4.3 Article

Tacrolimus Induced Thrombotic Microangiopathy (TMA) Presenting as Acute Macular Neuroretinopathy

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OCULAR IMMUNOLOGY AND INFLAMMATION
卷 31, 期 1, 页码 231-232

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TAYLOR & FRANCIS INC
DOI: 10.1080/09273948.2021.1998549

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Tacrolimus; hemolytic uremic syndrome; posterior reversible encephalopathy syndrome; thrombotic microangiopathy; acute macular neuroretinopathy

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This report describes a case of acute macular neuroretinopathy (AMN) associated with the use of tacrolimus. A 27-year-old woman with a history of diffuse proliferative membranous glomerulonephritis experienced abnormal body movements, loss of consciousness, and blurred vision in the left eye after 3 months of starting tacrolimus. Ocular examination revealed characteristic AMN findings.
This report highlights the association of tacrolimus use with acute macular neuroretinopathy (AMN). A 27-year-old woman, a known case of diffuse proliferative membranous glomerulonephritis, developed abnormal body movements, loss of consciousness, and blurring of vision in the left eye, after 3 months of starting tacrolimus. Blood investigations revealed anemia, thrombocytopenia, raised urea and creatinine levels, and raised LDH levels. A diagnosis of tacrolimus induced hemolytic uremic syndrome (HUS) with posterior reversible encephalopathy syndrome (PRES) was made. Ocular examination revealed a reddish-brown petaloid retinal lesion, which was better appreciated on red-free imaging as dark grey area pointing towards the fovea. OCT-A and SD-OCT revealed flow voids in deep retinal plexus, and disruption of ellipsoid and interdigitation zone, respectively, findings consistent with AMN. To the best of our knowledge, it is the first report of association of tacrolimus with AMN.

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