Atypical Mpox in a Nigerian Tertiary Health Facility
We describe diverse clinical characteristics and course of confirmed mpox cases managed in a Nigerian tertiary health facility. Clinical and epidemiologic data were analyzed, highlighting the unusual presentations of polymerase chain reaction (PCR)-confirmed mpox cases observed during the 2022 outbr...
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Veröffentlicht in: | The Journal of infectious diseases 2024-03, Vol.229 (Supplement_2), p.S181-S187 |
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creator | Chika-Igwenyi, Nneka M Unigwe, Uche S Ajayi, Nnennaya A Onwe, Ogah E Ewa, Richard L Ojide, Chiedozie K Una, Alfred F Igwenyi, Chikaodiri Chukwu, Kyrian S Okorie, Gabriel M Nnadozie, Ugochukwu U Ifebunandu, Ngozi A Ugwu, Collins N Emeka, Sampson Ibemesi, Desi Nnaji, Thomas O Primus, Nsikan O Odianosen, Ehiakhamen |
description | We describe diverse clinical characteristics and course of confirmed mpox cases managed in a Nigerian tertiary health facility.
Clinical and epidemiologic data were analyzed, highlighting the unusual presentations of polymerase chain reaction (PCR)-confirmed mpox cases observed during the 2022 outbreak.
Out of 17 suspected cases, 13 (76.4%) were PCR confirmed for mpox. The mean ± SD age for the participants was 28.62 ± 10.29 years (range, 2-55), of which 9 (64.3%) were male. Of the 13 PCR-confirmed cases, 5 (38.5%) had varicella zoster virus coinfection, 2 (15.4%) had HIV coinfection, and 1 (7.7%) had diabetes mellitus comorbidity. All patients experienced rash, with 6 (46.2%) having significant genital lesions and 1 (7.7%) having a severe perianal lesion. A lack of prodromal symptoms was reported in 3 (23.1%), and a prolonged prodrome (>1 week) occurred in 5 (38.5%). Skin lesions were polymorphic in 6 (46.2%), and solitary skin lesions occurred in 3 (23.1%), which persisted for >120 days in 7.7%.
Clinical recognition, diagnosis, and prevention remain a concern in resource-limited settings. Our findings highlight the need to further evaluate unusual skin lesions and to include mpox screening for genital skin lesions that are presumed to be sexually transmitted infections. Revision of clinical case definition and enhanced surveillance are key to early recognition and prevention of spread. |
doi_str_mv | 10.1093/infdis/jiad607 |
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Clinical and epidemiologic data were analyzed, highlighting the unusual presentations of polymerase chain reaction (PCR)-confirmed mpox cases observed during the 2022 outbreak.
Out of 17 suspected cases, 13 (76.4%) were PCR confirmed for mpox. The mean ± SD age for the participants was 28.62 ± 10.29 years (range, 2-55), of which 9 (64.3%) were male. Of the 13 PCR-confirmed cases, 5 (38.5%) had varicella zoster virus coinfection, 2 (15.4%) had HIV coinfection, and 1 (7.7%) had diabetes mellitus comorbidity. All patients experienced rash, with 6 (46.2%) having significant genital lesions and 1 (7.7%) having a severe perianal lesion. A lack of prodromal symptoms was reported in 3 (23.1%), and a prolonged prodrome (>1 week) occurred in 5 (38.5%). Skin lesions were polymorphic in 6 (46.2%), and solitary skin lesions occurred in 3 (23.1%), which persisted for >120 days in 7.7%.
