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Congenital absence of the left pericardium: a case report
Congenital absence of the pericardium (CAP) is rare in clinical practice, the symptoms vary among patients, and most doctors do not have enough knowledge of the condition. Most reported CAP cases are incidental findings. Therefore, this case report aimed to present a rare case of left partial CAP th...
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Published in: | BMC cardiovascular disorders 2023-05, Vol.23 (1), p.247-247, Article 247 |
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description | Congenital absence of the pericardium (CAP) is rare in clinical practice, the symptoms vary among patients, and most doctors do not have enough knowledge of the condition. Most reported CAP cases are incidental findings. Therefore, this case report aimed to present a rare case of left partial CAP that presented with non-specific, possibly cardiac-related symptoms.
The patient, male, 56 years old, Asian, was admitted on March 2, 2021. The patient complained of occasional dizziness in the past week. The patient was suffering from hyperlipidemia and hypertension (stage 2), both untreated. The patient reported chest pain, palpitations, discomfort in the precordium, and dyspnea in the lateral recumbent position after strenuous activities, all of which started when he was about 15 years old. ECG showed sinus rhythm, 76 bpm, premature ventricular beats, incomplete right bundle branch block, and clockwise rotation of the electrical axis. Most of the ascending aorta could be detected in the parasternal intercostal space 2-4 by transthoracic echocardiography in the left lateral position. Chest computed tomography revealed the absence of pericardium between the aorta and the pulmonary artery, and part of the left lung was extending into the space. No changes in his condition have been reported up to now (March 2023).
CAP should be considered when multiple examinations suggest heart rotation and a large moving range of the heart in the thoracic cavity. |
doi_str_mv | 10.1186/s12872-023-03262-3 |
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The patient, male, 56 years old, Asian, was admitted on March 2, 2021. The patient complained of occasional dizziness in the past week. The patient was suffering from hyperlipidemia and hypertension (stage 2), both untreated. The patient reported chest pain, palpitations, discomfort in the precordium, and dyspnea in the lateral recumbent position after strenuous activities, all of which started when he was about 15 years old. ECG showed sinus rhythm, 76 bpm, premature ventricular beats, incomplete right bundle branch block, and clockwise rotation of the electrical axis. Most of the ascending aorta could be detected in the parasternal intercostal space 2-4 by transthoracic echocardiography in the left lateral position. Chest computed tomography revealed the absence of pericardium between the aorta and the pulmonary artery, and part of the left lung was extending into the space. No changes in his condition have been reported up to now (March 2023).
CAP should be considered when multiple examinations suggest heart rotation and a large moving range of the heart in the thoracic cavity.</description><identifier>ISSN: 1471-2261</identifier><identifier>EISSN: 1471-2261</identifier><identifier>DOI: 10.1186/s12872-023-03262-3</identifier><identifier>PMID: 37173633</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Absence of pericardium ; Adolescent ; Analysis ; Aorta ; Asymptomatic ; Autopsies ; Bundle-Branch Block ; Cardiac arrest ; Care and treatment ; Case Report ; Case reports ; Chest ; Chest Pain ; Complications and side effects ; Computed tomography ; Congenital diseases ; Congenital heart defects ; Congenital heart disease ; Coronary vessels ; Defects ; Dyspnea ; Echocardiography ; EKG ; Electrocardiogram ; Electrocardiography ; Genetic aspects ; Heart ; Heart Defects, Congenital - diagnosis ; Hospitals ; Humans ; Hyperlipidemia ; Imprisonment ; Male ; Middle Aged ; Patients ; Pericardium ; Physicians ; Prevention ; Pulmonary arteries ; Pulmonary artery ; Respiration ; Risk factors ; Thoracic surgery ; Thorax ; Veins & arteries ; Ventricle</subject><ispartof>BMC cardiovascular disorders, 2023-05, Vol.23 (1), p.247-247, Article 247</ispartof><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c564t-8dd548e6c7b7068a3ad7f9c0d1acf3b6ccfde54b4ed8707485e7e7ac2fdd294b3</citedby><cites>FETCH-LOGICAL-c564t-8dd548e6c7b7068a3ad7f9c0d1acf3b6ccfde54b4ed8707485e7e7ac2fdd294b3</cites><orcidid>0000-0003-1453-3927</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/PMC10176923/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2815558863?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37173633$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Xiang-Yi</creatorcontrib><creatorcontrib>Jiang, Yan</creatorcontrib><creatorcontrib>Li, Hao-Wen</creatorcontrib><creatorcontrib>Liu, Yong-Kang</creatorcontrib><creatorcontrib>Bai, Jing</creatorcontrib><title>Congenital absence of the left pericardium: a case report</title><title>BMC cardiovascular disorders</title><addtitle>BMC Cardiovasc Disord</addtitle><description>Congenital absence of the pericardium (CAP) is rare in clinical practice, the symptoms vary among patients, and most doctors do not have enough knowledge of the condition. Most reported CAP cases are incidental findings. Therefore, this case report aimed to present a rare case of left partial CAP that presented with non-specific, possibly cardiac-related symptoms.
