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<articles>
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<front>
<journal-meta>
<journal-id pub-id-type="pid">S0001-600220020001</journal-id>
<journal-title>Acta Médica Costarricense</journal-title>
<abbrev-journal-title>Acta méd. costarric</abbrev-journal-title>
<issn>0001-6002</issn>
<publisher>
<publisher-name>Colegio de Médicos y Cirujanos de Costa Rica</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0001-60022002000100001</article-id>
<title-group>
<article-title xml:lang="es">El premio &quot;Aportes al mejoramiento de la calidad de vida&quot;</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Miranda</surname>
<given-names>Guido</given-names>
</name>
</contrib>
</contrib-group>
<aff id="A">
<institution>,  </institution>
<addr-line> </addr-line>
</aff>
<pub-date pub-type="pub">
<month>03</month>
<year>2002</year>
</pub-date>
<pub-date pub-type="epub">
<year>2002</year>
</pub-date>
<volume>44</volume>
<fpage>3</fpage>
<lpage>3</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http:/www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S0001-60022002000100001&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S0001-60022002000100001&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S0001-60022002000100001&amp;lng=en&amp;nrm=iso"></self-uri></article-meta>
</front>
</article>
<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 pub-id-type="pid">S0001-600220020001</journal-id>
<journal-title>Acta Médica Costarricense</journal-title>
<abbrev-journal-title>Acta méd. costarric</abbrev-journal-title>
<issn>0001-6002</issn>
<publisher>
<publisher-name>Colegio de Médicos y Cirujanos de Costa Rica</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0001-60022002000100002</article-id>
<title-group>
<article-title xml:lang="es">El papel de los anti-inflamatorios no esteroideos en la producción de fasceítis necrotizante</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Behm-López</surname>
<given-names>Bertrand</given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Salas-Herrera</surname>
<given-names>lsaías</given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution>,Centro Nacional de Control del Dolor y Cuidados Paliativos  </institution>
<addr-line>San José </addr-line>
</aff>
<aff id="A02">
<institution>,Centro Nacional de Control del Dolor y Cuidados Paliativos  </institution>
<addr-line> </addr-line>
</aff>
<pub-date pub-type="pub">
<month>03</month>
<year>2002</year>
</pub-date>
<pub-date pub-type="epub">
<year>2002</year>
</pub-date>
<volume>44</volume>
<fpage>5</fpage>
<lpage>9</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http:/www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S0001-60022002000100002&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S0001-60022002000100002&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S0001-60022002000100002&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p>La fasceítis necrotizante es una infección que afecta tejidos blandos, producida por estreptococos beta hemolíticos grupo A. Su diagnóstico temprano es difícil, siendo más fácil conforme avanza el curso de la enfermedad. Para determinar si existía una relación entre los anti-inflamatorios no esteroideos y la aparición de fasceítis necrotizante, fue analizada la literatura médica de estudios clínicos en los últimos 41 años (base de datos de MEDLINE), los cuales evidenciaron que el tamaño de las muestras era pequeño , no eran randomizadas, no tenían grupos control y no lograron demostrar evidencia científica de causa-efecto entre los anti-inflamatorios no esteroideos y la fasceítis necrotizante, sin importar las vías de administración utilizadas. Con el fin de determinar si existe una asociación entre los anti-inflamatorios no esteroideos y fasceítis necrotizante, deben llevarse a cabo en el futuro estudios clínicos bien diseñados.</p></abstract>
<abstract abstract-type="short" xml:lang="en"><p>Necrotizing fasceiitis, as a severe group A streptococcus infection generally originating from localizad skin infections or disruptions has increased worldwide in recent years. Early diagnosis is often difficult due to the appearance of characteristic soft tissue changes only late in the course of the disease. The medical literatura was analized to determine a possible association between non-setroidal antiinflammatory drugs and necrotizing fasceiitis and possible factors involved in necrotizing fasceiitis. Sample sizes of the clinical studies reviewed were small, non-randomized, without control groups. Thus, no clinical studies showed scientific evidence of a cause and effect relationship between non-setroidal anti-inflammatory drugs and necrotizing fasceiitis, regardless of the route of administration. Further well-designed clinical trials should be carried out to determine if there is a possible association between nonsetroidal anti-inflan-irnatory drugs and necrotizing fasceitis.</p></abstract>