Clinical recognition, diagnosis, and prevention remain a concern in resource-limited settings. Our findings highlight the need to further evaluate unusual skin lesions and to include mpox screening for genital skin lesions that are presumed to be sexually transmitted infections. Revision of clinical case definition and enhanced surveillance are key to early recognition and prevention of spread.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiad607</identifier><identifier>PMID: 38157416</identifier><language>eng</language><publisher>United States</publisher><ispartof>The Journal of infectious diseases, 2024-03, Vol.229 (Supplement_2), p.S181-S187</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c290t-44b605e0b6eccc028df7d879bc71e72297d33d20666d9718c0755d2f587643c63</cites><orcidid>0000-0002-4814-8384</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38157416$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chika-Igwenyi, Nneka M</creatorcontrib><creatorcontrib>Unigwe, Uche S</creatorcontrib><creatorcontrib>Ajayi, Nnennaya A</creatorcontrib><creatorcontrib>Onwe, Ogah E</creatorcontrib><creatorcontrib>Ewa, Richard L</creatorcontrib><creatorcontrib>Ojide, Chiedozie K</creatorcontrib><creatorcontrib>Una, Alfred F</creatorcontrib><creatorcontrib>Igwenyi, Chikaodiri</creatorcontrib><creatorcontrib>Chukwu, Kyrian S</creatorcontrib><creatorcontrib>Okorie, Gabriel M</creatorcontrib><creatorcontrib>Nnadozie, Ugochukwu U</creatorcontrib><creatorcontrib>Ifebunandu, Ngozi A</creatorcontrib><creatorcontrib>Ugwu, Collins N</creatorcontrib><creatorcontrib>Emeka, Sampson</creatorcontrib><creatorcontrib>Ibemesi, Desi</creatorcontrib><creatorcontrib>Nnaji, Thomas O</creatorcontrib><creatorcontrib>Primus, Nsikan O</creatorcontrib><creatorcontrib>Odianosen, Ehiakhamen</creatorcontrib><title>Atypical Mpox in a Nigerian Tertiary Health Facility</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>We describe diverse clinical characteristics and course of confirmed mpox cases managed in a Nigerian tertiary health facility.
Clinical and epidemiologic data were analyzed, highlighting the unusual presentations of polymerase chain reaction (PCR)-confirmed mpox cases observed during the 2022 outbreak.
Out of 17 suspected cases, 13 (76.4%) were PCR confirmed for mpox. The mean ± SD age for the participants was 28.62 ± 10.29 years (range, 2-55), of which 9 (64.3%) were male. Of the 13 PCR-confirmed cases, 5 (38.5%) had varicella zoster virus coinfection, 2 (15.4%) had HIV coinfection, and 1 (7.7%) had diabetes mellitus comorbidity. All patients experienced rash, with 6 (46.2%) having significant genital lesions and 1 (7.7%) having a severe perianal lesion. A lack of prodromal symptoms was reported in 3 (23.1%), and a prolonged prodrome (>1 week) occurred in 5 (38.5%). Skin lesions were polymorphic in 6 (46.2%), and solitary skin lesions occurred in 3 (23.1%), which persisted for >120 days in 7.7%.
Clinical recognition, diagnosis, and prevention remain a concern in resource-limited settings. Our findings highlight the need to further evaluate unusual skin lesions and to include mpox screening for genital skin lesions that are presumed to be sexually transmitted infections. Revision of clinical case definition and enhanced surveillance are key to early recognition and prevention of spread.</description><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kD1PwzAQhi0EoqWwMiKPLGnPduKPsaooRSqwlNlybAdcpUmwU4n--wa1MN3y3PvePQjdE5gSUGwWmsqFNNsG4ziICzQmBRMZ54RdojEApRmRSo3QTUpbAMgZF9doxCQpRE74GOXz_tAFa2r82rU_ODTY4Lfw6WMwDd742AcTD3jlTd1_4aWxoQ794RZdVaZO_u48J-hj-bRZrLL1-_PLYr7OLFXQZ3lecig8lNxba4FKVwknhSqtIF5QqoRjzFHgnDsliLQgisLRqpCC58xyNkGPp9wutt97n3q9C8n6ujaNb_dJDy0K5PAMGdDpCbWxTSn6Sncx7IbbNQH9a0qfTOmzqWHh4Zy9L3fe_eN_atgRUhRkqA</recordid><startdate>20240326</startdate><enddate>20240326</enddate><creator>Chika-Igwenyi, Nneka M</creator><creator>Unigwe, Uche S</creator><creator>Ajayi, Nnennaya A</creator><creator>Onwe, Ogah E</creator><creator>Ewa, Richard L</creator><creator>Ojide, Chiedozie K</creator><creator>Una, Alfred F</creator><creator>Igwenyi, Chikaodiri</creator><creator>Chukwu, Kyrian S</creator><creator>Okorie, Gabriel M</creator><creator>Nnadozie, Ugochukwu U</creator><creator>Ifebunandu, Ngozi A</creator><creator>Ugwu, Collins