Results 1 to 10 of about 434 (96)

Concomitant sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) and diffuse large B-cell lymphoma: a case report [PDF]

open access: goldJournal 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.
James C. Moore   +2 more
openalex   +3 more sources

Sinus Histiocytosis with Massive Lymphadenopathy (Rosai Dorfman Disease) and Anaplastic Large Cell Lymphoma

open access: goldEuropean Journal of Case Reports in Internal Medicine, 2017
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare and benign source of lymphadenopathy first described in 1969. This disease commonly presents in children and young adults with supra-diaphragmatic lymphadenopathy mainly at cervical nodal ...
Kapil Garg, Harpreet Singh
openalex   +3 more sources

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease): Report of a case in a Nigerian Teaching Hospital

open access: hybridNigerian Dental Journal, 2011
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare, benign disease of unknown aetiology. This disease typically presents with massive, painless cervical lymphadenopathy but may occur in a wide variety of extranodal sites.
O. F. Ajayi   +4 more
openalex   +4 more sources

Rosai-Dorfman disease: a report of eight cases in a tertiary care center and a review of the literature [PDF]

open access: yesBrazilian Journal of Medical and Biological Research, 2015
Rosai-Dorfman disease (RDD) is a nonmalignant histiocytic disorder of unknown origin that is extremely rare. By immunohistochemistry, the RDD cells are characteristically S-100 positive and CD1a negative.
R.C. Maia   +4 more
doaj   +3 more sources

Histocytopathological diagnosis of Rosai–Dorfman disease: Case report

open access: yesClinical Case Reports, 2022
Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) being a rare benign proliferative self‐limiting disease of the cells of macrophage‐histiocyte family is of unknown etiology and presents with massive lymphadenopathy.
Zephania Saitabau Abraham   +4 more
doaj   +1 more source

Rosai‐Dorfman disease in 6‐year‐old child: Presentation, diagnosis, and treatment

open access: yesClinical Case Reports, 2021
Rosai‐Dorfman disease is referred to as sinus histiocytosis massive lymphadenopathy. We are reporting a rare case of Rosai‐Dorfman disease, a case of 6‐year‐old boy with a history of multiple painless submandibular and cervical lymphadenopathy.
Kalpana Giri   +3 more
doaj   +1 more source

Rosai–Dorfman disease presenting as internal jugular vein thrombosis and middle lobe collapse-consolidation

open access: yesLung India, 2020
Rosai–Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy, is a rare and benign disease that usually presents as massive and painless cervical lymphadenopathy.
Ambika Sharma   +5 more
doaj   +1 more source

A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations

open access: yesJournal of Cutaneous Immunology and Allergy, 2023
Rosai–Dorfman disease (RDD) is a rare non‐Langerhans cell histiocytosis that was first described as sinus histiocytosis with massive lymphadenopathy by Rosai and Dorfman in 1969.
Shintaro Saito   +3 more
doaj   +1 more source

Patient with Rosai-Dorfman-Destombes disease: 18F-FDG-PET/CT scan as a diagnostic tool

open access: yesActa Médica Peruana, 2023
Rosai-Dorfman-Destombes disease (RDD) is a rare non-Langerhans cell histiocytosis, with sinus involvement and massive lymphadenopathy. RDD is usually self-limited; it can appear alone or related to other diseases. We present a 9-year-old male with biopsy
Luis C. Araujo Cachay
doaj   +1 more source

Intriguing nodules mimicking as leprosy: An interesting case report

open access: yesClinical Dermatology Review, 2023
The differential diagnosis of disseminated infiltrated cutaneous nodules includes a plethora of disorders ranging from the more frequently encountered infective and granulomatous conditions to the obscure ones with proliferative and malignant origin ...
Vasudha A Belgaumkar   +2 more
doaj   +1 more source

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