<?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>0120-2448</journal-id>
<journal-title><![CDATA[Acta Medica Colombiana]]></journal-title>
<abbrev-journal-title><![CDATA[Acta Med Colomb]]></abbrev-journal-title>
<issn>0120-2448</issn>
<publisher>
<publisher-name><![CDATA[Asociacion Colombiana de Medicina Interna]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-24482013000200012</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Accidente lonómico]]></article-title>
<article-title xml:lang="en"><![CDATA[Lonomiasis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ávila]]></surname>
<given-names><![CDATA[Albert Alejandro]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Moreno]]></surname>
<given-names><![CDATA[Atilio]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Garzón]]></surname>
<given-names><![CDATA[Andrés]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gómez]]></surname>
<given-names><![CDATA[Álvaro Andrés]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Hospital Universitario San Ignacio Pontificia Universidad Javeriana ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,Hospital Universitario San Ignacio Pontificia Universidad Javeriana Programa de especialización Medicina de Urgencias]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A03">
<institution><![CDATA[,Hospital Universitario San Ignacio Pontificia Universidad Javeriana ]]></institution>
<addr-line><![CDATA[Bogotá D.C.]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>04</month>
<year>2013</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>04</month>
<year>2013</year>
</pub-date>
<volume>38</volume>
<numero>2</numero>
<fpage>95</fpage>
<lpage>100</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0120-24482013000200012&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0120-24482013000200012&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0120-24482013000200012&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Se trata de un caso clínico de un adolescente masculino de 15 años de edad remitido del municipio de Arauca, Arauca Colombia por un cuadro clínico de hematuria macroscópica, equimosis y gingivorragia con antecedente de contacto previo con orugas de la familia Saturniidae. Presentaba prolongación de los tiempos de coagulación y disminución del fibrinógeno. El diagnóstico fue establecido por la anamnesis, las manifestaciones clínicas y los reportes de laboratorio. Las medidas terapéuticas tuvieron éxito. Las características fisiopatológicas y clínicas del accidente lonómico serán revisadas.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[This is a case report of a 15 years old male teenager referred from the municipality of Arauca, Arauca Colombia by a clinical picture of macroscopic hematuria, bruising and gingivorrhagia with a history of previous contact with caterpillars of the family saturniidae. clotting times were prolonged and fibrinogen was decreased. The diagnosis was established by history, clinical manifestations and laboratory reports. Therapeutic measures were successful. Pathophysiological and clinical characteristics of the lonimia accident have been reviewed.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[lepidópteros]]></kwd>
<kwd lng="es"><![CDATA[fibrinólisis]]></kwd>
<kwd lng="es"><![CDATA[larva]]></kwd>
<kwd lng="es"><![CDATA[Colombia]]></kwd>
<kwd lng="en"><![CDATA[lepidoptera]]></kwd>
<kwd lng="en"><![CDATA[fibrinolysis]]></kwd>
<kwd lng="en"><![CDATA[larva]]></kwd>
