M. Haedersdal et al., CHANGES IN SKIN REDNESS, PIGMENTATION, ECHOSTRUCTURE, THICKNESS, AND SURFACE CONTOUR AFTER 1 PULSED DYE-LASER TREATMENT OF PORT-WINE STAINSIN CHILDREN, Archives of dermatology, 134(2), 1998, pp. 175-181
Background: The pulsed dye laser is the treatment of choice for childr
en with port-wine stains (PWSs). Evaluation of treatment outcome and a
dverse effects is traditionally based on subjective clinical scoring s
ystems. We intend to objectify treatment results and adverse reactions
after 1 treatment with the pulsed dye laser. Design: A before-and-aft
er trial using skin reflectance to detect changes in skin redness and
pigmentation, ultrasonography to evaluate changes in echostructure and
skin thickness, and 3-dimensional surface contour analysis to detect
changes in surface texture. Patients: Twelve children with PWSs. Setti
ng: A university dermatological department. Results: The skin reflecta
nce-determined change in skin redness correlated with the clinical res
ponse (r=0.46, P<.002). The percentage of reflectance-determined light
ening was equal for pink, red, and dark red PWSs (median, 42.9%). Skin
pigmentation increased after laser treatment (P<.007). Ultrasonograph
y revealed lower dermal echogenicity of preoperative PWSs than of post
operative PWSs (P<.007) and healthy skin (P<.001). An increase in echo
genicity reflected a decrease in the dermal water (blood) content. Var
iations were found in the dermal localization of the PWS. Skin thickne
ss was significantly higher in the PWS before treatment than after (P<
.001). The preoperative lesional thickness correlated inversely with t
he ultrasound-assessed treatment response (r=0.35, P<.04). The surface
contour parameters decreased significantly after laser treatment, ind
icating a flattening of the skin surface. The contour changes correlat
ed positively with treatment response. By clinical evaluation, no hypo
pigmentation or texture changes were detected. Conclusion: The evaluat
ion of treatment outcome and adverse effects is refined by the use of
skin reflectance, ultrasonographic, and surface contour analysis.