منابع مشابه
Linear porokeratosis.
Linear porokeratosis is a rare variant. It can be present at birth or can develop in adult life. Lesions of linear porokeratosis are grouped and linearly arranged along the lines of Blaschko. On the extremities it affects the distal portion more than the proximal areas. On the trunk these can be zosteriform in distribution. Lesions of linear porokeratosis probably result from an abnormal clone ...
متن کامل[Generalized linear porokeratosis limited to one side of the body].
Poroqueratosis (PQ) refers to a group of disorders of keratinization with the common histological feature of the presence of cornoid lamellae, narrow columns of parakeratosis on a focally disorganized epidermis.1 We present 2 patients with lesions compatible with linear PQ, with extensive involvement of one side of the body. The first patient was a 23-year-old man with no past history of intere...
متن کاملLinear porokeratosis: a case report
Porokeratosis is a rare genodermatosis based on chronic keratinization disorder histologically characterized by the presence of a cornoid lamella and various clinical manifestations. Five most commonly described types of poroketarosis are porokeratosis of Mibelli or ”classic” porokeratosis, disseminated superfi cial actinic porokeratosis, disseminated palmoplantar porokeratosis, linear porokera...
متن کاملMulticentric Bowen disease in linear porokeratosis.
Linear porokeratosis is a genodermatosis, caused by a clonal proliferation of keratinocytes along the lines of Blaschko. This type of porokeratosis is particularly susceptible to malignant degeneration e.g. to Bowen disease, a squamous cell carcinoma (SCC) in situ with the potential for significant lateral spread. Here we report a case of linear porokeratosis on the left leg of a 56-year-old ma...
متن کاملA Case of Linear Porokeratosis Superimposed on Disseminated Superficial Actinic Porokeratosis
We present a female patient with linear porokeratosis of her right arm since childhood. At the age of 67 years she additionally developed disseminated superficial actinic porokeratosis (DSAP) involving both lower legs. This uncommon coexistence of two different types of porokeratosis fulfils the clinical criteria of a type 2 segmental manifestation of an autosomal dominant skin disorder, being ...
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ژورنال
عنوان ژورنال: Anais Brasileiros de Dermatologia
سال: 2018
ISSN: 1806-4841,0365-0596
DOI: 10.1590/abd1806-4841.20187798