Results 301 to 310 of about 50,269 (341)
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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
Philip R. Cohen +2 more
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Hyperkeratosis in Flegel's Disease
JAMA: The Journal of the American Medical Association, 1985Hyperkeratosis lenticularis perstans was first described by Flegel1in 1958. It may rightly be redefined as an autosomal dominant mucocutaneous syndrome of variable expressivity, characterized by an aberration in the keratinization process. A 67-year-old woman presented with numerous asymptomatic keratotic lesions, confined to the anterior aspect of ...
Rajagopala Swaminathan +1 more
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Hyperkeratosis of Nipple and Areola
Archives of Dermatology, 1977Hyperkeratosis of the nipple and areola is a rare condition that may occur in association with various forms of ichthyosis or as the result of extension of an epidermal nevus. The nevoid form is extremely rare and appears most commonly in women in their second or third decade of life.
Amir H. Mehregan, Homayoon Rahbari
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Hyperkeratosis of Nipple and Areola
Archives of Dermatology, 1978Hyperkeratosis of the nipple and areola is said to be rare. Mehregan and Rahbari presented two patients with it and reviewed the 13 other reported cases in the world literature.1They state that this eruption may occur in patients with ichthyosis or it may represent an epidermal nevus, with the latter form usually bilateral and in young women of ...
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Archives of Dermatology, 1979
To the Editor.— In the December 1977 issue of theArchives(113:1691-1692), Mehregan and Rahbari described two cases of hyperkeratosis of the nipple and areola of the nevoid type, and they mentioned that this is a very rare condition and, with their cases, there are only 15 reported cases in the literature.
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To the Editor.— In the December 1977 issue of theArchives(113:1691-1692), Mehregan and Rahbari described two cases of hyperkeratosis of the nipple and areola of the nevoid type, and they mentioned that this is a very rare condition and, with their cases, there are only 15 reported cases in the literature.
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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.
R. Marks, Caroline M. Mills
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Archives of Dermatology, 1978
To the Editor.— Recently I treated a patient with hyperkeratosis of the nipples who does not seem to fit the Levy-Franckel classification (Paris Med28:63-66, 1938) reviewed by Mehregan and Rahbari in their report of two cases in the DecemberArchives(113:1691-1692, 1977).
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To the Editor.— Recently I treated a patient with hyperkeratosis of the nipples who does not seem to fit the Levy-Franckel classification (Paris Med28:63-66, 1938) reviewed by Mehregan and Rahbari in their report of two cases in the DecemberArchives(113:1691-1692, 1977).
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Dermatomyositis with Follicular Hyperkeratosis
Dermatology, 1995We report 2 cases of dermatomyositis with follicular hyperkeratosis (FHK) in children. They occurred in a 10-year-old Vietnamese girl and a 9-year-old Caucasian boy. The girl's FHK disappeared after 2 months of treatment. The boy presented, 15 months after the onset of his dermatomyositis, with a generalised FHK which lasted for 6 months.
Emmanuel Delaporte +5 more
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