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Eruptive superficial porokeratosis in a patient with nephrotic syndrome()

A 34-year-old female was referred to our department, complaining of multiple asymptomatic lesions that appeared two weeks previously. The patient had active nephritis with nephrotic syndrome and was treated with immunosuppressive therapies. Physical examination revealed multiple well-circumscribed r...

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Detalles Bibliográficos
Autores principales: Ishikawa, Masato, Yamamoto, Toshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133250/
https://www.ncbi.nlm.nih.gov/pubmed/35321801
http://dx.doi.org/10.1016/j.abd.2020.08.038
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author Ishikawa, Masato
Yamamoto, Toshiyuki
author_facet Ishikawa, Masato
Yamamoto, Toshiyuki
author_sort Ishikawa, Masato
collection PubMed
description A 34-year-old female was referred to our department, complaining of multiple asymptomatic lesions that appeared two weeks previously. The patient had active nephritis with nephrotic syndrome and was treated with immunosuppressive therapies. Physical examination revealed multiple well-circumscribed rounds of flat brownish plaques with slightly elevated borders, some of which were covered by scales. The number of lesions was nine in total. Skin biopsy specimens showed dyskeratotic cells in the thinned epidermis with cornoid lamella, and the absence of a granular cell layer. The development of porokeratosis was considered to be related to immunosuppressive therapy or the activity of nephritis.
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spelling pubmed-91332502022-05-26 Eruptive superficial porokeratosis in a patient with nephrotic syndrome() Ishikawa, Masato Yamamoto, Toshiyuki An Bras Dermatol Case Letter A 34-year-old female was referred to our department, complaining of multiple asymptomatic lesions that appeared two weeks previously. The patient had active nephritis with nephrotic syndrome and was treated with immunosuppressive therapies. Physical examination revealed multiple well-circumscribed rounds of flat brownish plaques with slightly elevated borders, some of which were covered by scales. The number of lesions was nine in total. Skin biopsy specimens showed dyskeratotic cells in the thinned epidermis with cornoid lamella, and the absence of a granular cell layer. The development of porokeratosis was considered to be related to immunosuppressive therapy or the activity of nephritis. Sociedade Brasileira de Dermatologia 2022 2022-03-20 /pmc/articles/PMC9133250/ /pubmed/35321801 http://dx.doi.org/10.1016/j.abd.2020.08.038 Text en © 2022 Sociedade Brasileira de Dermatologia. Published by Elsevier España, S.L.U. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Letter
Ishikawa, Masato
Yamamoto, Toshiyuki
Eruptive superficial porokeratosis in a patient with nephrotic syndrome()
title Eruptive superficial porokeratosis in a patient with nephrotic syndrome()
title_full Eruptive superficial porokeratosis in a patient with nephrotic syndrome()
title_fullStr Eruptive superficial porokeratosis in a patient with nephrotic syndrome()
title_full_unstemmed Eruptive superficial porokeratosis in a patient with nephrotic syndrome()
title_short Eruptive superficial porokeratosis in a patient with nephrotic syndrome()
title_sort eruptive superficial porokeratosis in a patient with nephrotic syndrome()
topic Case Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133250/
https://www.ncbi.nlm.nih.gov/pubmed/35321801
http://dx.doi.org/10.1016/j.abd.2020.08.038
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