The patient, male, 56 years old, Asian, was admitted on March 2, 2021. The patient complained of occasional dizziness in the past week. The patient was suffering from hyperlipidemia and hypertension (stage 2), both untreated. The patient reported chest pain, palpitations, discomfort in the precordium, and dyspnea in the lateral recumbent position after strenuous activities, all of which started when he was about 15 years old. ECG showed sinus rhythm, 76 bpm, premature ventricular beats, incomplete right bundle branch block, and clockwise rotation of the electrical axis. Most of the ascending aorta could be detected in the parasternal intercostal space 2-4 by transthoracic echocardiography in the left lateral position. Chest computed tomography revealed the absence of pericardium between the aorta and the pulmonary artery, and part of the left lung was extending into the space. No changes in his condition have been reported up to now (March 2023).
CAP should be considered when multiple examinations suggest heart rotation and a large moving range of the heart in the thoracic cavity.</description><subject>Absence of pericardium</subject><subject>Adolescent</subject><subject>Analysis</subject><subject>Aorta</subject><subject>Asymptomatic</subject><subject>Autopsies</subject><subject>Bundle-Branch Block</subject><subject>Cardiac arrest</subject><subject>Care and treatment</subject><subject>Case Report</subject><subject>Case reports</subject><subject>Chest</subject><subject>Chest Pain</subject><subject>Complications and side effects</subject><subject>Computed tomography</subject><subject>Congenital diseases</subject><subject>Congenital heart defects</subject><subject>Congenital heart disease</subject><subject>Coronary vessels</subject><subject>Defects</subject><subject>Dyspnea</subject><subject>Echocardiography</subject><subject>EKG</subject><subject>Electrocardiogram</subject><subject>Electrocardiography</subject><subject>Genetic aspects</subject><subject>Heart</subject><subject>Heart Defects, Congenital - diagnosis</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hyperlipidemia</subject><subject>Imprisonment</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Patients</subject><subject>Pericardium</subject><subject>Physicians</subject><subject>Prevention</subject><subject>Pulmonary arteries</subject><subject>Pulmonary artery</subject><subject>Respiration</subject><subject>Risk factors</subject><subject>Thoracic surgery</subject><subject>Thorax</subject><subject>Veins & arteries</subject><subject>Ventricle</subject><issn>1471-2261</issn><issn>1471-2261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkktv1DAUhSMEog_4AyxQJDZsUvy2wwZVIwqVKrGBtXVjX089ysSDnanEv8fplNJByAtb1-d81746TfOGkgtKjfpQKDOadYTxjnCmWMefNadUaNoxpujzJ-eT5qyUDSFUG9K_bE64pporzk-bfpWmNU5xhrGFoeDksE2hnW-xHTHM7Q5zdJB93G8_ttA6KNhm3KU8v2peBBgLvn7Yz5sfV5-_r752N9--XK8ubzonlZg7470UBpXTgybKAAevQ--Ip-ACH5RzwaMUg0BvNNHCSNSowbHgPevFwM-b6wPXJ9jYXY5byL9sgmjvCymvLeQ5uhGtBFIthnJgQYCQIIkz2gsHQhnveGV9OrB2-2GL3uE0ZxiPoMc3U7y163RnaR2d6tlCeP9AyOnnHstst7E4HEeYMO2LZbW7VNQwUqXv_pFu0j5PdVaLSkppjOJ_VWuoP4hTSLWxW6D2UoueEqPMwrr4j6ouj9vo0oQh1vqRgR0MLqdSMobHT1Jil_TYQ3psTY-9T49d3vL26XgeLX_iwn8DtoS94g</recordid><startdate>20230512</startdate><enddate>20230512</enddate><creator>Li, Xiang-Yi</creator><creator>Jiang, Yan</creator><creator>Li, Hao-Wen</creator><creator>Liu, Yong-Kang</creator><creator>Bai, Jing</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>7QP</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>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1453-3927</orcidid></search><sort><creationdate>20230512</creationdate><title>Congenital absence of the left pericardium: a case report</title><author>Li, Xiang-Yi ; Jiang, Yan ; Li, Hao-Wen ; Liu, Yong-Kang ; Bai, Jing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c564t-8dd548e6c7b7068a3ad7f9c0d1acf3b6ccfde54b4ed8707485e7e7ac2fdd294b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Absence of pericardium</topic><topic>Adolescent</topic><topic>Analysis</topic><topic>Aorta</topic><topic>Asymptomatic</topic><topic>Autopsies</topic><topic>Bundle-Branch Block</topic><topic>Cardiac arrest</topic><topic>Care and treatment</topic><topic>Case Report</topic><topic>Case reports</topic><topic>Chest</topic><topic>Chest Pain</topic><topic>Complications and side effects</topic><topic>Computed