Samad Fatima, Nabi Ghulam, Ghazal Saadia
Ayub Medical College and Teaching Hospital Abbottabad.
J Ayub Med Coll Abbottabad. 2008 Oct-Dec;20(4):86-9.
Urbache-Wiethe disease (Lipoid Proteinosis) is a rare autosomal recessive disorder characterized by the deposition of an eosinophilic hyaline-like material in the skin, larynx, mucous membranes, brain, and other internal organs.
A survey of one year duration was carried out prospectively at the Department of Dermatology, Ayub Teaching Hospital Abbottabad to document cases of lipoid proteinosis. Cases were selected from the outpatients department on the basis of clinical presentation and were subjected to detailed examination and investigations after admission.
Five cases were diagnosed as suffering from Lipoid Proteinosis over the study period. All had typical features of hoarseness, skin lesions and tongue involvement. All were born of consanguineous parents. Three (60.0%) cases also gave a history of involvement of other family members, particularly cousins.
This rare disease occurs in Hazara Division of North West Frontier Province of Pakistan with an as yet undetermined frequency and clinical suspicion is warranted to diagnose cases with the typical presentation.
乌尔巴赫-维特病(类脂蛋白沉积症)是一种罕见的常染色体隐性疾病,其特征是嗜酸性透明样物质沉积于皮肤、喉部、黏膜、大脑及其他内脏器官。
在阿伯塔巴德阿尤布教学医院皮肤科进行了为期一年的前瞻性调查,以记录类脂蛋白沉积症病例。根据临床表现从门诊患者中选取病例,入院后进行详细检查和调查。
在研究期间,有5例被诊断为类脂蛋白沉积症。所有患者均有声音嘶哑、皮肤病变和舌部受累的典型特征。所有患者的父母均为近亲结婚。3例(60.0%)患者还提及其他家庭成员,尤其是堂兄弟姐妹患病史。
这种罕见疾病在巴基斯坦西北边境省哈扎拉地区有发生,发病频率尚未确定,对于具有典型表现的病例,有必要进行临床怀疑诊断。