<kwd-group>
<kwd>fasceítis necrotizante</kwd>
<kwd>anti-inflamatorios no esteroideos</kwd>
<kwd>infección</kwd>
<kwd>inmunosupresión</kwd>
</kwd-group>
</article-meta>
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<article-title xml:lang="es">Vertigo: una visión otorrinolaringológica para la medicina general</article-title>
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<copyright-statement/>
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<self-uri xlink:href="http:/www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S0001-60022002000100003&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S0001-60022002000100003&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S0001-60022002000100003&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p>Muchos padecimientos se presentan con diversos síntomas que son descritos como &quot;vértigo&quot; o &quot;mareo&quot;. Desde enfermedades inocentes hasta padecimientos potencialmente mortales pueden presentarlo, lo que genera cierta atmósfera de temor a enfrentarse con la tarea de llegar a un diagnóstico por parte del médico. Este trabajo trata de resumir la experiencia práctica del otorrinolaringólogo, dirigida a mejorar la capacidad resolutiva. Se describen las características y las causas del vértigo periférico y central, continuando con algunas recomendaciones para su tratamiento, y termina con la propuesta de un algoritmo general de cuatro pasos.</p></abstract>
<abstract abstract-type="short" xml:lang="en"><p>Many illnesses show themselves with various symptoms described as &quot;vertigo&quot; or &quot;dizziness&quot;. From very mild ailments to potentially mortal discases can present with this symptoms this generales some fear to face the tasks of reaching a diagnosis. This paper tries lo summarize the practicar experience of an otolaryngologist, aimed to improved the general physician's ability lo solve the diagnostic challenge. Central and peripheral vertigo's causes and characteristic are describes, followed by basic treatment recommendations. Finally, a general four steps algorithm is proposed.</p></abstract>
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<kwd>Vértigo</kwd>
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<journal-title>Acta Médica Costarricense</journal-title>
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<institution>,Universidad de Ciencias Médicas Departamento de Investigación Cátedra de Parasitología Médica</institution>
<addr-line>San José </addr-line>
<country>Costa Rica</country>
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<copyright-statement/>
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<self-uri xlink:href="http:/www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S0001-60022002000100004&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S0001-60022002000100004&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S0001-60022002000100004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p>Justificación: La mayoría de las infecciones por microsporidios en el ser humano se han reportado en el tracto gastrointestinal, sin embargo, es posible hallarlos parasitando otros sitios anatómicos como el tracto genitourinario, en donde las patologías pueden variar desde uretritis hasta falla renal. Tradicionalmente esas infecciones se deben al género Encephalitozoon, parásito contra el cual el Albendazol ha demostrado ser un medicamento efectivo. Objetivo: Determinar la prevalencia de microsporidios en personas que son referidas al laboratorio para urocultivo, dados los antecedentes clínicos que presentan. Métodos: El procesamiento de las muestras incluyó su toma con técnica aséptica, su cultivo en los medios de Agar Sangre, MacConkey y Manitol - sal para su estudio por presencia de bacterias y/u hongos y la realización del antibiograma, según los parámetros establecidos por la CCSS para los urocultivos. Adicional a esto se centrifugó una alícuota de 9 ml separando 50 microlitos del sedimento urinario, al cual se le añadió igual volumen de KOH al 5%. Se hicieron frotis los cuales se fijaron con alcohol metílico una vez secos, y se tiñeron con la técnica trierómica de Weber, obviando el paso de la decoloración y la deshidratación. Resultados: Se encontró un 25% de orinas positivas por microsporidios. Los pacientes con edades entre 26 y 55 años presentaron mayor positividad. Conclusiones: El porcentaje de prevalencia encontrado (25%) y el hecho de que estas infecciones pueden llegar a causar severos daños al ser humano, hacen imperativa la necesidad de realizar diagnósticos más certeros de esta parasitosis, para lo cual proponemos la tinción de Weber con la modificación presentada en este trabajo para el diagnóstico de las infecciones por microsporidios en el tracto urinario.</p></abstract>
