首页> 美国卫生研究院文献>Case Reports in Ophthalmological Medicine >Ocular Inflammatory Myofibroblastic Tumor in the Left Eye with Phthisis Right Eye: A Rare Occurrence in a Child
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Ocular Inflammatory Myofibroblastic Tumor in the Left Eye with Phthisis Right Eye: A Rare Occurrence in a Child

机译:左眼与Phthisis右眼的眼部炎症性肌纤维母细胞瘤:少见的儿童。

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摘要

Inflammatory myofibroblastic tumor (IMT) is a benign pseudoneoplastic inflammatory condition with the potential for persistent local growth and recurrence that rarely affects the orbit. We report a very rare case of anterior orbital IMT in a child who presented with gradually progressive mass in left eye for 16 months. Ocular examination showed a cauliflower like exophytic mass at 360 degrees of the perilimbal area covering the entire cornea and obscuring the visualization of anterior and posterior segments. The right eye was phthisical. CT scan showed a lobulated exophytic soft tissue mass in the preseptal region and along the anterior portion of the left globe extending from medial canthus to the lateral canthus. Enucleation of the left eye was performed and the histopathological examination confirmed the diagnosis of IMT. This report aims to raise awareness about this rare ocular entity and emphasizes its early treatment as delay can result in loss of the eye.
机译:炎性肌纤维母细胞瘤(IMT)是一种良性假肿瘤性炎性疾病,可能持续存在局部生长和复发,很少影响眼眶。我们报道了一个非常罕见的儿童眼眶前部IMT病例,该患儿左眼逐渐进行性肿块持续了16个月。眼部检查显示,在沿整个角膜覆盖的角膜周围区域360度处出现了菜花状外生块,并掩盖了前段和后段的图像。右眼发黄。 CT扫描显示在前中隔区和沿左球体的前叶部分,从内侧to延伸到外侧can,呈叶状外生软组织肿块。进行了左眼的去核,并且组织病理学检查证实了IMT的诊断。本报告旨在提高人们对这种罕见眼部实体的认识,并强调其早期治疗,因为延误会导致眼睛丧失。

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