<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1729-519X</journal-id>
<journal-title><![CDATA[Revista Habanera de Ciencias Médicas]]></journal-title>
<abbrev-journal-title><![CDATA[Rev haban cienc méd]]></abbrev-journal-title>
<issn>1729-519X</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Ciencias Médicas de la Habana]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1729-519X2007000100009</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[ECOENDOSCOPIA EN LA PATOLOGÍA BILIAR Y PANCREÁTICA]]></article-title>
<article-title xml:lang="en"><![CDATA[Endosonography in Pancreatobiliary Disorders]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Díaz-Canel Fernández]]></surname>
<given-names><![CDATA[Osvaldo]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Martínez López]]></surname>
<given-names><![CDATA[Rolando]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ruiz Torres]]></surname>
<given-names><![CDATA[Julián]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Anido Escobar]]></surname>
<given-names><![CDATA[Vivianne]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pernía González]]></surname>
<given-names><![CDATA[Liliana]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Centro Nacional de Cirugía Endoscópica  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2007</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2007</year>
</pub-date>
<volume>6</volume>
<numero>1</numero>
<fpage>0</fpage>
<lpage>0</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S1729-519X2007000100009&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S1729-519X2007000100009&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S1729-519X2007000100009&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[La ecoendoscopía o ultrasonografía endoscópica (USE) permite una buena visualización de la vesícula, vía biliar, del parénquima pancreático y de las estructuras vasculares vecinas a estos órganos. 1,2 Tiene una alta resolución debido a la cercanía del transductor y a las elevadas frecuencias. Junto con otras técnicas de imagen que se están desarrollando, como la tomografía computarizada (TC) helicoidal y la colangiopancreatografía por resonancia magnética (CPRM) son técnicas seguras y que ofrecen resultados prometedores en el estudio de los tumores, permitiendo la estadificación locoregional de éstos, llegar al diagnóstico de cálculos pequeños de la vía biliar principal que no son visualizados por US abdominal y lograr una visualización más fiel de la glándula pancreática y de las estructuras vasculares vecinas. 3,4, 5]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Endoscopic ultrasound is a minimally invasive imaging modality that provides high - resolution images of the extrahepatic biliary tree and the surrounding structures. It has been shown to be accurate for the detection and staging of bile duct and gallbladder cancer, and is especially useful for small tumors. Intraductal techniques, which are still in evolution, may provide even more information about the etiology and extent of biliary structures and mural tumors. EUS has also been shown to be useful for the detection of biliary stones and sludge when transabdominal ultrasound is not diagnostic. In many cases, diagnostic EUS is needed. 1, 2, 3 Endosonography produces detailed images of the pancreas and surrounding blood vessels and provides both accurate detection and staging of malignant lesions and the means for making a tissue diagnosis.The instruments and techniques for endosonography continue improving, and at present EUS can be considered a promising minimally invasive tool for evaluating the pancreatobiliary disorders. 4, 5]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Ecoendoscopía]]></kwd>
<kwd lng="es"><![CDATA[Afecciones pancreatobiliares]]></kwd>
<kwd lng="en"><![CDATA[Endosonography]]></kwd>
<kwd lng="en"><![CDATA[Pancreatobiliary Disorders]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="center" class="Estilo1">Centro Nacional de Cirug&iacute;a Endosc&oacute;pica </p>     <p class="Estilo1"><strong>&nbsp; </strong></p>     <p align="center" class="Estilo1"><strong>ECOENDOSCOPIA EN LA PATOLOGÍA BILIAR Y  PANCREÁTICA </strong></p>     <p class="Estilo1">&nbsp; </p>     <p class="Estilo1">*Dr. Osvaldo D&iacute;az–Canel Fern&aacute;ndez. Calle 13 N&uacute;m. 416 e/ G y F. El Vedado. Ciudad de La Habana. Tel&eacute;fono: 832-2958. </p>     <p class="Estilo1">* Dr. Rolando Mart&iacute;nez L&oacute;pez . Calle Mart&iacute; N&uacute;m. 630 e/ Rubiera y Perdomo. Regla. Ciudad de La Habana. Tel&eacute;fono: 94-2228  <a href=".%20rolando@cce.sld.cu">. rolando@cce.sld.cu </a></p>     <p class="Estilo1">** Dr. Juli&aacute;n Ruiz Torres. Calle 28 N&uacute;m. 116 e/ 1&ordf; y 3&ordf; Miramar. Ciudad de La Habana. Tel&eacute;fono: 203-1672.  <a href="julian@cce.sld.cu">julian@cce.sld.cu </a></p>     <p class="Estilo1">*** Dra. Vivianne Anido Escobar. Calle F N&uacute;m. 158 e/ Calzada y 9. El Vedado. Ciudad de La Habana.Tel&eacute;fono: 832-1418  <a href=".%20vivianne@cce.sld.cu">. vivianne@cce.sld.cu </a></p>     <p class="Estilo1">****Dra. Liliana Pern&iacute;a Gonz&aacute;lez. Calle Aguacate N&uacute;m.405. Apto. 402 e/ Teniente Rey y Amargura. Habana Vieja. Ciudad de La Habana. Tel&eacute;fono: 867-5080.  <a href="liliana@cce.sld.cu">liliana@cce.sld.cu </a></p>     <p class="Estilo1">&nbsp; </p>     ]]></body>
