摘要
目的探讨色素血管性斑痣性错构瘤病(PPV)的临床表现、特征及分型。方法收集并整理本院2007年至今收治的15例PPV患者的临床资料,总结其临床特点。结果 15例PPV患者中,Ⅱ型多见,占66.67%,其次为Ⅲ型(26.67%);5例有太田痣。结论色素血管性斑痣性错构瘤病临床少见,易导致误诊,同时应全面检查以排除系统损害的可能。
Objective To survey the clinical manifestations and features of 15 cases of phakomatosis pigmentovascu- laris（PPV）. Methods The clinical data of 15 cases of PPV treated in this hospital from 2007 were col- lected and collated, and their clinical features were summarized. Results Of the patients,type Ⅱ make up 66.67%,followed by type m （26.67%）, 5 patients combined with nevus of Ota. Conclusion PPV are clinically rare in and are easy to misdiagnoscd. The comprehensive physical examination are essencial to exclude the possibility of systematic damage.
出处
《中国皮肤性病学杂志》
CAS
北大核心
2012年第4期315-316,共2页
The Chinese Journal of Dermatovenereology
