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10.1136/bcr-2013-201764 http://scihub22266oqcxt.onion/10.1136/bcr-2013-201764 C3948389!3948389!24717855     free     free     free Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       BMJ+Case+Rep 2014 ; 2014 (ä): ä Nephropedia Template TP {{tp|p=24717855|t=2014. Atypical Henoch-Schonlein purpura? Consider polyarteritis nodosa!|pdf=|usr=}}{{24717855}} gab.com Text Atypical Henoch-Schonlein purpura Consider polyarteritis nodosa! JO: BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=24717855 #FOAvip We describe the case of a previously healthy 12-year-old boy admitted to a tertiary paediatric centre with the clinical diagnosis of Henoch-Schonlein purpura (HSP). Symptoms on admission included a generalised rash, colicky abdominal pain, hypertension, proteinuria and fresh rectal bleeding. Abdominal pain and distension worsened and serial ultrasounds suggested bowel ischaemia. He underwent repeat laparotomy and bowel resection, with slow improvement after the second laparotomy. The severity of systemic involvement (gastrointestinal, cardiac, renal and skin) made the initial diagnosis of HSP questionable. Immunohistochemistry of skin biopsies was negative for HSP. Histopathology of the bowel specimen revealed features of necrotising small and medium vessel vasculitis in keeping with polyarteritis nodosa. Twit Text FOAVip Atypical Henoch-Schonlein purpura Consider polyarteritis nodosa!????BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=24717855 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24717855 #FOAvip English Wikipedia <ref>{{Cite pmid|24717855}}</ref> Atypical Henoch-Schonlein purpura? Consider polyarteritis nodosa! #MMPMID24717855 Braungart S; Campbell A; Besarovic S BMJ Case Rep 2014[]; 2014 (ä): ä PMID24717855show ga We describe the case of a previously healthy 12-year-old boy admitted to a tertiary paediatric centre with the clinical diagnosis of Henoch-Schonlein purpura (HSP). Symptoms on admission included a generalised rash, colicky abdominal pain, hypertension, proteinuria and fresh rectal bleeding. Abdominal pain and distension worsened and serial ultrasounds suggested bowel ischaemia. He underwent repeat laparotomy and bowel resection, with slow improvement after the second laparotomy. The severity of systemic involvement (gastrointestinal, cardiac, renal and skin) made the initial diagnosis of HSP questionable. Immunohistochemistry of skin biopsies was negative for HSP. Histopathology of the bowel specimen revealed features of necrotising small and medium vessel vasculitis in keeping with polyarteritis nodosa. äAtypical Henoch-Schonlein purpura? Consider polyarteritis nodosa!(epmc).pdf DeepDyve Pubget Overpricing