<abstract abstract-type="short" xml:lang="en"><p>Urine samples from patients with clinical antecedents of suspicion genitourinary pathology were studied for bacteria, fungi and for the presence of microsporidia. Usual culture media and methods were used lo study bacteria and fungi organisms. To study for microsporidian parasites, nine ml were centrifuged and smears of the sediment were fixed, previous tratment with 5% KOH and then stained according to a modified Weber method. Groups of Microsporidia spores were foud in twenty five per cent of the samples, coming more frenquently from people between 26 to 55 five years old .</p></abstract>
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<self-uri xlink:href="http:/www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S0001-60022002000100005&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S0001-60022002000100005&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S0001-60022002000100005&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p>Las opciones terapéuticas y reconstructivas disponibles hoy en día para las mujeres con cáncer mamario son numerosas. De los métodos disponibles para la reconstrucción mamaria autóloga el colgajo recto abdominal ha sido el más popular. Es un colgajo que incluye la piel, el tejido graso y el músculo recto abdominal, este conjunto es llevado con su irrigación de la arteria epigástrica superior hasta el defecto de la mastectomía, en el tórax. El colgajo recto abdominal (TRAM) ha sido calificado por algunos líderes en el campo de la Cirugía Plástica como el procedimiento más ingenioso realizado en esta especialidad. Entre abril de 1999 y diciembre 2000 realizamos 15 reconstrucciones mamarias utilizando el TRAM. La reconstrucción fue unilateral en catorce casos y bilateral en un caso. En trece pacientes se utilizó un pedículo contralateral y en dos el pedículo fue ipsilateral. Como complicaciones tuvimos dos hernias abdominales, una necrosis grasa parcial y un hematoma, todas fueron resueltas satisfactoriamente. La reconstrucción inmediata ofrece ventajas sobre la reconstrucción retardada . En nuestro país podemos realizar tanto la reconstrucción retardada como inmediata y en los equipos de trabajo (oncólogos, cirujanos generales, cirujanos plásticos, psiquiatras, etc) se debe fomentar la reconstrucción inmediata.</p></abstract>
<abstract abstract-type="short" xml:lang="en"><p>Today, the therapeutic and reconstructive options for mastectomized women are numerous. Of the different methods for autologous breast reconstruction, the transversus rectus abdominis muscle &quot;TRAM&quot; flap has been the most popular. The flap includes skin, subcutancous tissue and the rectus abdominis muscle. This flap irrigated by the superior epigastric artery is taken lo the mastectomy defect in the thorax.. From April 1999 to December 2000 we performed 15 breast reconstructions using the rectus abdominis flap. The reconstruction was unilateral in fourteen cases and bilateral in one. In thirteen patients we utilized a contralateral pedicle and in two patients the pedicle was ipsilateral. The complications were two abdominal hernial, one partial fat necrosis and one hematoma, all of them resolved . Inmediate reconstruction offers advantages over delayed reconstruction. In our country we performed immediate and delayed reconstruction. Immediate reconstruction by comprensive teams of oncology and general surgeons, plastie surgeons, psychiatrics, etc.</p></abstract>
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<journal-title>Acta Médica Costarricense</journal-title>
<abbrev-journal-title>Acta méd. costarric</abbrev-journal-title>
<issn>0001-6002</issn>
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<article-id>S0001-60022002000100006</article-id>
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<article-title xml:lang="es">Diagnóstico directo de la mutación que causa el síndrome del cromosoma X frágil: experiencia en Costa Rica</article-title>
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<given-names>Patricia</given-names>
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<institution>,Instituto de Investigaciones en Salud  </institution>
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<fpage>27</fpage>
