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Revista Cubana de Pediatría

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2014, Number 3

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Rev Cubana Pediatr 2014; 86 (3)

Familial adenomatous polyposis found in cuban children

Amaya STA, García BE, Lazo VS, González FL, Torres FM, Sánchez GNL
Full text How to cite this article

Language: Spanish
References: 30
Page: 325-335
PDF size: 114.93 Kb.


Key words:

familial adenomatous polyposis.

ABSTRACT

Introduction: familial adenomatous polyposis is a dominant autosomal disease that evolves into colorectal cancer.
Objective: to characterize the Cuban children with familial adenomatous polyposis.
Methods: a prospective, descriptive case series study, who were seen at the Institute of Gastroenterology from February 2011 through May 2013. Fifteen children were diagnosed as adenomatous polyposis patients, based on colonoscopy and histological confirmation, respectively. All of them were performed upper digestive tract endoscopy, upper stomach ultrasonography, ortopantomography, bone survey, intestinal transit test, and ophthalmological and neurological exams.
Results: sixty percent were males and 60 % were Caucasians. Screening of asymptomatic patients and the rectal bleeding were the main causes of medical consultation (40 %, respectively). Full manifested disease prevailed and low-grade dysplasia was observed in 73.3 % of cases. In the study group, 26.7 % presented with polyps in their stomach, being this location the most observed one. The most common extraintestinal manifestation was congenital hypertrophy of the retinal epithelium (73.3 %) followed by supernumerary teeth and dentigerous cysts. On analyzing the age groups, 40 % of the 10 to 18 years old children had already undergone colectomy.
Conclusions: Most of the studied patients had family histories of the disease; the family screening and the rectal bleeding were the main reasons for the study. All of them presented with the fully manifested form of the disease and the vast majority had low grade dysplasia at the time of diagnosis. The polyps located out of the colon were more frequently found in the stomach and the most common extraintesinal manifestation was congenital hypertrophy of the retinal epithelium. The majority of the patients had not undergone colectomy at the time of study.


REFERENCES

  1. Itzkowitz S, Potack J. Colonic Polyps and Polyposis Syndromes. In: Feldman M, Friedman L, Brandt L. Sleisenger and Fordtran's Gastrointestinal and Liver Disease. 9th ed. Philadelphia: Editorial Saunders Elsevier; 2010. p. 2176-87.

  2. Shilyansky J. Tumores del tracto digestivo. En: Behrman RE, Kliegman RM, Jenson HB. Nelson. Tratado de Pediatría. 17a. ed. Philadelphia: Editorial Elsevier; 2004. p. 1290-1.

  3. Moreira L, Castells A, Castelví S. Pólipos y poliposis colorrectales. En: Montoro MA, García Pagán JC. Gastroenterología y Hepatología. Problemas Comunes en la Práctica Clínica. 2da. ed. Barcelona: Jarpyo Editores S.A.; 2012. p. 607-16.

  4. Arévalo F, Aragón V, Alva J, Pérez M, Cerrillo G, Montes P. Pólipos Colorectales: actualización en el diagnóstico [revisión]. Rev Gastroenterol Perú. 2012;32-2:123-33.

  5. Andreu M, Ferrández A. Pólipos colorrectales y poliposis intestinal. En: Ponce J, ed. Tratamiento de las enfermedades gastroenterológicas. 3era. ed. Barcelona: Doyma; 2011. p. 345-58.

  6. Graziano A, Gutiérrez A. Poliposis Adenomatosa Familiar. En: Reis Neto JA. Coloproctología Atual. Proctosite Colorectal Surgery At the Web [libro en Internet] Capítulo III; 2008 [citado 2 de enero de 2012]. Disponible en: http://www.proctosite.com/library/books/livro_reis_novo/cap03.pdf

  7. Erdman SH, Hoffenberg EJ. Polyps and Tumors of the Gastrointestinal Tract. In: Rudolph CD, Rudolph A, Lister GE, First L, Gershon A. Rudolph's Pediatrics Section 21. Disorders of the Gastrointestinal System. Parte 5. Disorders of the Stomach and Intestine. 22nd. ed. New York: McGraw-Hill; 2011. p. 414.

  8. Saab R, Furman WL. Epidemiology and Management Options for Colorectal Cancer in Children. Pediatr Drugs. 2008;10(3):177-92.

  9. McCart A, Latchford A, Volikos E, Rowan A, Tomlinson I, Silver A. A novel exon duplication event leading to a truncating germ-line mutation of the APC gene in a familial adenomatous polyposis family. Fam Cancer. 2006;5(2):205-8.

  10. Bisgaard ML, Bülow S. Familial adenomatous polyposis (FAP): genotype correlation to FAP phenotype with osteomas and sebaceous cysts. Am J Med Genet A. 2006 Feb 1;140(3):200-4.

