<?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>2448-9190</journal-id>
<journal-title><![CDATA[Revista alergia México]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. alerg. Méx.]]></abbrev-journal-title>
<issn>2448-9190</issn>
<publisher>
<publisher-name><![CDATA[Colegio Mexicano de Inmunología Clínica y Alergia A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2448-91902017000200235</article-id>
<article-id pub-id-type="doi">10.29262/ram.v64i2.194</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome de Good. Reporte de un caso]]></article-title>
<article-title xml:lang="en"><![CDATA[Good&#8217;s syndrome. Report of case]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Herrera-Sánchez]]></surname>
<given-names><![CDATA[Diana Andrea]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[León-Pedroza]]></surname>
<given-names><![CDATA[José Israel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vargas-Camaño]]></surname>
<given-names><![CDATA[María Eugenia]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Castrejón-Vázquez]]></surname>
<given-names><![CDATA[María Isabel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Instituto Mexicano del Seguro Social Centro Médico Nacional Siglo XXI Hospital de Especialidades]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado Centro Médico Nacional 20 de Noviembre ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2017</year>
</pub-date>
<volume>64</volume>
<numero>2</numero>
<fpage>235</fpage>
<lpage>240</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S2448-91902017000200235&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S2448-91902017000200235&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S2448-91902017000200235&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen:  Introducción:  El síndrome de Good es una asociación de timoma e inmunodeficiencia. Los síntomas son infecciones sinopulmonares recurrentes, además de los provocados por la compresión del timoma. Los exámenes paraclínicos se caracterizan por ausencia o disminución de linfocitos B, hipogammaglobulinemia, inversión de la relación CD4/CD8 y respuesta proliferativa anormal a mitógenos.  Caso clínico:  Mujer de 49 años de edad con edema de miembros inferiores, vómito posprandial, disfagia, diarrea crónica y pérdida ponderal. Con una segunda endoscopia se descartó cáncer gástrico. En la placa de tórax se observó ensanchamiento de mediastino y en la tomografía toracoabdominal, derrame pleural bilateral y tumor en mediastino anterior. El reporte histopatológico fue timoma B1. Exámenes paraclínicos: IgG, IgA e IgM de 349, 70.3 y 37.1 mg/dL, respectivamente; Ca125 631 UI/mL, leucocitos 7890 mm3 , hemoglobina 13.2 g/dL, linfocitos 2060 mm3 ; CD16+CD56+, CD19, CD3, CD4 y CD8 de 122, 77, 2052, 977 y 998 cel/µL, respectivamente; relación CD4/CD8 0.98; panel viral para hepatitis C, B y VIH negativo. La hipogammaglobulinemia confirmó síndrome de Good; se inició con 1 g/kg de gammaglobulina intravenosa, alcanzando meta de reemplazo a la tercera dosis, con mejoría clínica. La paciente falleció a los 4 meses por complicaciones cardiacas.  Conclusiones:  A pesar de la variabilidad de la presentación del síndrome de Good, debe sospecharse como parte de las manifestaciones paraneoplásicas del timoma.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract:  Background:  Good&#8217;s syndrome is an association of thymoma and immunodeficiency. The symptoms are recurrent sinopulmonary infections in addition to the compressive side of thymoma. A laboratory finding is notable for the absence or decrease of B lymphocytes, hypogammaglobulinemia, inversion ratio CD4/CD8 and abnormal proliferative response to mitogens.  Clinical case:  Female, 49-year-old started five months earlier with lower limb edema, postprandial vomiting, dysphagia, chronic diarrhea and weight loss. A second endoscopy ruled gastric neoplasia. Chest radiography with mediastinal widening, Thoraco-abdominal CT with bilateral pleural effusion and a mass in the anterior mediastinum, histopathological report of the tumor: B1 thymoma. Laboratory findings: IgG 349 mg/dL, IgA 70.3 mg/dL, 37.1 IgM mg/dL, Ca125 631 UI/mL, leukocytes 7890 mm3 , hemoglobin 13.2 g/dL, lymphocytes 2060 mm3 , CD16+CD56+ 122 cells/µL, CD19 77 cells/µL, CD3 2052 cells/µL, CD4 977 cells/µL, CD8 998 cells/µL; ratio CD4/ CD8 0.98, hepatitis C, B and HIV negative. They requested valuation to Clinical Immunology and Allergy due to hypogammaglobulinemia, the diagnosis of Good&#8217;s syndrome was confirmed and initiated with intravenous gamma globulin replacement to immunomodulatory dose of 1 g/ kg, she reached replacement goal in the third dose of immunoglobulin intravenous, with clinical improvement. She died four months later from cardiac complications.  Conclusions:  Despite the variability of presentation, Good&#8217;s syndrome should be suspected as part of the paraneoplastic manifestations of thymoma.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Timoma]]></kwd>
<kwd lng="es"><![CDATA[Hipogammaglobulinemia]]></kwd>
<kwd lng="es"><![CDATA[Gammaglobulina intravenosa]]></kwd>
<kwd lng="en"><![CDATA[Thymoma]]></kwd>
<kwd lng="en"><![CDATA[Hypogammaglobulinemia]]></kwd>
<kwd lng="en"><![CDATA[Intravenous gammaglobulin]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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