Recurrent Kawasaki disease in a child with retropharyngeal involvement: a case report and literature review
Kawasaki disease (KD) is a multisystemic vasculitic disease. Recurrent KD is rare and generally presents in a similar clinical picture as the first episode, and early diagnosis with prompt treatment is the key point in preventing associated cardiovascular morbidities. A 9-year-old boy, who was diagn...
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Veröffentlicht in: | Medicine (Baltimore) 2014-12, Vol.93 (29), p.e139-e139 |
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creator | Aldemir-Kocabaş, Bilge Kcal, Mücahit Murat Ramoğlu, Mehmet G Tutar, Ercan Fitöz, Suat Çiftçi, Ergin İnce, Erdal |
description | Kawasaki disease (KD) is a multisystemic vasculitic disease. Recurrent KD is rare and generally presents in a similar clinical picture as the first episode, and early diagnosis with prompt treatment is the key point in preventing associated cardiovascular morbidities. A 9-year-old boy, who was diagnosed with KD when he was 1.5 years' old, was referred to our hospital for surgical drainage of retropharyngeal abscess. He had a 7-day history of high fever, sore throat, left-sided neck swelling, and restricted neck movements. Subsequently, he was diagnosed with recurrent KD and retropharyngeal involvement. He was successfully treated with a single dose of intravenous immunoglobulin (IVIG) and acetyl salicylic acid. Recurrence is rare and occurs most commonly in children. Atypical presentation, incomplete disease, short duration of fever, and reduced response to IVIG treatment were found to be the risk factors for recurrence. KD can occasionally present with clinical and radiographic findings of deep neck bacterial infection. Unusual presentations in KD may cause delay in diagnosis and increase the risk of life-threatening complications. We describe a case of recurrent KD presenting with a clinical picture resembling retropharyngeal infection who fully recovered after 1 dose of IVIG instead of surgical drainage and antibiotic use. |
doi_str_mv | 10.1097/MD.0000000000000139 |
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Recurrent KD is rare and generally presents in a similar clinical picture as the first episode, and early diagnosis with prompt treatment is the key point in preventing associated cardiovascular morbidities. A 9-year-old boy, who was diagnosed with KD when he was 1.5 years' old, was referred to our hospital for surgical drainage of retropharyngeal abscess. He had a 7-day history of high fever, sore throat, left-sided neck swelling, and restricted neck movements. Subsequently, he was diagnosed with recurrent KD and retropharyngeal involvement. He was successfully treated with a single dose of intravenous immunoglobulin (IVIG) and acetyl salicylic acid. Recurrence is rare and occurs most commonly in children. Atypical presentation, incomplete disease, short duration of fever, and reduced response to IVIG treatment were found to be the risk factors for recurrence. KD can occasionally present with clinical and radiographic findings of deep neck bacterial infection. Unusual presentations in KD may cause delay in diagnosis and increase the risk of life-threatening complications. We describe a case of recurrent KD presenting with a clinical picture resembling retropharyngeal infection who fully recovered after 1 dose of IVIG instead of surgical drainage and antibiotic use.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000000139</identifier><identifier>PMID: 25546657</identifier><language>eng</language><publisher>United States: Wolters Kluwer Health</publisher><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Aspirin - therapeutic use ; Child ; Clinical Case Report ; Humans ; Immunoglobulins, Intravenous - therapeutic use ; Male ; Mucocutaneous Lymph Node Syndrome - complications ; Mucocutaneous Lymph Node Syndrome - diagnosis ; Mucocutaneous Lymph Node Syndrome - drug therapy ; Recurrence ; Retropharyngeal Abscess - etiology ; Retropharyngeal Abscess - therapy</subject><ispartof>Medicine (Baltimore), 2014-12, Vol.93 (29), p.e139-e139</ispartof><rights>Copyright © 2014 Wolters Kluwer Health, Inc. 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Recurrent KD is rare and generally presents in a similar clinical picture as the first episode, and early diagnosis with prompt treatment is the key point in preventing associated cardiovascular morbidities. A 9-year-old boy, who was diagnosed with KD when he was 1.5 years' old, was referred to our hospital for surgical drainage of retropharyngeal abscess. He had a 7-day history of high fever, sore throat, left-sided neck swelling, and restricted neck movements. Subsequently, he was diagnosed with recurrent KD and retropharyngeal involvement. He was successfully treated with a single dose of intravenous immunoglobulin (IVIG) and acetyl salicylic acid. Recurrence is rare and occurs most commonly in children. Atypical presentation, incomplete disease, short duration of fever, and reduced response to IVIG treatment were found to be the risk factors for recurrence. KD can occasionally present with clinical and radiographic findings of deep neck bacterial infection. Unusual presentations in KD may cause delay in diagnosis and increase the risk of life-threatening complications. We describe a case of recurrent KD presenting with a clinical picture resembling retropharyngeal infection who fully recovered after 1 dose of IVIG instead of surgical drainage and antibiotic use.