<body><![CDATA[<p class="Estilo1">* Especialista Primer Grado en Medicina General Integral y Especialista Segundo Grado en Gastroenterolog&iacute;a del </p>     <p class="Estilo1">CCE,  Asistente e Investigador Auxiliar, Aspirante a Dr. en Ciencias. </p>     <p class="Estilo1">** Especialista Segundo Grado en Gastroenterolog&iacute;a,  Asistente, Investigador Auxiliar y Director del CCE. </p>     <p class="Estilo1">*** Especialista Segundo Grado en Gastroenterolog&iacute;a del </p>     <p class="Estilo1">CCE, Investigadora Agregada. </p>     <p class="Estilo1">**** Especialista Primer Grado en Radiolog&iacute;a del CCE. </p>     <p class="Estilo1">&nbsp; </p>     <p class="Estilo1"><strong>RESUMEN </strong></p>     <p class="Estilo1">La ecoendoscop&iacute;a o ultrasonograf&iacute;a endosc&oacute;pica (USE) permite una buena visualizaci&oacute;n de la ves&iacute;cula, v&iacute;a biliar, del par&eacute;nquima pancre&aacute;tico y de las estructuras vasculares vecinas a estos &oacute;rganos. 1,2 Tiene una alta resoluci&oacute;n debido a la cercan&iacute;a del transductor y a las elevadas frecuencias. Junto con otras t&eacute;cnicas de imagen que se est&aacute;n desarrollando, como la tomograf&iacute;a computarizada (TC) helicoidal y la colangiopancreatograf&iacute;a por resonancia magn&eacute;tica (CPRM) son t&eacute;cnicas seguras y que ofrecen resultados prometedores en el estudio de los tumores, permitiendo la estadificaci&oacute;n locoregional de &eacute;stos, llegar al diagn&oacute;stico de c&aacute;lculos peque&ntilde;os de la v&iacute;a biliar principal que no son visualizados por US abdominal y lograr una visualizaci&oacute;n m&aacute;s fiel de la gl&aacute;ndula pancre&aacute;tica y de las estructuras vasculares vecinas. 3,4, 5 </p>     <p class="Estilo1"><strong>Palabras clave: </strong>Ecoendoscop&iacute;a, Afecciones pancreatobiliares. </p>     ]]></body>
<body><![CDATA[<p class="Estilo1">&nbsp; </p>     <p class="Estilo1"><strong>INTRODUCCION </strong></p>     <p class="Estilo1">La ecoendoscop&iacute;a (EE) o endoultrasonograf&iacute;a (EUS) gastrointestinal es una t&eacute;cnica de diagn&oacute;stico por imagen de introducci&oacute;n relativamente reciente. La primera publicaci&oacute;n se realiz&oacute; a principios de los a&ntilde;os ochenta. 1,2,3 Consiste en introducir, a trav&eacute;s del tubo digestivo, un endoscopio que lleva conectada una sonda ecogr&aacute;fica de alta frecuencia (5 MHz a 20 MHz) en su extremo distal. Su colocaci&oacute;n, en la proximidad de la v&iacute;a biliar y el p&aacute;ncreas, permite obtener im&aacute;genes de alta calidad, con gran precisi&oacute;n diagn&oacute;stica, evitando los artefactos relacionados con la interposici&oacute;n de &oacute;rganos y estructuras como el propio tubo digestivo. 4,5 En funci&oacute;n del tipo de transductor ecogr&aacute;fico cambia el eje de estudio y, por lo tanto, se modifica la imagen obtenida de un mismo objeto. 6,7 </p>     <p class="Estilo1">Se trata de una t&eacute;cnica m&iacute;nima invasiva, de baja morbilidad, con una tasa de complicaciones inferior a 1 /2 OOO. </p>     <p class="Estilo1">Los primeros ecoendoscopios eran de tipo radial y permit&iacute;an realizar una descripci&oacute;n morfol&oacute;gica, sin posibilidad de intervencionismo; no obstante, en sus comienzos, result&oacute; un claro avance diagn&oacute;stico, obteniendo m&aacute;s resoluci&oacute;n que las t&eacute;cnicas de imagen existentes entonces, especialmente en lo referente a la estadificaci&oacute;n locorregional del c&aacute;ncer de es&oacute;fago, est&oacute;mago, p&aacute;ncreas y recto. En el caso de la v&iacute;a biliar, especialmente en la detecci&oacute;n de coledocolitiasis, demostr&oacute; que ten&iacute;a la misma sensibilidad que la CPRE, sin la morbilidad asociada de &eacute;sta (Figura 1). </p>     <p class="Estilo1">La comercializaci&oacute;n, en 1991, de los ecoendoscopios sectoriales supuso un avance cualitativo; adem&aacute;s de introducir el Doppler en la EE, permite la realizaci&oacute;n de biopsias (punci&oacute;n aspiraci&oacute;n con aguja fina- PAAF) con control ecogr&aacute;fico permanente del recorrido de la punta de la aguja, y abri&oacute; el camino a la terap&eacute;utica en el campo de la patolog&iacute;a b&iacute;liopancre&aacute;tica. 8 </p>     <p class="Estilo1">La fase diagn&oacute;stica de la patolog&iacute;a biliopancre&aacute;tica se describe en la mayor&iacute;a de las publicaciones con equipos radiales; sin embargo, los equipos sectoriales son igualmente v&aacute;lidos, con la ventaja de aportar la posibilidad de la exploraci&oacute;n vascular mediante Doppler y recurrir a la PAAF en caso de lesiones dudosas. 9,10 </p>     <p class="Estilo1">&nbsp; </p>     <p class="Estilo1"><strong>DESARROLLO </strong></p>     <p class="Estilo1"><strong><em>La ecoendoscop&iacute;a en la patolog&iacute;a biliar </em></strong></p>     ]]></body>
