Juvenile Xanthogranuloma with Ocular Manifestations in a Nigerian Infant: A Case Report

Omololu Enigbokan, M. Ugalahi, Oluwatofunmi T. Eyekpegha, Valerie N. Abiola, Shakirat A Gold-Olufadi, E. Onebunne, B. Olusanya
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Abstract

Accurate diagnosis is the foundation of optimal care, which occasionally requires a multidisciplinary approach. Rare diseases may pose some diagnostic challenges, especially in the context of their similarity to other more common pathologies. We report a case of Juvenile Xanthogranuloma (JXG), a rare disease that had some initial diagnostic challenges due to its similarity with molluscum contagiosum.
尼日利亚婴儿伴有眼部表现的幼年黄疽:病例报告
准确诊断是最佳治疗的基础,有时需要采用多学科方法。罕见疾病可能会给诊断带来一些挑战,尤其是在它们与其他更常见的病症相似的情况下。我们报告了一例幼年黄疽(JXG)病例,这是一种罕见疾病,由于与软疣相似,最初的诊断遇到了一些挑战。
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