<kwd lng="en"><![CDATA[Colombia]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  <font size="2" face="Verdana">      <p align="center"><font size="4"><b>Accidente lon&oacute;mico</b></font></p>      <p align="center"><font size="3"><b>Lonomiasis</b></font></p>      <p align="center">Albert Alejandro &Aacute;vila, Atilio Moreno, Andr&eacute;s Garz&oacute;n, &Aacute;lvaro Andr&eacute;s G&oacute;mez, Bogot&aacute;, D.C. (Colombia)</p>  </font>    <p><font size="2" face="Verdana">Dr. Albert alejandro &Aacute;vila &Aacute;lvarez: residente de Medicina de Urgencias, Pontificia Universidad Javeriana, Hospital Universitario san ignacio;    <br>  Dr. Atilio Moreno carrillo: Medicina Interna P.U.J. Advanced Fellowship in emergency Medicine G.W.U. Director Programa de especializaci&oacute;n Medicina de Urgencias, Pontificia Universidad Javeriana, Hospital Universitario San Ignacio;    <br>  Dres. Andr&eacute;s Garz&oacute;n Forero y &Aacute;lvaro Andr&eacute;s G&oacute;mez Venegas: residentes de Medicina Interna. Pontificia Universidad Javeriana, Hospital Universitario San Ignacio, Bogot&aacute;, D.C. (Colombia).    <br>  Correspondencia. Dr. Albert Alejandro &Aacute;vila &Aacute;lvarez E-mail: <a href="mailto:alejandroavila2010@gmail.com">alejandroavila2010@gmail.com</a></font></p>  <font size="2" face="Verdana">    <p>Recibido: 29/IV/2012 Aceptado: 17/V/2013</p>   <hr>      <p><b>Resumen</b></p>      ]]></body>
<body><![CDATA[<p>Se trata de un caso cl&iacute;nico de un adolescente masculino de 15 a&ntilde;os de edad remitido del municipio de Arauca, Arauca Colombia por un cuadro cl&iacute;nico de hematuria macrosc&oacute;pica, equimosis y gingivorragia con antecedente de contacto previo con orugas de la familia <i>Saturniidae</i>. Presentaba prolongaci&oacute;n de los tiempos de coagulaci&oacute;n y disminuci&oacute;n del fibrin&oacute;geno. El diagn&oacute;stico fue establecido por la anamnesis, las manifestaciones cl&iacute;nicas y los reportes de laboratorio. Las medidas terap&eacute;uticas tuvieron &eacute;xito. Las caracter&iacute;sticas fisiopatol&oacute;gicas y cl&iacute;nicas del accidente lon&oacute;mico ser&aacute;n revisadas.</p>      <p><b>Palabras clave: </b><i>lepid&oacute;pteros, fibrin&oacute;lisis, larva, Colombia.</i></p>  <hr>      <p><b>Abstract</b></p>      <p>This is a case report of a 15 years old male teenager referred from the municipality of Arauca, Arauca Colombia by a clinical picture of macroscopic hematuria, bruising and gingivorrhagia with a history of previous contact with caterpillars of the family saturniidae. clotting times were prolonged and fibrinogen was decreased. The diagnosis was established by history, clinical manifestations and laboratory reports. therapeutic measures were successful. Pathophysiological and clinical characteristics of the lonimia accident have been reviewed.</p>      <p><b>Keywords: </b><i>lepidoptera, fibrinolysis, larva, Colombia.</i></p>  <hr>      <p><font size="3"><b>Introducci&oacute;n</b></font></p>      <p>El envenenamiento por orugas pertenecientes al g&eacute;nero lepid&oacute;ptera incluye los siguientes s&iacute;ndromes: erucismo, lepidopterismo, dendrolimiasis, oftalmia nodosa y coagulopat&iacute;a de consumo con fibrin&oacute;lisis secundaria. En el accidente lon&oacute;mico los s&iacute;ndromes descritos son el erucismo y la coagulopat&iacute;a de consumo con fibrin&oacute;lisis secundaria (1-5). El erucismo por <i>Saturniidae </i>es el envenenamiento resultante del contacto con orugas en la etapa larval de la especie Lonomia (<a href="#fig1">Figura 1. B</a>). Se estima que m&aacute;s de 250000 especies de lepid&oacute;pteras habitan la tierra, de las cuales unas 180000 han sido descritas hasta ahora (1, 3). Los lepid&oacute;pteros est&aacute;n divididos en 4 sub&oacute;rdenes: Zeugloptera, aglossata, Heterobathmiina y Glossata (1,2), con aproximadamente 100 familias, de las cuales 12 son de importancia m&eacute;dica (3, 5,6). La familia <i>Saturniidae </i>perteneciente al suborden Glossata incluye 26 especies de lonomia que se encuentran distribuidas en el continente americano (1, 2,7-9). Sin embargo, s&oacute;lo <i>Lonomia obliqua </i>y <i>Lonomia achelous </i>causan accidentes graves.