Genetic profile, risk factors and therapeutic approach of desmoid tumors in familial adenomatous polyposis

Detalhes bibliográficos
Autor(a) principal: Freitas,Ana Catarina Ribeiro
Data de Publicação: 2017
Outros Autores: Barbosa,Laura Elisabete Ribeiro
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of Coloproctology (Rio de Janeiro. Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2237-93632017000200163
Resumo: ABSTRACT Introduction: Desmoid tumors are the main extraintestinal manifestation of FAP, presenting high morbidity and mortality. It is a neoplasia without metastasis capacity, but with infiltrative growth and with a high rate of recurrence. In familial forms, these tumors are associated with a germinal mutation in the APC gene, with a genotype-phenotype correlation influenced by other risk factors. Materials and methods: A review of articles published since the year 2000 in Portuguese, English or Spanish on desmoid tumors in patients with FAP was carried out. A total of 49 publications were included. Results: The site of the mutation in the APC gene is related to the severity of FAP and to the frequency of desmoid tumor. Mutations located distally to codon 1309 are associated with a more attenuated polyposis, but with higher frequency of desmoid tumors. Clinically, these tumors may or may not be symptomatic, depending on their size and location. In their treatment, priority should be given to medical therapy, especially in intra-abdominal tumors, with surgery being the last option if there are no other complications. Discussion: These tumors are associated with certain risk factors: genetic (mutation site), hormonal (estrogenic environment) and physical (surgical trauma) ones. In young women, a later prophylactic colectomy is suggested. Moreover, the laparoscopic approach to prophylactic surgery seems to be an option that reduces surgical trauma and consequently the appearance of desmoid tumors. Conclusion: The step-up medical approach has been shown to be valid in the treatment of intra-abdominal desmoid tumors, and medical treatment should be the first therapeutic option.
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spelling Genetic profile, risk factors and therapeutic approach of desmoid tumors in familial adenomatous polyposisDesmoid disease, hereditaryFibromatosis, aggressiveAdenomatous polyposis coliRisk factors and therapeuticsABSTRACT Introduction: Desmoid tumors are the main extraintestinal manifestation of FAP, presenting high morbidity and mortality. It is a neoplasia without metastasis capacity, but with infiltrative growth and with a high rate of recurrence. In familial forms, these tumors are associated with a germinal mutation in the APC gene, with a genotype-phenotype correlation influenced by other risk factors. Materials and methods: A review of articles published since the year 2000 in Portuguese, English or Spanish on desmoid tumors in patients with FAP was carried out. A total of 49 publications were included. Results: The site of the mutation in the APC gene is related to the severity of FAP and to the frequency of desmoid tumor. Mutations located distally to codon 1309 are associated with a more attenuated polyposis, but with higher frequency of desmoid tumors. Clinically, these tumors may or may not be symptomatic, depending on their size and location. In their treatment, priority should be given to medical therapy, especially in intra-abdominal tumors, with surgery being the last option if there are no other complications. Discussion: These tumors are associated with certain risk factors: genetic (mutation site), hormonal (estrogenic environment) and physical (surgical trauma) ones. In young women, a later prophylactic colectomy is suggested. Moreover, the laparoscopic approach to prophylactic surgery seems to be an option that reduces surgical trauma and consequently the appearance of desmoid tumors. Conclusion: The step-up medical approach has been shown to be valid in the treatment of intra-abdominal desmoid tumors, and medical treatment should be the first therapeutic option.Sociedade Brasileira de Coloproctologia2017-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S2237-93632017000200163Journal of Coloproctology (Rio de Janeiro) v.37 n.2 2017reponame:Journal of Coloproctology (Rio de Janeiro. Online)instname:Sociedade Brasileira de Coloproctologia (SBCP)instacron:SBCP10.1016/j.jcol.2017.04.001info:eu-repo/semantics/openAccessFreitas,Ana Catarina RibeiroBarbosa,Laura Elisabete Ribeiroeng2017-06-27T00:00:00Zoai:scielo:S2237-93632017000200163Revistahttp://www.scielo.br/scielo.php?script=sci_serial&pid=2237-9363&lng=pt&nrm=isohttps://old.scielo.br/oai/scielo-oai.php||sbcp@sbcp.org.br2317-64232237-9363opendoar:2017-06-27T00:00Journal of Coloproctology (Rio de Janeiro. Online) - Sociedade Brasileira de Coloproctologia (SBCP)false
