Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient

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Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient*

Buschke-Fisher-Brauer keratoderma is a rare hereditary autosomal dominant disease of incomplete penetrance. Important differential diagnoses include other palmoplantar keratinization disorders, acquired or hereditary, which is done based on the histopathological findings. This diagnosis alerts especially about the possibility of associated neoplasms. Treatment involves topical keratolytic agent...

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Punctate Palmoplantar Keratoderma (Brauer-Buschke-Fisher Syndrome) - Report of a Case and Review of the Literature

Punctate palmoplantar keratoderma type 1, also known as Brauer-Buschke-Fisher syndrome, is an autosomal dominant inherited disorder with variable penetrance. The disorder is characterized by multiple punctate hyperkeratotic papules on the palms and soles. Although it is a clinical rarity, a spot diagnosis can usually be made provided one is familiar with the condition thereby unnecessary diagno...

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Watcher’s type of palmoplantar keratoderma

A 51-year-old man reported with progressive thickening of the skin of the hands and feet since the age of 6yrs. It was largely asymptoma c; however, brisk walking caused excessive swea ng, pain, and widening of the fissures on the soles of the feet. He also had scaly raised lesions on legs and knees. His mother, maternal aunt, cousin and nephew had similar lesions. Examination of the soles of f...

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Brunauer-Fuhs-Siemens palmoplantar keratoderma: A rare, striate type of focal palmoplantar keratoderma

Brunauer-Fuhs-Siemens palmoplantar keratoderma, commonly known as striate palmoplantar keratoderma, is a rare, autosomally inherited disease of linear hyperkeratosis in which patient usually presents with conspicuous longitudinal hyperkeratosis on volar surface of hands and feet. Mutations in 3 genes namely desmoglein 1, desmoplakin and keratin 1, have been identified and held responsible for t...

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Autosomal recessive epidermolytic palmoplantar keratoderma.

Palmoplantar keratoderma (PPK) is a heterogeneous group of disorders. Epidermolytic PPK is a well delineated autosomal dominant entity, but no recessive form is known. Here we report two sons of phenotypically normal, consanguineous, Arab parents with features suggestive of PPK. They presented with patchy eczematous skin lesions followed by PPK and raised serum levels of IgE. Skin biopsy from t...

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ژورنال

عنوان ژورنال: Anais Brasileiros de Dermatologia

سال: 2014

ISSN: 0365-0596

DOI: 10.1590/abd1806-4841.20142923