Anil S, Philip T, Jacob O, Beena V T
Dental College, Trivandrum, India.
J Pierre Fauchard Acad. 1993 Sep;7(3):89-92.
Hyalinosis cutis et mucosae is a rare genetic disease characterized by accumulation of glycoproteinaceous material at mucocutaneous sites, salivary glands, central and peripheral nervous systems, eyes, other organs and tissues. The course of the disease is protracted and not likely to regress either spontaneously or with therapy. The disease may produce considerable disfigurement and functional impairment. The morbid factors include disfiguring papulonodular lesions particularly of expose skin, hoarseness of voice due to vocal cord. Infiltration, nodular deformation of the eyelids and board like rigidity of tongue. A case of Hyalinosis cutis et mucosae in a 18 year old girl is reported here. The clinical features, histopathology and management are discussed in detail.
皮肤黏膜透明变性是一种罕见的遗传性疾病,其特征是糖蛋白物质在皮肤黏膜部位、唾液腺、中枢和周围神经系统、眼睛及其他器官和组织中蓄积。该病病程迁延,不太可能自发消退或经治疗后消退。该病可导致严重的毁容和功能障碍。致病因素包括尤其是暴露皮肤处的毁容性丘疹结节性病变、声带导致的声音嘶哑、眼睑浸润、结节变形以及舌板样僵硬。本文报告了一名18岁女孩患皮肤黏膜透明变性的病例。详细讨论了其临床特征、组织病理学及治疗方法。