<?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>S2448-91902025000400367</article-id>
<article-id pub-id-type="doi">10.29262/ram.v72i4.1467</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Cromoblastomicosis, una enfermedad tropical desatendida: reporte de caso y revisión narrativa]]></article-title>
<article-title xml:lang="en"><![CDATA[Overview of Chromoblastomycosis, a neglected tropical disease: case report and narrative review]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Paternina-Colorado]]></surname>
<given-names><![CDATA[Angie Juliana]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Melo-Maecha]]></surname>
<given-names><![CDATA[Yadira]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Velasco-Castro]]></surname>
<given-names><![CDATA[Julio César]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Garzon-Peñuela]]></surname>
<given-names><![CDATA[Angie Lizeth]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cubillos-Vega]]></surname>
<given-names><![CDATA[Hector Julián]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bernal-Otalora]]></surname>
<given-names><![CDATA[Sara Daniela]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[García-Agudelo]]></surname>
<given-names><![CDATA[Lorena]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Regional de la Orinoquía  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2025</year>
</pub-date>
<volume>72</volume>
<numero>4</numero>
<fpage>367</fpage>
<lpage>371</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S2448-91902025000400367&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S2448-91902025000400367&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S2448-91902025000400367&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Antecedentes: La cromoblastomicosis (CBM) es una micosis subcutánea crónica presente en regiones tropicales o subtropicales, causada por la inoculación traumática de varias especies de hongos melanizados, los más comunes son Fonsecaea pedrosoi y Cladophialophora carrionii, se caracteriza en etapas tempranas por máculas o pápulas eritematosas con aspecto verrugoso o hiperqueratósico, que progresan a morfologías nodulares, verrugosas, tumorales, en placa o cicatriciales.  Objetivo: describir una presentación clásica y realizar una revisión narrativa de la CMB con un tiempo de evolución prolongado y extensión multifocal.  Reporte de caso: Hombre de 69 años, de ocupación agricultor con antecedentes de hipertensión arterial, falla cardiaca con FEVI conservada, diverticulosis colónica y hernia umbilical. Ingresó al servicio de urgencias por cuadro de un día de disnea, escalofríos, astenia, adinamia y fiebre, compatible con neumopatía crónica exacerbada y neumonía; dado historial de 10 años de crecimiento progresivo de lesiones en piel tipo pápulas indoloras y pruriginosas que se extendieron con distintas presentaciones a otras áreas del cuerpo, se le practicó un estudio de hidróxido de potasio (KOH) evidenciando estructuras micóticas y presencia de levaduras, mientras que la biopsia de piel reportó hallazgos de hiperplasia pseudoepiteliomatosa, y abscesos intraepidérmicos con cuerpos de Medlar, patognomónicos de la CBM.  Conclusión: Se resalta la relevancia de un diagnóstico acertado de una enfermedad tropical desatendida y la instauración de tratamiento antimicótico personalizado, además de la necesidad de un monitoreo a largo plazo debido al carácter crónico de la patología por su marcada resistencia al tratamiento.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Background: Chromoblastomycosis (CBM) is a chronic subcutaneous mycosis present in tropical or subtropical regions, caused by the traumatic inoculation of various species of melanized fungi, the most common being Fonsecaea pedrosoi and Cladophialophora carrionii. It is characterized in early stages by erythematous macules or papules with a verrucous or hyperkeratotic appearance, which progress to nodular, verrucous, tumoral, plaque, or scar-like morphologies.  Objective: to describe a classic presentation and conduct a narrative review of CBM with a prolonged evolution time and multifocal extension.  Case report: 69-year-old man, a farmer by occupation, with a history of hypertension, heart failure with preserved ejection fraction, colonic diverticulosis, and umbilical hernia. He was admitted to the emergency department with a one-day history of dyspnea, chills, asthenia, adynamia, and fever, consistent with exacerbated chronic lung disease and pneumonia. Given a 10-year history of progressive growth of painless and pruritic papular skin lesions that spread with various presentations to other areas of the body, a potassium hydroxide (KOH) test was performed, revealing mycotic structures and the presence of yeasts. Meanwhile, the skin biopsy reported findings of pseudoepitheliomatous hyperplasia and intraepidermal abscesses with Medlar bodies, pathognomonic of CBM.  Conclusion: The case highlights the importance of an accurate diagnosis of an overlooked tropical disease and the establishment of personalized antifungal treatment, as well as the need for long-term monitoring due to the chronic nature of the pathology and its marked resistance to treatment.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Cromoblastomicosis]]></kwd>
<kwd lng="es"><![CDATA[Enfermedades desatendidas]]></kwd>
<kwd lng="es"><![CDATA[Dermatomicosis]]></kwd>
<kwd lng="en"><![CDATA[Chromoblastomycosis]]></kwd>
<kwd lng="en"><![CDATA[Neglected diseases]]></kwd>
<kwd lng="en"><![CDATA[Dermatomycoses]]></kwd>
</kwd-group>
</article-meta>
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