  11. Hegde MR, Roa BB. Detecting mutations in the APC gene in familial adenomatous polyposis (FAP). Curr Protoc Hum Genet. 2006 Aug;10:108.

  12. Kanter-Smoler G, Fritzell K, Rohlin A, Engwall Y, Hallberg B, Bergman A, et al. Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families. BMC Med. 2008 Apr 24;6:10.

  13. Stekrova J, Sulova M, Kebrdlova V, Zidkova K, Kotlas J, Ilencikova D, et al. Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects. BMC Med Genet. 2007 Apr 5;8:16.

  14. Vasen H, Möslein G, Alonso A, Aretz S, Bernstein I, Bertario L, et al. Guidelines for the clinical management of familial adenomatous polyposis (FAP). Gut. 2008;57:704- 13.

  15. Moraes Righetti AE, Jacomini C, Serafim Parra R, Ribeiro de Almeida Normanha AL, Ribeiro Rocha JJ. La poliposis adenomatosa familiar y tumores desmoides. Clínicas (Sao Paulo). 2011 Octubre;66(10):1839-42.

  16. Alfaro I, Ocaña T, Castells A, Cordero C, Ponce M, Cajal RY, et al. Características de los pacientes con poliposis adenomatosa familiar en España. Los primeros resultados del Registro Español de Poliposis Adenomatosa Familiar. Med Clin (Barc). 2010 Jun 19;135(3):103-8.

  17. Björk J. Epidemiología de la poliposis adenomatosa familiar en Suecia: evolución en el tiempo y las diferencias en el fenotipo entre varones y mujer. El Registro de Poliposis Sueco. Departamento de Gastroenterología y Hepatología. Hospital Karolinska Suecia. 1999;34(12):1230-5.

  18. Grau García C, Soto Gutiérrez A, Andrada Becerra E, Sánchez de las Heras B, Gallego Plazas J, Brotons Brotons A, et al. Paciente con poliposis adenomatosa familiar y metástasis hepáticas de tumor neuroendocrino. Gastroenterología y Hepatología. 2011;34(5):329-32.

  19. Half E, Bercovich D, Rozen P. Familial adenomatous polyposis. Orphanet Journal of Rare Diseases. 2009;4:22.

  20. Stella A, Resta N, Gentile M, Susca F, Mareni C, Montera MP, et al. Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP). Am J Hum Genet. 1993 Nov;53(5):1031-7.

  21. Bisgaard ML, Ripa R, Knudsen AL, Bülow S. Familial adenomatous polyposis patients without an identified APC germline mutation have a severe phenotype. Gut. 2004 Feb;53(2):266-70.

  22. Jiménez Rodríguez RM, Suárez Artacho G, Morcillo J, Díaz Pavón JM, Morales Méndez S. Adenocarcinoma de cuarta porción de duodeno en paciente con poliposis adenomatosa familiar. Rev Esp Enferm Dig. 2007 Ago;99(8):477-8.

  23. Katsinelos P, Kountouras J, Chatzimavroudis G, Zavos C, Pilpilidis I, Fasoulas K, et al. Wireless capsule endoscopy in detecting small-intestinal polyps in familial adenomatous polyposis. World Journal Gastroenterology. 2009;15(48):6075-9.

  24. Douma KFL, Bleiker EMA, Aaronson NK, Cats A, Gerritsma MA, Gundy CM. Longterm compliance with endoscopic surveillance for familial adenomatous polyposis. Colorectal Disease. 2010;12:1198-207.

  25. Pang CP, Keung JW, Tang NL, Fan DS, Lau JW, Lam DS. Congenital hypertrophy of the retinal pigment epithelium and APC mutations in two Chinese families with familial adenomatous polyposis. Eye (Lond). 2000 Feb;14(Pt 1):18-22.

  26. Valanzano R, Cama A, Volpe R, Curia MC, Mencucci R, Palmirotta R, et al. Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutations. Cancer. 1996 Dec 1;78(11):2400-10.

  27. Jiménez Mesa G, López Barbán MA, Hano García O. Valor de la ortopantomografía en la poliposis familiar de colon. Rev Cubana Med. 1996 Abr;35(1):24-9.

  28. Sxott RJ, Froggatt NJ, Trembath RC, Evans Evans DG, Hodgson SV, Maher ER. Familial infiltrative fibromatosis (desmoid tumours) (MI M135290) caused by a recurrent 3' APC gene mutation. Hum Mol Genet. 1996 Dec;5(12):1921-4.

  29. Groen EJ, Roos A, Muntinghe FL, Enting RH, de Vries J, Kleibeuker JH, et al. Extra-intestinal manifestations of familial adenomatous polyposis. Ann Surg Oncol. 2008 Sep;15(9):2439-50.

  30. Celta F, Dhamo A, Civitelli S, Zangari R. Comment on Extraintestinal manifestations of familial adenomatous polyposis. Ann Surg Oncol. 2009;16(5):1446-8.




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Rev Cubana Pediatr. 2014;86