Purpura Fulminans Due to Staphylococcus aureus
Background. Purpura fulminans is an acute illness commonly associated with meningococcemia or invasive streptococcal disease, and it is typically characterized by disseminated intravascular coagulation (DIC) and purpuric skin lesions. In this article, we report the first 5 cases (to our knowledge) o...
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Veröffentlicht in: | Clinical infectious diseases 2005-04, Vol.40 (7), p.941-947 |
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description | Background. Purpura fulminans is an acute illness commonly associated with meningococcemia or invasive streptococcal disease, and it is typically characterized by disseminated intravascular coagulation (DIC) and purpuric skin lesions. In this article, we report the first 5 cases (to our knowledge) of purpura fulminans directly associated with Staphylococcus aureus strains that produce high levels of the superantigens toxic shock syndrome toxin-1 (TSST-1), staphylococcal enterotoxin serotype B (SEB), or staphylococcal enterotoxin serotype C (SEC). Methods. Cases were identified in the Minneapolis-St. Paul, Minnesota, metropolitan area during 2000–2004. S. aureus infection was diagnosed on the basis of culture results, and susceptibility to methicillin was determined. The ability of the isolated organisms to produce TSST-1, SEB, SEC, and Panton-Valentine leukocidin (PVL) was determined. TSST-1, SEB, and SEC levels were also quantified after in vitro growth of the organisms. Results. In 3 of the 5 cases, the infecting S. aureus strain was isolated from the blood cultures. In 2 of the 5 cases, the infecting S. aureus strain was isolated only from the respiratory tract, indicating that purpura fulminans and toxic shock syndrome resulted from exotoxin and/or other host factors, rather than septicemia. One of these latter 2 patients also had necrotizing pneumonia, and the isolated S. aureus was a methicillin-resistant strain that produced both SEC and PVL. Only 2 of the 5 patients survived, and 1 of the survivors received activated protein C. Conclusions. Staphylococcal purpura fulminans may be a newly emerging illness associated with superantigen production. Medical practitioners should be aware of this illness. |
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Purpura fulminans is an acute illness commonly associated with meningococcemia or invasive streptococcal disease, and it is typically characterized by disseminated intravascular coagulation (DIC) and purpuric skin lesions. In this article, we report the first 5 cases (to our knowledge) of purpura fulminans directly associated with Staphylococcus aureus strains that produce high levels of the superantigens toxic shock syndrome toxin-1 (TSST-1), staphylococcal enterotoxin serotype B (SEB), or staphylococcal enterotoxin serotype C (SEC). Methods. Cases were identified in the Minneapolis-St. Paul, Minnesota, metropolitan area during 2000–2004. S. aureus infection was diagnosed on the basis of culture results, and susceptibility to methicillin was determined. The ability of the isolated organisms to produce TSST-1, SEB, SEC, and Panton-Valentine leukocidin (PVL) was determined. TSST-1, SEB, and SEC levels were also quantified after in vitro growth of the organisms. Results. In 3 of the 5 cases, the infecting S. aureus strain was isolated from the blood cultures. In 2 of the 5 cases, the infecting S. aureus strain was isolated only from the respiratory tract, indicating that purpura fulminans and toxic shock syndrome resulted from exotoxin and/or other host factors, rather than septicemia. One of these latter 2 patients also had necrotizing pneumonia, and the isolated S. aureus was a methicillin-resistant strain that produced both SEC and PVL. Only 2 of the 5 patients survived, and 1 of the survivors received activated protein C. Conclusions. Staphylococcal purpura fulminans may be a newly emerging illness associated with superantigen production. Medical practitioners should be aware of this illness.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1086/428573</identifier><identifier>PMID: 15824983</identifier><language>eng</language><publisher>United States: The University of Chicago Press</publisher><subject>Adult ; Anti-Bacterial Agents - therapeutic use ; Bacteremia ; Bacteria ; Bacterial Toxins - metabolism ; Blood ; Case studies ; Enterotoxins ; Enterotoxins - metabolism ; Exotoxins - metabolism ; Female ; Humans ; Illnesses ; Infections ; Leukocidins ; Major Articles ; Male ; Middle Aged ; Platelets ; Purpura ; Purpura fulminans ; Purpura, Schoenlein-Henoch - etiology ; Purpura, Schoenlein-Henoch - microbiology ; Purpura, Schoenlein-Henoch - pathology ; Sepsis - complications ; Sepsis - microbiology ; Shock, Septic - etiology ; Shock, Septic - pathology ; Staphylococcal Infections - complications ; Staphylococcal Infections - drug therapy ; Staphylococcal Infections - microbiology ; Staphylococcal Infections - pathology ; Staphylococcus ; Staphylococcus aureus ; Staphylococcus aureus - isolation & purification ; Staphylococcus aureus - metabolism ; Superantigens ; Superantigens - metabolism ; Toxicity</subject><ispartof>Clinical infectious diseases, 2005-04, Vol.40 (7), p.941-947</ispartof><rights>Copyright 2005 The Infectious Diseases Society of America</rights><rights>Copyright University of Chicago, acting through its Press Apr 1, 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-63af5de1000a451d8e124ef060a5b5cdcc4531c953a0459cf9e87dd1a58027ff3</citedby><cites>FETCH-LOGICAL-c394t-63af5de1000a451d8e124ef060a5b5cdcc4531c953a0459cf9e87dd1a58027ff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4463190$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4463190$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27922,27923,58015,58248</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15824983$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kravitz, Gary R.</creatorcontrib><creatorcontrib>Dries, David J.</creatorcontrib><creatorcontrib>Peterson, Marnie L.</creatorcontrib><creatorcontrib>Schlievert, Patrick M.</creatorcontrib><title>Purpura Fulminans Due to Staphylococcus aureus</title><title>Clinical infectious diseases</title><addtitle>Clinical Infectious Diseases</addtitle><description>Background. Purpura fulminans is an acute illness commonly associated with meningococcemia or invasive streptococcal disease, and it is typically characterized by disseminated intravascular coagulation (DIC) and purpuric skin lesions. In this article, we report the first 5 cases (to our knowledge) of purpura fulminans directly associated with Staphylococcus aureus strains that produce high levels of the superantigens toxic shock syndrome toxin-1 (TSST-1), staphylococcal enterotoxin serotype B (SEB), or staphylococcal enterotoxin serotype C (SEC). Methods. Cases were identified in the Minneapolis-St. Paul, Minnesota, metropolitan area during 2000–2004. S. aureus infection was diagnosed on the basis of culture results, and susceptibility to methicillin was determined. The ability of the isolated organisms to produce TSST-1, SEB, SEC, and Panton-Valentine leukocidin (PVL) was determined. TSST-1, SEB, and SEC levels were also quantified after in vitro growth of the organisms. Results. In 3 of the 5 cases, the infecting S. aureus strain was isolated from the blood cultures. In 2 of the 5 cases, the infecting S. aureus strain was isolated only from the respiratory tract, indicating that purpura fulminans and toxic shock syndrome resulted from exotoxin and/or other host factors, rather than septicemia. One of these latter 2 patients also had necrotizing pneumonia, and the isolated S. aureus was a methicillin-resistant strain that produced both SEC and PVL. Only 2 of the 5 patients survived, and 1 of the survivors received activated protein C. Conclusions. Staphylococcal purpura fulminans may be a newly emerging illness associated with superantigen production. Medical practitioners should be aware of this illness.</description><subject>Adult</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Bacteremia</subject><subject>Bacteria</subject><subject>Bacterial Toxins - metabolism</subject><subject>Blood</subject><subject>Case studies</subject><subject>Enterotoxins</subject><subject>Enterotoxins - metabolism</subject><subject>Exotoxins - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Illnesses</subject><subject>Infections</subject><subject>Leukocidins</subject><subject>Major Articles</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Platelets</subject><subject>Purpura</subject><subject>Purpura fulminans</subject><subject>Purpura, Schoenlein-Henoch - etiology</subject><subject>Purpura, Schoenlein-Henoch - microbiology</subject><subject>Purpura, Schoenlein-Henoch - pathology</subject><subject>Sepsis - complications</subject><subject>Sepsis - microbiology</subject><subject>Shock, Septic - etiology</subject><subject>Shock, Septic - pathology</subject><subject>Staphylococcal Infections - complications</subject><subject>Staphylococcal Infections - drug therapy</subject><subject>Staphylococcal Infections - microbiology</subject><subject>Staphylococcal Infections - pathology</subject><subject>Staphylococcus</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - isolation & purification</subject><subject>Staphylococcus aureus - metabolism</subject><subject>Superantigens</subject><subject>Superantigens - metabolism</subject><subject>Toxicity</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkE1LAzEURYMotlb9BSKDC3dT8ybfS2mtFQqKViluQprJYOu0U5MJ2H_vyJQKrt6Fc7g8LkLngPuAJb-hmWSCHKAuMCJSzhQcNhkzmVJJZAedhLDEGEBidow6wGRGlSRd1H-KfhO9SUaxXC3WZh2SYXRJXSUvtdl8bMvKVtbGkJjoXQyn6KgwZXBnu9tDr6O76WCcTh7vHwa3k9QSReuUE1Ow3AHG2FAGuXSQUVdgjg2bM5tbSxkBqxgxmDJlC-WkyHMwTOJMFAXpoeu2d-Orr-hCrVeLYF1ZmrWrYtAgJAciRCNe_ROXVfTr5jedgVIceCb-2qyvQvCu0Bu_WBm_1YD173y6na8RL3dtcb5y-Z-226sRLlphGerK7zmlnIDCDU5bvAi1-95j4z81F0QwPZ6966Gc8tkbZvqZ_AA6DoAq</recordid><startdate>20050401</startdate><enddate>20050401</enddate><creator>Kravitz, Gary R.</creator><creator>Dries, David J.</creator><creator>Peterson, Marnie L.</creator><creator>Schlievert, Patrick M.