Results 121 to 130 of about 12,699 (164)

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

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

SOX-10 and Melan-A Immunostaining in Areas of Focal Acantholytic Dyskeratosis and Epidermolytic Hyperkeratosis Within Dysplastic Nevi Biopsies: An Observational Study

American journal of dermatopathology
Background: Focal acantholytic dyskeratosis (FAD) and epidermolytic hyperkeratosis (EHK) are common incidental epidermal histologic findings within dysplastic nevi biopsies.
K. Erickson, Raghav Tripathi, Bethany R. Rohr   +2 more
semanticscholar   +1 more source

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

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

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

An interesting case of coincidental epidermolytic hyperkeratosis and erythema annulare centrifugum in the setting of latent tuberculosis in a 12‐year‐old female

International Journal of Dermatology, 2019
Erythema annulare centrifugum (EAC) is a chronic phenomenon of the skin that presents with annular gyrate erythematous patches or thin plaques that enlarge centrifugally and clear centrally. The interior border of the erythema has a “trailing scale”. EAC
P. Hirt, A. Price, Khalid M. Alwunais, L. Schachner   +3 more
semanticscholar   +1 more source