<?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>1028-4818</journal-id>
<journal-title><![CDATA[Multimed]]></journal-title>
<abbrev-journal-title><![CDATA[Multimed]]></abbrev-journal-title>
<issn>1028-4818</issn>
<publisher>
<publisher-name><![CDATA[Centro Provincial de Información de Ciencias Médicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1028-48182019000400786</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Hellp síndrome. Presentación de un caso y revisión de la entidad]]></article-title>
<article-title xml:lang="en"><![CDATA[Hellp syndrome. Presentation of a case and review of the entity]]></article-title>
<article-title xml:lang="pt"><![CDATA[Síndrome de Hellp. Apresentação de um caso e revisão da entidade]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Tamayo Milanes]]></surname>
<given-names><![CDATA[Glennis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Malcolm Suárez]]></surname>
<given-names><![CDATA[Adolfo Luis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mendoza Castro]]></surname>
<given-names><![CDATA[Isabel Milagros]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ttito Hurtado]]></surname>
<given-names><![CDATA[Johayra Marilia]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de Ciencias Médicas de Granma Hospital General Universitario Carlos Manuel de Céspedes ]]></institution>
<addr-line><![CDATA[Bayamo Granma]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2019</year>
</pub-date>
<volume>23</volume>
<numero>4</numero>
<fpage>786</fpage>
<lpage>794</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S1028-48182019000400786&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S1028-48182019000400786&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S1028-48182019000400786&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Introducción:  el síndrome Hellp es una complicación grave de la Preeclampsia que determina el aumento de la mortalidad y morbilidad materna y perinatal. Descrita inicialmente en 1954 por Pritchard quien mencionó la hemólisis, trombocitopenia y otras alteraciones en las pacientes con toxemia severa; pero es Weinstein que en el año 1982, reconoce una rara y grave variante de preeclampsia, y para denominarla tomó las iniciales de los hechos que consideró fundamentales, de dicho síndrome: (H) hemólisis; (EL) elevación de enzimas hepáticas y (LP) plaquetopenia.  Presentación del caso:  se diagnosticó un caso de Hellp síndrome en una paciente de 31 años de edad y 24 semanas de gestación gemelar. Se realizó interrupción de embarazo de urgencia por bienestar materno y evoluciona favorablemente hasta ahora sin complicaciones. Realizamos una revisión bibliográfica actualizada así como su epidemiologia, diagnostico y tratamiento de esta entidad.  Discusión:  el caso que se reporta es el de una paciente con Hellp síndrome, considerándose una patología grave con alto riesgo de morbimortalidad materno- fetal, después de esta descripción, el objetivo principal es la realización de un diagnostico oportuno y recurrir a tiempo a la interrupción del embarazo.  Conclusiones: la sospecha clínica fue baja al inicio del cuadro, cuya condición pudo empeorar aún más el resultado materno sino se hubiera realizado un diagnóstico adecuado. Según nuestro protocolo nacional se preconiza el parto transpelviano y tratamiento oportuno del mismo, así como homogeniza el manejo de estas pacientes con el fin de evitar complicaciones.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Introduction:  Hellp syndrome is a serious complication of pre-eclampsia that determines the increase in maternal and perinatal mortality and morbidity. Initially described in 1954 by Pritchard who mentioned haemolysis, thrombocytopenia and other alterations in patients with severe toxemia; but it is Weinstein who in 1982, recognizes a rare and serious variant of preeclampsia, and to name it took the initials of the facts that he considered fundamental, of said syndrome: (H) hemolysis; (EL) elevation of liver enzymes and (LP) plaquetopenia.  Case presentation:  A case of Hellp syndrome was diagnosed in a patient aged 31 years and 24 weeks of twin gestation. An emergency pregnancy interruption for maternal well-being was performed and it has progressed favorably until now without complications. We conducted an updated bibliographic review as well as its epidemiology, diagnosis and treatment of this entity.  Discussion:  the case reported is that of a patient with Hellp syndrome, considering a serious pathology with a high risk of maternal-fetal morbidity and mortality, after this description, the main objective is the realization of a timely diagnosis and timely recourse to the Interruption of pregnancy.  Conclusions:  the clinical suspicion was low at the beginning of the picture, whose condition could worsen the maternal result even more if an adequate diagnosis had not been made. According to our national protocol transpelvic birth and timely treatment is recommended, as well as homogenizes the management of these patients in order to avoid complications.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[RESUMO  Introdução:  A síndrome de Hellp é uma complicação grave da pré-eclâmpsia que determina o aumento da mortalidade e morbidade materna e perinatal. Inicialmente descrito em 1954 por Pritchard, que mencionou hemólise, trombocitopenia e outras alterações em pacientes com toxemia grave; mas é Weinstein quem, em 1982, reconhece uma variante rara e séria de pré-eclâmpsia, e para o nome tomou as iniciais dos fatos que considerava fundamentais, da referida síndrome: (H) hemólise; (EL) elevação das enzimas hepáticas e (PL) plaquetopenia.  Apresentação do caso:  Um caso de síndrome de Hellp foi diagnosticado em um paciente com 31 anos e 24 semanas de gestação gemelar. Uma interrupção de gravidez de emergência para o bem-estar materno foi realizada e progrediu favoravelmente até agora sem complicações. Foi realizada uma revisão bibliográfica atualizada, bem como sua epidemiologia, diagnóstico e tratamento desta entidade.  Discussão:  o caso relatado é de um paciente com síndrome de Hellp, considerando-se uma patologia grave com alto risco de morbimortalidade materno-fetal, após essa descrição, o objetivo principal é a realização de um diagnóstico oportuno e o uso oportuno da doença. interrupção da gravidez.  Conclusões:  a suspeita clínica foi baixa no início do quadro, cuja condição poderia piorar ainda mais o resultado materno se não houvesse diagnóstico adequado. De acordo com nosso protocolo nacional, o nascimento transpélvico e o tratamento oportuno são recomendados, assim como a homogeneização do manejo desses pacientes, a fim de evitar complicações.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Síndrome HELLP]]></kwd>
<kwd lng="en"><![CDATA[HELLP Syndrome]]></kwd>
<kwd lng="pt"><![CDATA[síndrome HELLP]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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