Generalized Form of Peeling Skin Syndrome: A Case Report
نویسندگان
چکیده مقاله:
Peeling skin syndrome (PSS) is a very rare keratinization disorder, characterized by spontaneous exfoliation of the stratum corneum. Herein, we report a case of non-inflammatory (type A) PSS.
منابع مشابه
Peeling Skin Syndrome: A Case Report
Observations: Peeling skin syndrome is a very rare autosomal recessive disease characterized by widespread painless peeling of the skin in superficial sheets. We present a 31-year-old man with a lifelong history of continuous, spontaneous, asymptomatic generalized peeling skin. Histologically, there was epidermal separation at the level of stratum corneum, just above the stratum granulosum. The...
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Peeling skin syndrome is a very rare autosomal recessive disease characterized by widespread painless peeling of the skin in superficial sheets. Etiology is still unknown with an autosomal recessive inheritance. Less than 100 cases have been reported in the medical literature. We present a 32-year-old man having asymptomatic peeling of skin since birth. Sheets of skin were peeling from his neck...
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متن کاملPeeling skin syndrome.
To cite: Bansal M, Mahajan S, Sankhwar S, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015210902 DESCRIPTION A 30-year-old man born of a non-consanguineous marriage presented with asymptomatic peeling of skin throughout his body, sparing palms and soles, since birth. There was no preceding history of redness or fluid-filled lesions over the affected are...
متن کاملHypercalciuria in a child with acral peeling skin syndrome: a case report.
We present a case of 3-year-old Caucasian boy who developed monthly cyclic attacks of skin peeling of the palms and soles over 1.5 years. The skin peeling was associated with hypercalciuria. No mutation was present in TGM5 and CSTA genes, but the typical clinical picture and the biopsy from flaccid blisters on the feet confirmed the acral peeling skin syndrome (APSS). The possible associations ...
متن کاملA Case of Inflammatory Generalized Type of Peeling Skin Syndrome Possibly Caused by a Homozygous Missense Mutation of CDSN
A 54-year-old Japanese woman had repetitive superficial skin peeling and ensuing erythematous changes in the sites since infancy. Her parents had a consanguineous marriage, and she was the only individual affected in her family tree. The erythematous changes seemed to worsen in the summer. Histologically, hyperkeratosis and splitting of the epidermis within the stratum corneum was noted, and el...
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عنوان ژورنال
دوره 13 شماره 2
صفحات 60- 61
تاریخ انتشار 2010-07-01
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