dc.title.none.fl_str_mv Genetic profile, risk factors and therapeutic approach of desmoid tumors in familial adenomatous polyposis
title Genetic profile, risk factors and therapeutic approach of desmoid tumors in familial adenomatous polyposis
spellingShingle Genetic profile, risk factors and therapeutic approach of desmoid tumors in familial adenomatous polyposis
Freitas,Ana Catarina Ribeiro
Desmoid disease, hereditary
Fibromatosis, aggressive
Adenomatous polyposis coli
Risk factors and therapeutics
title_short Genetic profile, risk factors and therapeutic approach of desmoid tumors in familial adenomatous polyposis
title_full Genetic profile, risk factors and therapeutic approach of desmoid tumors in familial adenomatous polyposis
title_fullStr Genetic profile, risk factors and therapeutic approach of desmoid tumors in familial adenomatous polyposis
title_full_unstemmed Genetic profile, risk factors and therapeutic approach of desmoid tumors in familial adenomatous polyposis
title_sort Genetic profile, risk factors and therapeutic approach of desmoid tumors in familial adenomatous polyposis
author Freitas,Ana Catarina Ribeiro
author_facet Freitas,Ana Catarina Ribeiro
Barbosa,Laura Elisabete Ribeiro
author_role author
author2 Barbosa,Laura Elisabete Ribeiro
author2_role author
dc.contributor.author.fl_str_mv Freitas,Ana Catarina Ribeiro
Barbosa,Laura Elisabete Ribeiro
dc.subject.por.fl_str_mv Desmoid disease, hereditary
Fibromatosis, aggressive
Adenomatous polyposis coli
Risk factors and therapeutics
topic Desmoid disease, hereditary
Fibromatosis, aggressive
Adenomatous polyposis coli
Risk factors and therapeutics
description ABSTRACT Introduction: Desmoid tumors are the main extraintestinal manifestation of FAP, presenting high morbidity and mortality. It is a neoplasia without metastasis capacity, but with infiltrative growth and with a high rate of recurrence. In familial forms, these tumors are associated with a germinal mutation in the APC gene, with a genotype-phenotype correlation influenced by other risk factors. Materials and methods: A review of articles published since the year 2000 in Portuguese, English or Spanish on desmoid tumors in patients with FAP was carried out. A total of 49 publications were included. Results: The site of the mutation in the APC gene is related to the severity of FAP and to the frequency of desmoid tumor. Mutations located distally to codon 1309 are associated with a more attenuated polyposis, but with higher frequency of desmoid tumors. Clinically, these tumors may or may not be symptomatic, depending on their size and location. In their treatment, priority should be given to medical therapy, especially in intra-abdominal tumors, with surgery being the last option if there are no other complications. Discussion: These tumors are associated with certain risk factors: genetic (mutation site), hormonal (estrogenic environment) and physical (surgical trauma) ones. In young women, a later prophylactic colectomy is suggested. Moreover, the laparoscopic approach to prophylactic surgery seems to be an option that reduces surgical trauma and consequently the appearance of desmoid tumors. Conclusion: The step-up medical approach has been shown to be valid in the treatment of intra-abdominal desmoid tumors, and medical treatment should be the first therapeutic option.
publishDate 2017
dc.date.none.fl_str_mv 2017-06-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.relation.none.fl_str_mv 10.1016/j.jcol.2017.04.001
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Coloproctologia
publisher.none.fl_str_mv Sociedade Brasileira de Coloproctologia
dc.source.none.fl_str_mv Journal of Coloproctology (Rio de Janeiro) v.37 n.2 2017
reponame:Journal of Coloproctology (Rio de Janeiro. Online)
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reponame_str Journal of Coloproctology (Rio de Janeiro. Online)
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repository.name.fl_str_mv Journal of Coloproctology (Rio de Janeiro. Online) - Sociedade Brasileira de Coloproctologia (SBCP)
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