Información de la revista
Vol. 58. Núm. 2.
Páginas 168-173 (febrero 2003)
Vol. 58. Núm. 2.
Páginas 168-173 (febrero 2003)
Acceso a texto completo
Atresia de vías biliares
Visitas
111741
E. Donat Aliaga
, B. Polo Miquel, C. Ribes-Koninckx
Autor para correspondencia
ribes_car@qva.es
Correspondencia: Sección de Gastroenterología. Hospital Infantil La Fe.Avda. Campanar, 21. 46009 Valencia. España.
Correspondencia: Sección de Gastroenterología. Hospital Infantil La Fe.Avda. Campanar, 21. 46009 Valencia. España.
Sección de Gastroenterología. Hospital Infantil La Fe. Valencia. España.
Este artículo ha recibido
Información del artículo
El Texto completo está disponible en PDF
Bibliografía
[1.]
J. Vázquez, A.M. Hernández-Cano, J.A. Díez, J.R. Lilly.
Atresia de vías biliares. Estado actual.
An Esp Pediatr, 26 (1987), pp. 407-409
[2.]
P.W. Yoon, J.S. Bresee, R.S. Olney, L.M. James, M.J. Khoury.
Epidemiology of biliary atresia: A population-based study.
Pediatrics, 99 (1997), pp. 376-382
[3.]
P.F. Whitington.
Chronic Cholestasis of infancy.
Pediatr Clin North Am, 43 (1996), pp. 1-27
[4.]
I.D. D’Agata, W.F. Balistreri.
Evaluation of liver disease in the pediatric patient.
Pediatr Rev, 20 (1999), pp. 376-390
[5.]
M. Davenport, M. Savage, A.P. Mowat, E.R. Howard.
Biliary atresia splenic malformation syndromes: An etiologic and prognostic subgroup.
Surgery, 113 (1993), pp. 662-668
[6.]
H.H. A-Kader, M.J. Nowicki, K.I. Kuramoto, B. Baroudy, J.B. Zeldis, W.F. Balistreri.
Evaluation of the role of hepatitis C virus in biliary atresia.
Pediatr Infect Dis J, 13 (1994), pp. 657-658
[7.]
R.J. Sokol, C. Mack.
Etiopathogenesis of biliary atresia.
Semin Liver Dis, 21 (2001), pp. 517-524
[8.]
B. Fischler, B. Haglund, A. Hjern.
A population-based study on the incidence and possible pre-and perinatal etiologic risk factors of biliary atresia.
J Pediatr, 141 (2002), pp. 217-222
[10.]
J.F. Fitzgerald.
Cholestatic disorders of infancy.
Pediatr Clin North Am, 35 (1988), pp. 357-375
[11.]
T.R. Silveria, F.M. Salzano, P.T. Donaldson, P.T. Donaldson, G. Mieli-Vergani, E.R. Howard.
Association between HLA and extrahepatic biliary atresia.
J Pediatr Gastroenterol Nutr, 16 (1993), pp. 114-117
[12.]
R.A. Schreiber, R.E. Kleinman.
Genetics, immunology and biliary atresia: An opening or a diversionα.
J Pediatr Gastroenterol Nutr, 16 (1993), pp. 111-113
[13.]
L. Camillus, M.D. Witzleben, D.A. Piccoli.
Extrahepatic bile ducts.
Pediatric gastrointestinal disease, 3rd ed, pp. 915-927
[14.]
K.P. Fung, S.P. Lau.
Gamma-glutamyl transpeptidase activity and its serial measurament in differentation between extrahepatic biliary atresia and neonatal hepatitis.
J Pediatr Gastroenterol Nutr, 4 (1985), pp. 208-213
[15.]
G. Maggiore, O. Bernard, M. Hadchouel, A. Lemmonier, D. Alagille.
Diagnostic value of serum gamma-glutamyl transpeptidase activity in liver diseases in children.
J Pediatr Gastroenterol Nutr, 12 (1991), pp. 21-26
[16.]
R.P. Altman, S. Abramson.
Potential errors in the diagnosis and surgical management of neonatal jaundice.
J Pediatr Surg, 20 (1985), pp. 529-534
[17.]
S.O. Choi, W.H. Park, H.J. Lee.
Ultrasonographic Triangular Cord: the most definitive finding for noninvaisve diagnosis of extrahepatic.
Eur J Pediatr Surg, 8 (1998), pp. 12-16
[18.]
W.H. Park, S.O. Choi, H.J. Lee, S.P. Kim, S.K. Zeon, S.L. Lee.
A new diagnostic approach to biliary atresia with emphasis on the ultrasonographic triangular cord sign: comparison ultrasonography, hepatobiliary scintigraphy, and liver need biopsy in the evaluation of infantile cholestasis.
J Pediatr Surg, 32 (1997), pp. 1555-1559
[19.]