</p>      <p align="center"><a name="fig1"></a><img src="img/revistas/amc/v38n2/v38n2a11f1.jpg"></p>      <p><i>L. achelous </i>se encuentra principalmente en Venezuela y la Guyana Francesa (10,11) y existen reportes en Paraguay, Per&uacute; y Ecuador. otra variedad se encuentra en el norte de Brasil, donde se clasifica como <i>L. diabolous </i>(3,10). <i>L. obliqua </i>se encuentra en el sur y sureste de Brasil (12-16). <i>L. obliqua </i>tambi&eacute;n se encuentra en Uruguay, Paraguay y Argentina (3). Donde los casos reportados por accidente lon&oacute;mico arrojan una incidencia de ocho casos por cada 100.000 habitantes (17).</p>      <p>En Colombia se han reportado casos por <i>L. descimoni</i>, <i>L. rufescens</i>, <i>L. claucina</i>, <i>L. occidentalis</i>, <i>L. armata</i>, <i>L. inexpectata </i>y <i>L. Saturniidae</i>. De los casos reportados provenientes de los departamentos del Casanare y de la amazonia se ha identificado como responsable a <i>L. achelous </i>(18).</p>      ]]></body>
<body><![CDATA[<p>La importancia del accidente lon&oacute;mico no radica &uacute;nicamente en su incidencia, sino en las tasas de morbilidad y mortalidad asociadas (19). En las &uacute;ltimas d&eacute;cadas algunas especies est&aacute;n adquiriendo importancia por la gravedad de los casos y su expansi&oacute;n geogr&aacute;fica. Representantes del g&eacute;nero lonomia est&aacute;n migrando a otras zonas en las que no se hallaban, desplaz&aacute;ndose desde las &aacute;reas rurales a las &aacute;reas urbanas debido a la deforestaci&oacute;n, colonizaci&oacute;n, eliminaci&oacute;n de predadores naturales y al cambio clim&aacute;tico global (4,20,21).</p>      <p><b>Presentaci&oacute;n del caso</b></p>      <p>Paciente masculino de 15 a&ntilde;os de edad, procedente y remitido del hospital local de Arauca, Arauca (Colombia), quien ingresa al servicio de urgencias del Hospital Universitario San Ignacio de Bogot&aacute; -HUSI, por presentar un cuadro cl&iacute;nico de cinco d&iacute;as de evoluci&oacute;n, que inicia con el contacto en la palma izquierda con orugas que se encontraban en el tallo de un &aacute;rbol. Presentando dolor de intensidad moderada en el sitio de contacto. Dos d&iacute;as despu&eacute;s presenta sangrado en laceraciones recientes de miembros inferiores, hematuria, gingivorragia y equimosis. Consulta al hospital local de Arauca, Arauca donde toman paracl&iacute;nicos que evidencian prolongaci&oacute;n en los tiempos de coagulaci&oacute;n e inician manejo m&eacute;dico con la administraci&oacute;n endovenosa de una unidad de plasma fresco congelado. Ante la persistencia de la prolongaci&oacute;n de los tiempos de coagulaci&oacute;n de etiolog&iacute;a desconocida deciden remitir.</p>      <p align="center"><a name="tab1"></a><img src="img/revistas/amc/v38n2/v38n2a11t1.jpg"></p>      <p>A su ingreso al HUSI, se encontr&oacute; a un paciente con los siguientes signos vitales: TA 110/60 mmHg, frecuencia cardiaca de 72 lpm, frecuencia respiratoria de 16 rpm y saturaci&oacute;n de ox&iacute;geno de 96%, mucosas h&uacute;medas, con estigmas de gingivorragia. A la auscultaci&oacute;n ruidos cardiacos r&iacute;tmicos sin soplos, ruidos respiratorios normales. En la mano izquierda presentaba edema y calor local de forma difusa. Adem&aacute;s de un hematoma en cara interna del muslo y pierna izquierda y varios hematomas peque&ntilde;os en extremidades superiores e inferiores. el examen neurol&oacute;gico era normal.</p>      <p>Se comienza hidrataci&oacute;n con cristaloides endovenosos y se solicitan paracl&iacute;nicos con los siguientes resultados:</p>      <p>TP &gt; 120 segundos, TPT &gt; 180 segundos, INR &gt; de 11, Fibrin&oacute;geno &lt; 60 mg/dL: hemoglobina: 13,5g/dL, hematocrito: 39.2%, plaquetas: 212000.</p>      <p>Uroan&aacute;lisis: hemoglobina 1000 xc, hemat&iacute;es incontables.</p>      <p>BUN 10,7 mg/dL, creatinina 0,87 mg/dL, sodio 141,4 mmol/L, potasio 4,06 mmol/L.