Devlin H, Sloan P, Thakkar N S
Turner Dental School, University of Manchester, England.
J Oral Pathol Med. 1995 Mar;24(3):140-3. doi: 10.1111/j.1600-0714.1995.tb01155.x.
Oral manifestations of infantile systemic hyalinosis in a child of Asian origin are presented. Infantile systemic hyalinosis is a rare fatal condition with probably an autosomal recessive mode of inheritance. The symptoms become apparent soon after birth and death usually occurs before the age of two years. The systemic features are essentially due to widespread deposition of hyaline material in tissues. These include thickening and nodularity of skin, growth failure, joint contractures, osteoporosis, diarrhoea and recurrent infections. The oral changes in the case reported here included thickening of the oral mucosa, extensive overgrowth of gingival tissue, osteoporosis, marked curvature of the dental roots, and replacement of periodontal ligament by hyaline fibrous material. Immunohistochemistry revealed widespread presence of Type VI collagen in the connective tissue with particularly intense staining in the hyaline material.
本文报道了一名亚洲裔儿童的婴儿全身性透明变性的口腔表现。婴儿全身性透明变性是一种罕见的致命疾病,可能为常染色体隐性遗传模式。症状在出生后不久就会显现,通常在两岁前死亡。全身特征主要是由于透明物质在组织中广泛沉积所致。这些特征包括皮肤增厚和结节形成、生长发育迟缓、关节挛缩、骨质疏松、腹泻和反复感染。此处报道病例的口腔变化包括口腔黏膜增厚、牙龈组织广泛增生、骨质疏松、牙根明显弯曲,以及牙周韧带被透明纤维材料替代。免疫组织化学显示,结缔组织中广泛存在VI型胶原蛋白,在透明物质中染色尤为强烈。