<body><![CDATA[<p class="Estilo1">La exploraci&oacute;n de la v&iacute;a biliar principal (VBP) se realiza desde el bulbo duodenal hasta la papila. La exploraci&oacute;n del hep&aacute;tico com&uacute;n y col&eacute;doco se consigue aspirando e instilando agua en la rodilla duodenal, y manteniendo el bal&oacute;n del ecoendoscopio con m&iacute;nimo relleno, con la finalidad de permitir los movimientos de introducci&oacute;n y retirada, que deben ser muy suaves, asociados a rotaci&oacute;n y tensi&oacute;n del mando anteroposterior del endoscopio y s&oacute;lo ocasionalmente del mando lateral. La regi&oacute;n ampular y el col&eacute;doco distal precisan la introducci&oacute;n del ecoendoscopio en la segunda porci&oacute;n duodenal hasta la regi&oacute;n ampular mediante control endosc&oacute;pico, y desde aqu&iacute; y mediante una maniobra similar a la retirada de la CPRE podemos explorar la papila, el col&eacute;doco distal, y al continuar la retirada se puede apreciar la totalidad del col&eacute;doco. 11, 12 </p>     <p class="Estilo1">La ves&iacute;cula biliar se explora desde la proximidad del bulbo duodenal (distal o proximal) en funci&oacute;n de las variantes anat&oacute;micas que presente el individuo explorado. 13, 14 </p>     <p class="Estilo1">La v&iacute;a biliar puede explorarse pr&aacute;cticamente en 100 % de los pacientes sin intervenciones quir&uacute;rgicas previas. 15, 16 </p>     <p class="Estilo1"><em>Existen algunas limitaciones de la EE en el estudio de la v&iacute;a biliar </em> </p>     <p class="Estilo1">Resulta t&eacute;cnicamente imposible en caso de gastrectom&iacute;a total y B-II, as&iacute; como en presencia de estenosis gastroduodenales. </p>     <p class="Estilo1">Pueden ser dif&iacute;cil de interpretar tras una CPRE, especialmente si se ha colocado una pr&oacute;tesis, debido a la presencia de aerobilia y al engrosamiento parietal de la v&iacute;a biliar. </p>     <p class="Estilo1">La presencia de aire dentro de un divert&iacute;culo duodenal, yuxtaampular. </p>     <p class="Estilo1">La distancia al hilio hep&aacute;tico puede hacer dif&iacute;cil la adecuada estadificaci&oacute;n de los tumores hiliares. </p>     <p class="Estilo1">Finalmente, existe una marcada dificultad en la diferenciaci&oacute;n entre una Odditis y un Ampuloma T1. </p>     <p class="Estilo1">En general, podemos afirmar que la EE tiene la misma sensibilidad en la detecci&oacute;n de las neoplasias de p&aacute;ncreas que la TAC. 17 </p>     ]]></body>
<body><![CDATA[<p class="Estilo1">Sin embargo, la EE resulta superior en la detecci&oacute;n de tumores peque&ntilde;os (&lt; 25 mm) entre los que encontramos aquellos con mayores posibilidades de resecci&oacute;n. 18 </p>     <p class="Estilo1">En cuanto a la valoraci&oacute;n global de la infiltraci&oacute;n vascular, la EE resulta similar a la TC helicoidal (o algo superior, aunque sin alcanzar significado estad&iacute;stico). </p>     <p class="Estilo1">En estudios previos se mantiene la idea de que la EE es inferior a la TC en el estudio de la invasi&oacute;n vascular de los vasos mesent&eacute;ricos y en general de la infiltraci&oacute;n de vasos arteriales; sin embargo, el empleo de ecoendoscopios sectoriales con eco-Doppler mejora la calidad del estudio vascular por EE y esta superioridad de la TC deber&aacute; ser demostrada. </p>     <p class="Estilo1">Estudios recientes apuntan a la TC helicoidal como la mejor t&eacute;cnica para determinar el estadio TNM con una sensibilidad de 67 % y una seguridad diagn&oacute;stica de 83 % (Tabla 1). La EE permite el estudio locorregional, y por lo tanto la determinaci&oacute;n de su estadio M quedar&iacute;a fuera de sus posibilidades. Sin embargo, salvo en el caso del estadio M, la EE resulta m&aacute;s sensible que la TC para detectar la irresecabilidad, en funci&oacute;n de criterios locoregionales. 19 </p>     <p align="center" class="Estilo1"><img src="/img/revistas/rhcm/v6n1/f0109107.jpg" width="573" height="210">  </p>     
