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Drug reaction with eosinophilia and systemic symptoms syndrome in a patient taking lamotrigine
Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare adverse drug reaction characterised by skin eruption and multiple organ involvement. Diagnosing this entity is challenging due to the variability of clinical manifestations, late onset and relapse even after stopping th...
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Published in: | BMJ case reports 2019-10, Vol.12 (10), p.e229180 |
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description | Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare adverse drug reaction characterised by skin eruption and multiple organ involvement. Diagnosing this entity is challenging due to the variability of clinical manifestations, late onset and relapse even after stopping the causative drug. It is potentially life-threatening; thus, it must be promptly recognised and the causative drug withdrawn. We describe a case of a 50-year-old man with an acute diffuse rash, fever and eosinophilia 4 weeks after having started lamotrigine. The suspected eliciting drug was suspended and systemic corticoid treatment was initiated (prednisolone 0.5 mg/kg/day). Symptoms relapsed under corticoid tapering with greater severity. The patient developed an exuberant rash associated with peripheral lymphadenopathies, marked eosinophilia and hepatic cytolysis. The diagnosis of DRESS syndrome to lamotrigine was made. Prednisolone dosage was increased to 1 mg/kg/day, and the subsequent taper was performed slowly over the course of 10 weeks. Full clinical remission was observed. |
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Diagnosing this entity is challenging due to the variability of clinical manifestations, late onset and relapse even after stopping the causative drug. It is potentially life-threatening; thus, it must be promptly recognised and the causative drug withdrawn. We describe a case of a 50-year-old man with an acute diffuse rash, fever and eosinophilia 4 weeks after having started lamotrigine. The suspected eliciting drug was suspended and systemic corticoid treatment was initiated (prednisolone 0.5 mg/kg/day). Symptoms relapsed under corticoid tapering with greater severity. The patient developed an exuberant rash associated with peripheral lymphadenopathies, marked eosinophilia and hepatic cytolysis. The diagnosis of DRESS syndrome to lamotrigine was made. Prednisolone dosage was increased to 1 mg/kg/day, and the subsequent taper was performed slowly over the course of 10 weeks. Full clinical remission was observed.</description><identifier>ISSN: 1757-790X</identifier><identifier>EISSN: 1757-790X</identifier><identifier>DOI: 10.1136/bcr-2019-229180</identifier><identifier>PMID: 31653619</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd</publisher><subject>Anticonvulsants - adverse effects ; Antigens ; Blood diseases ; Case reports ; Cytomegalovirus ; Dermatitis ; Diagnosis, Differential ; Drug dosages ; Drug Hypersensitivity Syndrome - drug therapy ; Drug Hypersensitivity Syndrome - etiology ; Edema ; emergency medicine ; Epilepsy - drug therapy ; Fever ; Glucocorticoids - therapeutic use ; Hepatitis ; Humans ; immunology ; Laboratories ; Lamotrigine - adverse effects ; Liver ; Male ; Middle Aged ; neurology (drugs and medicines) ; Patients ; Prednisolone - therapeutic use ; Reminder of Important Clinical Lesson ; Salmonella ; unwanted effects / adverse reactions</subject><ispartof>BMJ case reports, 2019-10, Vol.12 (10), p.e229180</ispartof><rights>BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2019 BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b520t-fc1ad6d2173794a645f109085cb0d8440df73ce8d72d635e5390b862316d6d1a3</citedby><cites>FETCH-LOGICAL-b520t-fc1ad6d2173794a645f109085cb0d8440df73ce8d72d635e5390b862316d6d1a3</cites><orcidid>0000-0001-8302-3037</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827764/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827764/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31653619$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lameiras, Catarina</creatorcontrib><creatorcontrib>Ornelas, Énia</creatorcontrib><creatorcontrib>Mendes Lopes, Marta</creatorcontrib><creatorcontrib>Dória, Maria do Céu</creatorcontrib><title>Drug reaction with eosinophilia and systemic symptoms syndrome in a patient taking lamotrigine</title><title>BMJ case reports</title><addtitle>BMJ Case Rep</addtitle><addtitle>BMJ Case Rep</addtitle><description>Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare adverse drug reaction characterised by skin eruption and multiple organ involvement. Diagnosing this entity is challenging due to the variability of clinical manifestations, late onset and relapse even after stopping the causative drug. It is potentially life-threatening; thus, it must be promptly recognised and the causative drug withdrawn. We describe a case of a 50-year-old man with an acute diffuse rash, fever and eosinophilia 4 weeks after having started lamotrigine. The suspected eliciting drug was suspended and systemic corticoid treatment was initiated (prednisolone 0.5 mg/kg/day). Symptoms relapsed under corticoid tapering with greater severity. The patient developed an exuberant rash associated with peripheral lymphadenopathies, marked eosinophilia and hepatic cytolysis. The diagnosis of DRESS syndrome to lamotrigine was made. Prednisolone dosage was increased to 1 mg/kg/day, and the subsequent taper was performed slowly over the course of 10 weeks. Full clinical remission was observed.</description><subject>Anticonvulsants - adverse effects</subject><subject>Antigens</subject><subject>Blood diseases</subject><subject>Case reports</subject><subject>Cytomegalovirus</subject><subject>Dermatitis</subject><subject>Diagnosis, Differential</subject><subject>Drug dosages</subject><subject>Drug Hypersensitivity Syndrome - drug therapy</subject><subject>Drug Hypersensitivity Syndrome - etiology</subject><subject>Edema</subject><subject>emergency medicine</subject><subject>Epilepsy - drug therapy</subject><subject>Fever</subject><subject>Glucocorticoids - therapeutic use</subject><subject>Hepatitis</subject><subject>Humans</subject><subject>immunology</subject><subject>Laboratories</subject><subject>Lamotrigine - adverse effects</subject><subject>Liver</subject><subject>Male</subject><subject>Middle Aged</subject><subject>neurology (drugs and medicines)</subject><subject>Patients</subject><subject>Prednisolone - therapeutic use</subject><subject>Reminder of Important Clinical Lesson</subject><subject>Salmonella</subject><subject>unwanted effects / adverse reactions</subject><issn>1757-790X</issn><issn>1757-790X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqNkc1LBCEYxiWKiurcLYRuxZQfMzpegtg-IehS0ClxRmfXbUcndYv--4ytrQ5BXnzA3_u8jzwA7GJ0hDFlx00bCoKwKAgRuEYrYBPzihdcoIfVH3oD7MQ4RflQXNYlXQcbFLOKMiw2weNZmI9hMKpN1jv4atMEGh-t88PEzqyCymkY32IyvW2z6Ifk-5iF08H3BloHFRxUssYlmNSTdWM4U71PwY6tM9tgrVOzaHY-7y1wf3F-N7oqbm4vr0enN0VTEZSKrsVKM00wp1yUipVVh5FAddU2SNdliXTHaWtqzYlmtDIVFaipGcn_yGNY0S1wsvAd5k1vdJvTBDWTQ7C9Cm_SKyt_vzg7kWP_IllNOGdlNtj_NAj-eW5iklM_Dy5nloQiIRhiJc_U8YJqg48xmG65ASP50YnMnciPTuSikzyx9zPYkv9qIAMHC6Dpp_9wO_yGlwH_ot8Btn2j6w</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Lameiras, Catarina</creator><creator>Ornelas, Énia</creator><creator>Mendes Lopes, Marta</creator><creator>Dória, Maria do Céu</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8302-3037</orcidid></search><sort><creationdate>20191001</creationdate><title>Drug reaction with eosinophilia and systemic symptoms syndrome in a patient taking lamotrigine</title><author>Lameiras, Catarina ; Ornelas, Énia ; Mendes Lopes, Marta ; Dória, Maria do Céu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b520t-fc1ad6d2173794a645f109085cb0d8440df73ce8d72d635e5390b862316d6d1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Anticonvulsants - adverse effects</topic><topic>Antigens</topic><topic>Blood diseases</topic><topic>Case reports</topic><topic>Cytomegalovirus</topic><topic>Dermatitis</topic><topic>Diagnosis, Differential</topic><topic>Drug dosages</topic><topic>Drug Hypersensitivity Syndrome - drug therapy</topic><topic>Drug Hypersensitivity Syndrome - etiology</topic><topic>Edema</topic><topic>emergency medicine</topic><topic>Epilepsy - drug therapy</topic><topic>Fever</topic><topic>Glucocorticoids - therapeutic use</topic><topic>Hepatitis</topic><topic>Humans</topic><topic>immunology</topic><topic>Laboratories</topic><topic>Lamotrigine - adverse effects</topic><topic>Liver</topic><topic>Male</topic><topic>Middle Aged</topic><topic>neurology (drugs and medicines)</topic><topic>Patients</topic><topic>Prednisolone - therapeutic use</topic><topic>Reminder of Important Clinical Lesson</topic><topic>Salmonella</topic><topic>unwanted effects / adverse reactions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lameiras, Catarina</creatorcontrib><creatorcontrib>Ornelas, Énia</creatorcontrib><creatorcontrib>Mendes Lopes, Marta</creatorcontrib><creatorcontrib>Dória, Maria do Céu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMJ case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lameiras, Catarina</au><au>Ornelas, Énia</au><au>Mendes Lopes, Marta</au><au>Dória, Maria do Céu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Drug reaction with eosinophilia and systemic symptoms syndrome in a patient taking lamotrigine</atitle><jtitle>BMJ case reports</jtitle><stitle>BMJ Case Rep</stitle><addtitle>BMJ Case Rep</addtitle><date>2019-10-01</date><risdate>2019</risdate><volume>12</volume><issue>10</issue><spage>e229180</spage><pages>e229180-</pages><issn>1757-790X</issn><eissn>1757-790X</eissn><abstract>Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare adverse drug reaction characterised by skin eruption and multiple organ involvement. Diagnosing this entity is challenging due to the variability of clinical manifestations, late onset and relapse even after stopping the causative drug. It is potentially life-threatening; thus, it must be promptly recognised and the causative drug withdrawn. We describe a case of a 50-year-old man with an acute diffuse rash, fever and eosinophilia 4 weeks after having started lamotrigine. The suspected eliciting drug was suspended and systemic corticoid treatment was initiated (prednisolone 0.5 mg/kg/day). Symptoms relapsed under corticoid tapering with greater severity. The patient developed an exuberant rash associated with peripheral lymphadenopathies, marked eosinophilia and hepatic cytolysis. The diagnosis of DRESS syndrome to lamotrigine was made. Prednisolone dosage was increased to 1 mg/kg/day, and the subsequent taper was performed slowly over the course of 10 weeks. Full clinical remission was observed.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd</pub><pmid>31653619</pmid><doi>10.1136/bcr-2019-229180</doi><orcidid>https://orcid.org/0000-0001-8302-3037</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anticonvulsants - adverse effects Antigens Blood diseases Case reports Cytomegalovirus Dermatitis Diagnosis, Differential Drug dosages Drug Hypersensitivity Syndrome - drug therapy Drug Hypersensitivity Syndrome - etiology Edema emergency medicine Epilepsy - drug therapy Fever Glucocorticoids - therapeutic use Hepatitis Humans immunology Laboratories Lamotrigine - adverse effects Liver Male Middle Aged neurology (drugs and medicines) Patients Prednisolone - therapeutic use Reminder of Important Clinical Lesson Salmonella unwanted effects / adverse reactions |
title | Drug reaction with eosinophilia and systemic symptoms syndrome in a patient taking lamotrigine |
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