A.G. Manolaki, V.F. Larcher, A.P. Mowat, J.J. Barrett, B. Portmann, E.R. Howard.
The prelaparotomy diagnosis of extrahepatic biliary atresia.
Arch Dis Child, 58 (1983), pp. 591-594
[20.]
G. Azar, D. Benecck, B. Lane, J. Markowitz, F. Daum, E. Kahn.
Atypical morphologic presentation of biliary atresia and value of serial liver biopsies.
J Pediatr Gastroenterol Nutr, 34 (2002), pp. 212-215
[21.]
M.B. Heyman, H.L. Shapiro, M.M. Thaler.
Endoscopic retrograde cholangiography in the diagnosis of biliary malformations in children.
Gastrointest Endosc, 34 (1988), pp. 449-453
[22.]
M. Guelrud, D. Jean, S. Mendoza, J. Plaz, P. Torres.
ERCP in the diagnosis of extrahepatic biliary atresia.
Gastrointest Endosc, 37 (1991), pp. 522-526
[24.]
J.R. Lilly.
The surgery of “correctable“ biliary atresia.
J Pediatr Surg, 20 (1985), pp. 522-525
[25.]
K. Suruga, S. Tsunoda, E. Deguchi, K. Kimura, T. Miyano.
The future role of hepatic portoenterostomy as treatment of biliary atresia.
J Pediatr Surg, 20 (1992), pp. 707-709
[26.]
M. Oh, M. Hobeldin, T. Chen, D.W. Thomas, J.B. Atkinson.
The kasai procedure in the treatment of biliary atresia.
J Pediatr Surg, 30 (1995), pp. 1077-1081
[27.]
R. Emblem, Shake, I. Monclan.
Progress in the treatment of biliary atresia: A plea for surgical intervention within the first two months of life in infants with persistent cholestasis.
Acta Pediatr, 82 (1993), pp. 971-974
[28.]
V. Martinez, J. Boix-Ochoa, J. Lloret, J. Broto.
Paediatric liver transplantation: Life after portoenterostomy in biliary atresia.
J Pediatr Surg, 27 (1992), pp. 830-832
[29.]
P.J. Mc Kiernan, A.J. Backer, D.A. Kelly.
The frecuency and outcome of biliary atresia in the UK and Ireland.
Lancet, 355 (2000), pp. 25-29
[30.]
J.N. Lin, K.L. Wang, J.H. Chuang.
The efficacy of Kasai operation for biliary atresia: A single institutional experience.
J Pediatr Surg, 20 (1992), pp. 704-706
[31.]
R.W. DeConti, R.D. Craver, G.W. Willis, C.B. Hill, D.H. Hayes, R.M. Arensman.
Extrahepatic biliary atresia: From diagnosis to liver transplantation.
Pediatr Surg Int, 7 (1992), pp. 337-340
[32.]
T. Muraji, Y. Higgashimoto.
The inproved outlook of biliary atresia with corticosteroid therapy.
J Pediatr Surg, 9 (1997), pp. 1103-1106
[33.]
J. Manzanares, P. Urruzuno, E. Medina.
Tratamiento médico del niño con enfermedad colestática crónica. Soporte nutricional y tratamiento sustitutivo.
An Esp Pediatr, 116 (1998), pp. 18-21
[34.]
V. Ramaccioni, H.E. Soriano, R. Arumugam, W.J. Klish.
Nutritional aspects of chronic liver disease and liver transplantation in children.
J Pediatr Gastroenterol Nutr, 30 (2000), pp. 361-367
[35.]
P. Vajro, M. Couturier, F. Lemmonier, M. Odievre.
Effects of post-operative cholerstyramine and phenobarbital administration on bile flow restoration in infants with extrahepatic biliary atresia.
J Pediatr Surg, 21 (1986), pp. 36235-36236
[36.]
E.A. Jones, N.V. Bregaza.
The pruritus of colestasis.
Hepatology, 29 (1999), pp. 1003-1006
[37.]
A.F. Hofmann.
Cholestatic liver disease: pathophysiology and therapeutic options.
Liver, 22 (2002), pp. 14-19
[38.]
B. Yerushalmi, R.J. Sokol, M.R. Narkewicz, D. Smith, F.M. Karrer.
Use of rifampicin for severe pruritus in children with cronic cholestasis.
J Pediatr Gastroenterol Nutr, 29 (1999), pp. 442-447
[39.]
C. Steiner, S. Mitzner.
Experiences with MARS liver support therapy in liver failure: Analysis of 176 patients of the International MARS Registry.
Liver, 2 (2002), pp. 20-25
[40.]
C. Ribes-Koninckx, B. Polo, R. Sanchis, E. Donat.
Application of an extracorporeal hepatic support device (MARS) in pediatric patients.
J Paediatr Gastroenterol Nutr, 34 (2002), pp. 440
Copyright © 2003. Asociación Española de Pediatría