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                <text>Archivos de la Sociedad Española de Oftalmología; Madrid, may.1997. ISSN: 0365-6691</text>
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                <text>Objetivo. La glomerulopatía proliferativa mesangial (GPM), se caracteriza por la proliferación de las células mesangiales con acumulación de matriz mesangial extracelular.&#13;
&#13;
El objetivo del presente artículo es describir  los hallazgos retinales en el fondo de ojo de una paciente con GPM.&#13;
&#13;
Caso clínico. Una paciente de 34 años concurrió para realizar control de rutina. Tenía antecedentes de asma bronquial, hipertensión arterial (HTA) y GPM con depósitos de IgM que requirió trasplante renal. En su exploración se constató una agudeza visual de 10/10 en ambos ojos. Como hallazgo, en el fondo de ojo (FO) se detectaron múltiples lesiones redondeadas de menos de ¼ de diámetro papilar en polo posterior con compromiso macular, perifoveales y en retina periférica 360°. En la tomografía de coherencia óptica, se observaron alteraciones del perfil posterior compatibles con depósitos drusenoides a nivel del epitelio pigmentario retinal (EPR) y como múltiples imágenes hiperreflectivas por alteración del EPR a nivel de la retinofluoresceinografía. &#13;
&#13;
Se realizaron además estudios de campo visual que evidenciaron escotomas aislados en ambos ojos y electroretinograma de características normales.&#13;
&#13;
Conclusión. Como hemos visto en el presente caso, los hallazgos retinales en la GPM brindan información sobre la afectación ocular de la glomerulopatía proliferativa mesangial y nos permiten realizar el seguimiento de estos pacientes para la detección temprana y/o prevención de sus posibles complicaciones.</text>
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                <text>Oftalmología Clínica y Experimental, vol. 18, nro. 3, sep. de 2025, p. 244-350</text>
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