Results 71 to 80 of about 6,090 (177)

[Keratoderma with epidermolytic hyperkeratosis].

Medicina cutanea ibero-latino-americana, 1987
Three members of one family with keratoderma Thost-Unna and histopathological picture of epidermolytic hyperkeratosis are reported. Several dermatoses with this abnormality of the keratinization are mentioned and the literature cases with keratoderma are reviewed.
A, Woscoff, J G, Casas, E, Dancziger
openaire   +1 more source

A novel keratin 10 gene mutation causing epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma) in a term neonate

, 2017
Epidermolytic hyperkeratosis (EHK) is a rare skin condition characterized by erythroderma and blistering at birth, leading to generalized hyperkeratosis of varying severity in adulthood. EHK is frequently mistaken for staphylococcal scalded skin syndrome
Edmond G. Lemire, Jaya. P. Bodani, Karen I. Holfeld, Satyaranjan Pegu   +3 more
core   +1 more source

Epidermal nevi and epidermolytic hyperkeratosis: A review of cases, highlighting indications for biopsy and genetics referral

Epidermal nevi are common benign cutaneous hamartomas that may rarely demonstrate histopathologic evidence of epidermolytic hyperkeratosis (EHK), representing cutaneous mosaicism for pathogenic keratin variants.
Cha, Kelly B., Mancuso, Jennifer B., Isaac, Jacqueline M., Nelson, Jessie M., Mervak, Julie E., Arreola, Amanda, Chan, May P.   +6 more
core   +1 more source

Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family

Therapeutics and Clinical Risk Management, 2014
Zhiliang Li,1,* Qiao Liu,2,* Aimin Wang,2 Hongsheng Wang,1 Chengrang Li1 1Department of Dermatology, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, People's Republic of China; 2Hainan ...
Li Z, Liu Q, Wang A, Wang H, Li C
doaj  

Late-Onset Nevus Comedonicus With Follicular Epidermolytic Hyperkeratosis-Case Report and Review of the Literature

, 2019
Nevus comedonicus is a rare cutaneous follicular hamartoma, characterized by the clustering of papules with firm, blackened horny buffers. It is usually present at birth or during childhood, although few cases of late-onset disease have been described ...
Ramona Zanniello, Pilloni, Luca, Gavino Faa, Brunella Conti, Faa, Gavino, Conti, Brunella, Rongioletti, Franco, Luca Pilloni, Franco Rongioletti, Zanniello, Ramona   +9 more
core   +1 more source

Autosomal dominant non-epidermolytic palmoplantar hyperkeratosis in a Nigerian girl

Nigerian Journal of Paediatrics
Palmoplantar keratoderma (PPK) is a hereditary cutaneous disorder characterized by a marked hyperkeratosis of the palms and soles. A variant that was inherited in an autosomal dominant form was highlighted in a 20-month-old girl-child.
Anigilaje EA, Dzuachii DO
doaj  

Nevus Unius Lateris With Epidermolytic Hyperkeratosis Managed With Radiofrequency Ablation: A Case Report. [PDF]

Cureus
Jack J, Raviprakash D, Joseph L, Sundaram M.   +3 more
europepmc   +1 more source

Nevoid follicular epidermolytic hyperkeratosis in a blaschkoid epidermal nevus. [PDF]

JAAD Case Rep
Raihane AS, Chiu LW, Elwood HR, Durkin JR.   +3 more
europepmc   +1 more source

Scrotal Paget disease with epidermolytic acanthoma. [PDF]

JAAD Case Rep
Li JF, Tan ZH, Zhuang YC, Sun YZ.
europepmc   +1 more source

Epidermolytic Hyperkeratosis: A Challenging Pathology for Clinical Correlation

Balkan Medical Journal, 2019
Hala M. El Hanbuli, Mohamed H. Elmahdi, Marwa A. Salem   +2 more
doaj   +1 more source