Results 201 to 210 of about 11,448 (231)
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Disseminated Epidermolytic Acanthoma
Journal of Cutaneous Pathology, 1979A 65‐year‐old Japanese male suffered from numerous brownish papules on his back for 6 months. Clinical appearance resembled seborrheic keratosis, but light microscopic examination revealed epidermolytic hyperkeratosis. Electron microscopic findings were the same as those of epider‐molytic hyperkeratosis and systemic nevus verrucosus.
Y, Miyamoto, K, Ueda, M, Sato, H, Yasuno
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Incidental Epidermolytic Hyperkeratosis
The American Journal of Dermatopathology, 1995Epidermolytic hyperkeratosis is the distinctive histopathologic change that has been described as the main feature of bullous congenital ichthyosiform erythroderma and as an incidental finding in other cutaneous disorders. We retrospectively evaluated our cases of incidental epidermolytic hyperkeratosis over a 5-year period, and reviewed the conditions
P, Mahaisavariya +2 more
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Acral epidermolytic hyperkeratosis
British Journal of Dermatology, 1993We present a family with a distinctive pattern of epidermolytic hyperkeratosis which is mild, restricted to the distal parts of the limbs, and non-disabling. Features of the other variants of epidermolytic hyperkeratosis are discussed.
C M, Mills, R, Marks
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Disseminated Epidermolytic Acanthoma
The American Journal of Dermatopathology, 1993A 57-year-old man developed hundreds of light brown, slightly atrophic papules, which were distributed diffusely over the back. Although clinically the lesions resembled seborrheic keratoses, histologic examination demonstrated changes of epidermolytic hyperkeratosis.
J E, Knipper, J A, Hud, C J, Cockerell
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Solitary epidermolytic acanthoma
Journal of Cutaneous Pathology, 2013BackgroundSolitary epidermolytic acanthoma is thought to be an uncommon lesion. It can present as a solitary, localized or disseminated process that is unrelated to the genetic form of icthyosis.MethodsA retrospective review of solitary epidermolytic acanthomas was performed at the Ackerman Academy of Dermatopathology, NY, over a 2 year period.
Viktoryia, Kazlouskaya +2 more
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Acrosyringial Epidermolytic Papulosis neviformis
Dermatology, 1985A 42-year-old woman showed multiple verrucous papules on her right ringfinger. Histology revealed a hyperkeratotic plug and epidermal foci of epidermolytic hyperkeratosis exclusively involving the intraepidermal sweat duct units. We propose the term acrosyringial epidermolytic papulosis neviformis or epidermolytic sweat duct nevus to define this unique
A M, Zina, S, Bundino, M G, Pippione
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Epidermolytic Palmo‐plantar Keratoderma
International Journal of Dermatology, 1984ABSTRACT: An 11–year‐old girl who at 91/2 months was diagnosed as having keratoderma of the palms and soles, present since birth, developed typical granuloma annulare at the age of 11 years. To the authors’knowledge, this is the first report of epidermolytic palmo‐plantar keratoderma associated with granuloma annulare.
J R, Thomas, S L, Greene, W P, Su
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Epidermolytic Palmo‐plantar Keratoderma
International Journal of Dermatology, 1986An 11-year-old girl who at 9 1/2 months was diagnosed as having keratoderma of the palms and soles, present since birth, developed typical granuloma annulare at the age of 11 years. To the authors' knowledge, this is the first report of epidermolytic palmo-plantar keratoderma associated with granuloma annulare.
E, van Dijk +3 more
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Persistent actinic epidermolytic hyperkeratosis
Journal of the American Academy of Dermatology, 1995Epidermolytic hyperkeratosis is a distinctive histologic change noted in a variety of acquired and congenital dermatoses. Its pathogenesis is unknown. We have observed acquired epidermolytic hyperkeratosis in four Japanese men.Our purpose was to report four cases of acquired epidermolytic hyperkeratosis induced by sun exposure.Four cases were studied ...
H, Suzuki +3 more
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