Results 181 to 190 of about 13,745 (220)

Epidermolytic hyperkeratosis: one more pattern of Grover disease

International Journal of Dermatology, 2020
ing. Indeed, the physiopathology remains elusive. One suggested hypothesis involves an adrenaline-induced constriction of periglandular vessels, followed by an exacerbated dilatation which allows blood to fill the eccrine ducts.
F. Bardazzi, F. Pepe, M. Malosso, C. Loi, C. Baraldi, C. Misciali, A. Patrizi   +6 more
semanticscholar   +1 more source

Incidental Epidermolytic Hyperkeratosis

The American Journal of Dermatopathology, 1995
Epidermolytic 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, Ronald P. Rapini, Punkae Mahaisavariya   +2 more
openaire   +3 more sources

Acral epidermolytic hyperkeratosis

British Journal of Dermatology, 1993
We 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
openaire   +3 more sources

Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis)

British Journal of Dermatology, 1994
To evaluate the role of filaggrin in keratin filament aggregation in epidermolytic ichthyosis (epidermolytic hyperkeratosis, EH), we studied EH skin by light and electron microscopic immunohistochemistry, and biochemical analysis using sodium dodecylsulphate-polyacrylamide gel electrophoresis and immunoblotting.
Robin A.J. Eady, Karen A. Holbrook, R.A. Underwood, Beverly A. Dale, A. Ishida-Yamamoto   +4 more
openaire   +3 more sources

Persistent actinic epidermolytic hyperkeratosis

Journal of the American Academy of Dermatology, 1995
Epidermolytic 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 ...
Tsukasa Takemura, Hukiko Takahashi, Mitsuo Miyashita, Hiroyuki Suzuki   +3 more
openaire   +3 more sources

A family with palmoplantar epidermolytic hyperkeratosis

Clinical and Experimental Dermatology, 1989
Familial epidermolytic hyperkeratosis confined to the palms and soles was first characterized by Klaus and Weinstein in 1970. This entity has been the subject of only four subsequent reports. We report a family previously diagnosed as suffering from tylosis (Thost Unna syndrome), in which eleven members have been affected, and review the literature on ...
P.E. Hutchinson, J. Berth-Jones
openaire   +3 more sources

Incidental focal epidermolytic hyperkeratosis in rosacea

The Journal of Dermatology, 2017
Hee-Chul Chung, Jin-Wook Lee, H. Bak, S. Ahn   +3 more
semanticscholar   +3 more sources

Nevus comedonicus with Epidermolytic Hyperkeratosis

Dermatology, 1987
A 7-year-old girl had a linear nevus comedonicus affecting the right upper limb. Histologic examination of two biopsies specimens showed both the common changes of nevus comedonicus and the presence of epidermolytic hyperkeratosis. Therefore, nevus comedonicus should be included in the list of dermatoses having the distinctive histologic pattern of ...
A. Molinero, F.G. Aloi
openaire   +3 more sources

Epidermolytic Hyperkeratosis Type 1 with a New Heterozygous Mutation in KRT1 Gene: A Case Report

GenoMed Connect
Background: Epidermolytic hyperkeratosis (EHK) formerly known as bullous ichthyosiform erythroderma, is a rare autosomal dominant inheritance condition with a prevalence ranging from 1:200,000 to 1:300,000.
Maitha Abdulla Aljuwaied, Waqas Saad Abdulwahha, Mays Alrim Mustafa Al Moukdad, Moza Kamil Bin Kamil Alshamsi, Sham Zain AlAbdin, Ahmed Elbarkouky, Omar El Khatib, Salahdein Aburuz   +7 more
semanticscholar   +1 more source

Clinical Heterogeneity in Epidermolytic Hyperkeratosis

Archives of Dermatology, 1994
Epidermolytic hyperkeratosis (EHK) is a rare autosomal dominant disorder of cornification. While different clinical presentations of EHK have been described, the distinctions have not been clear. We have examined 52 patients with EHK from 21 families in an effort to define and characterize the specific clinical features of this disorder.We found that ...
Sherri J. Bale, John J. DiGiovanna
openaire   +3 more sources