[Retroperitoneal haemorrhage after traumatic rupture of a phaechromocytoma].

نویسندگان

  • María Teresa Gómez Hernández
  • Guzmán Franch-Arcas
  • Carmen González Sánchez
  • Raúl Sánchez-Jiménez
  • María Cerro-Martínez
چکیده

1. Thull DL, Vogel VG. Recognition and management of hereditary breast cancer syndromes. Oncologist. 2004;9:13–24. 2. Aretz S, Stienen D, Uhlhaas S, Loff S, Back W, Pagenstecher C, et al. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome. Hum Mutat. 2005;26:513–9. 3. Volikos E, Robinson J, Aittomaki K, Mecklin JP, Järvinen H, Westerman AM, et al. LKB1 exonic and whole gene delection are a common cause of Peutz-Jeghers syndrome. J Med Genet. 2006;43:18–9. 4. Bruwer A, Bargen JA, Kierland RR. Surface pigmentation and generalized intestinal polyposis; (Peutz-Jeghers syndrome). Proc Staff Meet May Clin. 1954;29:168–71. 5. Calva D, Howe JR. Sı́ndromes de poliposis hamartomatosa. Surg Clin N Am. 2008;88:779–817. 6. Espin Basany E, Garcı́a Aguilar J. Cáncer colorrectal: aspectos generales y lesiones precancerosas. Manual de la Asociación Española de Cirujanos. Madrid: Panamericana; 2010. p. 502. 7. Jansen M, de Leng WW, Baas AF, Myoshi H, Mathus-Vliegen L, Taketo MM, et al. Mucosal prolapse in the pathogenesis of Peutz-Jeghers polyposis. Gut. 2006;55:1–5. 8. Kinzler KW, Vogelstein B. Landscaping the cancer terrain. Science. 1998;280:1036–7. 9. Beggs AD, Latchford AR, Vasen HF, Moslein G, Alonso A, Aretz S, et al. Peutz-Jeghers syndrome: a systematic review and recommendations for management. Gut. 2010;59:975–86.

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عنوان ژورنال:
  • Cirugia espanola

دوره 91 3  شماره 

صفحات  -

تاریخ انتشار 2013