</p>      <p>Se consider&oacute; que el paciente presentaba un accidente lon&oacute;mico con una coagulopat&iacute;a secundaria asociada. dado que los casos de los &uacute;ltimos a&ntilde;os en el pa&iacute;s involucran a <i>L. achelous, </i>que posee un veneno con un mecanismo de predominio fibrinol&iacute;tico asociado al consumo de factores de coagulaci&oacute;n, y ante la ausencia del suero antilon&oacute;mico en el pa&iacute;s se inicia el manejo con &aacute;cido tranex&aacute;mico 500 mg/IV/6 h y complejo protromb&iacute;nico 1800 unidades intravenoso (30 mg/kg) (48). El control de paracl&iacute;nicos demostraba persistencia en la prolongaci&oacute;n de los tiempos de coagulaci&oacute;n con consumo del fibrin&oacute;geno. Al siguiente d&iacute;a de su ingreso se logra la consecuci&oacute;n por parte del ministerio de la Protecci&oacute;n social de Colombia de cinco ampollas de suero antilon&oacute;mico que se administraron inmediatamente (48). Treinta minutos despu&eacute;s de la infusi&oacute;n el paciente comienza a presentar lesiones maculopapulares pruriginosas de 4mm en el t&oacute;rax (47, 48, 53), que ceden con la aplicaci&oacute;n de hidrocortisona 300 mg y difenhidramina 50 mg endovenosos. Se complementa el manejo con la aplicaci&oacute;n de 10 unidades de crioprecipitados (47, 48).</p>      ]]></body>
<body><![CDATA[<p>Posterior a la aplicaci&oacute;n del suero antilon&oacute;mico el paciente comienza a presentar correcci&oacute;n progresiva de los tiempos de coagulaci&oacute;n. Cuatro d&iacute;as despu&eacute;s de observaci&oacute;n, los controles de paracl&iacute;nicos se encontraban dentro de l&iacute;mites normales y se da de alta (<a href="#tab2">Tabla 2</a>).</p>      <p align="center"><a name="tab2"></a><img src="img/revistas/amc/v38n2/v38n2a11t2.jpg"></p>      <p><font size="3"><b>Discusi&oacute;n</b></font></p>      <p>El contacto con la oruga suele ocurrir de forma accidental ya que las orugas se agrupan en los tallos y ramas de los &aacute;rboles cercanos a las residencias (<a href="#fig1">Figura 1. A</a>) (3, 7). La oruga de lonomia tiene cerdas de color verde pardusco de diferentes tama&ntilde;os en el cuerpo, &eacute;stas son evaginaciones duras y espinosas de la cut&iacute;cula y est&aacute;n presentes en todas las etapas larvales (16, 17, 22). Las cerdas tienen en el extremo distal una punta fina rica en quitina que se rompe f&aacute;cilmente para liberar el veneno presente en el canal hueco interno que lo almacena (22).</p>      <p>La gravedad del envenenamiento se relaciona principalmente con el contacto con una colonia que contiene al menos 40-50 orugas. Cada oruga produce aproximadamente 2.56 mg de veneno (4,17-22).</p>       <p><b>Caracter&iacute;sticas del veneno. </b>Los venenos de las especies <i>L. obliqua </i>y <i>L. achelous </i>tienen efectos similares, pero los mecanismos por el que causan sus efectos son diferentes (23).</p>      <p><b>Veneno de <i>L. Obliqua. </i></b>Est&aacute; compuesto por toxinas entre las que se encuentran factores activadores del factor de coagulaci&oacute;n II, del factor X, <b>a </b>-fibrogenasas, hialuronidasas, lipocalinas, serpinas y fosfolipasa A2 (22, 24-30).</p>      <p>El veneno de <i>L. obliqua </i>provoca una forma especial de coagulaci&oacute;n intravascular diseminada (CID) con coagulopat&iacute;a de consumo, agotamiento de los factores V y XIII, as&iacute; como fibrin&oacute;lisis secundaria (15, 17, 29-32). Esto es diferente de CID observada en otras situaciones cl&iacute;nicas, como traumatismo, neoplasia o sepsis (4, 17, 26, 29, 33-37).</p>      <p>De las cerdas de <i>L. obliqua </i>se han extra&iacute;do dos toxinas procoagulantes: un activador del factor X, llamado losac (factor activador Stuart de <i>L. obliqua) </i>y un activador de la protrombina llamado lopap (proteasa activadora de protrombina de lonomia obliqua). Lopap realiza un papel importante en el s&iacute;ndrome hemorr&aacute;gico inducido por contacto con la oruga <i>L. oblicua </i>(26, 29, 35, 37-39).</p>      <p><b>Toxinas procoagulantes. </b>1. Lopap, es una serinoproteasa de 69 kDa, activadora de protrombina independiente de los cofactores de protrombinasa (Factor V activado, fosfol&iacute;pidos).</p>      ]]></body>
