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>Journals >Cirujano General >Year 2001, Issue 3


Nari GA, Nassar M, Moreno E, Ponce O
Congenital cystic dilation of the biliary tract. Report on six patients
Cir Gen 2001; 23 (3)

Language: Español
References: 16
Page: 168-172
PDF: 4. Kb.


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ABSTRACT

Objective: To inform our experience in the diagnosis and treatment of six patients with cystic dilation of the biliary tract.
Setting: Third level health care hospital.
Description of patients: There were four women and two men, their ages ranged from 45 to 57 years, average 50 years. Predominating symptoms were pain and jaundice. Four patients received surgical treatment, in two a cholecystectomy plus resection of the cyst and hepato-jejuno-anastomosis were performed and, for the other two, cholecystectomy plus choledochotomy with extraction of gallstones. The other two patients were treated medically.
Conclusion: Although congenital cystic dilation of the choledochus is an infrequent entity, it should be taken into account by the surgeon to reach a diagnosis.


Key words: Gallbladder, bile ducts, cysts.


REFERENCIAS

  1. Baumann R, Duclos B, Adolf M. Dilatations kistiques congenitales du Choledoque. Encyclopedie Med-Chir. Editorial Elsevier-Paris 1992.

  2. Facciuto E, Sechi M, Todeschini F. Dilatación congénita y litiasis intrahepática. Enfermedad de Caroli. Pren Med Argent 1988; 55: 42-6.

  3. Miller W, Sechtin A, Campbell W, Pieters P. Imaging findings in Caroli’s disease. Am J Roentgenol 1995; 165: 333-7.

  4. Viaggio J, Iza J, Ciardullo M, Evens L. Dilatación quística congénita del colédoco. Rev Argent Cirug 1978; 36: 98-9.

  5. Balsells J, Margarit C, Murio E, Lazaro J, Cherco R. Adenocarcinome in Caroli’s disease treated by liver transplantation. HPB Surg 1993; 7: 81-6.

  6. Orsoni O, Vadenbossche D, Boukaya V, Verrier C, Audibert B, Picaud R. Un cas de maladie de Caroli pure unilobaire. J Chir 1994; 131: 532-7.

  7. Parcerisa R, Degani J, Ferraroti J, Beret N. Dilatación quística de las vías biliares. Pren Med Argent 1993; 80: 322-6.

  8. Molinari E, Alche S, Segura J, Caorsi S, Banga E. Dilataciones quísticas de la vía biliar. Rev Argent Cirug 1984; 47: 33-5.

  9. Valayer J, Moreaux J. Kystes de la voie biliaire. Encyclopedie Med-Chir. Editorial Elsevier-Paris 1992.

  10. Suchida Y, Sato T, Sanjo K, Etoh T, Hata K, Terawaki K et al. Evaluation of long term results of Caroli’s disease, 21 years observation of a family with autosomal. “Dominant” inheritance and review of literature. Hepatogastroenterology 1995; 42: 175-181.

  11. Benhijeb T, Muller J, Gellert K, Zanow J, Rudolph B. Aktuelle therapie der Gallencysten II. Intrahepatische Cysten (Caroli Syndrom). Chirurg 1996; 67: 238-43.

  12. Blumgart LH. Cirugía de hígado y vías biliares. Ed. Panamericana, Buenos Aires, 1990: 1167-77.

  13. Desroches J, Spahr L, Leduce F, Pomier Layfargues G, Picard M, Picard D. Noninvasive diagnosis of Caroli’s syndrome associated with congenital fibrosis using hepatobiliary scintigraphy. Clin Nucl Med 1995; 20: 512-4.

  14. Espinosa Aguilar M, Lopez de Hierro Ruiz M, Pinel Julian L, Gonzalez Galilea A, Suarez Crespo J. Síndrome de Caroli: una entidad variable. Rev Esp Enferm Dig 1994; 86: 849-52.

  15. Nari G, Moreno E, Nassar M, Mana R, Lopez Vinuesa F. Dilataciones quísticas congénitas de la vía biliar extrahepática. Acta Gastroenterol Latinoam 1998; 28: 33-5.

  16. Nari G, Prenna J, Moreno E, Oliva F, Olivares S. Enfermedad de Caroli: Presentación de un caso y revisión de la literatura. Acta Gastroenterol Latinoam 1998; 28: 209-11.






>Journals >Cirujano General >Year 2001, Issue 3
 

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