<?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>2221-2434</journal-id>
<journal-title><![CDATA[Revista Finlay]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Finlay]]></abbrev-journal-title>
<issn>2221-2434</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Ciencias Médicas de Cienfuegos. Centro Provincial de información de Ciencias Médicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2221-24342022000100100</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Diagnóstico de un síndrome de Morgagni-Stewart-Morel en una paciente con ictus isquémico. Reporte de un caso]]></article-title>
<article-title xml:lang="en"><![CDATA[Diagnosis of a Morgagni-Stewart-Morel Syndrome in a Patient with Ischemic Stroke. Report of a Case]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Valladares Valle]]></surname>
<given-names><![CDATA[Masleidy]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[García Leonard]]></surname>
<given-names><![CDATA[Juan Ibrahim]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sánchez Lozano]]></surname>
<given-names><![CDATA[Ada]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital General Universitario Dr. Gustavo Aldereguía Lima  ]]></institution>
<addr-line><![CDATA[Cienfuegos ]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2022</year>
</pub-date>
<volume>12</volume>
<numero>1</numero>
<fpage>100</fpage>
<lpage>105</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S2221-24342022000100100&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S2221-24342022000100100&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S2221-24342022000100100&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN El síndrome de Morgagni-Stewart-Morel es una rara enfermedad que se caracteriza por hiperostosis frontal interna bilateral asociada a alteraciones metabólicas, psiquiátricas, hipertensión arterial y disfunción de pares craneales de etiología no definida. Se presenta el caso de una paciente de 77 años con historia de diabetes mellitus tipo 2, hipertensión arterial sistémica y trastorno psiquiátrico, que ingresó en el Servicio de Neurología del Hospital General Universitario Dr. Gustavo Aldereguía Lima de Cienfuegos con cuadro de disartria y hemiparesia derecha. Se realizaron estudios de diagnóstico por imagen de cráneo donde se observó la presencia de hiperostosis frontal interna extensa, atrofia cortical y un infarto talámico izquierdo. Durante su estancia hospitalaria se documentó la presencia de obesidad grado I, hirsutismo e hipercolesterolemia. La paciente cumplió con los criterios del síndrome de Morgagni-Stewart-Morel al manifestar la presencia de hiperostosis frontal interna con manifestaciones, endocrinológicas y neuropsiquiátricas. Se presenta el caso con el objetivo de evidenciar el diagnóstico de una enfermedad de baja incidencia en pacientes cerebrovasculares isquémicos con la presencia de una sintomatología que incluye varios factores de riesgo vasculares bien documentados.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT Morgagni-Stewart-Morel syndrome is a rare disease characterized by bilateral internal frontal hyperostosis associated with metabolic and psychiatric disorders, arterial hypertension, and dysfunction of the cranial nerves of undefined etiology. The case of a 77-year-old patient with a history of type 2 diabetes mellitus, systemic arterial hypertension and psychiatric disorder, who was admitted to the Neurology Service of the Dr. Gustavo Aldereguía Lima University Hospital in Cienfuegos with dysarthria and right hemiparesis is presented. Diagnostic skull imaging studies were performed where the presence of extensive internal frontal hyperostosis, cortical atrophy and a left thalamic infarction was observed. During his hospital stay, the presence of grade I obesity, hirsutism and hypercholesterolemia was documented. The patient met the criteria for Morgagni-Stewart-Morel syndrome by manifesting the presence of internal frontal hyperostosis with endocrinological and neuropsychiatric manifestations. The case is presented in order to demonstrate the diagnosis of a low incidence disease in ischemic cerebrovascular patients with the presence of symptoms that include several well-documented vascular risk factors.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[síndrome de Morgagni-Stewart-Morel]]></kwd>
<kwd lng="es"><![CDATA[hiperostosis frontal interna]]></kwd>
<kwd lng="es"><![CDATA[accidente cerebrovascular]]></kwd>
<kwd lng="es"><![CDATA[reporte de casos]]></kwd>
<kwd lng="en"><![CDATA[Morgagni-Stewart-Morel syndrome]]></kwd>
<kwd lng="en"><![CDATA[hyperostosis frontalis internal]]></kwd>
<kwd lng="en"><![CDATA[stroke]]></kwd>
<kwd lng="en"><![CDATA[case reports]]></kwd>
</kwd-group>
</article-meta>
</front><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Medrano]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Medrano]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Medrano]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Medrano]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Ajo de los Reyes]]></surname>
<given-names><![CDATA[LM.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Presentación de una paciente con síndrome de Morgagni-Stewart-Morel]]></article-title>
<source><![CDATA[CCM]]></source>
<year>2016</year>
<volume>20</volume>
<numero>4</numero>
<issue>4</issue>
</nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Castilla]]></surname>
<given-names><![CDATA[C.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Cuadro clínico, en especial el psiquiátrico del Síndrome de Morgagni-Stewart- Morel.]]></article-title>
<source><![CDATA[Arq Neuro-Psiquiatr]]></source>
<year>1953</year>
<volume>11</volume>
<numero>4</numero>
<issue>4</issue>
</nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Barcat]]></surname>
<given-names><![CDATA[JA.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enfermedades raras. El síndrome de Morgagni Stewart Morel.]]></article-title>
<source><![CDATA[Medicina]]></source>
<year>2012</year>
<volume>72</volume>
<numero>6</numero>
<issue>6</issue>
</nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Attanasio]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Granziera]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Giantin]]></surname>
<given-names><![CDATA[V]]></given-names>
</name>
<name>
<surname><![CDATA[Manzato]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Full Penetrance of Morgagni-Stewart- Morel Syndrome in a 75-year-old woman case report and review of the literature]]></article-title>
<source><![CDATA[J Clin Endocrinol Metab]]></source>
<year>2013</year>
<volume>98</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>453-7</page-range></nlm-citation>
</ref>
<ref id="B5">
<label>5</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rodríguez]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Roldán]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Trinidad]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[García]]></surname>
<given-names><![CDATA[JR]]></given-names>
</name>
<name>
<surname><![CDATA[Ramírez]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Hiperostosis frontal interna (HFI). Síndrome de Morgagni-Stewart-Morel (HSH).]]></article-title>
<source><![CDATA[Rev ORL]]></source>
<year>2011</year>
<volume>2</volume>
<numero>17</numero>
<issue>17</issue>
</nlm-citation>
</ref>
<ref id="B6">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[She]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Szakacs]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Hyperostosis frontalis internal case report and review of literature]]></article-title>
<source><![CDATA[An Clin Lab Science]]></source>
<year>2004</year>
<volume>34</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>206-8</page-range></nlm-citation>
</ref>
<ref id="B7">
<label>7</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Subirana]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Ortega]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Galtés]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Castellà]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Hallazgo incidental de hiperostosis frontal interna o síndrome de Morgagni asociado a meningiomas.]]></article-title>
<source><![CDATA[Cuad Med Forense]]></source>
<year>2012</year>
<volume>18</volume>
<numero>2</numero>
<issue>2</issue>
</nlm-citation>
</ref>
<ref id="B8">
<label>8</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[García]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Síndrome de Morgagni-Stewart-Morel. Reporte de caso y revisión de la literatura.]]></article-title>
<source><![CDATA[Rev Méd Inst Mex Seg Soc]]></source>
<year>2016</year>
<volume>54</volume>
<numero>5</numero>
<issue>5</issue>
</nlm-citation>
</ref>
</ref-list>
</back>
</article>
