Results 71 to 80 of about 1,868 (215)

Rosai and Dorfman Disease with Pleural Involvement: Case Report

open access: yesThe Scientific World Journal, 2008
Sinus histiocytosis with massive lymphadenopathy (SHLM) disease is considered to be an indolent and self-limiting pathology. However, severe morbidity and mortality have been attributed to complications of SHLM.
Jouda Cherif   +5 more
doaj   +1 more source

Toxoplasma IgG Expressed in a Patient With Rosai-Dorfman Disease

open access: yesKaohsiung Journal of Medical Sciences, 2010
Rosai-Dorfman Disease (RDD) is a rare benign disease characterized by sinus histiocytosis with massive lymphadenopathy. RDD can be differentiated from other types of histiocytosis by immunochemical analysis, as RDD is positive for S100.
Hung-Ju Liao, Ching-Wen Chiang
doaj   +1 more source

Sinus histiocytosis with massive lymphadenopathy [PDF]

open access: yes, 2019
Two cases of a recently described entity, 'sinus histiocytosis with massive lymphadenopathy,' occurring in Black males, are reported. Prominent cervical adenopathy was the main presenting feature in both. Histologically, these nodes were characterised by
Kahn, L.B.   +2 more
core   +1 more source

Fine-needle aspiration cytology of Rosai-Dorfman disease of bone [PDF]

open access: yes, 2008
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a rare, benign self-limiting condition of unknown etiology. Less than a quarter of cases have only extranodal involvement and a few cases of skeletal involvement of Rosai-Dorfman
Jing, Xin   +2 more
core   +1 more source

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): a case report and review of Literature

open access: yesJournal of Health Science and Medical Research (JHSMR), 2003
Sinus histiocytosis with massive lymphadenopathy (SHML) or Rosai-Dorfman disease is an unusual, benign, selflimited condition of unknown etiology which generally presents as massive bilateral cervical lymphadenopathy in children.
R Tangsathitporn, A Nitiruangjarus
doaj  

International Consensus Statement on Allergy and Rhinology: Sinonasal Tumors

open access: yesInternational Forum of Allergy &Rhinology, Volume 14, Issue 2, Page 149-608, February 2024.
Abstract Background Sinonasal neoplasms, whether benign and malignant, pose a significant challenge to clinicians and represent a model area for multidisciplinary collaboration in order to optimize patient care. The International Consensus Statement on Allergy and Rhinology: Sinonasal Tumors (ICSNT) aims to summarize the best available evidence and ...
Edward C. Kuan   +158 more
wiley   +1 more source

Synchronous occurrence of primary cutaneous B‐cell lymphoma and cutaneous Rosai–Dorfman disease in distinct lesions: A unique association

open access: yesJournal of Cutaneous Pathology, Volume 51, Issue 1, Page 7-10, January 2024.
Abstract Rosai–Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy (SHML), is a rare subtype of reactive histiocytosis which is seldom associated with Hodgkin's and non‐Hodgkin's lymphomas. To date, the coexistence in the same patient of extra nodal SHML and primary cutaneous B‐cell lymphoma (PCBCL) has been reported in the ...
Gabriele Roccuzzo   +8 more
wiley   +1 more source

A case of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) in a patient with diffuse large B-cell lymphoma and chronic hepatitis B virus infection

open access: yesТерапевтический архив, 2012
The paper describes a case of diffuse large B-cell lymphoma detected in a patient 13 months after sinus histiocytosis with massive lymphadenopathy (SHML) or Rosai-Dorfman disease (RDD) being diagnosed together with active hepatitis B virus infection ...
A L Melikian   +3 more
doaj  

Unique Presentation of Rosai-Dorfman Disease as Concomitant Appendiceal and Rectal Masses with IgG4-Positive Plasma Cells Diagnosed by Core Needle Biopsy

open access: yesCase Reports in Oncological Medicine, 2020
Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a rare non-Langerhans cell histiocytosis. We report a case of a 69-year-old male with concurrent appendiceal and rectal masses who underwent CT-guided percutaneous ...
Jenna J. Poldemann   +2 more
doaj   +1 more source

Paranasal Rosai-Dorfman Disease with Osseous Destruction [PDF]

open access: yes, 2017
Rosai-Dorfman disease is a rare histiocytic proliferative disorder of unknown etiology typically characterized by cervical lymphadenopathy. Extranodal involvement often manifests in the head and neck region. We present a 10-year-old male who presented to
Changxing Liu   +2 more
core   +2 more sources

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