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Information Journal Paper

Title

A CASE REPORT OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP)

Pages

  63-66

Abstract

 BACKGROUND AND OBJECTIVE: FAMILIAL ADENOMATOUS POLYPOSIS (FAP) is an autosomal dominant disease that caused by mutation of the APC gene and in addition to COLON, it can involve stomach and duodenum. Since, the risk of MALIGNANCY in FAP is high, early diagnosis and treatment can prevent colorectal cancer. CASE: The patient was a 55 year old man who referred for rectal bleeding and proctalgia from 6 weeks ago. He was examined with anoscope, and rectal mass was observed. In pathological study, rectal adenocarcinoma was reported. B. Enema and total coloscopy were performed for patient and multiple polyps in colorectal were seen. For patient with FAP, total procto colectomy and permanent ileostomy were performed. There were malignant changes in one sessile polyps with >2.5 cm diameter. In COLONoscopic examination of patients family, 4 of 6 children were with FAP. CONCLUSION: Although, only 0.5% of all colorectal cancers caused by FAP but early diagnosis and screening in patients family can prevent the progress of disease and MALIGNANCY

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    APA: Copy

    GHOLIZADEH PASHA, A.A.R., SAVADKOOHI, SH., & SHAFIGH, E.. (2003). A CASE REPORT OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP). JOURNAL OF BABOL UNIVERSITY OF MEDICAL SCIENCES (JBUMS), 5(3 (19)), 63-66. SID. https://sid.ir/paper/73695/en

    Vancouver: Copy

    GHOLIZADEH PASHA A.A.R., SAVADKOOHI SH., SHAFIGH E.. A CASE REPORT OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP). JOURNAL OF BABOL UNIVERSITY OF MEDICAL SCIENCES (JBUMS)[Internet]. 2003;5(3 (19)):63-66. Available from: https://sid.ir/paper/73695/en

    IEEE: Copy

    A.A.R. GHOLIZADEH PASHA, SH. SAVADKOOHI, and E. SHAFIGH, “A CASE REPORT OF FAMILIAL ADENOMATOUS POLYPOSIS (FAP),” JOURNAL OF BABOL UNIVERSITY OF MEDICAL SCIENCES (JBUMS), vol. 5, no. 3 (19), pp. 63–66, 2003, [Online]. Available: https://sid.ir/paper/73695/en

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