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                <text>vol. 65, (2005), p. 226-230. Título: Medicina|773x|0025-7680</text>
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                <text>López, María de los Angeles.</text>
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                <text>vol. 64, n. 4 (2003), p. 247-51. Título: Anales de la Facultad de Medicina Univ. Nacional Mayor de San Marcos|773x|1025-5583</text>
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                <text>Espinoza, Yrma.</text>
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                <text>iv, paginación varía : il. ; 26 cm.</text>
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&#13;
Materiales y métodos. Estudio retrospectivo donde se evaluaron historias clínicas de pacientes con diagnóstico clínico de toxoplasmosis ocular, atendidos entre junio de 2023 y junio de 2025. Se identificaron los casos atípicos según criterios clínicos: retinocoroiditis pseudomúltiple, retinitis extensa, papilitis sin foco adyacente, necrosis retiniana aguda o inmunosupresión. Se recopilaron datos clínicos, serológicos y de tratamiento, analizados de forma descriptiva.&#13;
&#13;
Resultados. Se encontraron 23 pacientes con toxoplasmosis ocular, de los cuales 6 (26,1%) presentaron formas atípicas. El motivo de consulta más frecuente fue disminución de agudeza visual. Todos los pacientes presentaron IgG positiva y solo 7 IgM positiva. El tratamiento incluyó antiparasitarios y en casos seleccionados, corticosteroides sistémicos. Las complicaciones observadas fueron catarata, glaucoma, membrana epirretinal y desprendimiento de retina.&#13;
&#13;
Conclusión. En nuestra serie las formas atípicas de toxoplasmosis ocular fueron infrecuentes, pero clínicamente relevantes por su dificultad diagnóstica y tipo de complicaciones. Su identificación requiere un alto índice de sospecha, especialmente en pacientes inmunocomprometidos. El abordaje terapéutico debe ser individualizado y con seguimiento estrecho.</text>
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                <text>En nuestro país, la toxoplasmosis ocular es la principal causa de uveítis posterior, siendo la seroprevalencia en América Latina mayor al 50%.  Es considerada una patología endémica, y existe gran variabilidad en su prevalencia, siendo mayor en zonas de menor ingreso económico. En pacientes inmunocompetentes la retinocoroiditis es generalmente una infección autolimitada que resuelve espontáneamente en un perÍodo de 4 a 8 semanas.</text>
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