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10.1007/s11926-017-0656-6 http://scihub22266oqcxt.onion/10.1007/s11926-017-0656-6 C5388731!5388731!28401384     free     free     free Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Curr+Rheumatol+Rep 2017 ; 19 (5): ä Nephropedia Template TP {{tp|p=28401384|t=2017. Bone Involvement in Rosai-Dorfman Disease (RDD): a Case Report and Systematic Literature Review |pdf=|usr=}}{{28401384}} gab.com Text Bone Involvement in Rosai-Dorfman Disease (RDD): a Case Report and Systematic Literature Review JO: Curr Rheumatol Rep http://www.kidney.de/pget.php?&tw=1&pmid=28401384 #FOAvip Purpose of Review: Rosai-Dorfman disease (RDD) is a rare histiocytic disorder typically presenting as painless cervical lymphadenopathy. Extranodal involvement is common and may also affect bones. Here, we present a patient with typical nodal disease and multifocal bone manifestations. Further, a systematic literature review was performed to better understand the phenotype, clinical course and treatment options of such patients. Recent Findings: RDD is a nonmalignant, classically sporadic histiocytosis. Nevertheless, increasing evidence also suggests familial forms of the disease. According to our literature review, bone involvement is exceedingly rare and heterogeneous. Clinical outcome in terms of mortality seems to be favorable in most cases. Currently, therapy strategies include surgical and immunosuppressive treatments, but the optimal treatment of osseous RDD remains to be defined. Summary: Patients with osseous RDD may present to rheumatologists with arthralgia or arthritis. Due to the rarity of the disease, diagnosis and treatment remain challenging. Electronic supplementary material: The online version of this article (doi:10.1007/s11926-017-0656-6) contains supplementary material, which is available to authorized users. Twit Text FOAVip Bone Involvement in Rosai-Dorfman Disease (RDD): a Case Report and Systematic Literature Review ????Curr Rheumatol Rep http://www.kidney.de/pget.php?&tw=1&pmid=28401384 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28401384 #FOAvip English Wikipedia <ref>{{Cite pmid|28401384}}</ref> Bone Involvement in Rosai-Dorfman Disease (RDD): a Case Report and Systematic Literature Review #MMPMID28401384 Mosheimer BA; Oppl B; Zandieh S; Fillitz M; Keil F; Klaushofer K; Weiss G; Zwerina J Curr Rheumatol Rep 2017[]; 19 (5): ä PMID28401384show ga Purpose of Review: Rosai-Dorfman disease (RDD) is a rare histiocytic disorder typically presenting as painless cervical lymphadenopathy. Extranodal involvement is common and may also affect bones. Here, we present a patient with typical nodal disease and multifocal bone manifestations. Further, a systematic literature review was performed to better understand the phenotype, clinical course and treatment options of such patients. Recent Findings: RDD is a nonmalignant, classically sporadic histiocytosis. Nevertheless, increasing evidence also suggests familial forms of the disease. According to our literature review, bone involvement is exceedingly rare and heterogeneous. Clinical outcome in terms of mortality seems to be favorable in most cases. Currently, therapy strategies include surgical and immunosuppressive treatments, but the optimal treatment of osseous RDD remains to be defined. Summary: Patients with osseous RDD may present to rheumatologists with arthralgia or arthritis. Due to the rarity of the disease, diagnosis and treatment remain challenging. Electronic supplementary material: The online version of this article (doi:10.1007/s11926-017-0656-6) contains supplementary material, which is available to authorized users. äBone Involvement in Rosai-Dorfman Disease (RDD): a Case Report and Sys(epmc).pdf DeepDyve Pubget Overpricing