Retrospective analysis of the correlation between dermoscopic vascular features and the response to hemoporfin-mediated photodynamic therapy in previously untreated children with port wine stains.
Sheng Zhang, Xiuwei Wang, Yijing Chen, Yuhan Wang, Jianyou Chen, Xiaoyan Liu, Gao Lei Zhang, Wei Su
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引用次数: 0
Abstract
Background: Port wine stains (PWS) are congenital capillary malformations that affect the quality of life for children. Hemoporfin-mediated photodynamic therapy (HMME-PDT) is a promising therapeutic modality for patients with PWS. However, the variability in the clinical efficacy of HMME-PDT has necessitated further investigations into the factors influencing the therapeutic efficacy of this modality.
Objectives: To explore the correlation between dermoscopic vascular features and the efficacy of HMME-PDT in previously untreated children with PWS.
Methods: Clinical data were collected from children with PWS who were treated with HMME-PDT. Correlations between clinical efficacy and gender, age, lesion location, lesion color and dermoscopic vascular features were analyzed retrospectively in previously untreated children with PWS.
Results: A total of 100 previously untreated children with PWS were enrolled, including 52 males and 48 females aged between 1 and 14 years. The efficacy of HMME-PDT differed significantly in relation to lesion location and color of the PWS (P<0.05). Sausage-like vessels (66.67%), dotted and globular vessels (87.50%) and linear vessels (50.00%) were associated with excellent treatment outcomes. Reticular vessels (65.00%) showed improved outcomes. HMME-PDT was not effective in some cases with homogeneous reddish background (35.71%) features. No serious adverse events and recurrences were observed following HMME-PDT.
Conclusion: The dermoscopic vascular features showed a significant correlation with the effectiveness of HMME-PDT in previously untreated children with PWS. Thus, the vascular features of PWS classified by dermoscopy can provide helpful clinical information to evaluate the efficacy of HMME-PDT and develop individualized treatment program for children with PWS.