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- W2895033862 abstract "<p><span lang=ES>El síndrome de Sjögren primario es una enfermedad autoinmune sistémica de evolución crónica. </span><span lang=ES-AR>Puede presentar compromiso renal hasta en un 30% de los pacientes.</span><span lang=ES>La incidencia de tubulopatías varía de 2.6 a 33%. Se manifiestan por defectos en la concentración de la orina y alteraciones hidroelectrolíticas, principalmente acidosis tubular distal y de manera excepcional acidosis tubular proximal. Estos trastornos pueden asociarse a Nefrocalcinosis y litiasis renal. </span></p><p><span lang=ES>Reportamos el caso de una paciente con Sjögren primario que presentó acidosis tubular renal proximal asociada a cólicos renales recurrentes por litiasis renal y nefrocalcinosis. </span></p><p><span lang=ES>Destacamos la importancia de diagnosticar acidosis tubular renal en pacientes con síndrome de Sjögren que presenten alteraciones en el sedimento urinario y desórdenes electrolíticos para evitar la nefrocalcinosis medular y las nefrolitiasis asociadas. La terapia para la corrección de la acidosis tiene como objetivo evitar la progresión del trastorno y preservar la función renal.</span></p><p> </p>" @default.
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- W2895033862 date "2018-06-30" @default.
- W2895033862 modified "2023-10-17" @default.
- W2895033862 title "Nefrocalcinosis y acidosis tubular renal proximal en síndrome de Sjögren" @default.
- W2895033862 doi "https://doi.org/10.31053/1853.0605.v75.n2.19161" @default.
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