<p align="center" class="Estilo1">&nbsp; </p>     <p align="left" class="Estilo1">Donde la TC helicoidal se demuestra superior a la EUS, en lo referente a la estadificaci&oacute;n; es en presencia de grandes tumoraciones (&gt;4 cm), en las que las deformidades anat&oacute;micas y la mayor distancia desde la sonda ecogr&aacute;fica a las estructuras vasculares, no permitir&aacute;n su adecuada visualizaci&oacute;n. En general, estos tumores son irresecables y la EUS se limitar&aacute; a la obtenci&oacute;n de una muestra citol&oacute;gica que confirme su naturaleza tumoral (Figura 2). 20 </p>     <p class="Estilo1">El empleo de algoritmos diagn&oacute;sticos, a partir de la informaci&oacute;n obtenida de la TC y la EE, permite seleccionar los pacientes resecables, reduce el coste y evita laparotom&iacute;as innecesarias. No obstante, cerca de 20 % de los pacientes considerados como resecables por TC helicoidal y EE, finalmente ser&aacute;n irresecables, debido a la presencia de micromet&aacute;stasis hep&aacute;ticas o carcinomatosis peritoneal (Figura 3, 4). </p>     <p class="Estilo1">Los tumores ampulares merecen un an&aacute;lisis separado, ya que la pr&aacute;ctica de la EE resulta t&eacute;cnicamente m&aacute;s dif&iacute;cil; pero, por otro lado, la TC tambi&eacute;n encuentra m&aacute;s dificultades en el estudio de esta zona; globalmente la EE resulta &uacute;til, y obtiene una seguridad de 80-90 % en la estadificaci&oacute;n de los tumores grandes, y una seguridad de 70 % en los menores de 2 cm. En el caso de tumores peque&ntilde;os, la evaluaci&oacute;n de la infiltraci&oacute;n de la pared debe realizarse sin comprimir el tumor con el bal&oacute;n relleno de agua, y probablemente con interposici&oacute;n de agua en el duodeno. 21 </p>     <p class="Estilo1">Ya se ha mencionado la limitaci&oacute;n de la EE para determinar las met&aacute;stasis a distancia, por lo que el estadio M no puede sistematizarse por EE debido a la imposibilidad de exploraci&oacute;n de la propia sonda ecogr&aacute;fica, aunque existen casos anecd&oacute;ticos de met&aacute;stasis hep&aacute;ticas y suprarrenales detectadas y biopsiadas por EE, as&iacute; como peque&ntilde;as colecciones de ascitis periduodenales y retrog&aacute;stricas, que tambi&eacute;n podr&iacute;an ser aspiradas mediante PAAF y diagnosticar o excluir una carcinomatosis peritoneal. 22 </p>     ]]></body>
<body><![CDATA[<p class="Estilo1"><strong><em>Otros tumores de p&aacute;ncreas </em></strong></p>     <p class="Estilo1">Otros tipos de tumores, como los cistoadenomas del p&aacute;ncreas constituyen 10 -15 % de las lesiones qu&iacute;sticas. La EE permite diferenciarlos, tanto por sus diferentes patrones ecogr&aacute;ficos, como por el an&aacute;lisis bioqu&iacute;mico de su contenido que resulta f&aacute;cil de obtener gracias a la PAAF guiada por EUS. La seguridad diagn&oacute;stica var&iacute;a alrededor de 92 % (Figura 4). 23 </p>     <p class="Estilo1"><em><strong>S</strong></em><strong><em>e han descrito diferentes patrones de tumores qu&iacute;sticos </em></strong></p>     <p class="Estilo1">La presencia de quistes simples o de un fino septo son indicativos de benignidad, especialmente si son menores de 2 cm. 24 </p>     <p class="Estilo1">Por el contrario, la pared gruesa, la presencia de tumoraci&oacute;n intraqu&iacute;stica, septos de grueso calibre o patr&oacute;n macroqu&iacute;stico son indicativos de malignidad. </p>     <p class="Estilo1">En un estudio reciente, Brugge demuestra que los criterios morfol&oacute;gicos aislados son poco sensibles y espec&iacute;ficos para diferenciar lesiones potencialmente malignas. La citolog&iacute;a, aunque muy espec&iacute;fica, contin&uacute;a siendo poco sensible, mientras que la determinaci&oacute;n del CEA aumenta la sensibilidad de 65 a 89 %; por el contrario, el estudio de Sedlack no encuentra una clara ventaja en el estudio citol&oacute;gico o la determinaci&oacute;n de CEA. Probablemente, en la mayor&iacute;a de los casos el aspecto ecoendosc&oacute;pico es suficiente para aventurar un diagn&oacute;stico sobre benignidad o malignidad, aunque existen casos en los que el an&aacute;lisis del contenido qu&iacute;stico puede ser determinante para definir el tratamiento que debe seguirse. 25 </p>     <p class="Estilo1">En el caso de los tumores endocrinos, la EE ha demostrado su utilidad, incluyendo los gastrinomas, que pueden ser adecuadamente diagnosticados en 80 % de los casos. La serie de Anderson con 82 pacientes que presentaban tumores neuroendocrinos, probablemente la mayor serie de un &uacute;nico centro, obtienen una sensibilidad y seguridad diagn&oacute;stica de 93 % y una especificidad de 95 %, lo que demuestra que la EE es una t&eacute;cnica diagn&oacute;stica de primera l&iacute;nea en el manejo de los tumores neuroendocrinos. 26, 27 </p>     <p class="Estilo1"><strong><em>Pancreatitis aguda </em></strong></p>     <p class="Estilo1">La EUS fue equivalente a la TC en la diferenciaci&oacute;n entre pancreatitis edematosa (difusamente hipoecoica y aumentada de tama&ntilde;o) y necrohemorr&aacute;gica (masas intrapancre&aacute;ticas hipoecoicas y focales) y superior en la detecci&oacute;n de coledocolitiasis, resulta similar a la CPRE en este &uacute;ltimo punto. En ocasiones, los cambios inflamatorios del antro y duodeno pueden impedir la adecuada exploraci&oacute;n de la cabeza pancre&aacute;tica. 28, 29 </p>     <p class="Estilo1"><strong><em>Pancreatitis cr&oacute;nica </em></strong></p>     ]]></body>
