Page 147 - Read Online
P. 147

Page 12 of 13                                         Ambe et al. Mini-invasive Surg 2018;2:37  I  http://dx.doi.org/10.20517/2574-1225.2018.45


                   pectations and reality. Minim Invasive Ther Allied Technol 2016;25:241-6.
               23.  Kneist W, Wachter N, Paschold M, Kauff DW, Rink AD, et al. Midterm functional results of taTME with neuromapping for low rectal
                   cancer. Tech Coloproctol 2016;20:41-9.
               24.  Aretz S, Uhlhaas S, Sun Y, Pagenstecher C, Mangold E, et al. Familial adenomatous polyposis: aberrant splicing due to missense or si-
                   lent mutations in the APC gene. Hum Mutat 2004;24:370-80.
               25.  Bisgaard ML, Fenger K, Bülow S, Niebuhr E, Mohr J. Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation
                   rate. Hum mutat 1994;3:121-5.
               26.  Knudsen AL, Bülow S, Tomlinson I, Möslein G, Heinimann K, et al. Attenuated familial adenomatous polyposis: results from an inter-
                   national collaborative study. Colorectal Dis 2010;12:e243-9.
               27.  Bülow S. Diagnosis of familial adenomatous polyposis. World J Surg 1991;15:41-6.
               28.  Dörner J, Fallahpour MT, Möslein G. Surgical management of hereditary colorectal cancer syndromes. In: Valle L, Gruber S, Capellá G,
                   editors. Hereditary colorectal cancer. Cham: Springer; 2018. pp. 327-47.
               29.  De Cosse JJ, Bülow S, Neale K, Järvinen H, Alm T, et al. Rectal cancer risk in patients treated for familial adenomatous polyposis. The
                   Leeds Castle polyposis group. Br J Surg 1992;79:1372-5.
               30.  Lynch HT, Smyrk T, McGinn T, Lanspa S, Cavalieri J, et al. Attenuated familial adenomatous polyposis (AFAP). A phenotypically and
                   genotypically distinctive variant of FAP. Cancer 1995;76:2427-33.
               31.  Knudsen AL, Bisgaard ML, Bülow S. Attenuated familial adenomatous polyposis (AFAP): a review of the literature. Fam cancer
                   2003;2:43-55.
               32.  Groen EJ, Roos A, Muntinghe FL, Enting RH, de Vries J, et al. Extra-intestinal manifestations of familial adenomatous polyposis. Ann
                   Surg Oncol 2008;15:2439-50.
               33.  Traboulsi EI, Krush AJ, Gardner EJ, Booker SV, Offerhaus GJ, et al. Prevalence and importance of pigmented ocular fundus lesions in
                   Gardner’s syndrome. N Engl J Med 1987;316:661-7.
               34.  Naylor EW, Gardner EJ, Richards RC. Desmoid tumors and mesenteric fibromatosis in Gardner’s syndrome: report of kindred 109.
                   Arch Surg 1979;114:1181-5.
               35.  Vasen HF, Möslein G, Alonso A, Aretz S, Bernstein I, et al. Guidelines for the clinical management of familial adenomatous polyposis
                   (FAP). Gut 2008;57:704-13.
               36.  Lynch PM, Morris JS, Wen S, Advani SM, Ross W, et al. A proposed staging system and stage-specific interventions for familial adeno-
                   matous polyposis. Gastrointest Endosc 2016;84:115-25.
               37.  Ambe PC, Möslein G. Ileoanal pouch. Coloproctology 2018;40:130-5.
               38.  Remzi FH, Fazio VW, Delaney CP, Preen M, Ormsby A, et al. Dysplasia of the anal transitional zone after ileal pouch-anal anastomosis:
                   results of prospective evaluation after a minimum of ten years. Dis Colon Rectum 2003;46:6-13.
