نتایج جستجو برای: palmoplantar keratodermas

تعداد نتایج: 1515  

Journal: :Photomedicine and laser surgery 2009
Steven Paul Nisticò Rosita Saraceno Caterina Schipani Antonio Costanzo Sergio Chimenti

BACKGROUND Ultraviolet radiation has been used for curative purposes in dermatologic conditions, especially in the last 30 years. OBJECTIVES We analyzed the efficacy of monochromatic excimer light in psoriasis, palmoplantar pustulosis, vitiligo, mycosis fungoides and alopecia areata, and to examine potential new indications. METHODS Two hundred seventy-nine patients with common and persiste...

2017
S. Burillo-Martínez F. Tous-Romero J. L. Rodríguez-Peralto C. Postigo-Llorente

administration of multiple cycles of topical and systemic corticosteroid therapy, topical tazarotene, ciclosporin at a dose of 3 mg/kg/d (whose efficacy cannot be adequately evaluated due to treatment interruption after a month because of failure to attend follow-up), and methotrexate at a maximum dose of 20 mg/wk, which the patient continues to receive. Interestingly, despite hypertrophic LP b...

Journal: :Journal of immunology 2008
Lone Skov Frank J Beurskens Claus O C Zachariae Sakari Reitamo Jessica Teeling David Satijn Kim M Knudsen Elmieke P J Boot Debra Hudson Ole Baadsgaard Paul W H I Parren Jan G J van de Winkel

IL-8 is a chemokine that has been implicated in a number of inflammatory diseases involving neutrophil activation. HuMab 10F8 is a novel fully human mAb against IL-8, which binds a discontinuous epitope on IL-8 overlapping the receptor binding site, and which effectively neutralizes IL-8-dependent human neutrophil activation and migration. We investigated whether interference in the cytokine ne...

Journal: :Acta dermatovenerologica Croatica : ADC 2013
Paulo Morais Lígia Peralta Manuela Loureiro Sónia Coelho

Pachyonychia congenita (PC) is a rare genodermatosis caused by mutations in any of the four genes KRT6A, KRT6B, KRT16, or KRT17, which can lead to dystrophic, thickened nails and focal palmoplantar keratoderma, among other manifestations. Although classically subdivided into two major variants, PC-1 (Jadassohn-Lewandowski syndrome) and PC-2 (Jackson-Lawler syndrome), according to the localizati...

Journal: :Indian Dermatology Online Journal 2014

Journal: :Cochrane Database of Systematic Reviews 2020

Journal: :acta medica iranica 0
vitorino modesto dos santos catholic university medical course, brasília-df, brazil . and department of internal medicine, armed forces hospital, brasília-df, brazil. thiago pereira loures department of internal medicine, armed forces hospital, brasília-df, brazil. joão daniel bringel rego division of pneumology, armed forces hospital, brasília-df, brazil. christiane aires teixeira division of pneumology, armed forces hospital, brasília-df, brazil. kayursula dantas de carvalho department of internal medicine, armed forces hospital, brasília-df, brazil. afonso lucas oliveira nascimento department of internal medicine, armed forces hospital, brasília-df, brazil.

pachyonychia congenital (pc) is a rare autosomal dominant genodermatosis characterized hyperkeratosis affecting the nails and palmoplantar areas, oral leukokeratosis, and cystic lesions. a 39-year-old woman with pc type 1 (jadassohn-lewandowsky syndrome) and b-cell lymphoma is described. no similar disorders or parental consanguinity were found in her family. typical features of pc developed si...

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