Comparative histochemistry of port-wine stains after copper vapor laser (578 nm) and argon laser treatment.

The present study compared the histologic changes occurring 15 min after copper vapor laser (CVL; operating at 578 nm) and argon laser (488/514 nm) treatment of port-wine stains (PWS) over a range of energy densities (8-32 J/cm2) with corresponding pulse widths of 50-200 ms. Frozen tissue sections were stained with nitroblue tetrazolium chloride (NBTC). This histochemical method permits an accurate color differentiation between blue-stained viable and unstained thermally damaged cells. At 8, 10, and 12 J/cm2 the argon-laser injury was confined to epidermal cell layers; none to superficial dermal effects were found. Fluences of at least 15 J/cm2 produced a diffuse NBTC-negative coagulation necrosis. Exposure of PWS skin to 8-12 J/cm2 at 578 nm did not alter the integrity of epidermal cells. In the dermis, damage was confined to blood vessels and surrounding collagen, showing a clear demarcation from adjacent viable structures. The maximum penetration depth achieved with these vessel selective energy densities was 0.44 mm. At 15 J/cm2, besides vascular injury, damage to the basal cell layer also occurred. At fluences of 17-20 J/cm2 a diffuse necrosis similar to that induced by the argon laser was found. Vessel selectivity of the 578 nm wave band was achieved with pulse widths from 50-74 ms, exceeding the estimated "ideal" exposure time (0.1-10.0 ms) for a vascular selective laser effect. The NBTC method allowed identification of subtle laser-induced tissue changes providing accurate quantitative data relating to the extent of vascular injury.

[1]  J. Pickering,et al.  Copper vapour laser treatment of port-wine stains and other vascular malformations. , 1990, British journal of plastic surgery.

[2]  J M Garden,et al.  The treatment of port-wine stains by the pulsed dye laser. Analysis of pulse duration and long-term therapy. , 1988, Archives of dermatology.

[3]  P. Morrison,et al.  585 nm for the treatment of port-wine stains. , 1990, Plastic and reconstructive surgery.

[4]  G. Spector The ultrastructural cytochemistry of lactic dehydrogenase, succinic dehydrogenase, dihydro-nicotinamide adenine dinucleotide diaphorase and cytochrome oxidase activities in hair cell mitochondria of the guinea pig cochlea. , 1975, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[5]  J. Pickering,et al.  Histology of port wine stains after copper vapour laser treatment , 1989, The British journal of dermatology.

[6]  S Mordon,et al.  Hexascan: a new robotized scanning laser handpiece. , 1990, Cutis.

[7]  A. Welch,et al.  Is there an optimal laser treatment for port wine stains? , 1986, Lasers in surgery and medicine.

[8]  J. Pickering,et al.  Computed temperature distributions around ectatic capillaries exposed to yellow (578 nm) laser light. , 1989, Physics in medicine and biology.

[9]  A. Seligman,et al.  A Histochemical Method for the Demonstration of Diphosphopyridine Nucleotide Diaphorase , 1958, The Journal of biophysical and biochemical cytology.

[10]  A. Pearse,et al.  The cytochemical localization of oxidative enzymes. I. Diphosphopyridine nucleotide diaphorase and triphosphopyridine nucleotide diaphorase. , 1958 .

[11]  B. Cosman Experience in the Argon Laser Therapy of Port Wine Stains , 1980, Plastic and reconstructive surgery.

[12]  K. Arndt,et al.  Argon laser-port-wine stain interaction. Immediate effects. , 1984, Archives of dermatology.

[13]  A. Welch,et al.  Time constants in thermal laser medicine , 1989, Lasers in surgery and medicine.

[14]  Robert Knobler,et al.  Histochemical evaluation of the coagulation depth after argon laser impact on a port‐wine stain , 1991 .

[15]  R. Knobler,et al.  Enzyme histochemical analysis of cell viability after argon laser-induced coagulation necrosis of the skin. , 1991, Journal of the American Academy of Dermatology.

[16]  K. Wolff,et al.  ENZYME-HISTOCHEMICAL STUDIES ON THE HEALING-PROCESS OF SPLIT SKIN GRAFTS. I. AMINOPEPTIDASE, DIPHOSPHOPYRIDINE-NUCLEOTIDE-DIAPHORASE AND SUCCINIC DEHYDROGENASE IN AUTOGRAFTS. , 1966, The Journal of investigative dermatology.

[17]  M. V. van Gemert,et al.  Clinical and histological evaluation of portwine stain treatment with a microsecond‐pulsed dye‐laser at 577 NM , 1984, Lasers in surgery and medicine.

[18]  K. Arndt Treatment technics in argon laser therapy. , 1984, Journal of the American Academy of Dermatology.

[19]  A J Welch,et al.  Spotsize effects on guinea pig skin following pulsed irradiation. , 1988, The Journal of investigative dermatology.

[20]  B. Gilchrest,et al.  Treatment of children with port-wine stains using the flashlamp-pulsed tunable dye laser. , 1989, The New England journal of medicine.

[21]  R. Knobler,et al.  Photoelectric quantitative evaluation of argon laser treatment of port wine stains , 1991, The British journal of dermatology.

[22]  J. Parrish,et al.  Microvasculature Can Be Selectively Damaged Using Dye Lasers: A Basic Theory and Experimental Evidence in Human Skin , 1981, Lasers in surgery and medicine.

[23]  R. Anderson,et al.  Comparative histological studies of the tunable dye (at 577 nm) laser and argon laser: the specific vascular effects of the dye laser. , 1981, The Journal of investigative dermatology.

[24]  W. Waidelich,et al.  Effects of argon, dye, and Nd: YAG lasers on epidermis, dermis, and venous vessels , 1986, Lasers in surgery and medicine.

[25]  S. Mordon,et al.  Robotized scanning laser handpiece for the treatment of port wine stains and other angiodysplasias , 1988, Lasers in surgery and medicine.

[26]  K. Wolff,et al.  Enzyme-histochemical studies on the healing process of split skin grafts. 3. Oxidative and hydrolytic enzymes in homografts. , 1966, The Journal of investigative dermatology.

[27]  O. Tan,et al.  Histologic comparison of the pulsed dye laser and copper vapor laser effects on pig skin , 1990, Lasers in surgery and medicine.

[28]  R. Anderson,et al.  Histologic responses of port-wine stains treated by argon, carbon dioxide, and tunable dye lasers. A preliminary report. , 1986, Archives of dermatology.

[29]  J. Parrish,et al.  Ultrastructure: effects of melanin pigment on target specificity using a pulsed dye laser (577 nm). , 1987, The Journal of investigative dermatology.

[30]  Lasers in dermatology. , 1982, Archives of dermatology.

[31]  A. Seligman,et al.  Syntheses of Some p-Nitrophenyl Substituted Tetrazolium Salts as Electron Acceptors for the Demonstration of Dehydrogenases1 , 1956 .

[32]  Cutaneous vascular disorders: advances in laser treatment. , 1990 .

[33]  J M Garden,et al.  Effect of dye laser pulse duration on selective cutaneous vascular injury. , 1986, The Journal of investigative dermatology.

[34]  S. Jacques,et al.  Light distributions in artery tissue: Monte Carlo simulations for finite‐diameter laser beams , 1989, Lasers in surgery and medicine.

[35]  M. Landthaler,et al.  [Treatment of naevi flammei with the argon laser]. , 1987, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.