منابع مشابه
Peeling skin syndrome
The coexistence of neurofibromatosis with partial unilateral lentigines raises the possibility that partial unilateral lentigines could be a variant or forme fruste of segmental neurofibromatosis. Our patient had no cutaneous lesions of neurofibromatosis but had bilateral Lisch nodules in the eyes. Since Lisch nodules are characteristic of neurofibromatosis, we conclude that the partial unilate...
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 کاملGeneralized Form of Peeling Skin Syndrome: A Case Report
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.
متن کاملA Case of Peeling Skin Syndrome
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...
متن کاملPeeling 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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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2015
ISSN: 1757-790X
DOI: 10.1136/bcr-2015-210902