<body><![CDATA[<p class="Estilo1">El par&eacute;nquima pancre&aacute;tico normal presenta un patr&oacute;n ecogr&aacute;fico homog&eacute;neo con una distribuci&oacute;n uniforme de un fino punteado de diferentes gamas de grises. 30, 31 </p>     <p class="Estilo1">En las pancreatitis cr&oacute;nicas graves se transforma en un patr&oacute;n heterog&eacute;neo, con focos hiperecog&eacute;nicos repartidos por toda la gl&aacute;ndula, y tabiques de aspecto fibr&oacute;tico que separan peque&ntilde;os focos hipoecog&eacute;nicos de aspecto nodular. Pueden verse calcificaciones y lesiones qu&iacute;sticas de diferentes tama&ntilde;os (Figura 5). </p>     <p class="Estilo1">Se ha descrito que la presencia de estos cambios parenquimatosos en los pacientes sin riesgo de pancreatitis cr&oacute;nica es infrecuente; por el contrario, en los pacientes con ingesti&oacute;n excesiva de alcohol, independientemente de que presenten s&iacute;ntomas o permanezcan sintom&aacute;ticos, se encuentra una alta prevalenc&iacute;a de estos cambios parenquimatosos, y se postula sobre la utilidad de la EE en el diagn&oacute;stico precoz de la pancreatitis cr&oacute;nica. La sensibilidad y la especificidad de los cambios parenquimatosos son dif&iacute;ciles de evaluar, debido a la poca frecuencia con la que se dispone de confirmaci&oacute;n histol&oacute;gica (Tabla 2). 32 </p>     <p class="Estilo1">&nbsp; </p>     <p align="center" class="Estilo1"><img src="/img/revistas/rhcm/v6n1/f0209107.jpg" width="562" height="182"></p>     
<p class="Estilo1">&nbsp; </p>     <p class="Estilo1">La EE puede detectar los cambios ductales asociados a la pancreatitis cr&oacute;nica, siendo el m&aacute;s precoz la dilataci&oacute;n con aumento en la ecogenicidad de sus paredes y, posteriormente, la irregularidad con estenosis y presencia de c&aacute;lculos en su interior. 33, 34, 35 </p>     <p class="Estilo1">En este sentido, se ha podido comprobar su utilidad en el diagn&oacute;stico diferencial de la presencia de calcificaciones focales en la cabeza de p&aacute;ncreas y su diferenciaci&oacute;n con coledocolitiasis. 36 </p>     <p class="Estilo1">La pancreatitis cr&oacute;nica es uno de los principales problemas al diagnosticar una neoplasia pancre&aacute;tica. Resulta frecuente que se solicite una EE para descartar un tumor maligno en presencia de un crecimiento de la cabeza del p&aacute;ncreas. Los artefactos asociados a la presencia de calcificaciones pancre&aacute;ticas, y la dificultad para moverse en un duodeno deformado por los cambios inflamatorios pancre&aacute;ticos, as&iacute; como la incapacidad de los ultrasonidos para diferenciar cambios neopl&aacute;sicos de cambios inflamatorios, explican muchos de los diagn&oacute;sticos incorrectos; s&oacute;lo la PAAF dirigida por EUS permite paliar en parte estas carencias. 37 </p>     <p class="Estilo1"><b><em>Otras anomal&iacute;as pancre&aacute;ticas </em></b></p>     ]]></body>
<body><![CDATA[<p class="Estilo1">Algunas anomal&iacute;as cong&eacute;nitas que pueden ser sospechadas mediante EE, como el p&aacute;ncreas ect&oacute;pico, p&aacute;ncreas anular o la presencia de un conducto com&uacute;n pancre&aacute;tico-biliar de longitud superior a 15 mm, tienden a asociarse con patolog&iacute;a pancre&aacute;tica. 38, 39, 40 </p>     <p class="Estilo1">Haciendo referencia a este &uacute;ltimo supuesto, la presencia por ecoendoscopia de un canal com&uacute;n de al menos 12 mm obtiene una sensibilidad de 88 % y una especificidad de 100 % comparada con la CPRE. 41, 42, 43 </p>     <p class="Estilo1"><strong><em>La exploraci&oacute;n pancre&aacute;tica y biliar mediante sondas-cateter o minisondas </em></strong></p>     <p class="Estilo1">Tambi&eacute;n denominada ultrasonograf&iacute;a intraductal (UID). B&aacute;sicamente consiste en introducir en los conductos biliar y pancre&aacute;tico, con una t&eacute;cnica similar a la CPRE o por v&iacute;a transhep&aacute;tica, unos cat&eacute;teres que llevan un transductor ultras&oacute;nico que gira por un mecanismo mec&aacute;nico y genera una imagen radial, perpendicular al eje de la sonda, aunque en determinadas circunstancias puede simular una imagen lineal. 44, 45, 46, 47 </p>     <p class="Estilo1">La UID ofrece dificultades t&eacute;cnicas y riesgos asociados a la canulaci&oacute;n biliopancre&aacute;tica, adem&aacute;s existe un alto riesgo de rotura de este material y disminuye el n&uacute;mero de exploraciones por sonda. Teniendo en cuenta estos inconvenientes, debemos preguntarnos: </p>     <p class="Estilo1"><strong><em>&iquest;Qu&eacute; ventajas ofrece la UID sobre la EE? </em></strong></p>     <p class="Estilo1">Hay autores que defienden la superioridad de la UID sobre cualquier otra t&eacute;cnica para detectar la presencia de coledocolitiasis incluso en presencia de colangiograf&iacute;a normal por CPRE. </p>     <p class="Estilo1">En el caso de los ampulomas, la UID es la &uacute;nica t&eacute;cnica que permite descartar la invasi&oacute;n submucosa y definir el grupo de pacientes susceptibles de resecci&oacute;n endosc&oacute;pica. </p>     <p class="Estilo1">&nbsp; </p>     <p class="Estilo1"><b>CONCLUSIONES </b> </p>     ]]></body>
