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Iodinated contrast-induced Stevens-Johnson syndrome: A report of a rare complication for a common imaging agent

Steven-Johnson syndrome (SJS) is a rare condition commonly associated with exposure to antibiotics. We have presented the case of a 76-year-old man with end-stage renal disease who had developed SJS after endovascular thrombectomy of hemodialysis access. He had developed epithelial erosions of the m...

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Detalles Bibliográficos
Autores principales: Carrera, Daniel, Ulloa, Jesus G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395747/
https://www.ncbi.nlm.nih.gov/pubmed/36016706
http://dx.doi.org/10.1016/j.jvscit.2022.06.015
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author Carrera, Daniel
Ulloa, Jesus G.
author_facet Carrera, Daniel
Ulloa, Jesus G.
author_sort Carrera, Daniel
collection PubMed
description Steven-Johnson syndrome (SJS) is a rare condition commonly associated with exposure to antibiotics. We have presented the case of a 76-year-old man with end-stage renal disease who had developed SJS after endovascular thrombectomy of hemodialysis access. He had developed epithelial erosions of the mucosal membranes, hemorrhagic bullae to the palmar and plantar surfaces, and erosions of the genitalia. The findings from biopsies of the lip and palm were suggestive of a drug reaction. He developed SJS three times after exposure to iodinated contrast. The one time he did not develop SJS, he had undergone open thrombectomy with no contrast exposure.
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spelling pubmed-93957472022-08-24 Iodinated contrast-induced Stevens-Johnson syndrome: A report of a rare complication for a common imaging agent Carrera, Daniel Ulloa, Jesus G. J Vasc Surg Cases Innov Tech Case report Steven-Johnson syndrome (SJS) is a rare condition commonly associated with exposure to antibiotics. We have presented the case of a 76-year-old man with end-stage renal disease who had developed SJS after endovascular thrombectomy of hemodialysis access. He had developed epithelial erosions of the mucosal membranes, hemorrhagic bullae to the palmar and plantar surfaces, and erosions of the genitalia. The findings from biopsies of the lip and palm were suggestive of a drug reaction. He developed SJS three times after exposure to iodinated contrast. The one time he did not develop SJS, he had undergone open thrombectomy with no contrast exposure. Elsevier 2022-07-16 /pmc/articles/PMC9395747/ /pubmed/36016706 http://dx.doi.org/10.1016/j.jvscit.2022.06.015 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case report
Carrera, Daniel
Ulloa, Jesus G.
Iodinated contrast-induced Stevens-Johnson syndrome: A report of a rare complication for a common imaging agent
title Iodinated contrast-induced Stevens-Johnson syndrome: A report of a rare complication for a common imaging agent
title_full Iodinated contrast-induced Stevens-Johnson syndrome: A report of a rare complication for a common imaging agent
title_fullStr Iodinated contrast-induced Stevens-Johnson syndrome: A report of a rare complication for a common imaging agent
title_full_unstemmed Iodinated contrast-induced Stevens-Johnson syndrome: A report of a rare complication for a common imaging agent
title_short Iodinated contrast-induced Stevens-Johnson syndrome: A report of a rare complication for a common imaging agent
title_sort iodinated contrast-induced stevens-johnson syndrome: a report of a rare complication for a common imaging agent
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395747/
https://www.ncbi.nlm.nih.gov/pubmed/36016706
http://dx.doi.org/10.1016/j.jvscit.2022.06.015
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