Primary Ovarian Carcinoid Tumors

Primary ovarian carcinoid tumors were reviewed from Mayo Clinic and Colorado Tumor Registry data. A total of 17 patients with this diagnosis were identified. Histologic analysis of these carcinoid tumors revealed 9 (53%) were insular, 5 (29%) were trabecular, and 4 (26%) were strumal carcinoid with...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Gynecologic oncology 1996-05, Vol.61 (2), p.259-265
Hauptverfasser: Davis, Kevin P., Hartmann, Lynn K., Keeney, Gary L., Shapiro, Howard
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 265
container_issue 2
container_start_page 259
container_title Gynecologic oncology
container_volume 61
creator Davis, Kevin P.
Hartmann, Lynn K.
Keeney, Gary L.
Shapiro, Howard
description Primary ovarian carcinoid tumors were reviewed from Mayo Clinic and Colorado Tumor Registry data. A total of 17 patients with this diagnosis were identified. Histologic analysis of these carcinoid tumors revealed 9 (53%) were insular, 5 (29%) were trabecular, and 4 (26%) were strumal carcinoid with or without a mature dermoid component. There were 11 patients with stage I and 6 patients with stage III or IV disease at diagnosis. Carcinoid syndrome was found in 29% of patients. Pressure or pain with defecation was noted in 41% of cases. Recurrence of tumor occurred in 1 of 11 patients with suspected stage I disease 13 years after initial diagnosis. Overall survival was excellent in the 11 patients whose disease was confined to one ovary (100% 5-year survival), but only 1 of 6 patients survived (33% 5-year survival) if advanced stage at diagnosis. Systemic chemotherapy for advanced disease achieved a complete response in 1 patient and stable disease in another. Although rare, primary ovarian carcinoid tumors treated with surgery alone and found to be confined to the ovary can be expected to have an excellent overall outcome.
doi_str_mv 10.1006/gyno.1996.0136
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_78005686</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0090825896901365</els_id><sourcerecordid>78005686</sourcerecordid><originalsourceid>FETCH-LOGICAL-c368t-c670b2db10eb074ff351f2390971837b1eec8195991a59808dac4f415655fadc3</originalsourceid><addsrcrecordid>eNp1kD1PwzAQhi0EKqWwsiFlQGwJ5zh27BFVfEmVylBmy3FsZJTExW4q8e9JlKgb0w3vc6_uHoRuMWQYgD1-_XY-w0KwDDBhZ2iJQdCUcSrO0RJAQMpzyi_RVYzfAEAA5wu04CxnuCiWKPkIrlXhN9keVXCqS9YqaNd5Vye7vvUhXqMLq5pobua5Qp8vz7v1W7rZvr6vnzapJowfUs1KqPK6wmAqKAtrCcU2JwJEiTkpK2yM5lhQIbCiggOvlS5sgSmj1KpakxV6mHr3wf_0Jh5k66I2TaM64_soSw5AGWcDmE2gDj7GYKzcTy9IDHJUIkclclQiRyXDwt3c3FetqU_47GDI7-dcRa0aG1SnXTxhBLgQfMT4hJnBwtGZIKN2ptOmdsHog6y9---CPxKoes0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>78005686</pqid></control><display><type>article</type><title>Primary Ovarian Carcinoid Tumors</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Davis, Kevin P. ; Hartmann, Lynn K. ; Keeney, Gary L. ; Shapiro, Howard</creator><creatorcontrib>Davis, Kevin P. ; Hartmann, Lynn K. ; Keeney, Gary L. ; Shapiro, Howard</creatorcontrib><description>Primary ovarian carcinoid tumors were reviewed from Mayo Clinic and Colorado Tumor Registry data. A total of 17 patients with this diagnosis were identified. Histologic analysis of these carcinoid tumors revealed 9 (53%) were insular, 5 (29%) were trabecular, and 4 (26%) were strumal carcinoid with or without a mature dermoid component. There were 11 patients with stage I and 6 patients with stage III or IV disease at diagnosis. Carcinoid syndrome was found in 29% of patients. Pressure or pain with defecation was noted in 41% of cases. Recurrence of tumor occurred in 1 of 11 patients with suspected stage I disease 13 years after initial diagnosis. Overall survival was excellent in the 11 patients whose disease was confined to one ovary (100% 5-year survival), but only 1 of 6 patients survived (33% 5-year survival) if advanced stage at diagnosis. Systemic chemotherapy for advanced disease achieved a complete response in 1 patient and stable disease in another. Although rare, primary ovarian carcinoid tumors treated with surgery alone and found to be confined to the ovary can be expected to have an excellent overall outcome.