Cardiac Surgery in Homozygous Familial Hypercholesterolemia
Homozygous familial hypercholesterolemia is a rare metabolic disorder with characteristic clinical presentations, such as tendon xanthomas, hypercholesterolemia, and significant cardiovascular disease including premature coronary artery disease. We describe a case of a 56-year-old woman with homozyg...
Gespeichert in:
| Veröffentlicht in: | Japanese Journal of Cardiovascular Surgery 2013/07/15, Vol.42(4), pp.307-311 |
|---|---|
| Hauptverfasser: | , , , , , |
| Format: | Artikel |
| Sprache: | eng ; jpn |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 311 |
|---|---|
| container_issue | 4 |
| container_start_page | 307 |
| container_title | Japanese Journal of Cardiovascular Surgery |
| container_volume | 42 |
| creator | Kawamura, Tomonori Mogi, Kenji Enomoto, Yoshinori Sakurai, Manabu Matsuura, Kaoru Takahara, Yoshiharu |
| description | Homozygous familial hypercholesterolemia is a rare metabolic disorder with characteristic clinical presentations, such as tendon xanthomas, hypercholesterolemia, and significant cardiovascular disease including premature coronary artery disease. We describe a case of a 56-year-old woman with homozygous familial hypercholesterolemia. She had been treated with low-density lipoprotein apheresis for 23 years. Preoperative echocardiography and coronary angiography showed severe aortic valve stenosis and right coronary artery stenosis. Aortic valve replacement with patch enlargement of the aortic valve annulus, and coronary artery bypass grafting were successfully performed. She was discharged uneventfully. |
| doi_str_mv | 10.4326/jjcvs.42.307 |
| format | Article |
| fullrecord | <record><control><sourceid>jstage_cross</sourceid><recordid>TN_cdi_crossref_primary_10_4326_jjcvs_42_307</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>article_jjcvs_42_4_42_307_article_char_en</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1317-c58f3b3c38a7c449e732643dcba5424966035fcf73389b387796e5896688a483</originalsourceid><addsrcrecordid>eNpFj8FKw0AQhhdRsNTefIA8gKm7mUl2gweRYK1Q8GDvy2S7STckTdlthfj0Rlvq6YeZ7x_mY-xe8DlCkj02jfkKc0zmwOUVmwilIEbB1TWb8ESlsUCJt2wWgis5TzIpuMAJeyrIbxyZ6PPoa-uHyO2iZd_130PdH0O0oM61jtpoOeytN9u-teFg_Ridozt2U1Eb7OycU7ZevK6LZbz6eHsvXlaxESBkbFJVQQkGFEmDmFs5vouwMSWlmGCeZRzSylQSQOUlKCnzzKZqnCtFqGDKHk5nje9D8LbSe-868oMWXP-q6z91jYke1Uf8-YQ34UC1vcDkD8609h_Gc-OyMVvy2u7gBxDaY6s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Cardiac Surgery in Homozygous Familial Hypercholesterolemia</title><source>J-STAGE Free</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Kawamura, Tomonori ; Mogi, Kenji ; Enomoto, Yoshinori ; Sakurai, Manabu ; Matsuura, Kaoru ; Takahara, Yoshiharu</creator><creatorcontrib>Kawamura, Tomonori ; Mogi, Kenji ; Enomoto, Yoshinori ; Sakurai, Manabu ; Matsuura, Kaoru ; Takahara, Yoshiharu</creatorcontrib><description>Homozygous familial hypercholesterolemia is a rare metabolic disorder with characteristic clinical presentations, such as tendon xanthomas, hypercholesterolemia, and significant cardiovascular disease including premature coronary artery disease. We describe a case of a 56-year-old woman with homozygous familial hypercholesterolemia. She had been treated with low-density lipoprotein apheresis for 23 years. Preoperative echocardiography and coronary angiography showed severe aortic valve stenosis and right coronary artery stenosis. Aortic valve replacement with patch enlargement of the aortic valve annulus, and coronary artery bypass grafting were successfully performed. She was discharged uneventfully.</description><identifier>ISSN: 0285-1474</identifier><identifier>EISSN: 1883-4108</identifier><identifier>DOI: 10.4326/jjcvs.42.307</identifier><language>eng ; jpn</language><publisher>The Japanese Society for Cardiovascular Surgery</publisher><subject>aortic valve stenosis ; familial hypercholesterolemia ; homozygote ; low-density lipoprotein</subject><ispartof>Japanese Journal of Cardiovascular Surgery, 2013/07/15, Vol.42(4), pp.307-311</ispartof><rights>2013 The Japanese Society for Cardiovascular Surgery</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1881,27923,27924</link.rule.ids></links><search><creatorcontrib>Kawamura, Tomonori</creatorcontrib><creatorcontrib>Mogi, Kenji</creatorcontrib><creatorcontrib>Enomoto, Yoshinori</creatorcontrib><creatorcontrib>Sakurai, Manabu</creatorcontrib><creatorcontrib>Matsuura, Kaoru</creatorcontrib><creatorcontrib>Takahara, Yoshiharu</creatorcontrib><title>Cardiac Surgery in Homozygous Familial Hypercholesterolemia</title><title>Japanese Journal of Cardiovascular Surgery</title><addtitle>J. J. C. V. S.