P262 Pulmonary benign metastasing leiomyoma: an single-institution case series
IntroductionPulmonary benign metastasizing leiomyoma (BML) is a rare and often asymptomatic presentation of smooth muscle tumour of uterine origin, occurring within the lung. Just over a hundred individual cases have been described in the literature; with two series of ten patients each, from contin...
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Veröffentlicht in: | Thorax 2017-12, Vol.72 (Suppl 3), p.A225 |
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description | IntroductionPulmonary benign metastasizing leiomyoma (BML) is a rare and often asymptomatic presentation of smooth muscle tumour of uterine origin, occurring within the lung. Just over a hundred individual cases have been described in the literature; with two series of ten patients each, from continental Europe and North America.ObjectivesWe sought to present the first comprehensive descriptive series from a contemporary U.K. population.MethodologyPatients at a single U.K. thoracic surgical centre, between 2003 and 2017, were identified from prospective histology databases. Retrospective data was collected from physical and electronic data sources, and cross-referenced for accuracy.Results6 patients – all postmenopausal females – were identified over a 15 year period. Average age was 44±8 years (mean ±SD). Half of the patients were asymptomatic with an incidental finding of pulmonary nodules, whilst the remaining 50% complained of nonspecific respiratory symptomatology. Plain imaging of the chest failed to reveal any abnormality in 2 (33.3%) patients. 5 (88.3%) patients had multiple lesions – median of 9 (range 2 to 12) – with bilateral distribution; measuring a median 11 mm (range 7 to 27) in size on cross-sectional imaging. All patients underwent diagnostic surgical wedge biopsy, with 5 (88.3%) procedures completed thoracoscopically; and no perioperative morbidity. 4 (66.7%) patients had a history of previous hysterectomy, and a further patient underwent a hysterectomy following the diagnosis of BML – all for uterine leiomyomata. 4 (66.7%) patients underwent oophorectomy, whilst one patient required hormonal suppression therapy. Survival was 100% at a median follow up of 37 months (range 4 to 150).ConclusionBML is a rare clinical entity accounting for a small proportion of patients presenting with pulmonary nodules. Following successful tissue diagnosis, outcomes with conservative or medical management are excellent. |
doi_str_mv | 10.1136/thoraxjnl-2017-210983.404 |
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Just over a hundred individual cases have been described in the literature; with two series of ten patients each, from continental Europe and North America.ObjectivesWe sought to present the first comprehensive descriptive series from a contemporary U.K. population.MethodologyPatients at a single U.K. thoracic surgical centre, between 2003 and 2017, were identified from prospective histology databases. Retrospective data was collected from physical and electronic data sources, and cross-referenced for accuracy.Results6 patients – all postmenopausal females – were identified over a 15 year period. Average age was 44±8 years (mean ±SD). Half of the patients were asymptomatic with an incidental finding of pulmonary nodules, whilst the remaining 50% complained of nonspecific respiratory symptomatology. Plain imaging of the chest failed to reveal any abnormality in 2 (33.3%) patients. 5 (88.3%) patients had multiple lesions – median of 9 (range 2 to 12) – with bilateral distribution; measuring a median 11 mm (range 7 to 27) in size on cross-sectional imaging. All patients underwent diagnostic surgical wedge biopsy, with 5 (88.3%) procedures completed thoracoscopically; and no perioperative morbidity. 4 (66.7%) patients had a history of previous hysterectomy, and a further patient underwent a hysterectomy following the diagnosis of BML – all for uterine leiomyomata. 4 (66.7%) patients underwent oophorectomy, whilst one patient required hormonal suppression therapy. Survival was 100% at a median follow up of 37 months (range 4 to 150).ConclusionBML is a rare clinical entity accounting for a small proportion of patients presenting with pulmonary nodules. Following successful tissue diagnosis, outcomes with conservative or medical management are excellent.</description><identifier>ISSN: 0040-6376</identifier><identifier>EISSN: 1468-3296</identifier><identifier>DOI: 10.1136/thoraxjnl-2017-210983.404</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Fibroids ; Patients</subject><ispartof>Thorax, 2017-12, Vol.72 (Suppl 3), p.A225</ispartof><rights>2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2017 © 2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</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>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Chandarana, K</creatorcontrib><creatorcontrib>Rizzo, V</creatorcontrib><creatorcontrib>Caruana, EJ</creatorcontrib><creatorcontrib>Dawson, AG</creatorcontrib><creatorcontrib>Rathinam, S</creatorcontrib><creatorcontrib>Nakas, A</creatorcontrib><title>P262 Pulmonary benign metastasing leiomyoma: an single-institution case series</title><title>Thorax</title><description>IntroductionPulmonary benign metastasizing leiomyoma (BML) is a rare and often asymptomatic presentation of smooth muscle tumour of uterine origin, occurring within the lung. Just over a hundred individual cases have been described in the literature; with two series of ten patients each, from continental Europe and North America.ObjectivesWe sought to present the first comprehensive descriptive series from a contemporary U.K. population.MethodologyPatients at a single U.K. thoracic surgical centre, between 2003 and 2017, were identified from prospective histology databases. Retrospective data was collected from physical and electronic data sources, and cross-referenced for accuracy.Results6 patients – all postmenopausal females – were identified over a 15 year period. Average age was 44±8 years (mean ±SD). Half of the patients were asymptomatic with an incidental finding of pulmonary nodules, whilst the remaining 50% complained of nonspecific respiratory symptomatology. Plain imaging of the chest failed to reveal any abnormality in 2 (33.3%) patients. 