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10.1590/abd1806-4841.20164778 http://scihub22266oqcxt.onion/10.1590/abd1806-4841.20164778 C5087226!5087226!27828641     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       An+Bras+Dermatol 2016 ; 91 (5): 646-8 Nephropedia Template TP {{tp|p=27828641|t=2016. Ofuji disease: a rare dermatosis and its challenging therapeutic approach* |pdf=|usr=}}{{27828641}} gab.com Text Ofuji disease: a rare dermatosis and its challenging therapeutic approach* JO: An Bras Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=27828641 #FOAvip Eosinophilic pustular folliculitis (EPF) or Ofuji disease is a rare dermatosis, prone to recurrence and chronicity. The peak incidence occurs in the third decade of life and its exact etiology remains unknown. Evidence suggests that the expression of adhesion molecules and the production of cytokines activate the follicular unit, but the stimulus that triggers these changes remains unclear. The three clinical variants reported in the literature include classic EPF, immunosuppression-associated EPF, and infancy-associated EPF. We report a case of eosinophilic pustular folliculitis with peculiar epidemiological characteristics, which represents a challenging therapeutic scenario. Twit Text FOAVip Ofuji disease: a rare dermatosis and its challenging therapeutic approach* ????An Bras Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=27828641 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27828641 #FOAvip English Wikipedia <ref>{{Cite pmid|27828641}}</ref> Ofuji disease: a rare dermatosis and its challenging therapeutic approach* #MMPMID27828641 de Brito FF; Martelli ACC; Cavalcante MLLL; Pinto ACVD; Itimura G; Soares CT An Bras Dermatol 2016[Sep]; 91 (5): 646-8 PMID27828641show ga Eosinophilic pustular folliculitis (EPF) or Ofuji disease is a rare dermatosis, prone to recurrence and chronicity. The peak incidence occurs in the third decade of life and its exact etiology remains unknown. Evidence suggests that the expression of adhesion molecules and the production of cytokines activate the follicular unit, but the stimulus that triggers these changes remains unclear. The three clinical variants reported in the literature include classic EPF, immunosuppression-associated EPF, and infancy-associated EPF. We report a case of eosinophilic pustular folliculitis with peculiar epidemiological characteristics, which represents a challenging therapeutic scenario. äOfuji disease: a rare dermatosis and its challenging therapeutic appro(epmc).pdf DeepDyve Pubget Overpricing