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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2022
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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. |
format | Online Article Text |
id | pubmed-9133250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ishikawamasato eruptivesuperficialporokeratosisinapatientwithnephroticsyndrome AT yamamototoshiyuki eruptivesuperficialporokeratosisinapatientwithnephroticsyndrome |