Results 11 to 20 of about 6,572 (224)

Rosai-Dorfman Disease in a 4-Month-Old Female Presenting With Cervical Lymphadenopathy. [PDF]

open access: yesClin Case Rep
ABSTRACT Rosai‐Dorfman disease is a rare histiocytic disorder that can mimic malignancies. This case highlights the importance of immunohistochemistry in distinguishing RDD from lymphoproliferative neoplasms, ensuring accurate diagnosis and management.
Khan A   +5 more
europepmc   +2 more sources

Neuropsychological Aspects of a Patient With Intracranial Rosai-Dorfman Disease: Case Report. [PDF]

open access: yesClin Case Rep
ABSTRACT Intracranial Rosai‐Dorfman disease (RDD) is rarely reported in the literature. Up to the present date, there are no documented studies regarding the neuropsychological aspects of a patient with this diagnosis. This study fills this gap, reporting a case of a patient with petroclival RDD, emphasizing the importance of cognitive investigation.
Veras C   +6 more
europepmc   +2 more sources

Temporal bone manifestation of primary extranodal Rosai–Dorfman disease: a case report

open access: yesJournal of Medical Case Reports, 2023
Background Rosai–Dorfman disease is a rare benign histiocytic disorder characterized in most cases by painless cervical adenopathy. Less than 10% of extranodal cases involve bony lesions. Primary bone Rosai–Dorfman disease in the absence of nodal disease
E. Koonar   +3 more
doaj   +1 more source

Intracranial Rosai-Dorfman Disease: pathophysiology, diagnosis and treatment [PDF]

open access: yes, 2022
Introduction and purpose: ​Rosai-Dorfman Disease (RDD), known also as sinus histiocytosis with massive lymphadenopathy(SHML) is a benign histiocytic proliferative syndrome. The etiology and pathogenesis of RDD remains unclear.
Dryla, Aleksandra   +3 more
core   +2 more sources

Rosai Dorfman Disease - A Rare Presentation of Cervical Lymphadenopathy - A Case Report [PDF]

open access: yes, 2023
Rosai Dorfman disease is an uncommon histiocytic disorder presenting as bilateral cervical lymphadenopathy in children and young adults. Under the revised classification of histiocytic disorders, it is classified in the` R’ group of histiocytosis ...
C. P. Luck   +4 more
core   +3 more sources

Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement

open access: yesSouth African Journal of Radiology, 2023
Rosai Dorfman disease is a rare but benign and self-limiting disorder. A case of Rosai Dorfman disease in a 16-year-old female with classic radiological and pathological findings is presented.
Smily Sharma   +3 more
doaj   +1 more source

Histological variability and the importance of clinicopathological correlation in cutaneous Rosai-Dorfman disease [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2016
: Rosai-Dorfman disease is a benign histiocytic proliferative disorder of unknown etiology. The disease mainly affects lymph node tissue, although it is rarely confined to the skin.
Ana Gameiro   +3 more
doaj   +1 more source

Systemic and Craniospinal Rosai Dorfman Disease with Intraparenchymal, Intramedullary and Leptomeningeal Disease

open access: yesInternational Journal of Hematology-Oncology and Stem Cell Research, 2021
Rosai Dorfman disease is a rare histiocytic disorder of over-production of non-Langerhans histiocytes, which typically manifests with massive lymphadenopathy and sinonasal involvement.
Yi Li   +5 more
doaj   +1 more source

Cytological diagnosis of Rosai–Dorfman disease: A study of twelve cases with emphasis on diagnostic challenges

open access: yesJournal of Cytology, 2020
Context: Rosai–Dorfman disease, also known as Sinus histiocytosis with massive lymphadenopathy, is a benign proliferative disorder of histiocytes. It typically affects lymph nodes; however, extranodal disease is being increasingly reported.
Rallapalli Rajyalakshmi   +5 more
doaj   +1 more source

Doença de Rosai-Dorfman cutânea Cutaneous Rosai-Dorfman Disease

open access: yesAnais Brasileiros de Dermatologia, 2009
Doença de Rosai-Dorfman é uma doença benigna e autolimitada. Tem etiologia desconhecida e foi descrita pela primeira vez por Rosai e Dorfman em 1969. As manifestações clássicas incluem linfadenopatia cervical usualmente acompanhada por febre, leucocitose
Fábio Machado Landim   +5 more
doaj   +1 more source

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