Histopathologic Changes in Congenital Corneal Stromal Dystrophy: Report of 4 Cases in 2 Families.

IF 1.3 4区 医学 Q3 ANATOMY & MORPHOLOGY
Ana M Colino Gallardo, Montserrat De la Torre Serrano, Lorenzo Alarcón García, Isabel Casado Fariñas, David De Pablo Velasco, Javier Martínez-Useros, Rodrigo Barderas, María J Fernández-Aceñero
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引用次数: 0

Abstract

Corneal dystrophies are hereditary diseases affecting the corneal tissue; they are bilateral, symmetrical and unrelated to environmental or systemic conditions. Congenital corneal stromal dystrophy is a very rare autosomal dominant dystrophy that is caused by a mutation in the DCN gene that encodes decorin (a proteoglycan of the extracellular matrix). We herein report 4 cases of congenital stromal corneal dystrophy in 2 families, highlighting the previously undescribed histopathologic features, the possible differential diagnosis of this entity and the key role played by decorin staining in its diagnosis.

先天性角膜基质营养不良的组织病理学改变:附2个家族4例报告。
角膜营养不良是影响角膜组织的遗传性疾病;它们是双边的、对称的,与环境或系统条件无关。先天性角膜基质营养不良是一种非常罕见的常染色体显性营养不良,由编码decorin(细胞外基质的蛋白聚糖)的DCN基因突变引起。我们在此报告了2个家族的4例先天性基质性角膜营养不良病例,强调了以前未描述的组织病理学特征、该实体的可能鉴别诊断以及decorin染色在其诊断中发挥的关键作用。
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来源期刊
Applied Immunohistochemistry & Molecular Morphology
Applied Immunohistochemistry & Molecular Morphology ANATOMY & MORPHOLOGY-MEDICAL LABORATORY TECHNOLOGY
CiteScore
3.20
自引率
0.00%
发文量
153
期刊介绍: ​Applied Immunohistochemistry & Molecular Morphology covers newly developed identification and detection technologies, and their applications in research and diagnosis for the applied immunohistochemist & molecular Morphologist. Official Journal of the International Society for Immunohistochemisty and Molecular Morphology​.
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