Potential role of 18F-FDG PET/CT in a case of progressive Rosai Dorfman disease [PDF]
Asia Oceania Journal of Nuclear Medicine and Biology, 2021 Rosai Dorfman disease is a rare form of nonlangerhans cell histiocytosis, presenting with extensive lymphadenopathies. Treatment in most cases of nodal disease, involves close observation; however, extranodal involvement requires a more definitive ...
Armaghan Fard-Esfahani +4 more
doaj +1 more source
Sinus Histiocytosis: An Uncommon Presentation of an Uncommon Condition [PDF]
, 2015 Introduction Rosai–Dorfman Disease (RDD), also known as Sinus Histiocytosis with Massive Lymphadenopathy (SHML), is a rare, benign, proliferative disorder of macrophages and monocytes that was first described by Rosai and Dorfman in 1969.
Greco, MD, Allison, Kane, MD, Gregory
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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
Rosai Dorfman Disease - A Rare Presentation of Cervical Lymphadenopathy - A Case Report [PDF]
, 2023 Rosai Dorfman disease is an uncommon histiocytic disorder presenting as bilateral cervical lymphadenopathy in children and young adults. Under the revised classification of histiocytic disorders, it is classified in the` R’ group of histiocytosis ...
C. P. Luck +4 more
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Rosai-Dorfman disease presenting as stridor and hoarseness in a young female patient
Radiology Case Reports, 2023 Rosai-Dorfman disease is a non-Langherans cell histiocytosis typically revealed by lymphadenopathy. Extranodal involvement occurs in 43% and most commonly involves the head and neck, skin, and bones. Few reports have described laryngeal lesions.
Vivianne Kokje, MD, PhD +6 more
doaj +1 more source
Fine-needle aspiration cytology of Rosai-Dorfman disease of bone [PDF]
, 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
Unusual presentation of Rosai-Dorfman disease in a 14-month-old Italian child: a case report and review of the literature [PDF]
, 2016 Background: Rosai-Dorfman disease (RDD) is a rare form of histiocytosis characterized by histiocyte proliferation within lymph nodes and extranodal tissue. Here we report an unusual presentation of RDD in an Italian toddler.
Bruzzi, Patrizia +5 more
core +2 more sources
Neuropsychological Aspects of a Patient With Intracranial Rosai-Dorfman Disease: Case Report. [PDF]
Clin Case RepABSTRACT Intracranial Rosai‐Dorfman disease (RDD) is rarely reported in the literature. Up to the present date, there are no documented studies regarding the neuropsychological aspects of a patient with this diagnosis. This study fills this gap, reporting a case of a patient with petroclival RDD, emphasizing the importance of cognitive investigation.
Veras C +6 more
europepmc +2 more sources
Rosai Dorfman disease- A rare entity: Case report in North Indian male
Asian Journal of Medical Sciences, 2014 Rosai Dorfman disease is a rare disease characterized by histiocytic proliferation of lymph node in young adults. We present here the case of a 67 years old Indian male presenting with lymphadenopathy and pyrexia of unknown origin for 16 months duration.
Ankur Baruah
doaj +1 more source
A Rare Case of a Systemic Non-Langerhans Histiocytosis Presenting with Diabetes Insipidus and a Tentorial Mass [PDF]
, 2015 Introduction The histiocytoses are a group of clinically diverse diseases distinguished from one another based on the specific immunophenotype of the lesional cells, implying derivation from the same precursor cell.
Barros, MS, Guilherme +5 more
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