DAPSONE-INDUCED TOXIC MACULOPATHY IN LEPROSY PATIENT

Sita Paramita Ayuningtyas, A. Djatikusumo, S. Nusanti, Salmarezka Dewiputri, M. Sidik
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Abstract

Introduction: Dapsone has been widely used as a part of multidrug therapy for leprosy patients. Ocular side effects are rare. Ocular toxicity manifestations include retinal necrosis, optic atrophy, macular infarction, bilateral exudative retinal detachment, and choroidal detachment. We reported a rare case of dapsone-induced toxic maculopathy in a leprosy patient. Case Report: A 32-year-old male complained of blurred vision and a gray spot in central vision in the left eye (LE) for one month prior to admission. He had been treated with multidrug therapy (MDT) for leprosy for seven months. The MDT consists of dapsone, clofazimine, and rifampicin. The best-corrected visual acuity (BCVA) of the right eye (RE) and the LE were 6/6 and 6/12, respectively. A funduscopy of the LE showed decreased macular reflex. A color vision defect following the tritan axis was found in the LE. The Humphrey visual field (HVF) test of the LE revealed a central scotoma. Macular optical coherence tomography (OCT) showed intraretinal hyperreflectivity and subretinal fluid. Dapsone was then stopped in collaboration with a dermatologist. Two months after the discontinuation of Dapsone, the BCVA of the LE improved to 6/7.5, then 6/6 three months later. Color vision, macular OCT, and HVF tests revealed improvements. Multifocal ERG of both eyes (BE) also showed improvement in N1 and P1 wave amplitude in both eyes on 9-month follow-up after dapsone discontinuation. Discussion: Instead of direct drug toxicity, the mechanism of ocular side effects is thought to be ischemia caused by two distinct mechanisms. Macular ischemia is caused by acute, severe peripheral hypoxia and the physical effect of red cell fragmentation due to the hemolytic process. After discontinuation of dapsone, this case showed improvement in visual function and macular structure. Conclusion: Toxic maculopathy may be present in leprosy patients receiving dapsone treatment, although it is uncommon. Regular follow-up and evaluation of visual function and macular involvement are essential. Early detection of dapsone-induced toxic maculopathy and prompt discontinuation of dapsone may result in an improvement of visual functions.
氨苯砜致麻风病患者中毒性黄斑病变
氨苯砜作为麻风病多药治疗的一部分已被广泛应用。眼部副作用很少。眼部毒性表现包括视网膜坏死、视神经萎缩、黄斑梗死、双侧渗出性视网膜脱离和脉络膜脱离。我们报告了一例罕见的氨苯砜引起的麻风病患者中毒性黄斑病变。病例报告:一名32岁男性,入院前一个月主诉视力模糊,左眼中心视力有灰斑。他接受了7个月的麻风病多药治疗(MDT)。MDT由氨苯砜、氯法齐明和利福平组成。右眼最佳矫正视力(BCVA)为6/6,LE为6/12。眼底镜显示黄斑反射减弱。在LE中发现三轴以下的色觉缺陷。LE的Humphrey视野(HVF)检查显示中心暗斑。黄斑光学相干断层扫描(OCT)显示视网膜内高反射率和视网膜下积液。然后在皮肤科医生的协助下停用了氨苯砜。停用氨苯砜2个月后,LE的BCVA改善至6/7.5,3个月后改善至6/6。色觉、黄斑OCT和HVF测试显示改善。停药9个月后,双眼多焦ERG (BE)的N1、P1波幅度均有改善。讨论:眼部副作用的机制被认为是由两种不同的机制引起的缺血,而不是直接的药物毒性。黄斑缺血是由急性、严重的外周缺氧和溶血过程引起的红细胞碎裂的物理效应引起的。停用氨苯砜后,本例视力及黄斑结构均有改善。结论:中毒性黄斑病变可能存在于接受氨苯砜治疗的麻风病患者中,尽管这种情况并不常见。定期随访和评估视力功能和黄斑受累是必要的。早期发现氨苯砜引起的中毒性黄斑病变并及时停用氨苯砜可改善视觉功能。
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