medigraphic.com
Órgano oficial de la Sociedad Mexicana de Cirugía Dermatológica y Oncológica, AC

2012, Number 4

<< Back Next >>

Dermatología Cosmética, Médica y Quirúrgica 2012; 10 (4)

Peutz-Jeghers syndrome: a case report with multiple surgical procedures due to hamartomatous polyposis

Aquino FCJ, Rodríguez ISA

Language: Spanish
References: 13
Page: 267-270
PDF size: 208.97 Kb.


ABSTRACT

Peutz-Jeghers syndrome (PJS) is a hereditary autosomal dominant disease, characterized by pigmentation involving oral mucosa, palms and soles, and also associated to gastrointestinal hamartomatous polyposis. The clinical features ranges from asymptomatic cases to, intestinal obstruction, high risk of gastrointestinal cancer and extra-gastrointestinal neoplasm. We report a 21 year-old woman with Peutz-Jeghers syndrome from childhood with mucocutaneus pigmentation and several previous surgeries due to multiple polyposis.


REFERENCES

  1. Amos CI, Keitheri-Cheteri MB, Sabripour M, Wei C, McGarrity TJ, Seldin MF, Nations L, Lynch PM, Fidder HH, Friedman E, Frazier ML. “Peutz-Jeghers Syndrome”. J MedGenet 2004;41:327–333.

  2. Abdo FJ, Pérez TE, Bernal SF, Dzib SJ. “Síndrome de Peutz-Jeghers”. Rev Med Hosp Gen Mex 2005; 68 (2): 99-105.

  3. Gutiérrez BA, Rojo J, Aguilera MA, García C, Casanovas LJ y Aguayo MJ. “Síndrome de Peutz-Jeghers”. An Esp Pediatría 2001; 55: 161-164.

  4. Buck J, Harned R, Llcbtenstein J, Sobin LH. “From the Archives of the AFIP; Peutz-Jeghers Syndrome”. Radiographics 1992; 12:365-378.

  5. Cureton E, and Kim S. “Peutz-Jeghers Syndrome”. N Engl J Med 2007; 357:8.

  6. Arenas R. Dermatología. Atlas, diagnóstico y tratamiento. McGraw-Hill Interamericana. México, DF. 3a. ed. 2005:299.

  7. Lampe A K, Hampton P J, Woodford-Richens K, et al. “Laugier-Hunziker syndrome: an important differential diagnosis for Peutz-Jeghers síndrome”. J Med Genet 2003;40:e77.

  8. Choi HS. “Peutz-Jeghers Syndrome, a new understanding”. J Korean Med Sci 1999; 14: 2-7.

  9. Anaya DM, López TA. “Síndrome de Peutz-Jeghers, A propósito de un caso”. Gaceta Médica Boliviana 2010;33 (2): 59-63.

  10. Pinto SJ, Rebaza VS, Muñoz MS, Cárdenas M. “Síndrome de Peutz- Jeghers y adenocarcinoma de colon”. Rev. Gastroenterol Peru 2004; 24: 363-367.

  11. Pérez EA, Del Pino RG, López SM. “Síndrome de Laugier-Hunziker: Revisión bibliográfica y presentación de 3 casos infantiles”. Revista Mexicana de Cirugía Bucal y Maxilofacial 2010;6 (1): 14-18.

  12. McGarrity TJ, Peiffer LP, Billingsley ML. “Overexpression of Epidermal Growth Factor Receptor in Peutz-Jeghers Syndrome”. Dig Dis Sci 1999; 44 (6): 1136-1141.

  13. Rangwala S, Doherty CB, Katta R. “Laugier-Hunziker syndrome: A case report and review of the literature”. Dermatology Online Journal 2010; 16(12):9.




2020     |     www.medigraphic.com