Results 131 to 140 of about 2,541 (165)

Intracranial Rosai–Dorfman disease

Journal of Clinical Neuroscience, 2016
Rosai-Dorfman disease (RDD) is a rare histioproliferative disorder that only occasionally involves the central nervous system. We present the diagnosis and treatment of five patients with intracranial RDD. The patients were preoperatively misdiagnosed as meningioma or eosinophilic granuloma.
Bo Yuan, Huang   +5 more
openaire   +2 more sources

Rosai-Dorfman Disease

American Journal of Gastroenterology, 2017
Rosai–Dorfman disease (RDD) is a benign non-Langerhans cell histiocytic disorder that usually presents with massive lymphadenopathy and sinus histiocytosis, although at least 40% of patients can have extranodal involvement. Recent studies found NRAS, KRAS, and ARAF mutations in a subset of patients with RDD, but no BRAF-V600E mutations have been ...
G. Petur Nielsen   +5 more
  +4 more sources

Rosai-Dorfman Disease

Cutis, 2015
Rosai-Dorfman disease is a rare systemic disease characterized by a histiocyte proliferation which presents with lymphadenopathy. Some patients present with extranodal disease.
Alyssa, Miceli   +2 more
  +5 more sources

Cerebral Rosai–Dorfman disease

Child's Nervous System, 2015
Sinus histiocytosis (Rosai-Dorfman disease) with massive lymphadenopathy is a rare nonneoplastic and nonlangerhans cell proliferation disorder of the histiocytes. Extranodal location with or without lymphadenopathy occurs in about 40 % of the cases. Intracranial location is rare in children often mimicking meningiomas. The parasphenoidal region is more
Wolf, Lüdemann   +4 more
openaire   +2 more sources

Rosai-Dorfman Disease

Singapore medical journal, 2011
Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease, is a rare histiocytic proliferative disorder of unknown aetiology. The classic presentation of Rosai-Dorfman disease is massive, bilateral, painless cervical lymphadenopathy.
Nooshin K. Brinster   +3 more
openaire   +3 more sources

Giant intracranial Rosai–Dorfman disease

Journal of Clinical Neuroscience, 2004
Rosai-Dorfman disease is a rare, non-neoplastic disease characterized by an unusual proliferation of histiocytic cells. It rarely manifests intracranially, and only 50 cases of intracranial lesions have been reported. We describe an unusual case of a huge, solid mass in the paranasal sinuses, orbits, cavernous sinuses, and suprasellar cisterns.
Ture, U   +5 more
openaire   +3 more sources

Rosai-Dorfman disease

The Journal of the Association of Physicians of India, 2018
A young male presented with recurrent neck swellings with initial leucocyte count of 16800/mm3, with non-caseating glands on ultrasonography neck. FNAC showed mixed cellularity with histiocytic and marked lymphophagocytosis as seen in Rosai Dorfman Disease. Immunohistochemistry demonstrated CD 25, Ki 67 and CD 68 in histiocytes.
Facchetti F, Zelger B.
  +8 more sources

Rosai-Dorfman Disease

Ophthalmology, 2023
Benjamin Zhou   +2 more
openaire   +2 more sources

Rosai-Dorfman Disease

Annals of Plastic Surgery, 2019
Abstract Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare and benign proliferative disease that affects histiocytes. Its etiology remains unclear. Rosai-Dorfman disease primarily affects lymph nodes with many extranodal manifestations present, including cutaneous, pulmonary, ophthalmic ...
Reem, Karami   +3 more
openaire   +2 more sources

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