<body><![CDATA[<p>Los estudios <i>in vivo </i>apoyan la hip&oacute;tesis de que lopap a trav&eacute;s de la generaci&oacute;n de trombina contribuye a la presentaci&oacute;n de la coagulopat&iacute;a de consumo. La fragmentaci&oacute;n de la protrombina por lopap es similar a la inducida por el factor X activado, en ausencia de protrombinasa, formando pretrombina 2, fragmentos 1 + 2 y trombina, sin formaci&oacute;n de meizotrombina (39, 40).</p>      <p>Lopap estimula el aumento de la interleuquina 8, de la mol&eacute;cula de adhesi&oacute;n intercelular-1(ICAM-1) y selectina E, as&iacute; como tambi&eacute;n aumenta la secreci&oacute;n de &oacute;xido n&iacute;trico (NO) y prostaglandinas (PGI 2). El NO puede participar por varios mecanismos (15, 31, 34): puede inducir da&ntilde;o en los tejidos al generar peroxinitritos y radicales hidroxilo, contribuyendo a la hipotensi&oacute;n, a la inhibici&oacute;n de la agregaci&oacute;n plaquetaria, a la inhibici&oacute;n del fosfoinositol 3 quinasa (PI3K) y a la supresi&oacute;n de la v&iacute;a del flujo de calcio intracelular. Tambi&eacute;n puede suprimir la expresi&oacute;n de selectina P y el cambio conformacional de la glicoprote&iacute;na IIb-IIIa (GPIIb-IIIa) (31). en modelos <i>in vitro </i>se ha podido demostrar que en el envenenamiento por <i>L. obliqua </i>la disminuci&oacute;n de la agregaci&oacute;n plaquetaria coincide con la elevaci&oacute;n de los niveles s&eacute;ricos de no, sobre todo despu&eacute;s de seis horas, momento en que se observa la m&aacute;xima inhibici&oacute;n (31, 33, 34, 41).</p>      <p>2. Losac, es una serino-proteasa de 43 kDa. Capaz de activar el Factor X de una forma dependiente de la concentraci&oacute;n. Losac no activa otros factores de coagulaci&oacute;n (15).</p>      <p><b>Trombocitopenia. </b>Se detecta en algunos de los pacientes, sobre todo en los casos m&aacute;s graves (17, 42). La agregaci&oacute;n plaquetaria disminuye seis horas despu&eacute;s de la exposici&oacute;n al veneno. Alteraci&oacute;n que se acompa&ntilde;a de la prolongaci&oacute;n de los tiempos de coagulaci&oacute;n. Las manifestaciones hemorr&aacute;gicas tales como gingivorragia o sangrado de las heridas indican que hay alteraci&oacute;n de la adhesi&oacute;n plaquetaria. Los estudios <i>in vivo </i>evidencian una reducci&oacute;n de aproximadamente 26-30% en el recuento plaquetario a las seis horas, normaliz&aacute;ndose despu&eacute;s de las 24 horas. El consumo de plaquetas no parece ocurrir, ya que s&oacute;lo hay reducci&oacute;n leve en su n&uacute;mero (17, 22, 43, 44). Probablemente, la inhibici&oacute;n de la agregaci&oacute;n puede prevenir el consumo de plaquetas y la formaci&oacute;n de trombos en los lechos vasculares. Por lo tanto, la disminuci&oacute;n de la agregaci&oacute;n puede contribuir a la presentaci&oacute;n del s&iacute;ndrome hemorr&aacute;gico observado en el envenenamiento por <i>L. obliqua </i>(22, 42, 43).</p>      <p><b>Hem&oacute;lisis intravascular. </b>El veneno de <i>L. obliqua </i>provoca hem&oacute;lisis intravascular en ratas, con una reducci&oacute;n en el n&uacute;mero de eritrocitos circulantes, aumento de la hemoglobina plasm&aacute;tica en las primeras seis horas y una disminuci&oacute;n en los niveles de la hemoglobina total a las 24 horas (37, 43, 45). La hem&oacute;lisis intravascular se ha observado s&oacute;lo en los casos severos que tienen como antecedente el contacto con un gran n&uacute;mero de orugas (46, 47). Se cree que la responsable de la acci&oacute;n hemol&iacute;tica es la fosfolipasa A2 (43), enzima que induce actividad hemol&iacute;tica exclusivamente indirecta y responsable de provocar reacciones locales, como el dolor y la infamaci&oacute;n (17, 22, 30, 39).