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Porokeratosis plantaris palmaris et disseminata  [cached]
Sawheny M,Mahatachar V,Bisht Y
Indian Journal of Dermatology, Venereology and Leprology , 1995,
Abstract: A 65-year-old man presented with typical lesions of porokeratosis palmaris et disseminata clinically and histopathologically. Although this disease has autosomal dominant mode of inheritance, no family history of similar illness was seen in our case.
Porokeratosis Plantaris, Palmaris Et Disseminata  [cached]
Chatterjee Tapas Kumar,Sadhu Sisir Kumar
Indian Journal of Dermatology , 1997,
Abstract: A 14 year old girl developed dark, keratotic lesions all over the body for the last 9 years. The lesions were mostly linear but some were oval with keratotic border and atrophied center. The lesions were almost symmetrical in distribution. Homy and warty lesions appeared over soles for the last 2 years. An unusual presentation of porokeratosis plantaris, palmaris to disseminata is described.
Porokeratosis Palmaris, Plantaris Et Disseminata with a Mucous Membrane Lesion  [cached]
Gangopadhyay Ashok Kumar
Indian Journal of Dermatology, Venereology and Leprology , 2000,
Abstract: Porokeratosis affecting the mucous membrane of the tongue is reported in a young man.
Two Cases of Different Types of Porokeratosis: Improvement with Acitretin Treatment  [PDF]
Mine G?kdemir,Aysun ?ikar Aktürk,Kür?at Y?ld?z,Rebiay K?ran
Turkderm , 2011,
Abstract: There are five different types in the group of porokeratosis which is one of the keratinization disorders: disseminated superficial actinic porokeratosis, punctate porokeratosis, porokeratosis palmaris et plantaris disseminata, linear porokeratosis and porokeratosis of Mibelli (PM). PM is classic and the most common type that can be seen anywhere on the body skin. Disseminated superficial actinic porokeratosis is another type of porokeratosis which is characterized by widespread, bilateral and symmetric eruptions seen on sun-exposed areas. Although they are asemptomatic, treatment is recommended because of the possibility of developing skin malignancies. However, none of the current treatment approaches is fully effective. Here, we report two male patients diagnosed with PM and disseminated superficial actinic porokeratosis who demonstrated improvement with acitretin treatment.
Solitary Porokeratosis of Mibelli at an unusual site  [cached]
Nithya Raghunath,Metikurke Vijayashankar
Our Dermatology Online , 2012,
Abstract: Porokeratosis is an assorted group of five genetic disorders. These include porokeratosis of Mibelli, DSAP, punctate porokeratosis, porokeratosis palmaris et plantaris disseminata, and linear porokeratosis.They are disorders of abnormal keratinization characterized by the appearance of atrophic patches. Porokeratosis of Mibelli is referred to the more localized form of this disorder usually manifesting as solitary or a small group of lesions. It was first described by Mibelli in 1893 who described atrophic patches surrounded by a clinically and histologically unique ridge like border termed the cornoid lamella. The cornoid lamella is formed by rapidly proliferating atypical keratinocytes that expands peripherally to form a raised boundary at the junction of abnormal and normal cells. These lesions are most commonly found on the extremities, but can also be found on genitalia, face, oral mucosa and cornea. Though the patches are generally asymptomatic they can often lead to ulcerative, verrucous, giant, and malignant lesions. We describe a case of Porokeratosis of Mibelli at an unusual site in a 22 yr old male. The presenting history, clinical findings, biopsy results and available literature are reviewed.
Keratosis punctata palmaris et plantaris  [cached]
Mohanty Sandip,Gandhi Vijay,Baruah M
Indian Journal of Dermatology, Venereology and Leprology , 1999,
Abstract: A 30-year-old man presented with multiple keratotic papules on palms and soles. The lesions started at the age of 15 from soles. Family history was positive with members in preceding two generations being affected. Cutaneous examination revealed multiple discrete hyperkeratotic papules of variable size on palms and soles. Parakeratosis was absent in histopathology and this ruled out the diagnosis of porokeratosis punctata palmaris et plantaris.
Porokeratosis Of Mibelli  [cached]
Hawalia Dinesh Kumar
Indian Journal of Dermatology , 1995,
Abstract: A 30 year old male having lesions of Porokeratosis of Mibelli is described. Histopathology is consistent with the diagnosis.
Hyperkeratotic Verrucous Porokeratosis  [cached]
Rao Mummidi Venkateswara,Singh Ajit,Thappa Devinder Mohan,Ratnakar Chaganti
Indian Journal of Dermatology , 1998,
Abstract: A 40 year old male having porokeratosis of mibelli with its rare variant, hyperkeratotic verrucous porokeratosis, is reported here.
Linear Porokeratosis
Ramanan Cherukot,Ghorpade Ashok,Methi Vanita
Indian Journal of Dermatology , 1998,
Abstract: A case of linear porokeratosis in a 3 year old male child is reported for its rarity and clinical interest. The clinical features and histopathological features were classical.
Porokeratosis of mibelli  [cached]
Prasad A,Singh Gurmohan
Indian Journal of Dermatology, Venereology and Leprology , 1990,
Abstract: Twenty two cases of porokeratosis of Mibelli belonging to two separate families having 18 and 4 cases respectively were studied. Their pedigress traced in three generations followed an autosomal dominant pattern.
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