<lpage>33</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http:/www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S0001-60022002000100006&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S0001-60022002000100006&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S0001-60022002000100006&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p>Justificación y objetivo: el síndrome del cromosoma X frágil es la principal causa de retardo mental hereditario. Afecta a 1:4 000 varones y a 1:6 000 mujeres. La mayoría de las personas afectadas aún no han sido diagnosticadas y en sus familias suele haber más de un miembro con &quot;retardo mental de origen oscuro&quot;. Si estas personas conocieran el diagnóstico y el carácter hereditario del padecimiento, el asesoramiento genético adecuado y oportuno, podría contribuir a reducir la ocurrencia o la recurrencia de esta patología en las familias. El objetivo por lo tanto fue hacer diagnóstico directo de la mutación que causa el síndrome, para confirmar o descartar el diagnóstico clínico o citogenético en los probandos, para encontrar a los portadores y portadoras en las familias de estas personas y de esa manera poder brindar prevención a través del asesoramiento genético. Métodos: se realizaron los análisis moleculares mediante hibridaciones de Southem, con las sondas Ox 1.9 y StB 12.3 previa digestión del ADN genómico con las enzimas Hind III, EcoRI y Eagl. Además de confirmar la presencia o ausencia de la mutación completa en los afectados por el retardo mental, se ha determinado el tamaño de la premutación en algunos portadores y confirmado a individuos libres de mutación mediante el uso de la reacción en cadena de la polimerasa. Resultados: se han realizado estudios moleculares en niños con examen citogenético positivo (grupo uno, N = 13), sus familiares cercanos (grupo dos, N = 30) y niños referidos por maestros, pediatras y sicólogos (grupo tres, N = 15). En nueve de los niños del grupo uno se confirmó la presencia de la mutación completa del gen FMRI, en los otros cuatro se descartó, al encontrarse resultados normales en todas las pruebas moleculares. En el grupo dos se encontraron dos mujeres con la mutación completa y doce personas con la premutación: un varón transmisor fenotípicamente normal y once mujeres portadoras. El resto de los familiares estudiados resultaron normales. En el grupo tres se detectó una niña con la mutación, el resto fueron normales, tanto mediante estudios citogenéticos como moleculares. Conclusión: el diagnóstico preciso de la mutación permite, por un lado el abordaje correcto de los niños afectados desde el punto de vista psicopedagógico. Por otro lado, la identificación de los portadores de premutaciones y de los individuos libres de la mutación en una familia donde está segregando la enfermedad permite un consejo genético preciso de acuerdo al hallazgo molecular. Los métodos moleculares, además de más exactos, resultan más baratos que los citogenéticos cuando se cuenta con un laboratorio equipado y el personal capacitado.</p></abstract>
<abstract abstract-type="short" xml:lang="en"><p>Fragile X syndrome is the most common hereditary type of mental retardation, affecting 1:4 000 males and 1:6 000 females. Unfortunately, most persons with this syndrome have not bcen diagnosed and are classified as cases of mental retardation of unknown origin. The correct etiological classification of these patients would allow their families lo avoid recurrence of this disease through adequate genetic counseling. As a result, this study intended to provide accurate molecular diagnosis of fragile X syndrome in mentally retarded patients with clinical or cytogenetic suspicion of the disease, to detect the normal transmitting males and female carriers in each of the proband's families and to promote prevention after proper genetic counseling. To achieve this, genomic DNA was digested with Hind 111, EcoRI and Eagl and Southern blotting was performed with probes Oxl.9 and StB 12.3. To asses the size of the trinucleotide repeat, PCR was used in some of the cases. Three groups were studied: group one with 13 children with the cytogenetic marker, 30 of their close relativas conformes group two and group three with 15 clinically suspicious fragile X syndrome children. Results: of the 13 probands, four proved not to be fragile X cases since their average repeat number was 30. In group two, two females with the full mutation, one normal transmitting male and eleven female carriers with the premutation were found. In group three an additional female with the full mutation was identified, the rest had normal DNA and cytogenetic test results. In summary, DNA studies are a better way to accurately asses the full mutation and premutation carriers. The right diagnosis renders benefits to fragile X cases in terms of the interventions they need and to carriers since this information is a must for proper genetic counseling and prevention. Moreover, molecular studies are cheaper than cytogenetie diagnosis in well equipped laboratories with trained personnel.</p></abstract>
<kwd-group>
<kwd>genética humana</kwd>
<kwd>diagnóstico molecular</kwd>
<kwd>FRAXA</kwd>
<kwd>cromosoma X</kwd>
<kwd>retardo mental hereditario</kwd>
<kwd>FMRI</kwd>
<kwd>mutaciones inestables</kwd>
</kwd-group>
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