The epidemiological and clinical features of familial adenomatous polyposis in Ribeirão Preto

Abstract Purpose to study 75 familial adenomatous polyposis (FAP) patients treated in a single insti- tution in Ribeirão Preto/SP, from January 1981 to December 2011. Methods this is a retrospective study and the following data were collected: gender, age, main symptoms, familial history, coexisting...

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Published in:Journal of Coloproctology Vol. 33; no. 3; pp. 126 - 130
Main Authors: Feitosa, Marley Ribeiro, Oliveira, Tais Helena Garcia Fernandes de, Kondo, Bruno Ravenna Pinheiro, Lira, Haline Gomes de, Abissamra, André Antonio, Parra, Rogério Serafim, Féres, Omar, Rocha, Jose Joaquim Ribeiro da
Format: Journal Article
Language:English
Published: Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil Elsevier Editora Ltda 01-09-2013
Thieme Revinter Publicações Ltda
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Summary:Abstract Purpose to study 75 familial adenomatous polyposis (FAP) patients treated in a single insti- tution in Ribeirão Preto/SP, from January 1981 to December 2011. Methods this is a retrospective study and the following data were collected: gender, age, main symptoms, familial history, coexisting malignancies, surgical treatment, surgical morbidity and mortality, factors related to life quality. Results median age was 29 years. Male-to-female ratio was 1.2:1. Bleeding was the most common symptom (62.6%). Colorectal cancer incidence was 25.5% (n = 19). Extracolonic neoplasia incidence was 8%. Colectomy with ileorectal anastomosis (IRA) was performed in 72% of the patients. Eighteen patients (24%) were submitted to proctocolectomy with “J-pouch” ileoanal anastomosis. In three patients (4%) proctocolectomy with terminal il- eostomy was performed. Early and late complication rate were similar (22.7% × 24%). Ileal pouch surgery exhibited tendency to a higher morbidity and mortality but no significance could be found. Overall mortality rate was 7.46%. Malignant neoplasia was the main cause of mortality, accounting for 60% of deaths. Conclusion FAP is a rare pathology in our country. Genetic counseling and proper screening programs are essential tools to early diagnosis and follow-up. Surgery is the most effective treatment and the best option to prevent malignant neoplasia.
ISSN:2237-9363
2317-6423
DOI:10.1016/j.jcol.2013.06.003