Naha Kushal, Shastry Ananthakrishna B, Saravu Kavitha, Bhatia Sumit
Department of Medicine, Kasturba Medical College, Manipal 576104 India.
Australas Med J. 2011;4(3):155-9. doi: 10.4066/AMJ.2011.635. Epub 2011 Mar 31.
Lipoid proteinosis is a rare congenital disorder that can present with a variety of symptoms. A nineteen year old Indian male with dysmorphic features was admitted with a twelve year history of recurrent ulcerations over the upper limbs and oral cavity. Although the initial presentation was strongly suggestive of a congenital immune-deficiency syndrome, all investigations for immunodeficiency disorders were negative. Subsequent evaluation yielded a diagnosis of lipoid proteinosis.
类脂蛋白沉积症是一种罕见的先天性疾病,可表现出多种症状。一名19岁有畸形特征的印度男性因上肢和口腔反复溃疡12年入院。尽管最初的表现强烈提示先天性免疫缺陷综合征,但所有免疫缺陷疾病的检查均为阴性。随后的评估得出类脂蛋白沉积症的诊断。