Results 81 to 90 of about 283,013 (233)
Rosai-Dorfman Disease: Self-Resolving Unilateral Lymphadenopathy and a Brief Review of Literature
Case Reports in Oncological Medicine, 2018 Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy (SHML), is a disease of histiocytic proliferation with no known pathogenesis.
Joshua Feriante, Richard T. Lee
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Toxoplasma IgG Expressed in a Patient With Rosai-Dorfman Disease
Kaohsiung Journal of Medical Sciences, 2010 Rosai-Dorfman Disease (RDD) is a rare benign disease characterized by sinus histiocytosis with massive lymphadenopathy. RDD can be differentiated from other types of histiocytosis by immunochemical analysis, as RDD is positive for S100.
Hung-Ju Liao, Ching-Wen Chiang
doaj +1 more source
Rosai-Dorfman disease: a report of eight cases in a tertiary care center and a review of the literature [PDF]
Brazilian Journal of Medical and Biological Research, 2014 Rosai-Dorfman disease (RDD) is a nonmalignant histiocytic disorder of unknown origin that is extremely rare. By immunohistochemistry, the RDD cells are characteristically S-100 positive and CD1a negative.
R.C. Maia +4 more
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Bagaimana Prognosis Histiocytosis? Sebuah Laporan Kasus [PDF]
, 2013 Penderita histiocytosis dengan keterlibatan multiorgan dan disertai gangguan fungsi organ mempunyai prognosis buruk dan tingkat mortalitas tinggi. Dilaporkan seorang penderita histiocytosis, usia 1 tahun 1 bulan yang datang dengan kelainan di kulit ...
Lestari, R. D. (Rini) +1 more
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Diagnostic challenges in Rosai-Dorfman-Destombes disease (case description and literature review) [PDF]
, 2018 The described clinical case presents 39-year-old patient with no clinically significant accompanying diseases. Since the beginning of October 2015, the patient has complained of fever, abdominal pain and generalized enlarged lymph nodes.
Gercheva, Liana +3 more
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Journal of Gastrointestinal Cancer, 2012 Sinus histiocytosis with massive lymphadenopathy (SHML) was first described in 1969 by Rosai and Dorfman [1]. It is a rare inflammatory disorder with key clinicopathological characteristics such as emperipolesis and positive immunostaining for S-100 ...
Minerva A. Romero Arenas +3 more
semanticscholar +1 more source
Case Reports in Neurological Medicine, 2017 Polyostotic sclerosing histiocytosis, also known as Erdheim-Chester disease (ECD), is a rare form of non-Langerhans histiocytosis. ECD has wide clinical spectrums which mainly affect skeletal, neurological, dermatological, retroperitoneal, cardiac, and ...
Roaa Ridha Amer +2 more
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Rosai and Dorfman Disease with Pleural Involvement: Case Report
The Scientific World Journal, 2008 Sinus histiocytosis with massive lymphadenopathy (SHLM) disease is considered to be an indolent and self-limiting pathology. However, severe morbidity and mortality have been attributed to complications of SHLM.
Jouda Cherif +5 more
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Pulsatile tinnitus —a review of 84 patients [PDF]
, 2018 Pulsatile tinnitus can be annoying for a patient and can also be the only clue to a potentially devastating and life-threatening disease. In order to understand its clinical spectrum and management better we analysed the files of 84 patients seen at our ...
Mattle, Heinrich +3 more
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Rosai dorfman disease of the orbit [PDF]
, 2008 This is an Open Access article distributed under the terms of the Creative Commons Attribution ...
Honavar, Santosh G +2 more
core +4 more sources