</p>      <p><b>Veneno de <i>L. Achelous. </i></b>El contacto con orugas de <i>L. achelous </i>produce s&iacute;ndrome fibrinol&iacute;tico. Pruebas de laboratorio realizadas en los pacientes muestran una intensa actividad fibrinol&iacute;tica. El veneno y las fracciones fibrinol&iacute;ticas degradan la fibrina <i>in vitro. </i>Sin embargo, los productos de la degradaci&oacute;n obtenidos son completamente diferentes de la plasmina o productos de la degradaci&oacute;n de tripsina. El veneno degrada los co&aacute;gulos preformados a un ritmo m&aacute;s lento que la plasmina. Adem&aacute;s, los inhibidores de la proteasa del plasma del sistema fibrinol&iacute;tico (a2-antiplasmina, <b>a </b>2-macroglobulina) s&oacute;lo inhiben d&eacute;bilmente el efecto l&iacute;tico del veneno (47, 48).</p>      <p>El veneno de <i>L. achelous </i>tiene actividad tanto procoagulante como anticoagulante. Las principales toxinas del veneno de <i>L. achelous </i>son lonomin II, que tiene actividad fibrinol&iacute;tica directa, lonomin III, que es un activador de protrombina, lonomin IV, que act&uacute;a como activador del Factor X, lonomin V, enzima proteol&iacute;tica que ejerce su actividad sobre el zim&oacute;geno del Factor XIII activo y sobre sus subunidades A y B, inactiv&aacute;ndolo, y tambi&eacute;n tiene actividad similar a la uroquinasa (activando el plasminogeno), lonomin VII a y lonomin VIII, que act&uacute;an como activadores o inhibidores del Factor V. Lonomin VII, tiene actividad similar a la calicre&iacute;na y a lonomin I, achelasa I y achelasa II tienen acci&oacute;n fibrinol&iacute;tica similares a las de la plasmina (11, 47-49) (<a href="#fig2">Figura 2</a>).</p>      <p align="center"><a name="fig2"></a><img src="img/revistas/amc/v38n2/v38n2a11f2.jpg"></p>      <p><b>Signos y s&iacute;ntomas. </b>Los s&iacute;ntomas cl&iacute;nicos por el envenenamiento de <i>L. obliqua </i>son muy similares a los observados por <i>L. achelous</i>. Estos s&iacute;ntomas y signos inician con dolor local, eritema y edema en la zona de contacto, posteriormente aparece cefalea, n&aacute;useas y v&oacute;mito. Seis a 72 horas despu&eacute;s del envenenamiento puede aparecer hipotensi&oacute;n, hematomas, hematuria, equimosis, epistaxis, gingivorragia, sangrado de heridas recientes y melenas(4, 41-43, 47-49).</p>      <p>El tipo de reacci&oacute;n depende de la especie de la oruga involucrada, el grado de exposici&oacute;n, el estadio de desarrollo del lepid&oacute;ptero y de las caracter&iacute;sticas del paciente. Los s&iacute;ntomas los podemos clasificar como leves, moderados o severos (<a href="#tab1">Tabla 1</a>). Las complicaciones potencialmente mortales incluyen insuficiencia renal aguda (IRA) y hemorragias intracerebrales, alveolares o peritoneales (15-40-45-50-52).</p>      ]]></body>
<body><![CDATA[<p align="center"><a name="tab1"></a><img src="img/revistas/amc/v38n2/v38n2a11t1.jpg"></p>      <p>La incoagulabilidad de la sangre se demuestra por la significativa prolongaci&oacute;n de los par&aacute;metros hemost&aacute;ticos, como el tiempo de protrombina (TP), el tiempo de tromboplastina parcial activado (TPT), tiempo de trombina (TT), y trastornos asociados con el consumo de factores de la coagulaci&oacute;n, principalmente el consumo del fibrin&oacute;geno as&iacute; como los factores V, XIII, Prote&iacute;na C y antitrombina III. Los factores VIII:C, von Willebrand, productos de degradaci&oacute;n de fibrina y el d&iacute;mero D se encuentran elevados. El factor II esta disminuido en casos severos (16, 24, 21, 47, 53).