Coexisting variants of porokeratosis rarely occurs. Disseminated superficial porokeratosis (DSP) is characterized by multiple uniform small annular papules distributed all over body. DSP commonly coexist with linear porokeratosis (LP), but it is uncommon for DSP to coexist with porokeratosis of Mibelli (PM). PM presents with central atrophic erythematous plaques and thread-like elevated border....

Porokeratosis is characterized clinically by annular plaques with a distinct peripheral keratotic ridge and histologically by the cornoid lamella. Porokeratosis with follicular involvement is rarely reported. To provide the basis of that follicular porokeratosis is a clinical variant or not. Biopsy was taken from three patients who were diagnosed porokeratosis. Routine stain was made and review...

Porokeratosis (PK) is an uncommon disorder of epidermal keratinization characterized by annular plaques with an atrophic center surrounded by a raised, keratotic wall, with unknown aetiology and an unpredictable outcome. It has several clinical forms including porokeratosis of Mibelli, giant porokeratosis, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar ...

Porokeratosis (PK) is an uncommon disorder of epidermal keratinization characterized by annular plaques with an atrophic center surrounded by a raised, keratotic wall, with unknown aetiology and an unpredictable outcome. It has several clinical forms including porokeratosis of Mibelli, giant porokeratosis, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar poroke...

Observations: Porokeratosis is a dyskeratotic disorder of the skin characterized by hyperkeratotic papule or plaque with an annular appearance and usually diagnosed easily, both histopathologically and clinically. We present a case of linear porokeratosis which was most likely suggesting the linear epidermal nevus and linear lichen planus. We observed a tiny brown border in the dermoscopic exam...

Porokeratosis of Mibelli is a disorder of epidermal proliferation in which many different clinical forms can be distinguished. Two male patients with a localized type of porokeratosis limited to the genitalia are reported. Later in life they developed an annular skin lesion with peripheral keratotic ridge. The histological examination of a biopsy specimen showed the characteristic features of p...

Porokeratosis represents a spectrum of clinical diseases. Multiple variants have been described including porokeratosis ptychotropica, a rare subtype. The coexistence of two or more variants of porokeratosis in a single patient is regarded as a rare occurrence. Here we report a patient with porokeratosis ptychotropica with coexistent porokeratosis of Mibelli. The patient was a 47-year-old man w...

Porokeratoses are uncommon hereditary or acquired keratinization disorders due to abnormal clones of keratinocytes in the epidermis. Porokeratoses have several clinical features which may occur simultaneously. A rare type is verrucous porokeratosis (VPK). Herein, we present a 47-year-old man with a 4-year history of perianal verrucous lesions and one year history of annular pruritic lesions on ...

More than a century ago, two Italian dermatologists independently described a new keratotic disorder [1,2] which was called porokeratosis by Mibelli [1]. After these first descriptions, at least four variants of porokeratosis have been recognized. Clinically all these dermatological disorders are characterized by diffuse annular lesions surrounded by a raised, sharply marginated, keratotic bord...

Porokeratosis is a rare epidermal disorder characterized by annular or linear hyperkeratotic plaques with slightly raised thread-like borders, and in most cases, atrophic centers. Disseminated superficial porokeratosis and disseminated superficial actinic porokeratosis (DSAP), which primarily involve sun-exposed areas, are common types of porokeratoses. Histologically, a column of parakeratotic...