</description><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Aspirin - therapeutic use</subject><subject>Child</subject><subject>Clinical Case Report</subject><subject>Humans</subject><subject>Immunoglobulins, Intravenous - therapeutic use</subject><subject>Male</subject><subject>Mucocutaneous Lymph Node Syndrome - complications</subject><subject>Mucocutaneous Lymph Node Syndrome - diagnosis</subject><subject>Mucocutaneous Lymph Node Syndrome - drug therapy</subject><subject>Recurrence</subject><subject>Retropharyngeal Abscess - etiology</subject><subject>Retropharyngeal Abscess - therapy</subject><issn>0025-7974</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUFtLwzAUDqK4Of0FguTRl84kTdLGB0HmFSeC6HNJ29M1rjeTtsN_b4tT5nk5cL4rB6FTSuaUqODi-WZOdof6ag9NqfClJ5Tk-2hKCBNeoAI-QUfOfYyUgPFDNGFCcClFMEXrV0g6a6Fq8ZPeaKfXBqfGgXaATYU1TnJTpHhj2hxbaG3d5Np-VSvQxYD3ddFDOYgvR-aosdDUtsW6SnFhWrC67ex47Q1sjtFBpgsHJ9s9Q-93t2-LB2_5cv-4uF56DZOy9TLOA5FykgpJmIwh47HiiocqSTTxA5kC0X4aEppwQkUckiykXBIlJGcJy6Q_Q1c_vk0Xl5AmQz-ri6ixphy6R7U20X-kMnm0qvuIj4FsNDjfGtj6swPXRqVxCRSFrqDuXEQlp4xQ5bOBerab9Rfy-2H_G4-CgCQ</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Aldemir-Kocabaş, Bilge</creator><creator>Kcal, Mücahit Murat</creator><creator>Ramoğlu, Mehmet G</creator><creator>Tutar, Ercan</creator><creator>Fitöz, Suat</creator><creator>Çiftçi, Ergin</creator><creator>İnce, Erdal</creator><general>Wolters Kluwer Health</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20141201</creationdate><title>Recurrent Kawasaki disease in a child with retropharyngeal involvement: a case report and literature review</title><author>Aldemir-Kocabaş, Bilge ; Kcal, Mücahit Murat ; Ramoğlu, Mehmet G ; Tutar, Ercan ; Fitöz, Suat ; Çiftçi, Ergin ; İnce, Erdal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p266t-f4475d40d56026bef4b949489cca0376de0a3d801c4015b80f8146095642c2f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Aspirin - therapeutic use</topic><topic>Child</topic><topic>Clinical Case Report</topic><topic>Humans</topic><topic>Immunoglobulins, Intravenous - therapeutic use</topic><topic>Male</topic><topic>Mucocutaneous Lymph Node Syndrome - complications</topic><topic>Mucocutaneous Lymph Node Syndrome - diagnosis</topic><topic>Mucocutaneous Lymph Node Syndrome - drug therapy</topic><topic>Recurrence</topic><topic>Retropharyngeal Abscess - etiology</topic><topic>Retropharyngeal Abscess - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aldemir-Kocabaş, Bilge</creatorcontrib><creatorcontrib>Kcal, Mücahit Murat</creatorcontrib><creatorcontrib>Ramoğlu, Mehmet G</creatorcontrib><creatorcontrib>Tutar, Ercan</creatorcontrib><creatorcontrib>Fitöz, Suat</creatorcontrib><creatorcontrib>Çiftçi, Ergin</creatorcontrib><creatorcontrib>İnce, Erdal</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aldemir-Kocabaş, Bilge</au><au>Kcal, Mücahit Murat</au><au>Ramoğlu, Mehmet G</au><au>Tutar, Ercan</au><au>Fitöz, Suat</au><au>Çiftçi, Ergin</au><au>İnce, Erdal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recurrent Kawasaki disease in a child with retropharyngeal involvement: a case report and literature review</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>93</volume><issue>29</issue><spage>e139</spage><epage>e139</epage><pages>e139-e139</pages><issn>0025-7974</issn><eissn>1536-5964</eissn><abstract>Kawasaki disease (KD) is a multisystemic vasculitic disease. Recurrent KD is rare and generally presents in a similar clinical picture as the first episode, and early diagnosis with prompt treatment is the key point in preventing associated cardiovascular morbidities. A 9-year-old boy, who was diagnosed with KD when he was 1.5 years' old, was referred to our hospital for surgical drainage of retropharyngeal abscess. He had a 7-day history of high fever, sore throat, left-sided neck swelling, and restricted neck movements. Subsequently, he was diagnosed with recurrent KD and retropharyngeal involvement. He was successfully treated with a single dose of intravenous immunoglobulin (IVIG) and acetyl salicylic acid. Recurrence is rare and occurs most commonly in children. Atypical presentation, incomplete disease, short duration of fever, and reduced response to IVIG treatment were found to be the risk factors for recurrence. KD can occasionally present with clinical and radiographic findings of deep neck bacterial infection. Unusual presentations in KD may cause delay in diagnosis and increase the risk of life-threatening complications. We describe a case of recurrent KD presenting with a clinical picture resembling retropharyngeal infection who fully recovered after 1 dose of IVIG instead of surgical drainage and antibiotic use.</abstract><cop>United States</cop><pub>Wolters Kluwer Health</pub><pmid>25546657</pmid><doi>10.1097/MD.0000000000000139</doi><oa>free_for_read</oa></addata></record> |
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subjects | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use Aspirin - therapeutic use Child Clinical Case Report Humans Immunoglobulins, Intravenous - therapeutic use Male Mucocutaneous Lymph Node Syndrome - complications Mucocutaneous Lymph Node Syndrome - diagnosis Mucocutaneous Lymph Node Syndrome - drug therapy Recurrence Retropharyngeal Abscess - etiology Retropharyngeal Abscess - therapy |
title | Recurrent Kawasaki disease in a child with retropharyngeal involvement: a case report and literature review |
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