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10.1093/omcr/omx024 http://scihub22266oqcxt.onion/10.1093/omcr/omx024 C5471450!5471450!28638624     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Oxf+Med+Case+Reports 2017 ; 2017 (6): ä Nephropedia Template TP {{tp|p=28638624|t=2017. Kikuchi?Fujimoto disease: a case report of a multi-drug resistant, grueling disease |pdf=|usr=}}{{28638624}} gab.com Text Kikuchi Fujimoto disease: a case report of a multi-drug resistant, grueling disease JO: Oxf Med Case Reports http://www.kidney.de/pget.php?&tw=1&pmid=28638624 #FOAvip Histiocytic necrotizing lymphadenitis or Kikuchi?Fujimoto disease (KFD) is characterized by its rare occurrence. Mostly prevalent among Asian women, KFD manifests with lymphadenopathy?affecting mostly cervical and rarely generalized or retroperitoneal regions?in addition to fever. It is a self-limited disease that resolves within 1?4 months, responding remarkably to glucocorticosteroids or hydroxychloroquine. However, some rare cases prove to be unresponsive to the previously mentioned therapies. Here is a description of a case of KFD affecting a 67-year-old Syrian woman with a history of hypothyroidism due to iodine-deficiency. The patient?s initial clinical picture was malaise, fever, pericarditis and generalized lymphadenopathy. As treatment, she was given glucocorticosteroids with no significant response, while hydroxychloroquine proved to be partially effective. Until the date of this report, she has been receiving hydroxychloroquine with only slight clinical improvement. This case is proving to be resistant unlike most KFD cases that generally respond very well to treatment. Twit Text FOAVip Kikuchi Fujimoto disease: a case report of a multi-drug resistant, grueling disease ????Oxf Med Case Reports http://www.kidney.de/pget.php?&tw=1&pmid=28638624 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28638624 #FOAvip English Wikipedia <ref>{{Cite pmid|28638624}}</ref> Kikuchi?Fujimoto disease: a case report of a multi-drug resistant, grueling disease #MMPMID28638624 Youssef A; Ali R; Ali K; AlShehabi Z Oxf Med Case Reports 2017[Jun]; 2017 (6): ä PMID28638624show ga Histiocytic necrotizing lymphadenitis or Kikuchi?Fujimoto disease (KFD) is characterized by its rare occurrence. Mostly prevalent among Asian women, KFD manifests with lymphadenopathy?affecting mostly cervical and rarely generalized or retroperitoneal regions?in addition to fever. It is a self-limited disease that resolves within 1?4 months, responding remarkably to glucocorticosteroids or hydroxychloroquine. However, some rare cases prove to be unresponsive to the previously mentioned therapies. Here is a description of a case of KFD affecting a 67-year-old Syrian woman with a history of hypothyroidism due to iodine-deficiency. The patient?s initial clinical picture was malaise, fever, pericarditis and generalized lymphadenopathy. As treatment, she was given glucocorticosteroids with no significant response, while hydroxychloroquine proved to be partially effective. Until the date of this report, she has been receiving hydroxychloroquine with only slight clinical improvement. This case is proving to be resistant unlike most KFD cases that generally respond very well to treatment. äKikuchi?Fujimoto disease: a case report of a multi-drug resistant, gru(epmc).pdf DeepDyve Pubget Overpricing