Results 121 to 130 of about 482 (157)
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Disseminated Superficial Porokeratosis with Amyloid Deposition
Journal of Dermatology, 1996AbstractTwo patients with disseminated superficial porokeratosis (DSP) with amyloid deposition are reported. The skin lesions were distributed over both sun‐exposed areas and sun‐protected areas. No exacerbation by sun exposure was noted. Abundant amyloid substances were deposited at the papillary dermis, not only beneath the cornoid lamellae but also ...
Masami Ikeda +2 more
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Dermoscopy of Disseminated Superficial Actinic Porokeratosis
Actas Dermo-sifiliográficas, 2017 We present a series of 6 cases of disseminated superficial actinic porokeratosis and describe their dermoscopic features. Dermoscopy is a noninvasive in vivo technique that is useful as a tool for the diagnosis and follow-up of porokeratosis. This condition has specific dermoscopic features that were observed in our series of cases and that are ...
A, Nicola, J, Magliano
exaly +3 more sources
Inflammatory Stage of Disseminated Superficial Porokeratosis
Journal of Dermatology, 2005Disseminated superficial porokeratosis (DSP) is a keratinization disorder characterized by multiple small lesions with a slightly elevated, sharply defined ridge over the whole body. Unusual DSP cases with acute exacerbation of their lesions accompanied by severe pruritus have been reported and designated as "eruptive pruritic papular porokeratosis" or
Makoto Inaoki +2 more
exaly +3 more sources
Coexistence of congenital linear porokeratosis and disseminated superficial porokeratosis
Australasian Journal of Dermatology, 2011ABSTRACTThe coexistence of two or more forms of porokeratosis in a single individual is rarely reported. We report here on a patient exhibiting the coexistence of congenital linear porokeratosis and disseminated superficial porokeratosis. To our knowledge, this entity has been previously reported only once.
Eujin, Cho +3 more
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Disseminated superficial porokeratosis in a patient with AIDS
British Journal of Dermatology, 2006We report the case of a 50-year-old male homosexual suffering from AIDS, who developed diffuse annular hyperkeratotic lesions on the arms and legs. Histopathological examination revealed typical features of porokeratosis, which clinically was of the disseminated superficial type. Ultrastructural examination showed a paucity of keratohyalin granules and
J, Kanitakis +8 more
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Dermoscopy of Disseminated Superficial Actinic Porokeratosis
Archives of Dermatology, 2004T HE LESIONS ARE FROM THE RIGHT ARM OF A 53-year-old man (Figure 1), the left leg of a 57-year-old woman (Figure 2), and the left arm of a 48-year-old man (Figure 3) (size bar, 3 mm) affected with a disseminated superficial actinic porokeratosis. All 3 lesions reveal a similar pattern. A “white track” structure can be identified at the periphery of the
Pedro, Zaballos +2 more
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Disseminated Superficial Actinic Porokeratosis
Dermatologica, 2009We report a case of a 45-year-old woman who had a 20-year history of disseminated superficial actinic porokeratosis with numerous lesions on sun-exposed areas that were for a long time misdiagnosed as atrophic lichen planus.
M. Harms +3 more
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Disseminated superficial actinic porokeratosis*
British Journal of Dermatology, 1976A family is analysed in which disseminated superficial actinic porokeratosis (DSAP) occurred in five members. All three children of one generation are affected. Clinical, histopathological and genetic aspects of DSAP are discussed. Disseminated superficial actinic porokeratosis appears to be a clinical variant of porokeratosis of Mibelli. Since DSAP is
D J, Pirozzi, A, Rosenthal
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Disseminated Superficial Actinic Porokeratosis
Archives of Dermatology, 1969A clinicogenetic study was made of ten famlies with disseminated superficial actinic porokeratosis (DSAP). Complete cutaneous examinations were conducted on 58 family members. Age significantly influenced the manifestation of DSAP; no cases were observed below 16 years of age, but after this age the frequency increased almost linearly with an increase ...
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Disseminated Superficial Actinic Porokeratosis (DSAP)
Archives of Dermatology, 1967This study of 31 patients presents disseminated superficial actinic porokeratosis (DSAP) as a distinctive and recognizable entity characterized by many uniformly small, minimal, annular, anhidrotic, keratotic lesions developing during the third or fourth decade of life on sun-exposed areas of skin. It is not a rare condition.
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