Computed tomography of retinoblastoma.

S Lindahl
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引用次数: 14

Abstract

Retinoblastoma is the most common primary malignant intraocular tumor in children. The clinical features are leucocoria and/or strabismus. The ophthalmic diagnosis is straight forward in clear eye media with a white gray mass in the fundus. With opaque ocular media, other diagnostic procedures such as CT and ultrasonography are important. In the present study the results of CT examinations of 23 patients with histologically proven retinoblastomas are presented. The mean age of the patients was two years. The characteristic CT finding is a partly calcified intravitreous mass lesion mostly confined within the eyeball. Two cases showed retrobulbar extension and two intracranial tumor extension. No metastasis was found in the brain, liver, spleen, long bones, chest or skull. The radiologic screening procedures for retinoblastoma metastasis are discussed. In patients suspected to have a retinoblastoma, it is recommended to perform CT of the orbits and brain in order to detect the tumor and its possible retrobulbar and intracranial extension.

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视网膜母细胞瘤的计算机断层扫描。
视网膜母细胞瘤是儿童最常见的原发性眼内恶性肿瘤。临床表现为白质和/或斜视。在眼底有白色灰色肿块的透明眼介质中,眼科诊断是直接的。对于不透明的眼内介质,其他的诊断程序如CT和超声检查是重要的。本文报告23例经组织学证实的视网膜母细胞瘤的CT检查结果。患者的平均年龄为两岁。特征性CT表现为部分钙化的玻璃体内肿块病变,主要局限于眼球内。2例肿瘤延伸至球后,2例肿瘤延伸至颅内。脑、肝、脾、长骨、胸、颅骨未见转移。本文讨论了视网膜母细胞瘤转移的放射学筛查方法。在怀疑患有视网膜母细胞瘤的患者中,建议进行眼眶和脑部CT检查,以发现肿瘤及其可能的球后和颅内扩张。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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