2015, Number 2
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Rev Hosp Jua Mex 2015; 82 (2)
Alteraciones cutáneas en las poliposis intestinales
Rodríguez-Medina U, Medina-Murillo GR, Rodríguez-Wong U
Language: Spanish
References: 18
Page: 114-117
PDF size: 165.32 Kb.
ABSTRACT
There are a group of syndromes characterized by the presence of intestinal hamartomas or premalignant intestinal
polyps associated with cutaneous hamartomas or some other skin disorders. The genetic defect in many of these
syndromes is a mutation in genes involved in tumor suppression. Is necessary that the clinician knows skin
alterations of these syndromes, to suspect the diagnosis thereof; since in many patients these manifestations occur
earliest so that intestinal disorders.
REFERENCES
Rodríguez-Wong U. Pólipos epiteliales neoplásicos del colon y recto. Rev Hosp Jua Mex 1993; 60(3): 36-9.
Jelsig AM, Qvist N, Brusgaard K, Nielsen CB, Hansen TP, Ousager LB. Hamartomatous polyposis syndromes: a review. Orphanet J Rare Dis 2014; 9: 101.
Desai D, Murday V, Phillips R, Neale K, Milla P, Hudgson S. A survey of phenotypic features in juvenile polyps. J Med Genet 1998; 35: 476-81.
Cervantes-Bustamante R, Ramírez-Mayans J, Mata-Rivera N, Zárate-Mondragón F, Munguía-Vanegas P, Soria-Garibay B, et al. Poliposis juvenil en niños mexicanos. Rev Gastroenterol Mex 2002; 67(3): 150-4.
Gondak RO, da Silva-Jorge R, Jorge J, Lopes MA, Vargas PA. Oral pigmented lesions: Clinicopathologic features and review of the literature. Med Oral Patol Oral Cir Bucal 2012; 17(6): e919-e924.
Eisen D, Voorhees JJ. Oral melanoma and other pigmented lesions of the oral cavity. J Am Acad Dermatol 1991; 24(4): 527-37.
Tomas C, Soyer P, Dohan A, Dray X, Boudiaf M, Hoeffel C. Update on imaging of Peutz-Jeghers syndrome. World J Gastroenterol 2014; 20(31): 10864-75.
Giardiello FM, Trimbath JD. Peutz-Jeghers syndrome and management recommendations. Clin Gastroenterol Hepatol 2006; 4: 408-15.
Almenar-Besó R, Bagán-Sebastían JV, Milián-Masanet MA, Jiménez-Soriano Y. Síndrome de Cowden: presentación de un caso clínico con lesiones orales. An Med Interna (Madrid) 2001; 18(8): 426-8.
Nuñez-Nuñez R, Galán-Gómez E, Moreno-Hurtado C, Romero- Albillo A, Santamaría JI. Poliposis adenomatosa familiar: síndrome de Gardner. Cir Pediatr 2006; 19: 111-4.
Fotiadis C, Tsekouras DK, Antonakis P, Sfiniadakis J, Genetzakis M, Zografos GC. Gardner’s syndrome: A case report and review of the literature. World J Gastroenterol 2005; 11(34): 5408-11.
Juhn E, Khachemoune A. Gardner syndrome: skin manifestations, differential diagnosis and management. Am J Clin Dermatol 2010; 11(2): 117-22.
Ward EM, Wolfsen HC. Review article: the non inherit gastrointestinal polyposis syndromes. Aliment Pharmacol Ther 2002; 16: 333-42.
Seshadri D, Karagiorgos N, Hyser MJ. A case of Cronkhite- Canada syndrome and a review of gastrointestinal polyposis syndromes. Gastroenterol Hepatol (NY) 2012; 8: 197-201.
Sweetser S, Boardman LA. Cronkhite-Canada syndrome an acquired condition of gastrointestinal polyposis and dermatologic abnormalities. Gastroenterol Hepatol 2012; 8(3): 201-3.
Bruce A, Ng CS, Wolfsen HC, Smallridge RC, Lookingbill DP. Cutaneous clues to Cronkhite-Canada syndrome: a case report. Arch Dermatol 1999; 135: 212.
Maraver-Zamora M, Pinto-Morales W, Sánchez D, García D, Martínez-García R, Romero Gómez M, et al. Síndrome de Cronkhite-Canadá: presentación de un nuevo caso de esta enigmática e infrecuente enfermedad. Rev Esp Enferm Dig 2010; 102(3).
Sweetser S, Ahlquist DA, Osborn NK, et al. Clinicopathologic features and treatment outcomes in Cronkhite-Canada syndrome: support for autoimmunity. Dig Dis Sci 2012; 57(2): 496-502.