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Histopathological study of a case with glaucoma due to sturge-weber syndrome.

机译:斯特格韦伯综合征引起的青光眼病例的组织病理学研究。

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PURPOSE: To investigate the cause of the secondary glaucoma in a case of Sturge-Weber syndrome by histopathology.CASE: A 10-year-old boy with Sturge-Weber syndrome and glaucoma in the right eye was studied. Trabeculectomy was performed because of uncontrolled intraocular pressure, and the trabeculectomy specimen was examined histologically by both light and electron microscopy.RESULTS: Histological examination of the trabeculectomy specimen showed that the ciliary muscle was dislocated anteriorly, and the Schlemm canal was not present. The spaces in the juxtacanalicular connective tissue (JCT) were replaced by vascular structures and connective tissue. There were two kinds of vascular structures: in one, the endothelium was surrounded by pericytes; and in the other, the endothelium was not surrounded by pericytes.CONCLUSIONS: Developmental abnormalities of the Schlemm canal and the JCT may have caused the glaucoma. These observations suggest that the developmental abnormalities of both the mesoderm andthe neural crest might be involved in the pathogenesis of the glaucoma in cases of Sturge-Weber syndrome.
机译:目的:通过组织病理学调查Sturge-Weber综合征的继发性青光眼的病因。案例:研究了一个10岁男孩患有Sturge-Weber综合征和青光眼的右眼。由于眼压不受控制而进行了小梁切除术,并通过光学和电子显微镜对小梁切除术标本进行了组织学检查。结果:小梁切除术标本的组织学检查显示睫状肌向前脱位,没有Schlemm管。颈管结缔组织(JCT)中的空间被血管结构和结缔组织取代。血管结构有两种:一种是内皮被周细胞包围;另一种是内皮被周细胞包围。结论:Schlemm管和JCT的发育异常可能引起了青光眼。这些观察结果表明,在Sturge-Weber综合征的情况下,中胚层和神经c的发育异常可能与青光眼的发病有关。

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