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Neuropsychiatric manifestations in an adolescent male with Rowell syndrome

A 15-year-old boy presented with fever, skin, and oral lesions for 4 weeks. The cutaneous lesions were suggestive of subacute cutaneous lupus erythematosus and erythema multiforme. His clinical, histopathological, and immunological features were indicative of Rowell syndrome and he satisfied the dia...

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Autores principales: Kadiru, RA, Hegde, SP, Mithun, HK, Rao, AC
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253327/
https://www.ncbi.nlm.nih.gov/pubmed/33835061
http://dx.doi.org/10.4103/jpgm.JPGM_879_20
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author Kadiru, RA
Hegde, SP
Mithun, HK
Rao, AC
author_facet Kadiru, RA
Hegde, SP
Mithun, HK
Rao, AC
author_sort Kadiru, RA
collection PubMed
description A 15-year-old boy presented with fever, skin, and oral lesions for 4 weeks. The cutaneous lesions were suggestive of subacute cutaneous lupus erythematosus and erythema multiforme. His clinical, histopathological, and immunological features were indicative of Rowell syndrome and he satisfied the diagnostic criteria of Rowell syndrome proposed by Zeitouni et al. He subsequently developed neurological manifestations and was diagnosed to have neuropsychiatric systemic lupus erythematosus. We report this case for the unusual occurrence of a rare entity like Rowell syndrome in an adolescent male with co-existence of neuropsychiatric systemic lupus erythematosus.
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spelling pubmed-82533272021-07-14 Neuropsychiatric manifestations in an adolescent male with Rowell syndrome Kadiru, RA Hegde, SP Mithun, HK Rao, AC J Postgrad Med Case Report A 15-year-old boy presented with fever, skin, and oral lesions for 4 weeks. The cutaneous lesions were suggestive of subacute cutaneous lupus erythematosus and erythema multiforme. His clinical, histopathological, and immunological features were indicative of Rowell syndrome and he satisfied the diagnostic criteria of Rowell syndrome proposed by Zeitouni et al. He subsequently developed neurological manifestations and was diagnosed to have neuropsychiatric systemic lupus erythematosus. We report this case for the unusual occurrence of a rare entity like Rowell syndrome in an adolescent male with co-existence of neuropsychiatric systemic lupus erythematosus. Wolters Kluwer - Medknow 2021 2021-04-07 /pmc/articles/PMC8253327/ /pubmed/33835061 http://dx.doi.org/10.4103/jpgm.JPGM_879_20 Text en Copyright: © 2021 Journal of Postgraduate Medicine https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Kadiru, RA
Hegde, SP
Mithun, HK
Rao, AC
Neuropsychiatric manifestations in an adolescent male with Rowell syndrome
title Neuropsychiatric manifestations in an adolescent male with Rowell syndrome
title_full Neuropsychiatric manifestations in an adolescent male with Rowell syndrome
title_fullStr Neuropsychiatric manifestations in an adolescent male with Rowell syndrome
title_full_unstemmed Neuropsychiatric manifestations in an adolescent male with Rowell syndrome
title_short Neuropsychiatric manifestations in an adolescent male with Rowell syndrome
title_sort neuropsychiatric manifestations in an adolescent male with rowell syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253327/
https://www.ncbi.nlm.nih.gov/pubmed/33835061
http://dx.doi.org/10.4103/jpgm.JPGM_879_20
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