Literature DB >> 11231455

Intestinal transplantation for the treatment of desmoid tumors associated with familial adenomatous polyposis.

M A Chatzipetrou1, A G Tzakis, A D Pinna, T Kato, E P Misiakos, A K Tsaroucha, D Weppler, P Ruiz, M Berho, T Fishbein, H O Conn, C Ricordi.   

Abstract

BACKGROUND: Desmoid tumors associated with familial adenomatous polyposis (FAP) are locally invasive. Often occurring in the mesentery of the intestine, they sometimes recur after resection. Complications can include intestinal failure and dependence on parenteral nutrition. We describe 9 patients who underwent intestinal transplantation for the treatment of desmoid tumors associated with FAP.
METHODS: Records of patients undergoing intestinal transplantation for desmoid tumors at 2 transplant centers were reviewed for patient age, sex, type of graft, procedure date, tumor site, desmoid complications, medications, extracolonic manifestations, status at follow-up, and length of survival.
RESULTS: Nine patients with FAP and intestinal failure caused by desmoid tumors were treated with isolated intestinal (n = 6), multivisceral (n = 2), or combined liver-intestinal transplantation (n = 1). Desmoid tumors recurred in the abdominal walls of 2 patients. Two patients died: one as a result of sepsis, the other because of a rupture of a mycotic aneurysm of the aortic anastomosis. One graft lost to severe rejection was replaced with a second intestinal graft. Eleven to 53 months after transplantation, 7 patients were alive, well, independent of parenteral treatment, and leading apparently normal lifestyles.
CONCLUSIONS: Transplantation of the intestine alone or as part of a multivisceral transplantation may help rescue otherwise untreatable patients with complicated desmoid tumors.

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Year:  2001        PMID: 11231455     DOI: 10.1067/msy.2001.110770

Source DB:  PubMed          Journal:  Surgery        ISSN: 0039-6060            Impact factor:   3.982


  9 in total

Review 1.  Small intestinal transplantation.

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2.  Surgical treatment of giant mesenteric fibromatosis presenting as a gastrointestinal stromal tumor: a case report.

Authors:  Christos N Stoidis; Basileios G Spyropoulos; Evangelos P Misiakos; Christos K Fountzilas; Panorea P Paraskeva; Constantine I Fotiadis
Journal:  J Med Case Rep       Date:  2010-09-23

Review 3.  Gardner's syndrome: a case report and review of the literature.

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Journal:  World J Gastroenterol       Date:  2005-09-14       Impact factor: 5.742

4.  Short bowel syndrome after continence-preserving procedures.

Authors:  Jon S Thompson; Richard Gilroy; Debra Sudan
Journal:  J Gastrointest Surg       Date:  2007-10-30       Impact factor: 3.452

5.  Mifepristone (RU486), a pure antiprogesterone drug, in combination with vinblastine for the treatment of progesterone receptor-positive desmoid tumor.

Authors:  A Halevy; I Samuk; Z Halpern; L Copel; J Sandbank; Y Ziv
Journal:  Tech Coloproctol       Date:  2010-06-29       Impact factor: 3.781

Review 6.  Current status of the organ replacement approach for malignancies and an overture for organ bioengineering and regenerative medicine.

Authors:  Taizo Hibi; Masahiro Shinoda; Osamu Itano; Yuko Kitagawa
Journal:  Organogenesis       Date:  2014-05-16       Impact factor: 2.500

7.  Surgical treatment of intra-abdominal desmoid tumors resulting in short bowel syndrome.

Authors:  Matthew Wheeler; David Mercer; Wendy Grant; Jean Botha; Alan Langnas; Jon Thompson
Journal:  Cancers (Basel)       Date:  2012-01-19       Impact factor: 6.639

8.  The first modified multivisceral transplantation in the middle East: a major advance in transplantation surgery in shiraz transplant center.

Authors:  S Nikeghalian; H R Davari; F Kakaei; A Shamsaeefar; B Sanei; B Geramizadeh; M Moini; M A Sahmeddini; S A Malek-Hosseini
Journal:  Int J Organ Transplant Med       Date:  2010

Review 9.  Intra-Abdominal and Abdominal Wall Desmoid Fibromatosis.

Authors:  J Harrison Howard; Raphael E Pollock
Journal:  Oncol Ther       Date:  2016-02-03
  9 in total

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