<body><![CDATA[<p class="Estilo1">--La ecoendoscopia es una t&eacute;cnica de diagn&oacute;stico muy &uacute;til en la patolog&iacute;a biliopancre&aacute;tica. </p>     <p class="Estilo1">--La combinaci&oacute;n de la TC helicoidal y la EE resulta &oacute;ptima en el manejo de la patolog&iacute;a biliopancre&aacute;tica. </p>     <p class="Estilo1"><strong>&nbsp; </strong></p>     <p class="Estilo1"><strong>ABSTRACT: </strong>Endosonography in Pancreatobiliary Disorders.</p>     <p class="Estilo1">Endoscopic ultrasound is a minimally invasive imaging modality that provides high – resolution images of the extrahepatic biliary tree and the surrounding structures. It has been shown to be accurate for the detection and staging of bile duct and gallbladder cancer, and is especially useful for small tumors. Intraductal techniques, which are still in evolution, may provide even more information about the etiology and extent of biliary structures and mural tumors. EUS has also been shown to be useful for the detection of biliary stones and sludge when transabdominal ultrasound is not diagnostic. In many cases, diagnostic EUS is needed. 1, 2, 3 Endosonography produces detailed images of the pancreas and surrounding blood vessels and provides both accurate detection and staging of malignant lesions and the means for making a tissue diagnosis.The instruments and techniques for endosonography continue improving, and at present EUS can be considered a promising minimally invasive tool for evaluating the pancreatobiliary disorders. 4, 5 </p>     <p class="Estilo1"><strong>Key words: </strong>Endosonography,&nbsp; Pancreatobiliary Disorders. </p>     <p class="Estilo1">&nbsp; </p>     <p class="Estilo1">&nbsp; </p>     <p align="center" class="Estilo1">&nbsp; </p>     <p align="center" class="Estilo1"><strong>REFERENCIAS BIBLIOGRAFICAS </strong></p>     ]]></body>
<body><![CDATA[<p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">1. Amouyal P, Pa lazzo L, Amouyal G. Endosonography: promising    method for diag&shy;nosis of extrahepatic cholestasis. Lancet. 1989;2:1195-8.  <p class="Estilo1">&nbsp; </p>     <p class="Estilo1">2. Jellouli F, Keriven-Souquet O, Henry L. Endoscopic ultrasound    and spiral CT scan for biliopancreatic cancer: preliminary prospective study    of 40 patients [abstract]. Endoscopy. 1996;28:55. </p>     <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">3. De Ledinghen V, Lecesne R, Raymond JM. Endoscopic ultrasonography    versus magnetic resonance cholangiography for the diagnosis of common bile duct    stones: preliminary results of a prospective controlled study. Hepatology. 1996;24:172.  <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">4. Giovannini M, Roche J, Lapuelle J, Rabbia I, Pauwells A.    Cholestasis of unknown ori&shy;gin. Results of a prospective study in 121 patients.    Gastroenterology. 1995;S:A-153. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">5. Prat F, Amouyal P, Amouyal G, Pelletier G, Fr&uuml;sch J,    Choury AD, <em>et al. </em> Prospective controlled study of endoscopic ultrasonography    and endoscopic retrograde cholan&shy;giography in patients with suspected common    bile duct lithiasis. Lancet. 1996;347:75-9. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">6. Lindsell DRM. Ultrasound imaging of the pancreas and biliary    tract. Lancet. 1990;335:330-3. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">7. Dufour B, Zins M, Vilgrain V, Levy P, Bernades P, Menu Y.    Comparison between spi&shy;ral X-ray computed tomography and endosonography    in the diagnosis and staging of adenocarcinoma o&iacute; the pancreas. Clinical    preliminary study. Gastroenterol Clin Biol. 1997;21:124-30. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">8. Legmann P, Vignaux O, Dousset B, Baraza AJ, Palazzo L, Dumontier    I, <em>et al. </em> Pancreatic tumors: comparison o&iacute; dual-phase helical    CT and endoscopic sonography. Am J Roentgenol. 1998;170:1315-22. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">9. Midwinter MJ, Beveridge CJ, Wilsdon JB, Bennett MK, Baudouin    CJ, Charnley RM. Correlation between spiral computed tomography, endoscopic    ultrasonography and fin&shy;dings at operation in pancreatic and ampullary tumours.    Br J Surg. 1999. <p class="Estilo1">&nbsp; </p>     <p class="Estilo1">10. Soriano A, Ayuso MC, Ayuso JR. Preoperative staging and    tumor resectability assess&shy;ment in pancreatic cancer: prospective study    comparing endoscopic ultrasonography (EUS) computed tomography (CT), magnetic    resonance imaging (MRI) and angiography [abstract]. Gastroenterology. 2001;120:A760.  </p>     ]]></body>
