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Purpura fulminans, TEN, and disseminated herpes simplex: An unexpected combination
Stevens–Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and purpura fulminans (PF) are all rare conditions. A combination of these 3 conditions together with a viral infection is very rare. A 52‐year‐old, previously healthy woman which developed SJS, potentially due to a reaction to CT con...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043719/ https://www.ncbi.nlm.nih.gov/pubmed/35498363 http://dx.doi.org/10.1002/ccr3.5784 |
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author | Holm, Sebastian Thurfjell, Viktoria Lara‐Valencia, Paola Huss, Fredrik |
author_facet | Holm, Sebastian Thurfjell, Viktoria Lara‐Valencia, Paola Huss, Fredrik |
author_sort | Holm, Sebastian |
collection | PubMed |
description | Stevens–Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and purpura fulminans (PF) are all rare conditions. A combination of these 3 conditions together with a viral infection is very rare. A 52‐year‐old, previously healthy woman which developed SJS, potentially due to a reaction to CT contrast, although this is still unknown. This developed into TEN on day 10 of the initial admission, the patient scored 3 points on SCORTEN. On day 12 from initial admission, she developed unexpected multiorgan failure and PF. The patient passed away 2 days later, the autopsy demonstrates herpes simplex virus in the bladder and lungs on immunohistological staining. Our clinical case encountered the challenge of differentiating TEN and PF. The microscopic and immunochemical examination confirmed the clinical suspicion of PF but also a disseminated herpes simplex infection. We speculate the clinical route of this case started SJS and TEN, leading to superimposed infection with three different types of bacteria, confirmed in blood cultures, and a disseminated viral infection. The combination of all these diagnoses are very rare, no similar case has been described in adults to the authors’ knowledge. We recommend a prompt diagnosis and early recognition of both bacterial and viral infections to prevent the development of PF. |
format | Online Article Text |
id | pubmed-9043719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90437192022-04-28 Purpura fulminans, TEN, and disseminated herpes simplex: An unexpected combination Holm, Sebastian Thurfjell, Viktoria Lara‐Valencia, Paola Huss, Fredrik Clin Case Rep Case Reports Stevens–Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and purpura fulminans (PF) are all rare conditions. A combination of these 3 conditions together with a viral infection is very rare. A 52‐year‐old, previously healthy woman which developed SJS, potentially due to a reaction to CT contrast, although this is still unknown. This developed into TEN on day 10 of the initial admission, the patient scored 3 points on SCORTEN. On day 12 from initial admission, she developed unexpected multiorgan failure and PF. The patient passed away 2 days later, the autopsy demonstrates herpes simplex virus in the bladder and lungs on immunohistological staining. Our clinical case encountered the challenge of differentiating TEN and PF. The microscopic and immunochemical examination confirmed the clinical suspicion of PF but also a disseminated herpes simplex infection. We speculate the clinical route of this case started SJS and TEN, leading to superimposed infection with three different types of bacteria, confirmed in blood cultures, and a disseminated viral infection. The combination of all these diagnoses are very rare, no similar case has been described in adults to the authors’ knowledge. We recommend a prompt diagnosis and early recognition of both bacterial and viral infections to prevent the development of PF. John Wiley and Sons Inc. 2022-04-26 /pmc/articles/PMC9043719/ /pubmed/35498363 http://dx.doi.org/10.1002/ccr3.5784 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Holm, Sebastian Thurfjell, Viktoria Lara‐Valencia, Paola Huss, Fredrik Purpura fulminans, TEN, and disseminated herpes simplex: An unexpected combination |
title | Purpura fulminans, TEN, and disseminated herpes simplex: An unexpected combination |
title_full | Purpura fulminans, TEN, and disseminated herpes simplex: An unexpected combination |
title_fullStr | Purpura fulminans, TEN, and disseminated herpes simplex: An unexpected combination |
title_full_unstemmed | Purpura fulminans, TEN, and disseminated herpes simplex: An unexpected combination |
title_short | Purpura fulminans, TEN, and disseminated herpes simplex: An unexpected combination |
title_sort | purpura fulminans, ten, and disseminated herpes simplex: an unexpected combination |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043719/ https://www.ncbi.nlm.nih.gov/pubmed/35498363 http://dx.doi.org/10.1002/ccr3.5784 |
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