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><general>Oxford University Press</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T2</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>20050401</creationdate><title>Purpura Fulminans Due to Staphylococcus aureus</title><author>Kravitz, Gary R. ; Dries, David J. ; Peterson, Marnie L. ; Schlievert, Patrick M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-63af5de1000a451d8e124ef060a5b5cdcc4531c953a0459cf9e87dd1a58027ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Bacteremia</topic><topic>Bacteria</topic><topic>Bacterial Toxins - metabolism</topic><topic>Blood</topic><topic>Case studies</topic><topic>Enterotoxins</topic><topic>Enterotoxins - metabolism</topic><topic>Exotoxins - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Illnesses</topic><topic>Infections</topic><topic>Leukocidins</topic><topic>Major Articles</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Platelets</topic><topic>Purpura</topic><topic>Purpura fulminans</topic><topic>Purpura, Schoenlein-Henoch - etiology</topic><topic>Purpura, Schoenlein-Henoch - microbiology</topic><topic>Purpura, Schoenlein-Henoch - pathology</topic><topic>Sepsis - complications</topic><topic>Sepsis - microbiology</topic><topic>Shock, Septic - etiology</topic><topic>Shock, Septic - pathology</topic><topic>Staphylococcal Infections - complications</topic><topic>Staphylococcal Infections - drug therapy</topic><topic>Staphylococcal Infections - microbiology</topic><topic>Staphylococcal Infections - pathology</topic><topic>Staphylococcus</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - isolation & purification</topic><topic>Staphylococcus aureus - metabolism</topic><topic>Superantigens</topic><topic>Superantigens - metabolism</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kravitz, Gary R.</creatorcontrib><creatorcontrib>Dries, David J.</creatorcontrib><creatorcontrib>Peterson, Marnie L.</creatorcontrib><creatorcontrib>Schlievert, Patrick M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kravitz, Gary R.</au><au>Dries, David J.</au><au>Peterson, Marnie L.</au><au>Schlievert, Patrick M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Purpura Fulminans Due to Staphylococcus aureus</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clinical Infectious Diseases</addtitle><date>2005-04-01</date><risdate>2005</risdate><volume>40</volume><issue>7</issue><spage>941</spage><epage>947</epage><pages>941-947</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><abstract>Background. Purpura fulminans is an acute illness commonly associated with meningococcemia or invasive streptococcal disease, and it is typically characterized by disseminated intravascular coagulation (DIC) and purpuric skin lesions. In this article, we report the first 5 cases (to our knowledge) of purpura fulminans directly associated with Staphylococcus aureus strains that produce high levels of the superantigens toxic shock syndrome toxin-1 (TSST-1), staphylococcal enterotoxin serotype B (SEB), or staphylococcal enterotoxin serotype C (SEC). Methods. Cases were identified in the Minneapolis-St. Paul, Minnesota, metropolitan area during 2000–2004. S. aureus infection was diagnosed on the basis of culture results, and susceptibility to methicillin was determined. The ability of the isolated organisms to produce TSST-1, SEB, SEC, and Panton-Valentine leukocidin (PVL) was determined. TSST-1, SEB, and SEC levels were also quantified after in vitro growth of the organisms. Results. In 3 of the 5 cases, the infecting S. aureus strain was isolated from the blood cultures. In 2 of the 5 cases, the infecting S. aureus strain was isolated only from the respiratory tract, indicating that purpura fulminans and toxic shock syndrome resulted from exotoxin and/or other host factors, rather than septicemia. One of these latter 2 patients also had necrotizing pneumonia, and the isolated S. aureus was a methicillin-resistant strain that produced both SEC and PVL. Only 2 of the 5 patients survived, and 1 of the survivors received activated protein C. Conclusions. Staphylococcal purpura fulminans may be a newly emerging illness associated with superantigen production. Medical practitioners should be aware of this illness.</abstract><cop>United States</cop><pub>The University of Chicago Press</pub><pmid>15824983</pmid><doi>10.1086/428573</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Anti-Bacterial Agents - therapeutic use Bacteremia Bacteria Bacterial Toxins - metabolism Blood Case studies Enterotoxins Enterotoxins - metabolism Exotoxins - metabolism Female Humans Illnesses Infections Leukocidins Major Articles Male Middle Aged Platelets Purpura Purpura fulminans Purpura, Schoenlein-Henoch - etiology Purpura, Schoenlein-Henoch - microbiology Purpura, Schoenlein-Henoch - pathology Sepsis - complications Sepsis - microbiology Shock, Septic - etiology Shock, Septic - pathology Staphylococcal Infections - complications Staphylococcal Infections - drug therapy Staphylococcal Infections - microbiology Staphylococcal Infections - pathology Staphylococcus Staphylococcus aureus Staphylococcus aureus - isolation & purification Staphylococcus aureus - metabolism Superantigens Superantigens - metabolism Toxicity |
title | Purpura Fulminans Due to Staphylococcus aureus |
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