Systematized epidermolytic epidermal nevus (ichthyosis hystrix)
نویسندگان
چکیده
منابع مشابه
Mosaic epidermolytic ichthyosis - Case report*
Epidermolytic ichthyosis is a rare autosomal dominant disease that manifests at birth with fragile blisters and erosions that evolve into hyperkeratotic lesions associated or not with erythroderma. When the disease is associated with a mutation in cytokeratin 1, it may be related to hyperkeratosis of palms and soles, but this is not usually found when cytokeratin 10 is mutated. The disease can ...
متن کاملEpidermal nevus syndrome: Report of a giant linear epidermal nevus
Linear epidermal nevi frequently follow the lines of Blaschko and may be confused with the verrucous stage of incontinentia pigmenti. Inflammatory epidermal nevus appears as a line array of pink to red papules usually on the lower limb (Buttock and hip) clinically resembling psoriasis or eczematous dermatitis. But inflammatory epidermal nevus has distinct histopathologic features. We report a c...
متن کاملIchthyosis Hystrix : a case report Qazi
A six year old female child with generalized hyperpigmented hyperkeratotic verrucous plaques with nail and dental abnormalities suggestive of ichthyosis hystrix type of epidermal nevus is being reported in view of the rarity of this condition.
متن کاملCurth-Macklin Ichthyosis Hystrix of Curth-Macklin
Ichthyosis hystrix of Curth-Macklin ( IHCM) is an extremely rare keratinization disorder, with verrucous to hystrixlike hyperkeratotic plaques of varying extent. The diagnosis is based on a distinctive pattern of epidermolytic hyperkeratosis and the presence of binucleate cells under light microscopy, as well as unique electron microscopic findings of continuous perinuclear tonofibril shells in...
متن کاملKeratin 1 gene mutation detected in epidermal nevus with epidermolytic hyperkeratosis.
Since 1994, four cases of epidermal nevus with epidermolytic hyperkeratosis (EH) caused by keratin 10 gene mutations have been reported, although no keratin 1 (K1) gene mutation has yet been reported. We detected a K1 gene (KRT1) mutation in epidermal nevus with EH in a 10-year-old Japanese male. The patient showed well-demarcated verrucous, hyperkeratotic plaques mainly on the trunk, covering ...
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ژورنال
عنوان ژورنال: Scripta Scientifica Medica
سال: 2015
ISSN: 1314-6408,0582-3250
DOI: 10.14748/ssm.v47i3.1292