Literature DB >> 18237870

Desmoid tumors in a dutch cohort of patients with familial adenomatous polyposis.

Marry H Nieuwenhuis1, Wouter De Vos Tot Nederveen Cappel, Akke Botma, Fokko M Nagengast, Jan H Kleibeuker, Elisabeth M H Mathus-Vliegen, Evelien Dekker, Jan Dees, Juul Wijnen, Hans F A Vasen.   

Abstract

BACKGROUND & AIMS: Desmoid tumors are a severe extracolonic manifestation in familial adenomatous polyposis (FAP). Identification of risk factors might be helpful in the management of FAP patients with such tumors. The aim of this study was to assess potential risk factors for the development of desmoids in a cohort of Dutch FAP patients.
METHODS: The medical records of 735 FAP patients were analyzed for the occurrence of desmoids. Relative risks and survival times were calculated to assess the influence of potential risk factors (female sex, family history, mutation site, abdominal surgery, and pregnancy) on desmoid development.
RESULTS: Desmoid tumors were identified in 66 of the 735 patients (9%). The cumulative risk of developing desmoids was 14%. No correlation was found between specific adenomatous polyposis coli mutation sites and desmoid development. Patients with a positive family history for desmoids had a significant increased risk to develop this tumor (30% vs 6.7%, P < .001). No association was found between female sex or pregnancy and desmoid development. Most desmoid patients (95%) had undergone previous abdominal surgery. In a substantial proportion of patients with an ileorectal anastomosis, it was impossible to convert the ileorectal anastomosis to an ileal pouch-anal anastomosis as a result of desmoid development.
CONCLUSIONS: A positive family history of desmoids is an evident risk factor for developing desmoids. Most desmoids develop after colectomy. No correlation was found between desmoids and the adenomatous polyposis coli gene mutation site, female sex, and pregnancy. Ileal pouch-anal anastomosis is the appropriate type of surgery in FAP patients with a positive family history for desmoids.

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Year:  2008        PMID: 18237870     DOI: 10.1016/j.cgh.2007.11.011

Source DB:  PubMed          Journal:  Clin Gastroenterol Hepatol        ISSN: 1542-3565            Impact factor:   11.382


  27 in total

Review 1.  Hereditary Colorectal Cancer: Genetics and Screening.

Authors:  Lodewijk A A Brosens; G Johan A Offerhaus; Francis M Giardiello
Journal:  Surg Clin North Am       Date:  2015-06-16       Impact factor: 2.741

2.  Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients.

Authors:  Daniel Robert Quast; Ralph Schneider; Emanuel Burdzik; Steffen Hoppe; Gabriela Möslein
Journal:  Fam Cancer       Date:  2016-01       Impact factor: 2.375

3.  Risk factors predicting intra-abdominal desmoids in familial adenomatous polyposis: a single centre experience.

Authors:  A Sinha; P P Tekkis; K F Neale; R K S Phillips; S K Clark
Journal:  Tech Coloproctol       Date:  2010-03-30       Impact factor: 3.781

4.  Pregnancy does not increase the local recurrence rate after surgical resection of desmoid-type fibromatosis.

Authors:  Justin M M Cates
Journal:  Int J Clin Oncol       Date:  2014-08-16       Impact factor: 3.402

5.  Subsequent Adenomas of Ileal Pouch and Anorectal Segment after Prophylactic Surgery for Familial Adenomatous Polyposis.

Authors:  A E M'Koma; A J Herline; S E Adunyah
Journal:  World J Colorectal Surg       Date:  2013

6.  Desmoid tumor of mesentery in familial adenomatous polyposis: a case report.

Authors:  G Basdanis; V N Papadopoulos; S Panidis; I Tzeveleki; E Karamanlis; A Mekras; S Apostolidis; A Michalopoulos
Journal:  Tech Coloproctol       Date:  2010-11       Impact factor: 3.781

7.  Desmoid tumors: clinical features and outcome of an unpredictable and challenging manifestation of familial adenomatous polyposis.

Authors:  Fábio Guilherme Campos; Carlos Augusto Real Martinez; Marleny Novaes; Sérgio Carlos Nahas; Ivan Cecconello
Journal:  Fam Cancer       Date:  2015-06       Impact factor: 2.375

8.  A Sporadic Desmoid Tumor: an Exceptional Pancreatic Cystic-Solid Mass.

Authors:  Jalal Vahedian Ardakani; Ali Zare Mehrjardi; Massoud Baghai Wadji; Amir Saraee
Journal:  Indian J Surg       Date:  2015-11-13       Impact factor: 0.656

9.  Extracolonic manifestations of hereditary colorectal cancer syndromes.

Authors:  Daniel A Anaya; George J Chang; Miguel A Rodriguez-Bigas
Journal:  Clin Colon Rectal Surg       Date:  2008-11

10.  Japanese Society for Cancer of the Colon and Rectum (JSCCR) guidelines 2020 for the Clinical Practice of Hereditary Colorectal Cancer.

Authors:  Naohiro Tomita; Hideyuki Ishida; Kohji Tanakaya; Tatsuro Yamaguchi; Kensuke Kumamoto; Toshiaki Tanaka; Takao Hinoi; Yasuyuki Miyakura; Hirotoshi Hasegawa; Tetsuji Takayama; Hideki Ishikawa; Takeshi Nakajima; Akiko Chino; Hideki Shimodaira; Akira Hirasawa; Yoshiko Nakayama; Shigeki Sekine; Kazuo Tamura; Kiwamu Akagi; Yuko Kawasaki; Hirotoshi Kobayashi; Masami Arai; Michio Itabashi; Yojiro Hashiguchi; Kenichi Sugihara
Journal:  Int J Clin Oncol       Date:  2021-06-29       Impact factor: 3.402

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