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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease rosai-dorfman disease
Comorbidity C0019618|histiocytosis
Sentences 36
PubMedID- 21475597 sinus histiocytosis with massive lymphadenopathy (shml) is a rare disorder that is characterized by non-malignant proliferation of distinctive histiocytic/phagocytic cells within lymph node sinuses and the lymphatic system in extranodal sites.
PubMedID- 21906971 Sinus histiocytosis with massive lymphadenopathy rosai-dorfman disease: a unique case presentation.
PubMedID- 23739703 sinus histiocytosis with massive lymphadenopathy is a rare self-limitedpseudolymphomatous disorder of unknown etiology.
PubMedID- 24797172 We searched the english literature using pubmed (national library of medicine, bethesda, md) and scopus (elsevier) for the period 1970 to july 2013. for the pubmed search we used the terms rosai-dorfman disease, sinus histiocytosis with massive lymphadenopathy, and central nervous system, and for the scopus search we used the keywords rosai dorfman and central nervous system.
PubMedID- 24249896 rosai-dorfman disease (rdd), also known as sinus histiocytosis with massive lymphadenopathy, is a benign multi-organ non-langerhans cell histiocytic proliferation that was first described in 1969 by rosai and dorfman.
PubMedID- 22028755 The first report of sinus histiocytosis with massive lymphadenopathy (shml) was described in 1959, by destombes as a lipid storage disorder developing after inflammation.4.
PubMedID- 23323110 We describe a rare case of sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease) associated with a six-year history of autoimmune pancreatitis, which was controlled by steroid treatment.
PubMedID- 21331166 sinus histiocytosis with massive lymphadenopathy (shml) involves primarily the cervical nodes, but its histiocytes are morphologically quite different from those of lch.
PubMedID- 24960676 rosai-dorfman disease, or sinus histiocytosis with massive lymphadenopathy (shml), is a rare benign, self-limited disease with a predilection for head and neck involvement.
PubMedID- 23049324 rosai-dorfman disease (rdd) or sinus histiocytosis with massive lymphadenopathy is characterized by non-neoplastic proliferation of histiocytes/phagocytes in the sinusoids of lymph nodes and in extranodal tissues.
PubMedID- 25080658 Sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease) of the true vocal cord.
PubMedID- 25673935 Rdd was first described by rosai and dorfman in 19692 as a sinus histiocytosis with massive lymphadenopathy.
PubMedID- 24966569 sinus histiocytosis with massive lymphadenopathy, also known as rdd, is a rare histiocytic proliferative disorder of unknown etiology.
PubMedID- 24707426 The disease was first described by destombes in 1965 and later, in 1969, rosai-dorfman disease was first reported by juan rosai and roland dorfman as sinus histiocytosis with massive lymphadenopathy in young black males.
PubMedID- 20121618 Primary pancreatic sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease): an unusual extranodal manifestation clinically simulating malignancy.
PubMedID- 20806072 Sinus histiocytosis with massive lymphadenopathy (shml) or rosai-dorfman disease (rdd) is a rare but well-defined benign self-limited clinicopathological entity.
PubMedID- 24610654 Sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease)--imaging manifestations of renal involvement.
PubMedID- 20140240 (abbreviations: shml = sinus histiocytosis with massive lymphadenopathy; iddm = insulin dependent diabetes mellitus; asd = atrial septal defect; ps = pulmonary stenosis; pda = patent ductus areteriosis; tcc = transitional cell carcinoma).
PubMedID- 21139947 In 1969, rosai and dorfman first established sinus histiocytosis with massive lymphadenopathy (shml or rdd) as a clinicopathological entry.1 it typically presents with slowly progressive painless massive cervical lymphadenopathy in young adults and resolves spontaneously.
PubMedID- 25780440 rosai-dorfman disease (rdd), originally known as sinus histiocytosis with massive lymphadenopathy, is a non-langerhans cell histiocytosis that was first described in 1965 by destombes (1) and subsequently recognized as a distinct entity by rosai and dorfman in 1969 (2).
PubMedID- 24145594 rosai-dorfman disease (rdd)-sinus histiocytosis with massive lymphadenopathy-represents a peculiar proliferation of histiocyte-like cells in patients.
PubMedID- 21816647 Sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease) and oligoarthritis.
PubMedID- 21771370 Background: sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease (rdd)) is a rare entity with pathological accumulation of specific, activated macrophages, mainly in cervical lymph nodes.
PubMedID- 21383958 Sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease): a case report and review of 49 cases with fine needle aspiration cytology.
PubMedID- 23252252 [a case of sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease) in a patient with diffuse large b-cell lymphoma and chronic hepatitis b virus infection].
PubMedID- 25992132 Sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease): a case report and literature review.
PubMedID- 23785592 Approximately 365 cases of sinus histiocytosis with massive lymphadenopathy, also known as rosai-dorfman disease, have been described in the literature [2].
PubMedID- 22389884 Sinus histiocytosis with massive lymphadenopathy (shml), also known as rosai-dorfman disease [1], is a rare pathological condition characterized by fever and lymph node enlargement.
PubMedID- 22224025 Rdd (sinus histiocytosis with massive lymphadenopathy) is characterized by massive painless bilateral lymph node enlargement in the neck.
PubMedID- 23267385 In 1969, rosai-dorfman disease first reported by juan rosai and ronald dorfman as sinus histiocytosis with massive lymphadenopathy in young black male.
PubMedID- 19819734 Sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease) is a rare disease that typically occurs in lymph nodes.
PubMedID- 24758864 Background: adrenal gland involvement is a very rare extranodal presentation of sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease).
PubMedID- 25281034 Extranodal sinus histiocytosis with massive lymphadenopathy (rosai-dorfman disease) is a non-neoplastic condition that has rarely been reported to involve the central nervous system.
PubMedID- 24353690 They described four cases called “sinus histiocytosis with massive lymphadenopathy” initially.
PubMedID- 24587931 Here we report a case in a 6-year-old boy of differential diagnoses including dermatopathic lymphadenitis (dl), parasitic infection, kimura's disease, hypersensitivity reactions, cat-scratch disease, sinus histiocytosis with massive lymphadenopathy (shml), hyperplasic lymph nodes, and lymphoma.
PubMedID- 22973396 Sinus histiocytosis with massive lymphadenopathy (shml), also known as rosai-dorfman disease (rdd), was first described by rosai and dorfman in 1969.1 it is a rare idiopathic proliferative disorder that is commonly characterized by painless, massive cervical lymphadenopathy.

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