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Telangiectasis in CREST syndrome and systemic sclerosis: correlation of clinical and pathological features with response to pulsed dye laser treatment

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Abstract

Telangiectasia are cardinal features of systemic sclerosis (SS) and calcinosis, Raynaud’s syndrome, esophageal motility, sclerodactyly, telangiectasias (CREST) syndrome. The etiology of telangiectasia in these syndromes is unknown, but vascular dysfunction has been proposed. However, the telangiectasia of CREST have anecdotally been considered relatively resistant to pulse dye laser (PDL), the treatment of choice for classic telangiectasia. The study was designed to test whether SS/CREST telangiectasia require more treatments than sporadic telangiectasia and to identify clinical and histological features that could explain such an effect. Nineteen skin biopsies from patients with SS or CREST and 10 control biopsies were examined and compared for features that may predict a differential response to PDL. Sixteen cases of SS or CREST treated with PDL between 1997 and 2007 were evaluated and response to treatment was compared with 20 patients with sporadic telangiectasis. Relative to normal skin, CREST/scleroderma telangiectasia exhibited thickened vessels in 17 out of 19 sections and thickened collagen fibers in the reticular or deep dermis in all sections. The number of treatments required to clear SS/CREST telangiectasia was approximately twofold higher. SS/CREST telangiectasia are more resistant to PDL but can be effectively cleared with more treatments.

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References

  1. Meyer O (1999) [From Thibierge–Weissenbach syndrome (1910) to anti-centromere antibodies (1980). Clinical and biological features of scleroderma]. Ann Med Interne (Paris) 150:47–52

    CAS  Google Scholar 

  2. Winterbauer RH (1964) Multiple telangiectasia, Raynaud’s phenomenon, sclerodactyly, and subcutanious calcinosis: a syndrome mimicking hereditary hemorrhagic telangiectasia. Bull Johns Hopkins Hosp 114:361–383

    CAS  PubMed  Google Scholar 

  3. Frayha RA, Scarola JA, Shulman LE (1973) Calcinosis in scleroderma: a reevaluation of the CRST syndrome, abstracted. Arthritis Rheum 16:542

    Google Scholar 

  4. Velayos EE, Masi AT, Stevens MB, Shulman LE (1979) The 'CREST' syndrome. Comparison with systemic sclerosis (scleroderma). Arch Intern Med 139:1240–1244

    Article  CAS  PubMed  Google Scholar 

  5. Rouquette-Gally AM, Stern MH, Prost AC, Abuaf N, Homberg JC, Combrisson A (1985) Anti-centromere antibody, biological marker of the CREST syndrome as distinct from scleroderma. Presse Med 14:1497–1500

    CAS  PubMed  Google Scholar 

  6. Cafagna D, Melon F, Balbi M, Ponte E (1998) Vascular manifestations in systemic sclerosis (scleroderma). Minerva Med 89:153–161

    CAS  PubMed  Google Scholar 

  7. Freemont AJ, Hoyland J, Fielding P, Hodson N, Jayson MI (1992) Studies of the microvascular endothelium in uninvolved skin of patients with systemic sclerosis: direct evidence for a generalized microangiopathy. Br J Dermatol 126:561–568

    Article  CAS  PubMed  Google Scholar 

  8. Chizzolini C, Parel Y, Scheja A, Dayer JM (2006) Polarized subsets of human T-helper cells induce distinct patterns of chemokine production by normal and systemic sclerosis dermal fibroblasts. Arthritis Res Ther 8:R10

    Article  PubMed Central  PubMed  Google Scholar 

  9. Oliver SJ (2000) The Th1/Th2 paradigm in the pathogenesis of scleroderma, and its modulation by thalidomide. Curr Rheumatol Rep 2:486–491

    Article  CAS  PubMed  Google Scholar 

  10. Walker JG, Stirling J, Beroukas D, Dharmapatni K, Haynes DR, Smith MD et al (2005) Histopathological and ultrastructural features of dermal telangiectasias in systemic sclerosis. Pathology 37:220–225

    Article  PubMed  Google Scholar 

  11. Braverman IM (1989) Ultrastructure and organization of the cutaneous microvasculature in normal and pathologic states. J Invest Dermatol 93:2S–9S

    Article  CAS  PubMed  Google Scholar 

  12. Anderson RR, Parrish JA (1983) Selective photothermolysis: precise microsurgery by selective absorption of pulsed radiation. Science 220:524–527

    Article  CAS  PubMed  Google Scholar 

  13. Polla LL, Tan OT, Garden JM, Parrish JA (1987) Tunable pulsed dye laser for the treatment of benign cutaneous vascular ectasia. Dermatologica 174:11–17

    Article  CAS  PubMed  Google Scholar 

  14. Eisen D, Alster TS (2002) Use of a 585 nm pulsed dye laser for the treatment of morphea. Dermatol Surg 28:615–616

    Article  PubMed  Google Scholar 

  15. Ciatti S, Varga J, Greenbaum SS (1996) The 585 nm flashlamp-pumped pulsed dye laser for the treatment of telangiectases in patients with scleroderma. J Am Acad Dermatol 35:487–488

    Article  CAS  PubMed  Google Scholar 

  16. Braverman IM, Ken-Yen A (1983) Ultrastructure and three-dimensional reconstruction of several macular and papular telangiectases. J Invest Dermatol 81:489–497

    Article  CAS  PubMed  Google Scholar 

  17. Anderson RR, Parrish JA (1981) Microvasculature can be selectively damaged using dye lasers: a basic theory and experimental evidence in human skin. Lasers Surg Med 1:263–276

    Article  CAS  PubMed  Google Scholar 

  18. Garden JM, Tan OT, Kerschmann R, Boll J, Furumoto H, Anderson RR et al (1986) Effect of dye laser pulse duration on selective cutaneous vascular injury. J Invest Dermatol 87:653–657

    Article  CAS  PubMed  Google Scholar 

  19. Paul BS, Anderson RR, Jarve J, Parrish JA (1983) The effect of temperature and other factors on selective microvascular damage caused by pulsed dye laser. J Invest Dermatol 81:333–336

    Article  CAS  PubMed  Google Scholar 

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Correspondence to Shlomit Halachmi.

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Halachmi, S., Gabari, O., Cohen, S. et al. Telangiectasis in CREST syndrome and systemic sclerosis: correlation of clinical and pathological features with response to pulsed dye laser treatment. Lasers Med Sci 29, 137–140 (2014). https://doi.org/10.1007/s10103-013-1298-1

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  • DOI: https://doi.org/10.1007/s10103-013-1298-1

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