</description><identifier>ISSN: 0090-8258</identifier><identifier>EISSN: 1095-6859</identifier><identifier>DOI: 10.1006/gyno.1996.0136</identifier><identifier>PMID: 8626144</identifier><identifier>CODEN: GYNOA3</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Carcinoid Tumor - pathology ; Carcinoid Tumor - surgery ; Female ; Female genital diseases ; Follow-Up Studies ; Gynecology. Andrology. Obstetrics ; Humans ; Medical sciences ; Middle Aged ; Neoplasm Recurrence, Local ; Neoplasm Staging ; Ovarian Neoplasms - pathology ; Ovarian Neoplasms - surgery ; Retrospective Studies ; Survival Analysis ; Tumors</subject><ispartof>Gynecologic oncology, 1996-05, Vol.61 (2), p.259-265</ispartof><rights>1996 Academic Press</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-c670b2db10eb074ff351f2390971837b1eec8195991a59808dac4f415655fadc3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/gyno.1996.0136$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3089984$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8626144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Davis, Kevin P.</creatorcontrib><creatorcontrib>Hartmann, Lynn K.</creatorcontrib><creatorcontrib>Keeney, Gary L.</creatorcontrib><creatorcontrib>Shapiro, Howard</creatorcontrib><title>Primary Ovarian Carcinoid Tumors</title><title>Gynecologic oncology</title><addtitle>Gynecol Oncol</addtitle><description>Primary ovarian carcinoid tumors were reviewed from Mayo Clinic and Colorado Tumor Registry data. A total of 17 patients with this diagnosis were identified. Histologic analysis of these carcinoid tumors revealed 9 (53%) were insular, 5 (29%) were trabecular, and 4 (26%) were strumal carcinoid with or without a mature dermoid component. There were 11 patients with stage I and 6 patients with stage III or IV disease at diagnosis. Carcinoid syndrome was found in 29% of patients. Pressure or pain with defecation was noted in 41% of cases. Recurrence of tumor occurred in 1 of 11 patients with suspected stage I disease 13 years after initial diagnosis. Overall survival was excellent in the 11 patients whose disease was confined to one ovary (100% 5-year survival), but only 1 of 6 patients survived (33% 5-year survival) if advanced stage at diagnosis. Systemic chemotherapy for advanced disease achieved a complete response in 1 patient and stable disease in another. Although rare, primary ovarian carcinoid tumors treated with surgery alone and found to be confined to the ovary can be expected to have an excellent overall outcome.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Carcinoid Tumor - pathology</subject><subject>Carcinoid Tumor - surgery</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Follow-Up Studies</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local</subject><subject>Neoplasm Staging</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Ovarian Neoplasms - surgery</subject><subject>Retrospective Studies</subject><subject>Survival Analysis</subject><subject>Tumors</subject><issn>0090-8258</issn><issn>1095-6859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kD1PwzAQhi0EKqWwsiFlQGwJ5zh27BFVfEmVylBmy3FsZJTExW4q8e9JlKgb0w3vc6_uHoRuMWQYgD1-_XY-w0KwDDBhZ2iJQdCUcSrO0RJAQMpzyi_RVYzfAEAA5wu04CxnuCiWKPkIrlXhN9keVXCqS9YqaNd5Vye7vvUhXqMLq5pobua5Qp8vz7v1W7rZvr6vnzapJowfUs1KqPK6wmAqKAtrCcU2JwJEiTkpK2yM5lhQIbCiggOvlS5sgSmj1KpakxV6mHr3wf_0Jh5k66I2TaM64_soSw5AGWcDmE2gDj7GYKzcTy9IDHJUIkclclQiRyXDwt3c3FetqU_47GDI7-dcRa0aG1SnXTxhBLgQfMT4hJnBwtGZIKN2ptOmdsHog6y9---CPxKoes0</recordid><startdate>19960501</startdate><enddate>19960501</enddate><creator>Davis, Kevin P.</creator><creator>Hartmann, Lynn K.</creator><creator>Keeney, Gary L.