Results 11 to 20 of about 1,427 (174)
A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations
Journal 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
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The Clinicopathologic Spectrum of Rosai-Dorfman-Destombes Disease in Adults: An Analysis of 16 Cases. [PDF]
Eur J HaematolABSTRACT Rosai–Dorfman–Destombes disease (RDD) is a rare histiocytic proliferation with protean clinical manifestations, resulting from the accumulation of activated histiocytes within nodal and extra‐nodal tissues. The diagnosis can be missed, particularly when biopsies are obtained from extra‐nodal sites, where histological features may be less ...
Trinder M +8 more
europepmc +2 more sources
Histocytopathological diagnosis of Rosai–Dorfman disease: Case report
Clinical 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
Clinical 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
Lung 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
British Journal of Haematology, Volume 203, Issue 3, Page 369-383, November 2023., 2023 The simultaneous existence of two classifications of haemato‐lymphoid tumours poses problems not only for diagnosis formulation but also for patients' management and design of clinical trials. Summary Since the publication in 2017 of the revised 4th Edition of the World Health Organization (WHO) classification of haematolymphoid tumours, here referred ...
Brunangelo Falini +2 more
wiley +1 more source
A case of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman syndrome) from western India. [PDF]
Mcgill J Med, 2008 Jani PA, Banjan D.
europepmc +3 more sources
Bilateral breast Rosai‐Dorfman disease screen detected by mammography
Clinical Case Reports, Volume 11, Issue 3, March 2023., 2023 Rosai‐Dorfman disease (RDD) is a rare proliferative disorder of histiocytes typically found in nodal sites, however, it can also present initially as an asymptomatic mass in the breast. Presenting symptoms may include fever, lymphadenopathy, and weight loss. Tissue sampling is definitive for diagnosis and close surveillance is recommended.
Christina Sumner +6 more
wiley +1 more source
Case Reports in Ophthalmological Medicine, Volume 2023, Issue 1, 2023., 2023 Background. This study is aimed at exploring a case of choroidal Langerhans cell histiocytosis (LCH) successfully treated with systemic corticosteroid and immunosuppressant. Case presentation. A 24‐year‐old man with known multisystem LCH developed loss of vision, ocular pain, conjunctival injection, panuveitis, and a ciliochoroidal mass.
Fariba Ghassemi +5 more
wiley +1 more source
Patient with Rosai-Dorfman-Destombes disease: 18F-FDG-PET/CT scan as a diagnostic tool
Acta 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