Caso clínico
Sangrado de angiomiolipoma renal en paciente con síndrome de genes contiguos (TSC2/PKD1) tras 17 años de tratamiento renal sustitutivo
Renal angiomyolipoma bleeding in a patient with TSC2/PKD1 contiguous gene syndrome after 17 years of renal replacement therapy
Mónica Furlanoa,f,g, Yaima Barreirob, Teresa Martíc, Carme Facundod,f,g, César Ruiz-Garcíae,f, Iara DaSilvae,f,g, Nadia Ayasreha,f,g, Cristina Cabrera-Lópezg,i, José Ballaríne,f,g, Elisabet Arsf,g,h, Roser Torraa,f,g,
Autor para correspondencia
a Enfermedades Renales Hereditarias, Servicio de Nefrología, Fundació Puigvert, Barcelona, España
b Servicio de Hemodiálisis, Avericum S.L., Las Palmas de Gran Canaria, España
c Servicio de Radiología, Fundació Puigvert, Barcelona, España
d Unidad de Trasplante Renal, Servicio de Nefrología, Fundació Puigvert, Barcelona, España
e Servicio de Nefrología, Fundació Puigvert, Barcelona, España
f Instituto de Investigaciones Biomédicas Sant Pau (IIB-Sant Pau), Barcelona, España
g Universitat Autònoma de Barcelona, REDinREN, Instituto de Investigación Carlos III, Barcelona, España
h Laboratorio de Biología Molecular, Fundació Puigvert, Barcelona, España
i Servicio de Nefrología, Hospital Moisés Broggi, Sant Joan Despí, Barcelona
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