Permanent treatment of aquagenic syringeal acrokeratoderma with endoscopic thoracic sympathectomy.

نویسندگان

  • Engin Sezer
  • Emel Öztörk Durmaz
  • Emel Çetin
  • Sedef Şahin
چکیده

1. van Osch LD, Oranje AP, Keukens FM, Voorst Vader van PC, Veldman E. Keratosis follicularis spinulosa decalvans: A family study of seven male cases and six female carriers. J Med Genet 1992;29:36-40. 2. Fong K, Wedgeworth EK, Lai-Cheong JE, Tosi I, Mellerio JE, Powell AM, et al. MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvans. Clin Exp Dermatol 2012;37:631-4. 3. Castori M, Covaciu C, Paradisi M, Zambruno G. Clinical and genetic heterogeneity in keratosis follicularis spinulosa decalvans. Eur J Med Genet 2009;52:53-8. 4. Baden HP, Byers HR. Clinical findings, cutaneous pathology, and response to therapy in 21 patients with keratosis pilaris atrophicans. Arch Dermatol 1994;130:469-75. 5. Richard G, Harth W. Keratosis follicularis spinulosa decalvans. Therapy with isotretinoin and etretinate in the inflammatory stage. Hautarzt 1993;44:529-34. Evidence for treatment of keratosis follicularis spinulosa decalvans is anecdotal. Topical keratolytic agents and emollients offer only symptomatic improvement. Antibiotics may be necessary during pustular flares of disease.[4] Oral retinoids are effective in the early phase of disease when active perifollicular infiltrate is present. It must be continued for 6 to 12 months for an optimum response. Retinoids decrease epidermal proliferation and cytokine production thereby reducing hyperkeratosis and inflammation.[5]

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عنوان ژورنال:
  • Indian journal of dermatology, venereology and leprology

دوره 81 6  شماره 

صفحات  -

تاریخ انتشار 2015