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10.14740/gr912w http://scihub22266oqcxt.onion/10.14740/gr912w C5827906!5827906!29511410     free     free     free       Gastroenterology+Res 2018 ; 11 (1): 64-7 Nephropedia Template TP {{tp|p=29511410|t=2018. A Case of Adolescent Cronkhite-Canada Syndrome |pdf=|usr=}}{{29511410}} gab.com Text A Case of Adolescent Cronkhite-Canada Syndrome JO: Gastroenterology Res http://www.kidney.de/pget.php?&tw=1&pmid=29511410 #FOAvip The Cronkhite-Canada syndrome (CCS) was first reported in 1955, since then more than 500 cases have been reported, indicating an estimated incidence of one case per 1 million inhabitants. The syndrome occurs predominantly in male, with a ratio of three males to two females. Because of the rarity of the syndrome, there are no evidence-based therapies and the treatments described include a combination of therapies, but none is consistently effective. Surgery is usually reserved for the treatment of complications. Herein, we present a case of adolescent CCS. The patient was a 15-year-old boy who presented with watery diarrhea with 20 episodes a day, vomiting and abdominal pain for 4 weeks, with a weight loss of 8.0 kg (15.0% of initial weight). Endoscopic examination revealed polyposis in the stomach, duodenum, and colon. CCS was diagnosed and the patient was treated with a combined corticosteroid and metronidazole. Followed up at 8 month after the diagnosis, the patient was asymptomatic. Twit Text FOAVip A Case of Adolescent Cronkhite-Canada Syndrome ????Gastroenterology Res http://www.kidney.de/pget.php?&tw=1&pmid=29511410 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29511410 #FOAvip English Wikipedia <ref>{{Cite pmid|29511410}}</ref> A Case of Adolescent Cronkhite-Canada Syndrome #MMPMID29511410 Faria MAG; Basaglia B; Nogueira VQM; de Mendonca TBGF; Kaiser Junior RL; Filho IJZ; de Quadros LG Gastroenterology Res 2018[Feb]; 11 (1): 64-7 PMID29511410show ga The Cronkhite-Canada syndrome (CCS) was first reported in 1955, since then more than 500 cases have been reported, indicating an estimated incidence of one case per 1 million inhabitants. The syndrome occurs predominantly in male, with a ratio of three males to two females. Because of the rarity of the syndrome, there are no evidence-based therapies and the treatments described include a combination of therapies, but none is consistently effective. Surgery is usually reserved for the treatment of complications. Herein, we present a case of adolescent CCS. The patient was a 15-year-old boy who presented with watery diarrhea with 20 episodes a day, vomiting and abdominal pain for 4 weeks, with a weight loss of 8.0 kg (15.0% of initial weight). Endoscopic examination revealed polyposis in the stomach, duodenum, and colon. CCS was diagnosed and the patient was treated with a combined corticosteroid and metronidazole. Followed up at 8 month after the diagnosis, the patient was asymptomatic. äA Case of Adolescent Cronkhite-Canada Syndrome (epmc).pdf DeepDyve Pubget Overpricing