Mixed polyposis coli: Report of a rare entity with review of literature

Journal of Digestive Endoscopy

Kartar Singh¹  Vinita Chaudhary¹  Deepak Kumar Bhasin¹  Manish Manrai¹  Chalapathi Rao¹  Surinder Singh Rana¹  Ritambhra Nada²  Rajesh Gupta³ 

[1] Department of Gastroenterology, Post Graduate Institute of Medical Education and Research (PGIMER), Sector 12, Chandigarh – 160012, India;Department of Histopathology Post Graduate Institute of Medical Education and Research (PGIMER), Sector 12, Chandigarh – 160012, India;Department of Surgery, Post Graduate Institute of Medical Education and Research (PGIMER), Sector 12, Chandigarh – 160012, India;

关键词: rectal bleeding;    hereditary mixed polyposis syndrome;    adenomatous polyps;    hyperplastic polyps;    juvenile polyps;   

DOI  :  10.1055/s-0039-1700270

来源: DOAJ

【 摘 要 】

Colorectal polyps may be detected incidentally on a screening colonoscopy or when they present with symptoms like anemia or gastrointestinal bleeding. Early recognition and prompt management of polyps can cure the primary disease and prevent future risk of malignancies in the patient and provide an opportunity to screen the families in cases of inherited polyposis syndromes. We report a case of rectal bleeding due to colorectal polyps of varying histology. Histology showed hyperplastic polyp, juvenile polyps (JP) with focal dysplasia, adenomatous polyp and villous adenoma with dysplasia. He underwent total proctocolectomy with ileal pouch anal anastomosis (J-pouch) (TP-IPAA). Mixed polyposis syndrome is a rare entity. (J Dig Endosc 2013;4(2):39-41)

【 授权许可】

Unknown