5 (88.3%) patients had multiple lesions – median of 9 (range 2 to 12) – with bilateral distribution; measuring a median 11 mm (range 7 to 27) in size on cross-sectional imaging. All patients underwent diagnostic surgical wedge biopsy, with 5 (88.3%) procedures completed thoracoscopically; and no perioperative morbidity. 4 (66.7%) patients had a history of previous hysterectomy, and a further patient underwent a hysterectomy following the diagnosis of BML – all for uterine leiomyomata. 4 (66.7%) patients underwent oophorectomy, whilst one patient required hormonal suppression therapy. Survival was 100% at a median follow up of 37 months (range 4 to 150).ConclusionBML is a rare clinical entity accounting for a small proportion of patients presenting with pulmonary nodules. Following successful tissue diagnosis, outcomes with conservative or medical management are excellent.</description><subject>Fibroids</subject><subject>Patients</subject><issn>0040-6376</issn><issn>1468-3296</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNo9kE9LxDAQxYMouK5-h4jn6EySJo03WfwHC-5BzyHtpmtKm65NC-7Ni1_UT2KXFWHgwfB4M-9HyCXCNaJQN8N717vPOjaMA2rGEUwuriXIIzJDqXImuFHHZAYggSmh1Sk5S6kGgBxRz8hqxRX_-fpejU3bRdfvaOFj2ETa-sGlaULc0MaHrt11rbulLtL9qvEsxDSEYRxCF2npkqfJ98Gnc3JSuSb5iz-dk7eH-9fFE1u-PD4v7pasQC4ly7nI1TpTRVFA5QWU5fS-5GvjZSbKyivNM5lXDlBAVeYGufOK69KIQqATazEnV4fcbd99jD4Ntu7GPk4nLRoNhmca-eSSB1fR1nbbh3ZqaBHsnp39Z2f37OyBnZ3YiV-UjGXS</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Chandarana, K</creator><creator>Rizzo, V</creator><creator>Caruana, EJ</creator><creator>Dawson, AG</creator><creator>Rathinam, S</creator><creator>Nakas, A</creator><general>BMJ Publishing Group LTD</general><scope>3V.</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>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201712</creationdate><title>P262 Pulmonary benign metastasing leiomyoma: an single-institution case series</title><author>Chandarana, K ; Rizzo, V ; Caruana, EJ ; Dawson, AG ; Rathinam, S ; Nakas, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1244-82386d56bbb0fe30cc01742d9e453cfe672548fa0130fc8912ae627c93b31a3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Fibroids</topic><topic>Patients</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chandarana, K</creatorcontrib><creatorcontrib>Rizzo, V</creatorcontrib><creatorcontrib>Caruana, EJ</creatorcontrib><creatorcontrib>Dawson, AG</creatorcontrib><creatorcontrib>Rathinam, S</creatorcontrib><creatorcontrib>Nakas, A</creatorcontrib><collection>ProQuest Central (Corporate)</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>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>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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><jtitle>Thorax</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chandarana, K</au><au>Rizzo, V</au><au>Caruana, EJ</au><au>Dawson, AG</au><au>Rathinam, S</au><au>Nakas, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>P262 Pulmonary benign metastasing leiomyoma: an single-institution case series</atitle><jtitle>Thorax</jtitle><date>2017-12</date><risdate>2017</risdate><volume>72</volume><issue>Suppl 3</issue><spage>A225</spage><pages>A225-</pages><issn>0040-6376</issn><eissn>1468-3296</eissn><abstract>IntroductionPulmonary benign metastasizing leiomyoma (BML) is a rare and often asymptomatic presentation of smooth muscle tumour of uterine origin, occurring within the lung. Just over a hundred individual cases have been described in the literature; with two series of ten patients each, from continental Europe and North America.ObjectivesWe sought to present the first comprehensive descriptive series from a contemporary U.K. population.MethodologyPatients at a single U.K. thoracic surgical centre, between 2003 and 2017, were identified from prospective histology databases. Retrospective data was collected from physical and electronic data sources, and cross-referenced for accuracy.Results6 patients – all postmenopausal females – were identified over a 15 year period. Average age was 44±8 years (mean ±SD). Half of the patients were asymptomatic with an incidental finding of pulmonary nodules, whilst the remaining 50% complained of nonspecific respiratory symptomatology. Plain imaging of the chest failed to reveal any abnormality in 2 (33.3%) patients. 5 (88.3%) patients had multiple lesions – median of 9 (range 2 to 12) – with bilateral distribution; measuring a median 11 mm (range 7 to 27) in size on cross-sectional imaging. All patients underwent diagnostic surgical wedge biopsy, with 5 (88.3%) procedures completed thoracoscopically; and no perioperative morbidity. 4 (66.7%) patients had a history of previous hysterectomy, and a further patient underwent a hysterectomy following the diagnosis of BML – all for uterine leiomyomata. 4 (66.7%) patients underwent oophorectomy, whilst one patient required hormonal suppression therapy. Survival was 100% at a median follow up of 37 months (range 4 to 150).ConclusionBML is a rare clinical entity accounting for a small proportion of patients presenting with pulmonary nodules. Following successful tissue diagnosis, outcomes with conservative or medical management are excellent.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/thoraxjnl-2017-210983.404</doi><oa>free_for_read</oa></addata></record> |
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title | P262 Pulmonary benign metastasing leiomyoma: an single-institution case series |
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