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<body><![CDATA[<!-- ref --><p class="Estilo1">16. Brugge WR. Pancreatic cancer staging: Endoscopic ultrasonography    criterio for vascular invasion. Gastrointest Endosc Clin North Am. 1995;5:741-54.  <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">17. Brugge WR, lee NU, Kelsey PB. The use of EUS to diagnose    malignant portal venous system invasion by pancreatic cancer. Gastrointest Endosc.1996;43:561-7.  <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">18. Tio TL, Sie LH, Kallimanis G. Staging o&iacute; ampullary    and pancreatic carcinoma: com&shy;parison between endosonography and surgery.    Gastrointest Endosc. 1996;44:706-13. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">19. Chang KJ, Nguyen P, Erickson PA, Durbin TE, Katz K. The    clinical utility of endos&shy;copic-guided fine needle aspiration in the diagnosis    and staging of pancreatic cancer. Gastrointest Endosc. 1997;45:387-93. <p class="Estilo1">&nbsp; </p>     <p class="Estilo1">20. Brugge WR, Saltzman JR, Scheiman JM. Diagnosis of cystic    neoplasms of the pan&shy;creas by EUS: the report of the Cooperative Pancreatic    Cyst Study [abstract]. Gastrointest Endosc. 2001;53:AB 71. </p>     <p class="Estilo1">&nbsp; </p>     ]]></body>
<body><![CDATA[<p class="Estilo1">21. Sedlack RE, V&aacute;zquez Sequeiros E. Affi Ausefulness    of endosonography and fine needle aspiration in preoperative evaluation of pancreatic    cystic lesions [abstract]. Gastrointest Endosc. 2001;53:AB 175. </p>     <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">22. Rosch T, Lightdale CJ, Botet JF, Boyce GA, Sivak MV, Yasuda    K, <em>et al. </em> Localization of pancreatic endocrine tumors by endoscopic    ultrasonography. N Engl J Med. 1992;26:1721-b. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">23. Sugiyama M, Wada N, Atomi Y, Kuroda A, Muto T. Diagnosis    of acute pancrea&shy;titis. Value of endoscopic sonography. A1R 1995;165:867-72.  <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">24. Zuccaro G, Sivak MV. Endosonographic ultrasonography in    the diagnosis of chro&shy;nic pancreatitis: Value of chronic pancreatitis. Endoscopy.    1992;24(Suppl):347-9. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">25. Buscail L, Escorrou J, Moreau J, Delvaux M, Louvel D, Lapeyre    F, <em>et al </em>. Endoscopic ultrasonography in chronic pancreatitis: a comparative    prospective study with conven&shy;tional ultrasonography, computed tomography,    and ERCP. Pancreas. 1995;10:251-7. <p class="Estilo1">&nbsp; </p>     ]]></body>
<body><![CDATA[<!-- ref --><p class="Estilo1">26. Fritscher-Ravens A, Broering DC, Knoefel WT, Rogiers X,    Swain P, Thonke F, Bobrowski C, Topalidis T, Soehendra N . EUS-guided fine-needle    aspiration of suspected hilar cholangiocarcinoma in potentially operable patients    with negative brush cytology. Am J Gastroenterol. Jan 2004;99(1):45-51. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">27. Jacobson BC, Pitman MB, Brugge WR. EUS-guided FNA for the    diagnosis of gallbladder masses. Gastrointest Endosc. Feb 2003;57(2):251-4.  <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">28. Palazzo L. Which test for common bile ducts stones? Endoscopic    and intraductal ultrasonography. Endoscopy. 1997;29:655-65. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">29. Tseng U, Jao YT, Mo LR. Over the wire US catheter probe    as adjunct to ERCP in the detection o&iacute; choledocolithiasis. Gastrointest    . 2001;54:720-5. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">30. Tio TL, Cheng J, Wijers OB, Sars PRA, Tygat GNJ. Endosonographic    TNM staging o&iacute; extrahepatic bile duct cancer: comparison with pathological    staging. Gastroenterology. 1991;100:1351-b1. <p class="Estilo1">&nbsp; </p>     ]]></body>
<body><![CDATA[<!-- ref --><p class="Estilo1">31. Mirallie E, Pattou F, Malvaux P, Filoche B, Godchaux JM,    Maunoury V, Palazzo L, Lefebvre J, Huglo D, Paris JC, Carnaille B, Proye C.    Value of endoscopic ultrasonography and somatostatin receptor scintigraphy in    the preoperative localization of insulinomas and gastrinomas. Experience of    54 cases]. Gastroenterol Clin Biol. Apr 2002;26(4):360-6. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">32. Dahan P, Andant C, Levy P, Amouyal P, Amouyal G, Dumont    M. Prospective eva&shy;luation of endoscopic ultrasonography and microscopic    examinations of duodenal bile in the diagnosis o&iacute; cholecystolithiasis    in 45 patients with normal conventional ultraso&shy;nography. Gut 1996;38:277-81.  <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">33. Sugiyama M, Atomi Y, Yamato T. Endoscopic ultrasonography    for differential diag&shy;nosis of polypoid gallbladder lesions: analysis in    surgical and follow up series. Gut 2000;46:250-4. <p class="Estilo1">&nbsp; </p>     <p class="Estilo1">34. Napoleon B, Albis R, Saurin JC, Scoazec JY, Fumex J, Ponchon    T. Clinical impact of endoscopic ultrasound and intraductal ultrasonography    in the management o&iacute; ampu&shy;Ilary tumors [abstract]. Endoscopy. 2000;32:A27.  </p>     <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">35. Menzel J, Poremba C, Dietl KH. Preoperative diagnosis of    bile Duch strictures-com&shy;parison o&iacute; intraductal ultrasonography with    convencional endosonography. Scand J Gastroenterol. 2000;35:77-82. <p class="Estilo1">&nbsp; </p>     ]]></body>