N</creator><creator>Emeka, Sampson</creator><creator>Ibemesi, Desi</creator><creator>Nnaji, Thomas O</creator><creator>Primus, Nsikan O</creator><creator>Odianosen, Ehiakhamen</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4814-8384</orcidid></search><sort><creationdate>20240326</creationdate><title>Atypical Mpox in a Nigerian Tertiary Health Facility</title><author>Chika-Igwenyi, Nneka M ; Unigwe, Uche S ; Ajayi, Nnennaya A ; Onwe, Ogah E ; Ewa, Richard L ; Ojide, Chiedozie K ; Una, Alfred F ; Igwenyi, Chikaodiri ; Chukwu, Kyrian S ; Okorie, Gabriel M ; Nnadozie, Ugochukwu U ; Ifebunandu, Ngozi A ; Ugwu, Collins N ; Emeka, Sampson ; Ibemesi, Desi ; Nnaji, Thomas O ; Primus, Nsikan O ; Odianosen, Ehiakhamen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c290t-44b605e0b6eccc028df7d879bc71e72297d33d20666d9718c0755d2f587643c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chika-Igwenyi, Nneka M</creatorcontrib><creatorcontrib>Unigwe, Uche S</creatorcontrib><creatorcontrib>Ajayi, Nnennaya A</creatorcontrib><creatorcontrib>Onwe, Ogah E</creatorcontrib><creatorcontrib>Ewa, Richard L</creatorcontrib><creatorcontrib>Ojide, Chiedozie K</creatorcontrib><creatorcontrib>Una, Alfred F</creatorcontrib><creatorcontrib>Igwenyi, Chikaodiri</creatorcontrib><creatorcontrib>Chukwu, Kyrian S</creatorcontrib><creatorcontrib>Okorie, Gabriel M</creatorcontrib><creatorcontrib>Nnadozie, Ugochukwu U</creatorcontrib><creatorcontrib>Ifebunandu, Ngozi A</creatorcontrib><creatorcontrib>Ugwu, Collins N</creatorcontrib><creatorcontrib>Emeka, Sampson</creatorcontrib><creatorcontrib>Ibemesi, Desi</creatorcontrib><creatorcontrib>Nnaji, Thomas O</creatorcontrib><creatorcontrib>Primus, Nsikan O</creatorcontrib><creatorcontrib>Odianosen, Ehiakhamen</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chika-Igwenyi, Nneka M</au><au>Unigwe, Uche S</au><au>Ajayi, Nnennaya A</au><au>Onwe, Ogah E</au><au>Ewa, Richard L</au><au>Ojide, Chiedozie K</au><au>Una, Alfred F</au><au>Igwenyi, Chikaodiri</au><au>Chukwu, Kyrian S</au><au>Okorie, Gabriel M</au><au>Nnadozie, Ugochukwu U</au><au>Ifebunandu, Ngozi A</au><au>Ugwu, Collins N</au><au>Emeka, Sampson</au><au>Ibemesi, Desi</au><au>Nnaji, Thomas O</au><au>Primus, Nsikan O</au><au>Odianosen, Ehiakhamen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Atypical Mpox in a Nigerian Tertiary Health Facility</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2024-03-26</date><risdate>2024</risdate><volume>229</volume><issue>Supplement_2</issue><spage>S181</spage><epage>S187</epage><pages>S181-S187</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><abstract>We describe diverse clinical characteristics and course of confirmed mpox cases managed in a Nigerian tertiary health facility.
Clinical and epidemiologic data were analyzed, highlighting the unusual presentations of polymerase chain reaction (PCR)-confirmed mpox cases observed during the 2022 outbreak.
Out of 17 suspected cases, 13 (76.4%) were PCR confirmed for mpox. The mean ± SD age for the participants was 28.62 ± 10.29 years (range, 2-55), of which 9 (64.3%) were male. Of the 13 PCR-confirmed cases, 5 (38.5%) had varicella zoster virus coinfection, 2 (15.4%) had HIV coinfection, and 1 (7.7%) had diabetes mellitus comorbidity. All patients experienced rash, with 6 (46.2%) having significant genital lesions and 1 (7.7%) having a severe perianal lesion. A lack of prodromal symptoms was reported in 3 (23.1%), and a prolonged prodrome (>1 week) occurred in 5 (38.5%). Skin lesions were polymorphic in 6 (46.2%), and solitary skin lesions occurred in 3 (23.1%), which persisted for >120 days in 7.7%.
Clinical recognition, diagnosis, and prevention remain a concern in resource-limited settings. Our findings highlight the need to further evaluate unusual skin lesions and to include mpox screening for genital skin lesions that are presumed to be sexually transmitted infections. Revision of clinical case definition and enhanced surveillance are key to early recognition and prevention of spread.</abstract><cop>United States</cop><pmid>38157416</pmid><doi>10.1093/infdis/jiad607</doi><orcidid>https://orcid.org/0000-0002-4814-8384</orcidid><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current) |
title | Atypical Mpox in a Nigerian Tertiary Health Facility |
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