</creator><creator>Shapiro, Howard</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>19960501</creationdate><title>Primary Ovarian Carcinoid Tumors</title><author>Davis, Kevin P. ; Hartmann, Lynn K. ; Keeney, Gary L. ; Shapiro, Howard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-c670b2db10eb074ff351f2390971837b1eec8195991a59808dac4f415655fadc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Carcinoid Tumor - pathology</topic><topic>Carcinoid Tumor - surgery</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Follow-Up Studies</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Recurrence, Local</topic><topic>Neoplasm Staging</topic><topic>Ovarian Neoplasms - pathology</topic><topic>Ovarian Neoplasms - surgery</topic><topic>Retrospective Studies</topic><topic>Survival Analysis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Davis, Kevin P.</creatorcontrib><creatorcontrib>Hartmann, Lynn K.</creatorcontrib><creatorcontrib>Keeney, Gary L.</creatorcontrib><creatorcontrib>Shapiro, Howard</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Gynecologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Davis, Kevin P.</au><au>Hartmann, Lynn K.</au><au>Keeney, Gary L.</au><au>Shapiro, Howard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary Ovarian Carcinoid Tumors</atitle><jtitle>Gynecologic oncology</jtitle><addtitle>Gynecol Oncol</addtitle><date>1996-05-01</date><risdate>1996</risdate><volume>61</volume><issue>2</issue><spage>259</spage><epage>265</epage><pages>259-265</pages><issn>0090-8258</issn><eissn>1095-6859</eissn><coden>GYNOA3</coden><abstract>Primary ovarian carcinoid tumors were reviewed from Mayo Clinic and Colorado Tumor Registry data. A total of 17 patients with this diagnosis were identified. Histologic analysis of these carcinoid tumors revealed 9 (53%) were insular, 5 (29%) were trabecular, and 4 (26%) were strumal carcinoid with or without a mature dermoid component. There were 11 patients with stage I and 6 patients with stage III or IV disease at diagnosis. Carcinoid syndrome was found in 29% of patients. Pressure or pain with defecation was noted in 41% of cases. Recurrence of tumor occurred in 1 of 11 patients with suspected stage I disease 13 years after initial diagnosis. Overall survival was excellent in the 11 patients whose disease was confined to one ovary (100% 5-year survival), but only 1 of 6 patients survived (33% 5-year survival) if advanced stage at diagnosis. Systemic chemotherapy for advanced disease achieved a complete response in 1 patient and stable disease in another. Although rare, primary ovarian carcinoid tumors treated with surgery alone and found to be confined to the ovary can be expected to have an excellent overall outcome.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>8626144</pmid><doi>10.1006/gyno.1996.0136</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0090-8258
ispartof Gynecologic oncology, 1996-05, Vol.61 (2), p.259-265
issn 0090-8258
1095-6859
language eng
recordid cdi_proquest_miscellaneous_78005686
source MEDLINE; Elsevier ScienceDirect Journals
subjects Adult
Aged
Aged, 80 and over
Biological and medical sciences
Carcinoid Tumor - pathology
Carcinoid Tumor - surgery
Female
Female genital diseases
Follow-Up Studies
Gynecology. Andrology. Obstetrics
Humans
Medical sciences
Middle Aged
Neoplasm Recurrence, Local
Neoplasm Staging
Ovarian Neoplasms - pathology
Ovarian Neoplasms - surgery
Retrospective Studies
Survival Analysis
Tumors
title Primary Ovarian Carcinoid Tumors
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T18%3A32%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Primary%20Ovarian%20Carcinoid%20Tumors&rft.jtitle=Gynecologic%20oncology&rft.au=Davis,%20Kevin%20P.&rft.date=1996-05-01&rft.volume=61&rft.issue=2&rft.spage=259&rft.epage=265&rft.pages=259-265&rft.issn=0090-8258&rft.eissn=1095-6859&rft.coden=GYNOA3&rft_id=info:doi/10.1006/gyno.1996.0136&rft_dat=%3Cproquest_cross%3E78005686%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=78005686&rft_id=info:pmid/8626144&rft_els_id=S0090825896901365&rfr_iscdi=true