tomography</topic><topic>Congenital diseases</topic><topic>Congenital heart defects</topic><topic>Congenital heart disease</topic><topic>Coronary vessels</topic><topic>Defects</topic><topic>Dyspnea</topic><topic>Echocardiography</topic><topic>EKG</topic><topic>Electrocardiogram</topic><topic>Electrocardiography</topic><topic>Genetic aspects</topic><topic>Heart</topic><topic>Heart Defects, Congenital - diagnosis</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Hyperlipidemia</topic><topic>Imprisonment</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Patients</topic><topic>Pericardium</topic><topic>Physicians</topic><topic>Prevention</topic><topic>Pulmonary arteries</topic><topic>Pulmonary artery</topic><topic>Respiration</topic><topic>Risk factors</topic><topic>Thoracic surgery</topic><topic>Thorax</topic><topic>Veins & arteries</topic><topic>Ventricle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xiang-Yi</creatorcontrib><creatorcontrib>Jiang, Yan</creatorcontrib><creatorcontrib>Li, Hao-Wen</creatorcontrib><creatorcontrib>Liu, Yong-Kang</creatorcontrib><creatorcontrib>Bai, Jing</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>Calcium & Calcified Tissue Abstracts</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>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC cardiovascular disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xiang-Yi</au><au>Jiang, Yan</au><au>Li, Hao-Wen</au><au>Liu, Yong-Kang</au><au>Bai, Jing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Congenital absence of the left pericardium: a case report</atitle><jtitle>BMC cardiovascular disorders</jtitle><addtitle>BMC Cardiovasc Disord</addtitle><date>2023-05-12</date><risdate>2023</risdate><volume>23</volume><issue>1</issue><spage>247</spage><epage>247</epage><pages>247-247</pages><artnum>247</artnum><issn>1471-2261</issn><eissn>1471-2261</eissn><abstract>Congenital absence of the pericardium (CAP) is rare in clinical practice, the symptoms vary among patients, and most doctors do not have enough knowledge of the condition. Most reported CAP cases are incidental findings. Therefore, this case report aimed to present a rare case of left partial CAP that presented with non-specific, possibly cardiac-related symptoms.
The patient, male, 56 years old, Asian, was admitted on March 2, 2021. The patient complained of occasional dizziness in the past week. The patient was suffering from hyperlipidemia and hypertension (stage 2), both untreated. The patient reported chest pain, palpitations, discomfort in the precordium, and dyspnea in the lateral recumbent position after strenuous activities, all of which started when he was about 15 years old. ECG showed sinus rhythm, 76 bpm, premature ventricular beats, incomplete right bundle branch block, and clockwise rotation of the electrical axis. Most of the ascending aorta could be detected in the parasternal intercostal space 2-4 by transthoracic echocardiography in the left lateral position. Chest computed tomography revealed the absence of pericardium between the aorta and the pulmonary artery, and part of the left lung was extending into the space. No changes in his condition have been reported up to now (March 2023).
CAP should be considered when multiple examinations suggest heart rotation and a large moving range of the heart in the thoracic cavity.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>37173633</pmid><doi>10.1186/s12872-023-03262-3</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-1453-3927</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Absence of pericardium Adolescent Analysis Aorta Asymptomatic Autopsies Bundle-Branch Block Cardiac arrest Care and treatment Case Report Case reports Chest Chest Pain Complications and side effects Computed tomography Congenital diseases Congenital heart defects Congenital heart disease Coronary vessels Defects Dyspnea Echocardiography EKG Electrocardiogram Electrocardiography Genetic aspects Heart Heart Defects, Congenital - diagnosis Hospitals Humans Hyperlipidemia Imprisonment Male Middle Aged Patients Pericardium Physicians Prevention Pulmonary arteries Pulmonary artery Respiration Risk factors Thoracic surgery Thorax Veins & arteries Ventricle |
title | Congenital absence of the left pericardium: a case report |
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