</addtitle><description>Homozygous familial hypercholesterolemia is a rare metabolic disorder with characteristic clinical presentations, such as tendon xanthomas, hypercholesterolemia, and significant cardiovascular disease including premature coronary artery disease. We describe a case of a 56-year-old woman with homozygous familial hypercholesterolemia. She had been treated with low-density lipoprotein apheresis for 23 years. Preoperative echocardiography and coronary angiography showed severe aortic valve stenosis and right coronary artery stenosis. Aortic valve replacement with patch enlargement of the aortic valve annulus, and coronary artery bypass grafting were successfully performed. She was discharged uneventfully.</description><subject>aortic valve stenosis</subject><subject>familial hypercholesterolemia</subject><subject>homozygote</subject><subject>low-density lipoprotein</subject><issn>0285-1474</issn><issn>1883-4108</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpFj8FKw0AQhhdRsNTefIA8gKm7mUl2gweRYK1Q8GDvy2S7STckTdlthfj0Rlvq6YeZ7x_mY-xe8DlCkj02jfkKc0zmwOUVmwilIEbB1TWb8ESlsUCJt2wWgis5TzIpuMAJeyrIbxyZ6PPoa-uHyO2iZd_130PdH0O0oM61jtpoOeytN9u-teFg_Ridozt2U1Eb7OycU7ZevK6LZbz6eHsvXlaxESBkbFJVQQkGFEmDmFs5vouwMSWlmGCeZRzSylQSQOUlKCnzzKZqnCtFqGDKHk5nje9D8LbSe-868oMWXP-q6z91jYke1Uf8-YQ34UC1vcDkD8609h_Gc-OyMVvy2u7gBxDaY6s</recordid><startdate>20130715</startdate><enddate>20130715</enddate><creator>Kawamura, Tomonori</creator><creator>Mogi, Kenji</creator><creator>Enomoto, Yoshinori</creator><creator>Sakurai, Manabu</creator><creator>Matsuura, Kaoru</creator><creator>Takahara, Yoshiharu</creator><general>The Japanese Society for Cardiovascular Surgery</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20130715</creationdate><title>Cardiac Surgery in Homozygous Familial Hypercholesterolemia</title><author>Kawamura, Tomonori ; Mogi, Kenji ; Enomoto, Yoshinori ; Sakurai, Manabu ; Matsuura, Kaoru ; Takahara, Yoshiharu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1317-c58f3b3c38a7c449e732643dcba5424966035fcf73389b387796e5896688a483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; jpn</language><creationdate>2013</creationdate><topic>aortic valve stenosis</topic><topic>familial hypercholesterolemia</topic><topic>homozygote</topic><topic>low-density lipoprotein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawamura, Tomonori</creatorcontrib><creatorcontrib>Mogi, Kenji</creatorcontrib><creatorcontrib>Enomoto, Yoshinori</creatorcontrib><creatorcontrib>Sakurai, Manabu</creatorcontrib><creatorcontrib>Matsuura, Kaoru</creatorcontrib><creatorcontrib>Takahara, Yoshiharu</creatorcontrib><collection>CrossRef</collection><jtitle>Japanese Journal of Cardiovascular Surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawamura, Tomonori</au><au>Mogi, Kenji</au><au>Enomoto, Yoshinori</au><au>Sakurai, Manabu</au><au>Matsuura, Kaoru</au><au>Takahara, Yoshiharu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cardiac Surgery in Homozygous Familial Hypercholesterolemia</atitle><jtitle>Japanese Journal of Cardiovascular Surgery</jtitle><addtitle>J. J. C. V. S.</addtitle><date>2013-07-15</date><risdate>2013</risdate><volume>42</volume><issue>4</issue><spage>307</spage><epage>311</epage><pages>307-311</pages><issn>0285-1474</issn><eissn>1883-4108</eissn><abstract>Homozygous familial hypercholesterolemia is a rare metabolic disorder with characteristic clinical presentations, such as tendon xanthomas, hypercholesterolemia, and significant cardiovascular disease including premature coronary artery disease. We describe a case of a 56-year-old woman with homozygous familial hypercholesterolemia. She had been treated with low-density lipoprotein apheresis for 23 years. Preoperative echocardiography and coronary angiography showed severe aortic valve stenosis and right coronary artery stenosis. Aortic valve replacement with patch enlargement of the aortic valve annulus, and coronary artery bypass grafting were successfully performed. She was discharged uneventfully.</abstract><pub>The Japanese Society for Cardiovascular Surgery</pub><doi>10.4326/jjcvs.42.307</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0285-1474 |
| ispartof | Japanese Journal of Cardiovascular Surgery, 2013/07/15, Vol.42(4), pp.307-311 |
| issn | 0285-1474 1883-4108 |
| language | eng ; jpn |
| recordid | cdi_crossref_primary_10_4326_jjcvs_42_307 |
| source | J-STAGE Free; EZB-FREE-00999 freely available EZB journals |
| subjects | aortic valve stenosis familial hypercholesterolemia homozygote low-density lipoprotein |
| title | Cardiac Surgery in Homozygous Familial Hypercholesterolemia |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T22%3A02%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstage_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cardiac%20Surgery%20in%20Homozygous%20Familial%20Hypercholesterolemia&rft.jtitle=Japanese%20Journal%20of%20Cardiovascular%20Surgery&rft.au=Kawamura,%20Tomonori&rft.date=2013-07-15&rft.volume=42&rft.issue=4&rft.spage=307&rft.epage=311&rft.pages=307-311&rft.issn=0285-1474&rft.eissn=1883-4108&rft_id=info:doi/10.4326/jjcvs.42.307&rft_dat=%3Cjstage_cross%3Earticle_jjcvs_42_4_42_307_article_char_en%3C/jstage_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |