Extra nodal Rosai-Dorfman disease originating in the nasal and paranasal complex and gnathic bones: a systematic analysis of seven cases and review of literature

J Ojha, YB Rawal, JL Hornick, K Magliocca… - Head and Neck …, 2020 - Springer
Rosai-Dorfman disease (RDD) is a benign, self-limiting histiocytosis of unknown etiology.
The classic form of the condition includes a painless cervical lymphaenopathy accompanied …

Rosai–Dorfman disease: a rare clinicopathological presentation and review of the literature

A Azari-Yaam, MR Abdolsalehi, M Vasei… - Head and neck …, 2021 - Springer
Rosai–Dorfman disease (RDD) is a rare and self-limiting disease process that presents most
commonly in young patients as massive, painless, cervical lymphadenopathy. Extranodal …

Uncommon Fibroinflammatory Sinonasal Tract Lesions: Granulomatosis with Polyangiitis, Eosinophilic Angiocentric Fibrosis, and Rosai–Dorfman Disease

LDR Thompson - Surgical Pathology Clinics, 2024 - Elsevier
Understanding and including in the differential diagnoses of necro-inflammatory lesions that
affect the SNT, disorders like GPA, EAF, and RDD, will use a systematic approach to …

Isolated bilateral orbital and paranasal Rosai-Dorfman disease affecting two brothers: a case report and a systematic literature review

HM Alsulaiman, R Alanazi, S Elkhamary, A Maktabi… - Orbit, 2025 - Taylor & Francis
ABSTRACT A systematic literature review revealed 88 Rosai–Dorfman Disease (RDD)
cases affecting the orbit. We present a review of the literature on orbital RDD in addition to …

Atypical primary cutaneous Rosai Dorfman disease: A case report

AE Kinio, MA Sawchuk, M Pratt - Journal of Cutaneous …, 2017 - journals.sagepub.com
Background: Rosai Dorfman disease (RDD) is a rare disorder that typically presents with
bilateral cervical lymphadenopathy and follows a benign course. Objective: We present a …

[HTML][HTML] Rosai-Dorfman sphenoorbital histiocytosis with intraparenchymal invasion: Do we have to consider this skull base pathology as a malignant disease?

E Burgos-Sosa, JJJ Mendoza… - Surgical Neurology …, 2024 - pmc.ncbi.nlm.nih.gov
Background: Rosai-Dorfman disease (RDD) is a rare type of histiocytosis that can manifest
with diverse symptoms. It usually presents with systemic involvement, and only a few cases …

Rosai–Dorfman‐type histiocytes occur in eosinophilic chronic rhinosinusitis and potentially play a role in disease initiation and persistence

MJ Wilsher, F Bonar - Histopathology, 2016 - Wiley Online Library
Aims We recently identified the presence of Rosai–Dorfman‐type histiocytes (RDH) in
sinonasal tissue removed from individuals with eosinophilic chronic rhinosinusitis (ECR) …

Синусовый гистиоцитоз нелангенгарсного типа с поражением кожи челюстно-лицевой области (болезнь Розаи-Дорфмана). Клиническое наблюдение

НВ Калакуцкий, ИБ Баранова, ТН Овсепян… - Стоматология, 2021 - elibrary.ru
В челюстно-лицевой хирургии периодически встречаются случаи длительно
протекающего хронического воспаления мягких тканей без положительного эффекта от …

[PDF][PDF] SINONASAL ROSAI-DORFMAN DISEASE–IS IT A SURGICAL

I Hazkani, N Schwartz, T Kogan, F Kassem - medicalconnections.ro
Rezumat Introducere: Boala Rosai-Dorfman (BRD), cunoscută și sub numele de histiocitoză
sinusală cu limfadenopatie masivă, este o boală rară, idiopatică, benignă, caracterizată …

Extranodal Rosai–Dorfman Disease of Oropharynx: A Rare Disease with Unusual Site of Presentation

J Kumar, P Kaur, A Khurana… - … DISEASE & Health, 2016 - classical.goforpromo.com
Rosai–Dorfman disease is a rare histiocytic disease which is most frequently seen in
children and young adults. Extra nodal site of oropharynx is rare. A rare case of extranodal …