case Reports, 2008 Introduction Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman Disease, is a rare and benign source of lymphadenopathy first described in 1969, which mimics neoplastic processes.
Moore James C +2 more
doaj +1 more source
, 2019 Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare and benign proliferative disease that affects histiocytes. Its etiology remains unclear.
Fadi Ghieh +7 more
core +1 more source
Rosai-Dorfman disease presenting as stridor and hoarseness in a young female patient
Radiology Case Reports, 2023 Rosai-Dorfman disease is a non-Langherans cell histiocytosis typically revealed by lymphadenopathy. Extranodal involvement occurs in 43% and most commonly involves the head and neck, skin, and bones. Few reports have described laryngeal lesions.
Vivianne Kokje, MD, PhD +6 more
doaj +1 more source
Potential role of 18F-FDG PET/CT in a case of progressive Rosai Dorfman disease [PDF]
Asia Oceania Journal of Nuclear Medicine and Biology, 2021 Rosai Dorfman disease is a rare form of nonlangerhans cell histiocytosis, presenting with extensive lymphadenopathies. Treatment in most cases of nodal disease, involves close observation; however, extranodal involvement requires a more definitive ...
Armaghan Fard-Esfahani +4 more
doaj +1 more source
Rosai Dorfman disease- A rare entity: Case report in North Indian male
Asian Journal of Medical Sciences, 2014 Rosai Dorfman disease is a rare disease characterized by histiocytic proliferation of lymph node in young adults. We present here the case of a 67 years old Indian male presenting with lymphadenopathy and pyrexia of unknown origin for 16 months duration.
Ankur Baruah
doaj +1 more source
Nasal and Nasopharyngeal Rosai-Dorfman Disease
, 2022 Teaching Point: Nasal and nasopharyngeal Rosai-Dorfman disease is a rare cause of nasal ...
Di Dier, Kelly +2 more
core +1 more source
Emergency Airway Management of a Patient with Rosai-Dorfman Disease
Airway, 2021 Rosai-Dorfman disease is a rare histiocytic disorder that involves the over-production of non-Langerhans sinus histiocytes. It presents with cervical lymphadenopathy and huge neck swelling that could prove to be a challenging airway and a nightmare for ...
Chitta Ranjan Mohanty +4 more
doaj +1 more source