               39.  Carne PW, Pemberton JH. Technical aspects of ileoanal pouch surgery. Clin Colon Rectal Surg 2004;17:35-41.
               40.  Van Duijvendijk P, Slors JF, Taat CW, Oosterveld P, Sprangers MA, et al. Quality of life after total colectomy with ileorectal anastomo-
                   sis or proctocolectomy and ileal pouch-anal anastomosis for familial adenomatous polyposis. Br J Surg 2000;87:590-6.
               41.  DE Marchis ML, Tonelli F, Quaresmini D, Lovero D, Della-Morte D, et al. Desmoid tumors in familial adenomatous polyposis. Anti-
                   cancer Res 2017;37:3357-66.
               42.  Ambe PC, Zirngibl H, Möslein G. Routine virtual ileostomy following restorative proctocolectomy for familial adenomatous polyposis.
                   World J Surg 2018;42:1867-71.
               43.  Monson JR, Arsalanizadeh R. Transanal total mesorectal excision (TaTME) and quality of rectal cancer surgery: do we really know?
                   Ann Surg 2017;266:e88-9.
               44.  Ambe PC, Zirngibl H, Möslein G. Initial experience with taTME in patients undergoing laparoscopic restorative proctocolectomy for
                   familial adenomatous polyposis. Tech Coloproctol 2017;21:971-4.
               45.  Reilly WT, Pemberton JH, Wolff BG, Nivatvongs S, Devine RM, et al. Randomized prospective trial comparing ileal pouch-anal anas-
                   tomosis performed by excising the anal mucosa to ileal pouch-anal anastomosis performed by preserving the anal mucosa. Ann Surg
                   1997;225:666-76.
               46.  Rullier E, Laurent C, Garrelon JL, Michel P, Saric J, et al. Risk factors for anastomotic leakage after resection of rectal cancer. Br J Surg
                   1998;85:355-8.
               47.  Aziz O, Albeyatti A, Derias M, Varsani N, Ashrafian H, et al. PTU-202 A case-controlled study demonstrating that changes associated
                   with rectal anastomotic leakage are detectable within 48 hours of surgery. Gut 2015;64:A152.
               48.  Al-Tassan N, Chmiel NH, Maynard J, Fleming N, Livingston AL, et al. Inherited variants of MYH associated with somatic G:C-->T:A
                   mutations in colorectal tumors. Nat Genet 2002;30:227-32.
               49.  Mazzei F, Viel A, Bignami M. Role of MUTYH in human cancer. Mutat Res 2013;743-744:33-43.
               50.  Nielsen M, Joerink-van de Beld MC, Jones N, Vogt S, Tops CM, et al. Analysis of MUTYH genotypes and colorectal phenotypes in pa-
                   tients With MUTYH-associated polyposis. Gastroenterology 2009;136:471-6.
               51.  Nieuwenhuis MH, Vogt S, Jones N, Nielsen M, Hes FJ, et al. Evidence for accelerated colorectal adenoma--carcinoma progression in
                   MUTYH-associated polyposis? Gut 2012;61:734-8.
               52.  De Rosa M, Galatola M, Quaglietta L, Miele E, De Palma G, et al. Alu-mediated genomic deletion of the serine/threonine protein kinase
                   11 (STK11) gene in Peutz-Jeghers syndrome. Gastroenterology 2010;138:2558-60.
               53.  Howe JR, Roth S, Ringold JC, Summers RW, Järvinen HJ, et al. Mutations in the SMAD4/DPC4 gene in juvenile polyposis. Science
                   1998;280:1086-8.
               54.  Howe JR, Bair JL, Sayed MG, Anderson ME, Mitros FA, et al. Germline mutations of the gene encoding bone morphogenetic protein
                   receptor 1A in juvenile polyposis. Nat Genet 2001;28:184-7.
               55.  Orloff MS, Eng C. Genetic and phenotypic heterogeneity in the PTEN hamartoma tumour syndrome. Oncogene 2008;27:5387-97.
   142   143   144   145   146   147   148   149   150   151   152