A Novel Case of Acquired Isolated Left Ventricular Non-compaction in a Primigravida: Revisiting the Diagnostic Criteria of Left Ventricular Non-compaction
Left ventricular non-compaction (LVNC) is rare cardiomyopathy characterized by the presence of a two-layered myocardium with prominent trabeculations. It has high rates of mortality and morbidity. Clinical presentation could vary from asymptomatic patients to developing ventricular arrhythmias, thro...
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Veröffentlicht in: | Curēus (Palo Alto, CA) CA), 2023-01, Vol.15 (1), p.e33823 |
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creator | Akhigbe, Esiemoghie J Ezeh, Ebubechukwu Sebro, Nadew Olanipekun, Olalekan Rueda Rios, Carlos |
description | Left ventricular non-compaction (LVNC) is rare cardiomyopathy characterized by the presence of a two-layered myocardium with prominent trabeculations. It has high rates of mortality and morbidity. Clinical presentation could vary from asymptomatic patients to developing ventricular arrhythmias, thromboembolism, heart failure, and even sudden cardiac death. We present a 23-year-old primigravida with a childhood history of dilated cardiomyopathy secondary to post-viral myocarditis presenting at 32 weeks gestation with dyspnea on exertion. Initial 2-D echocardiogram revealed a mildly dilated left ventricle with apical trabeculation and a 2-layer distinction between compacted and noncompacted myocardium indicating non-compaction of the left ventricle. This case presents a peculiar confluence of cardiac genetics, normal physiology, and infection. We describe a rare form of acquired LVNC that transformed from another type of cardiomyopathy to LVNC during pregnancy drawing attention to the causality pathways of LVNC. |
doi_str_mv | 10.7759/cureus.33823 |
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It has high rates of mortality and morbidity. Clinical presentation could vary from asymptomatic patients to developing ventricular arrhythmias, thromboembolism, heart failure, and even sudden cardiac death. We present a 23-year-old primigravida with a childhood history of dilated cardiomyopathy secondary to post-viral myocarditis presenting at 32 weeks gestation with dyspnea on exertion. Initial 2-D echocardiogram revealed a mildly dilated left ventricle with apical trabeculation and a 2-layer distinction between compacted and noncompacted myocardium indicating non-compaction of the left ventricle. This case presents a peculiar confluence of cardiac genetics, normal physiology, and infection. 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This work is published under https://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2023, Akhigbe et al. 2023 Akhigbe et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c266t-79f7587ced3849f706c8fa8aa58be3a05f320cb3d8845eeef14d125ad8c921793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930369/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930369/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36819372$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Akhigbe, Esiemoghie J</creatorcontrib><creatorcontrib>Ezeh, Ebubechukwu</creatorcontrib><creatorcontrib>Sebro, Nadew</creatorcontrib><creatorcontrib>Olanipekun, Olalekan</creatorcontrib><creatorcontrib>Rueda Rios, Carlos</creatorcontrib><title>A Novel Case of Acquired Isolated Left Ventricular Non-compaction in a Primigravida: Revisiting the Diagnostic Criteria of Left Ventricular Non-compaction</title><title>Curēus (Palo Alto, CA)</title><addtitle>Cureus</addtitle><description>Left ventricular non-compaction (LVNC) is rare cardiomyopathy characterized by the presence of a two-layered myocardium with prominent trabeculations. 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We describe a rare form of acquired LVNC that transformed from another type of cardiomyopathy to LVNC during pregnancy drawing attention to the causality pathways of LVNC.</description><subject>Cardiac arrhythmia</subject><subject>Cardiology</subject><subject>Cardiomyopathy</subject><subject>Disease</subject><subject>Dyspnea</subject><subject>Edema</subject><subject>Electrocardiography</subject><subject>Heart failure</subject><subject>Magnetic resonance imaging</subject><subject>Medical diagnosis</subject><subject>Medicine</subject><subject>Mortality</subject><subject>Obstetrics/Gynecology</subject><subject>Patients</subject><subject>Physiology</subject><subject>Pleural effusion</subject><subject>Pregnancy</subject><subject>Preventive Medicine</subject><subject>Ultrasonic imaging</subject><subject>Womens health</subject><issn>2168-8184</issn><issn>2168-8184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqFUU1P3DAUtKqigmBvnCtLvTbgjyR2eqi0WsqHtAJUAVfrrfOyGGXjxXZW6l_h15J0AW1PPb2R3ryZeRpCjjk7UaqoTm0fsI8nUmohP5EDwUudaa7zzzt4n0xifGKMcaYEU-wL2Zel5pVU4oC8TOm132BLZxCR-oZO7XPvAtb0KvoW0gDm2CT6gF0KzvYthOGgy6xfrcEm5zvqOgr0NriVWwbYuBp-0N-4cdEl1y1pekR65mDZ-ZicpbPgEgYHo9V_hI_IXgNtxMnbPCT357_uZpfZ_ObiajadZ1aUZcpU1ahCK4u11PmAWWl1Axqg0AuUwIpGCmYXstY6LxCx4XnNRQG1tpXgqpKH5OdWd90vVljbMRC0Zj18BOGP8eDMv5vOPZql35iqkkyWo8C3N4Hgn3uMyTz5PnRDZiOUZmVesmpkfd-ybPAxBmw-HDgzY5lmW6b5W-ZA_7qb6oP8Xp18BecJn0c</recordid><startdate>20230116</startdate><enddate>20230116</enddate><creator>Akhigbe, Esiemoghie J</creator><creator>Ezeh, Ebubechukwu</creator><creator>Sebro, Nadew</creator><creator>Olanipekun, Olalekan</creator><creator>Rueda Rios, Carlos</creator><general>Cureus Inc</general><general>Cureus</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</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>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20230116</creationdate><title>A Novel Case of Acquired Isolated Left Ventricular Non-compaction in a Primigravida: Revisiting the Diagnostic Criteria of Left Ventricular Non-compaction</title><author>Akhigbe, Esiemoghie J ; 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It has high rates of mortality and morbidity. Clinical presentation could vary from asymptomatic patients to developing ventricular arrhythmias, thromboembolism, heart failure, and even sudden cardiac death. We present a 23-year-old primigravida with a childhood history of dilated cardiomyopathy secondary to post-viral myocarditis presenting at 32 weeks gestation with dyspnea on exertion. Initial 2-D echocardiogram revealed a mildly dilated left ventricle with apical trabeculation and a 2-layer distinction between compacted and noncompacted myocardium indicating non-compaction of the left ventricle. This case presents a peculiar confluence of cardiac genetics, normal physiology, and infection. 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subjects | Cardiac arrhythmia Cardiology Cardiomyopathy Disease Dyspnea Edema Electrocardiography Heart failure Magnetic resonance imaging Medical diagnosis Medicine Mortality Obstetrics/Gynecology Patients Physiology Pleural effusion Pregnancy Preventive Medicine Ultrasonic imaging Womens health |
title | A Novel Case of Acquired Isolated Left Ventricular Non-compaction in a Primigravida: Revisiting the Diagnostic Criteria of Left Ventricular Non-compaction |
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