一般型皮肤异色病样淀粉样变11例分析  

Analysis for 11 Cases of Poikiloderma-like Cutaneous Amyloidosis

作　　者：裴小平 王宇 李龙年 潘慧清 林尔艺 刘红芳 袁立燕 薛汝增 谷梅 

机构地区：[1]广东省皮肤病医院,广东广州510091

出　　处：《皮肤性病诊疗学杂志》2016年第5期314-317,共4页Journal of Diagnosis and Therapy on Dermato-venereology

基　　金：广东省中医药局科研课题(编号:20152027)

摘　　要：目的:分析一般型皮肤异色病样淀粉样变(PLCA)的临床特点。方法:收集总结我院11例经组织病理确诊的一般型皮肤异色病样淀粉样变患者的临床资料(病史、皮损特点、治疗及转归等)进行分析。结果:11例均为成人期发病。首发部位均在四肢,9例日晒后加重,7例伴有苔藓样丘疹,3例伴有水疱,3例有家族史。结论:在临床中,表现为皮肤异色、苔藓样丘疹,首发于四肢,无智力低下和身材矮小,需考虑一般型PLCA的可能。Objective：To investigate the clinical characteristics of general type poikiloderma- like cutaneous amyloidosis （PLCA）. Methods：Eleven patients with general type PLCA confirmed by histopathology were enrolled, and clinical data including medical history, cutaneous lesion fea- tures, therapy and prognosis were analyzed. Results：All of the 11 cases were onset at adult, and skin lesions first appeared on the limbs. Nine cases aggravated after insolation, 7 cases with li- chenification of pimples, 3 cases with blisters, 3 cases with family history. Conclusion：General type PLCA was rare in clinical. We should consider the possibility of PLCA when the patients pro- gressed with poikiloderma, liehenification of pimples, the initial skin lesion in limbs and without hypophrenia and microsomia.

关 键 词：皮肤异色病样 淀粉样变 

分 类 号：R758.6[医药卫生—皮肤病学与性病学]