</p>      <p>La IRA se observa en 2-5% de los pacientes despu&eacute;s del contacto con <i>L. obliqua </i>y 10% de &eacute;stos puede desarrollar enfermedad renal cr&oacute;nica (6, 34, 51). Los pacientes con IRA presentan una mayor frecuencia de hematuria y grandes cambios en los par&aacute;metros de coagulaci&oacute;n. Sin embargo, la patog&eacute;nesis de las complicaciones renales es desconocida. Cambios hemodin&aacute;micos, isquemia renal y la acci&oacute;n directa de las toxinas del veneno pueden contribuir a esta patog&eacute;nesis (6, 51).</p>      <p>La ira es m&aacute;s frecuente despu&eacute;s del contacto con <i>L. obliqua </i>que con <i>L. achelous.</i></p>      <p><b>Tratamiento. </b>El tratamiento con la terapia convencional con f&aacute;rmacos antifibrinol&iacute;ticos como la aprotinina 400000 KIU en una hora seguido de 200000 KIU cada seis horas en infusi&oacute;n continua, el &aacute;cido &eacute;psilon aminocaproico 20 gramos d&iacute;a (dosis iniciales de 30 mg/kg por v&iacute;a endovenosa continuando con 15 mg/kg/4 h), o el &aacute;cido tranex&aacute;mico 15 g/d (oral o endovenoso) se han utilizado con &eacute;xito para tratar a los pacientes envenenados por <i>L. achelous. </i>La administraci&oacute;n de fibrin&oacute;geno purificado o los crioprecipitados 4-8 U/24 h (48), contribuyen a la correcci&oacute;n de los tiempos de coagulaci&oacute;n. Por el contrario, la terapia de reemplazo, ya sea con sangre total o plasma fresco congelado ha demostrado que pueden agravar los s&iacute;ntomas cl&iacute;nicos del envenenamiento.</p>      <p>La administraci&oacute;n de &aacute;cido &eacute;psilon aminocaproico, para revertir las manifestaciones cl&iacute;nicas de los pacientes envenenados por <i>L. obliqua </i>no permite ni la recuperaci&oacute;n del fibrin&oacute;geno, ni la normalizaci&oacute;n de los par&aacute;metros hemost&aacute;ticos, pero s&iacute; aumenta la tasa de mortalidad (54).</p>      <p>En el envenenamiento por <i>L. obliqua </i>el suero antilon&oacute;mico es el &uacute;nico tratamiento efectivo, ya que obtiene la recuperaci&oacute;n del fibrin&oacute;geno y la normalizaci&oacute;n de los tiempos de protrombina (TP) y tiempo parcial de tromboplastina activado (TPT), independiente del tiempo de la administraci&oacute;n (6, 14, 30, 54). Los antifibrinol&iacute;ticos no deben ser administrados y la administraci&oacute;n de sangre total o plasma fresco congelado no est&aacute; indicada, ya que exacerban la coagulaci&oacute;n intravascular diseminada (42, 51 ,54).</p>      <p><font size="3"><b>Conclusi&oacute;n</b></font></p>      <p>Los accidentes con orugas de las especies lonomia cada vez son m&aacute;s frecuentes. Lo que probablemente est&eacute; relacionado con el desequilibrio ecol&oacute;gico constante causado por la deforestaci&oacute;n, el avance de la frontera agr&iacute;cola, la colonizaci&oacute;n y el calentamiento global.</p>      <p>Este reporte reafirma la importancia de la historia cl&iacute;nica y examen f&iacute;sico para el establecimiento del diagn&oacute;stico. Sin el antecedente obtenido del contacto previo con una oruga de la familia <i>Saturniidae </i>en una ciudad donde no se presentan estos accidentes, la posibilidad de retraso en el diagn&oacute;stico y en el tratamiento es alta. As&iacute; mismo se advierte la posibilidad de remisiones de nuevos casos a la red hospitalaria de la ciudad de Bogot&aacute; y se alerta sobre el ecoturismo que ha aumentado las tasas de accidentes en los parques de reserva natural. Los viajeros a zonas end&eacute;micas generalmente pertenecen a las ciudades principales del pa&iacute;s lo que hace necesario que el personal de salud de zonas no end&eacute;micas est&eacute; preparado para la atenci&oacute;n de este tipo de envenenamiento.</p>  <hr>      ]]></body>
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<ref-list>
<ref id="B1">
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