<?xml version="1.0" encoding="UTF-8"?> <!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2d1 20170631//EN" "JATS-journalpublishing1.dtd"> <ArticleSet> <Article> <Journal> <PublisherName>journal-jmsr</PublisherName> <JournalTitle>Journal of Medical and Surgical Research</JournalTitle> <PISSN>I</PISSN> <EISSN>S</EISSN> <Volume-Issue>Vol. II, n 2</Volume-Issue> <PartNumber/> <IssueTopic>Multidisciplinary</IssueTopic> <IssueLanguage>English</IssueLanguage> <Season>December, 2015</Season> <SpecialIssue>N</SpecialIssue> <SupplementaryIssue>N</SupplementaryIssue> <IssueOA>Y</IssueOA> <PubDate> <Year>-0001</Year> <Month>11</Month> <Day>30</Day> </PubDate> <ArticleType>JMSR Oncology</ArticleType> <ArticleTitle>Desmoid Tumors of the Abdominal Wall and the Therapeutic Management: a Case Report.</ArticleTitle> <SubTitle/> <ArticleLanguage>English</ArticleLanguage> <ArticleOA>Y</ArticleOA> <FirstPage>166</FirstPage> <LastPage>170</LastPage> <AuthorList> <Author> <FirstName>H.</FirstName> <LastName>Hachim</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>N</CorrespondingAuthor> <ORCID/> <FirstName>M.</FirstName> <LastName>Alaoui</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>M.</FirstName> <LastName>Mountassir</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>M. A.</FirstName> <LastName>Majbar</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>F.</FirstName> <LastName>Sabbah</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>M.</FirstName> <LastName>Raiss</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>A.</FirstName> <LastName>Hrora</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>M.</FirstName> <LastName>Ahallat</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> </Author> </AuthorList> <DOI/> <Abstract>Desmoid tumors are fibrous proliferations that have an aggressive and an infiltrating character which tend te reccur locally without gaving any metastasis. Ther are rare repressenting less than 0,03% of all tumors. Mostly, they are sporadic, but in 2% of the cases they come in a genetic context __doublequotosingThe Gardner Syndrome__doublequotosing. Desmoid tumors are localized, appearing in a decreasing order of frequency in the structures of the abdominal wall, the peripheral muscle fascia or more rarely in the intra-abdominal contents (mesentery, retroperitoneum). We report the case of a 32 years old female patient who had a desmoid tumor of the abdominal wall discovered during pregnancy. And from this clinical case we will focus on the difficulties of their therapeutic management, recalling through a literature review, the clinical, paraclinical and therapeutic features of these tumors.</Abstract> <AbstractLanguage>English</AbstractLanguage> <Keywords>Desmoid tumor, Aggressive fibromatosis, Abdominal wall, Infiltrated margins.</Keywords> <URLs> <Abstract>https://journal-jmsr.net/ubijournal-v1copy/journals/abstract.php?article_id=4769&title=Desmoid Tumors of the Abdominal Wall and the Therapeutic Management: a Case Report.</Abstract> </URLs> <References> <ReferencesarticleTitle>References</ReferencesarticleTitle> <ReferencesfirstPage>16</ReferencesfirstPage> <ReferenceslastPage>19</ReferenceslastPage> <References/> </References> </Journal> </Article> </ArticleSet>