Results 31 to 40 of about 7,279 (231)

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, Ashok Baral, Niva Tiwari, Krishna Sagar Sharma   +3 more
doaj   +1 more source

Cutaneous Rosai-Dorfman disease

Dermatology Online Journal, 2008
A 63-year-old woman developed multiple nodules at the site of a recently biopsied proliferation of CD 68+ histiocytes. Clinical lymphadenopathy was not present on physical examinaton or on computed tomography scans. A subsequent skin biopsy specimen showed changes consistent with Rosai-Dorfman disease.
Merola, Joseph F, Pulitzer, Melissa, Rosenman, Karla, Brownell, Isaac   +3 more
openaire   +4 more sources

Cutaneous Rosai-Dorfman disease

Dermatology Online Journal, 2006
Sinus histiocytosis with massive lymphadenopathy, or Rosai-Dorfman disease, is a benign idiopathic histiocytic proliferative disorder that commonly involves the lymph nodes but secondarily may involve the skin. However, purely cutaneous disease without lymphadenopathy or internal organ involvement rarely may occur.
Rubenstein, Melissa A, Farnsworth, Neil N, Pielop, Josie A, Orengo, Ida F, Curry, Jonathan L, Drucker, Carol R, Hsu, Sylvia   +6 more
openaire   +4 more sources

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, Claudio De Vito, MD, PhD, Flavia Costa Varela, MD, Yan Monnier, MD, PhD, Nicolas Dulguerov, MD, Minerva Becker, MD, Maxime Mermod, 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, McHugh, Jonathan B., Pu, Robert T.   +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, Coccolini, Elena, Di Dio, Francesco, Iughetti, Lorenzo, Mariotti, Ilaria, Predieri, Barbara   +5 more
core   +2 more sources

Neuropsychological Aspects of a Patient With Intracranial Rosai-Dorfman Disease: Case Report. [PDF]

Clin Case Rep
ABSTRACT 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, de Oliveira DS, Dos Santos SRZ, Ferreira LFL, Filho CAFA, Côrtes BA, Charchat-Fichman H.   +6 more
europepmc   +2 more sources

[Rosai-Dorfman disease].

Annales de dermatologie et de venereologie, 2013
Rosai–Dorfman disease is a benign disease characterized by a proliferation of histiocytes with distinctive cytologic and immunophenotypic features. Also known as sinus histiocytosis with massive lymphadenopathy, Rosai–Dorfman disease is a rare disorder that was described almost simultaneously by Destombes, who reported four cases, and by Rosai and ...
C, Vanhaecke, M-D, Vignon-Pennamen
  +6 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, Farrell, MD, Christopher J, Kenyon, MD, PhD, Lawrence C, Krupa, BS, Kelly, Krupa, BS, Kristin, Madineni, MD, Ravichandra   +5 more
core   +2 more sources