论文部分内容阅读
一、历史的误会——晶体后纤维增生症、Terry综合征 1941年深秋,美国波士顿一位眼科大夫转了一个3月龄的早产儿患者到哈佛医学院眼科请求Ver-hoeff及Chandler会诊。该患儿瞳孔呈灰白色,伴有明显的眼球震颤。当时Terry正在verhoeff领导下的哈佛Howe实验室学习眼病理。在Verhoeff的指导下Terry经过详细临床病理研究认为该患儿瞳孔内灰白膜和晶体后永存血管鞘膜有关,是鞘外原始间叶组织增生的产物。波士顿另一眼科名家HarryMesangers建议称此病为晶体后纤维增生症,这病送
First, the history of misunderstanding - crystal fibroplasia, Terry syndrome In the late autumn of 1941, an ophthalmologist in Boston, United States transferred a 3-month-old premature children to Harvard Medical School ophthalmology request Ver-hoeff and Chandler consultation. The pupil was gray, with significant nystagmus. Terry was studying eye pathology at Harvard-Howe Labs, led by verhoeff. Under the guidance of Verhoeff Terry detailed clinical and pathological studies suggest that the pupil of the gray membrane and post-crystalline persistent vascular sheath, is the product of primitive mesenchymal tissue outside the sheath. Boston, another ophthalmologist HarryMesangers suggested that the disease is crystal fibroplasia, the disease to send