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Journal Information
Vol. 25. Issue 8.
Pages 578-581 (January 2001)
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Vol. 25. Issue 8.
Pages 578-581 (January 2001)
Síndrome urofacial de ochoa: caso clínico
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M.E. Muñoz fernández1, J. Rodó salas, C. Grande moreillo, L. Morales fochs
Servicio de Cirugía Pediátrica. Unidad Integrada Hospital Sant Joan de Déu – Hospital Clinic. Barcelona
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Resumen

Se trata del caso de una paciente de 11 años de edad portadora de una derivación urinaria por una uropatía compleja debido a una disinergia vésico-esfinteriana. La facies inexpresiva, con mirada perdida y gesticulaciones forzadas sobre todo al sonreir (la sonrisa parecía un llanto) junto a la uropatía grave, permitió catalogarla como síndrome de Ochoa

Se le practicó una fijación psoica de la vejiga, un reimplante ureteral derecho, una liberación del cuello vesical y el cierre de la cistostomía. En la evolución empeoró la función renal. Recientemente ha recibido un trasplante renal en otro centro y la paciente se encuentra asintomática

Palabras clave:
Síndrome urofacial
Ochoa
Abstract

An 11 year-old girl had an urinary diversión because of a complex uropathy with vesical sphincter dyssinergism. Her inexpressive face with lost eyes and forced gestures, especially when smiling –her smile looking rather like weeping- was the clue to the diagnosis of Ochoa’s syndrome

She underwent psoic bladder fixation, right ureteral reimplantation, bladder neck losening and cystostomy undiversion. At follow-up, renal function deteriorated. She has recently received a kidney transplantation in another institution, and is now symptom-free

Key words:
Urofacial syndrome
Ochoa’s syndrome

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