Results 11 to 20 of about 4,878 (159)

Rosai-Dorfman Disease, Presenting as a Mass in the Trachea: A Case Report. [PDF]

open access: yesRespirol Case Rep
We present a rare case of Rosai–Dorfman disease (RDD) confined solely to the trachea. After initial bronchoscopic resection, systemic corticosteroid therapy was initiated due to lesion progression, successfully stabilizing the disease for 4 years. ABSTRACT A 45‐year‐old woman was referred to our clinic for evaluation of a 17 mm tracheal mass detected ...
Youn T, Lee B, Han J, Jeong BH.
europepmc   +2 more sources

Intrathoracic Rosai-Dorfman Disease in Elderly Patients: A Case Report. [PDF]

open access: yesClin Case Rep
ABSTRACT Rosai–Dorfman disease (RDD), a rare form of histiocytosis, predominantly affects young individuals. Clinically categorized into nodal and extranodal subtypes, the disease primarily involves systemic lymph nodes with possible involvement of other organs.
Xiao J, Ma L, Cao W.
europepmc   +2 more sources

Emergence of cutaneous Rosai–Dorfman disease during immunosuppressive treatment of follicular B-cell lymphoma: A case report

open access: yesSAGE Open Medical Case Reports, 2021
Background: Sinus histiocytosis with massive lymphadenopathy, also known as Rosai–Dorfman disease, is a rare proliferation of non-Langerhans histiocytes.
Sharon L Kipfer   +2 more
doaj   +1 more source

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

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

Orbital involvement in Rosai-Dorfman disease [PDF]

open access: yes, 2011
A doença de Rosai-Dorfman (DRD) ou histiocitose sinusal com linfadenopatia maciça é uma entidade clínica idiopática, rara e benigna, caracterizada pela proliferação histiocitária com linfofagocitose. Geralmente se apresenta com linfoadenomegalia cervical,
GONÇALVES, Allan C. Pieroni   +4 more
core   +2 more sources

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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