<body><![CDATA[<!-- ref --><p class="Estilo1">36. Tomado K, Tomiyama T, Wada S, Ohasi A, Satoh Y, Ido K,    Sugano K. Endoscopic transpapilary bile Duch biopsy Ruth the combination of    intraductal ultrasonography in the diagnosis of biliary strictures. Gut 2002;50:326-31.  <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">37. Tamada K, Kanai N, Wada S, Tomiyama T, Ohashi A, Satoh    Y, Ido K, Sugano K. Utility and limitations of intraductal ultrasonography in    distinguishing longitudinal cancer extension along the bile duct from inflammatory    wall thickening. Abdom Imaging. Nov-Dec 2001;26(6):623-31. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">38. Kohut M, Nowakowska-Dulawa E, Marek T, Kaczor R, Nowak    A. Accuracy o&iacute; line&shy;ar endoscopic ultrasonography in the evaluation    of patients with suspected common bile ducts stones. Endoscopy. 2002;34(4):299-303.  <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">39. Tandon M, Topazian M. Endoscopic Ultrasound in Idiophatic    Acute Pancreatitis. Am J Gastroenterol. 2001;96(3):705-9. <!-- ref --><p class="Estilo1">40. Norton SA, Alderson D. Endoscopic ultrasonography in the    evaluation of idiophatic acute pancreatitis. BrJ Surg. 2000;87:1650-5. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">41. Frossard JL, Sosa-Valencia L, Amouyal G, Marty O, Hadengue    A. Usefulness of endoscopic ultrasonography in patients with &quot;idiopathic&quot;    acute pancreatitis. Am J Gastroenterol. 2001;96(3):705-9. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">42. Scheiman JM, Carlos RC, Barnett JL, Elta GH, Nostrant TT,    Chey WD, <em>et al. </em> Can Endoscopic Ultrasound or Magnetic Resonance Cholangiopancreatography    replace ERCP in patients with suspected biliary disease? A prospective trial    and cost analysis. Am J Gastroenterol. 2001;96(10):2900-4. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">43. Gress FG, Hawes RH, Savides TJ, Ikenberry SO, Cummings    O, Kopecky K, et al. Role of EUS in the preoperative staging of pancreatic cancer:    a large single-center expe&shy;rience. Gastrointest Endosc. 1999;50:786-91.  <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">44. Sheridan MB, Ward J, Guthrie JA, Spencer JA, Craven CM,    Wilson D, et al. Dynamic contrast-en haced MR imaging and dual-phase helical    CT in the preoperative assessment of suspected pancreatic cancer: a comparative    study with receiver operating charac&shy;teristic analysis. AJR Am J Roentgenol.    1999;173:585-90. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">45. Materne R, Van Beers BE, Gigot JF, Jamart J, Geubel A,    Pringot J, Deprez P. Extra&shy;hepatic biliary obstruction: magnetic resonance    imaging comparec&iacute; with endoscopic ultrasonography. Endoscopy. 2000;32(1):3-9.  <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">46. Calvo MM, Bujanda L, Calder&oacute;n A, Heras I, Cabriada    ) L, Bernal A, <em>et al </em>. Role of magnetic resonance chola ng&iexcl;opa    ncreatography in patients with suspected choledo&shy;cholithiasis. Mayo Clin    Proc. 2002;77(5):407-12. <p class="Estilo1">&nbsp; </p>     <!-- ref --><p class="Estilo1">47. Anderson MA, Carpenter S, Thompson NW, Nostrant TT, Elta    GH, Scheiman JM. Endoscopic ultrasound is highly accurate and directs management    in patients with neu&shy;roendocrine tumors of the pancreas. Am l Gastroenterol.    2000;95(9):2271-7. <p class="Estilo1">&nbsp;</p>     <p class="Estilo1" align="center"><b>&nbsp; ANEXO</b></p>     <p class="Estilo1" align="center"><img width="264" height="210" src="/img/revistas/rhcm/v6n1/f0309107.jpg"></p>     
<p class="Estilo1" align="center">Fig. 1 . C&aacute;lculo del col&eacute;doco. </p>     <p class="Estilo1" align="center"><img width="254" height="210" src="/img/revistas/rhcm/v6n1/f0409107.jpg"></p>     
<p class="Estilo1" align="center">Fig. 2 . T. de cuerpo de p&aacute;ncreas y ADP </p>     <p class="Estilo1" align="center"><img width="276" height="206" src="/img/revistas/rhcm/v6n1/f0509107.jpg"></p>     
<p class="Estilo1" align="center">Fig. 3. T. de cabeza del p&aacute;ncreas &nbsp; </p>     ]]></body>
<body><![CDATA[<p class="Estilo1" align="center"><img width="276" height="224" src="/img/revistas/rhcm/v6n1/f0609107.jpg"></p>     
<p class="Estilo1" align="center">Fig. 4 . Tumor qu&iacute;stico del p&aacute;ncreas. </p>     <p class="Estilo1" align="center"><img width="277" height="247" src="/img/revistas/rhcm/v6n1/f0709107.jpg"></p>     
<p class="Estilo1" align="center">Fig. 5 . Pancreatitis cr&oacute;nica calcificada. </p>     <p class="Estilo1">&nbsp; </p>     <p class="Estilo1">&nbsp; </p>      ]]></body><back>
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