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Tratamiento quirúrgico de la dilatación quística congénita de la vía biliar
Surgical treatment of congenital cystic dilatation of the biliary tract
Enrique Artigues Sánchez de Rojas1
Autor para correspondencia
eartigues@hotmail.com

Correspondencia: Dr. E. Artigues Sánchez de Rojas. Avda. Autopista del Saler, 12-23. 46013 Valencia. España.
, Eugenia Pareja Ibars, Ricardo Fabra Ramis, Antonio Vázquez Prado, Francisco Cárdenas Cauqui, Ramón Trullenque Peris
Servicio de Cirugía General y Digestiva (Prof. R. Trullenque Peris). Hospital General Universitario. Valencia. España.
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        "resumen" => "<span class="elsevierStyleSectionTitle">Introducci&#243;n</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">La dilataci&#243;n qu&#237;stica cong&#233;nita de la v&#237;a biliar &#40;DQCVB&#41; es una afecci&#243;n poco frecuente en nuestro medio&#46; Pese a ser una enfermedad cong&#233;nita&#44; aproximadamente un tercio de los casos no se diagnostican en la infancia&#46; Se clasifican en varios tipos&#44; siendo el tipo I&#44; o dilataci&#243;n fusiforme de la v&#237;a biliar extrahep&#225;tica&#44; el m&#225;s frecuente&#44; present&#225;ndose en el 50-90&#37; de casos&#44; seg&#250;n las series&#46;</p> <span class="elsevierStyleSectionTitle">Pacientes y m&#233;todo</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Se presentan los resultados de una serie de pacientes adultos ingresados en nuestro hospital durante los &#250;ltimos 25 a&#241;os con el diagn&#243;stico de DQCVB&#59; dicha serie consta de 11 pacientes&#44; 8 mujeres y 3 varones&#44; con una edad media de 41&#44;8 a&#241;os&#46; Se revisan los antecedentes personales&#44; la cl&#237;nica&#44; las exploraciones complementarias realizadas&#44; la anatom&#237;a de la v&#237;a biliar y la encrucijada biliopancre&#225;tica&#44; la clasificaci&#243;n&#44; las t&#233;cnicas quir&#250;rgicas llevadas a cabo&#44; el an&#225;lisis histopatol&#243;gico de las piezas de resecci&#243;n&#44; la evoluci&#243;n postoperatoria y el seguimiento a medio y largo plazo&#46;</p> <span class="elsevierStyleSectionTitle">Resultados</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">La variante m&#225;s frecuente fue el tipo I &#40;8 casos&#41;&#59; el tama&#241;o medio de la dilataci&#243;n qu&#237;stica fue de 6&#44;2 cm&#59; la existencia de un canal com&#250;n largo se pudo objetivar en tres de los 11 casos &#40;27&#37;&#41;&#59; la t&#233;cnica quir&#250;rgica m&#225;s empleada fue la ex&#233;resis completa del quiste&#44; seguida de reconstrucci&#243;n mediante hepaticoyeyunostom&#237;a en Y de Roux &#40;7 casos&#41;&#59; en un caso&#44; la anatom&#237;a patol&#243;gica inform&#243; de un adenocarcinoma adenopapilar infiltrante en la pared del quiste&#44; y en otro de una metaplasia intestinal focal&#59; un paciente falleci&#243; en el postoperatorio a consecuencia de un cuadro de sepsis&#46;</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Reafirmar la implicaci&#243;n de la existencia de un canal com&#250;n largo en la fisiopatogenia de la DQCVB&#44; la necesidad de disponer preoperatoriamente de un conocimiento de la anatom&#237;a de la v&#237;a biliar y la uni&#243;n biliopancre&#225;tica&#44; y la indicaci&#243;n de elecci&#243;n de resecci&#243;n de la v&#237;a biliar afectada&#44; con reconstrucci&#243;n de la misma mediante hepaticoyeyunostom&#237;a en Y de Roux&#46;</p>"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Introduction</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Congenital cystic dilatation of the biliary tract is infrequent in Spain&#59; although the anomaly is congenital&#44; approximately one-third of cases are not diagnosed in childhood&#46; Various types of the anomaly have been classified and the most common is type I&#44; or fusiform dilatation of the extrahepatic biliary tract&#44; which accounts for 50-90&#37; of cases depending on the series&#46;</p> <span class="elsevierStyleSectionTitle">Material and methods</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">We present the results of a series of adult patients admitted to our hospital in the last 25 years with a diagnosis of congenital cystic dilatation of the biliary tract&#46; Our series consisted of 11 patients&#44; 8 women and 3 men&#44; with a mean age of 41&#46;8 years&#46;We reviewed the patients&#8217; personal history of previous diseases&#44; clinical features&#44; complementary investigations performed&#44; anatomy of the biliary tract and biliary-pancreatic junction&#44; classification&#44; surgical techniques used&#44; histopathological analysis of the surgical specimens&#44; postoperative course and medium- and long-term follow-up&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">The most frequent variant was type I &#40;eight patients&#41;&#46; The mean size of cystic dilatation was 6&#46;2 cm&#46; A long common canal was found in three of the eleven patients &#40;27&#37;&#41;&#46; The most frequently used surgical technique was total excision of the cyst followed by reconstruction through Yen- Roux hepaticojejunostomy &#40;seven patients&#41;&#46; Histopathological analysis revealed an infiltrating adenopapillary adenocarcinoma in the cystic wall in one patient and focal intestinal metaplasia in another&#46; One patient died in the postoperative period due to sepsis&#46;</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">we reaffirm the involvement of a long common canal in the physiopathogenesis of congenital cystic dilatation of the biliary tract and the need for preoperative knowledge of the anatomy of the biliary tract and biliary-pancreatic junction&#46; The surgical treatment of choice is total resection of the cyst with reconstruction through Y-en-Roux hepaticojejunostomy&#46;</p>"
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ISSN: 0009739X
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