Metastatic Malignant Thymoma to the Abdomen: A SEER Database Review and Assessment of Treatment Strategies
Thymoma is a neoplasm occurring in 0.15 of 100,000 persons/year. Abdominal metastases are rare. We report the incidence of malignant thymoma (MT) and suggest imaging and treatment options for cases of abdominal metastasis. A National Cancer Institute's Surveillance, Epidemiology and End Results...
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Veröffentlicht in: | World journal of oncology 2017-10, Vol.8 (5), p.147-150 |
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description | Thymoma is a neoplasm occurring in 0.15 of 100,000 persons/year. Abdominal metastases are rare. We report the incidence of malignant thymoma (MT) and suggest imaging and treatment options for cases of abdominal metastasis.
A National Cancer Institute's Surveillance, Epidemiology and End Results database review was conducted to identify MT cases, followed by a literature review examining cases of metastases to the abdomen. Incidence rates were calculated, and symptoms, treatments, size and location of tumors, disease-free interval (DFI), and survival time were recorded.
From 1973 to 2008, a total of 1,588 MT cases were identified (45.4 cases/year), which were extrapolated to 2,724 over 60 years. Incidence has risen from 17 cases in 1973 to 90 cases in 2008, with a larger incidence in males than females (0.23 vs. 0.17 per 100,000). There were 25 cases of abdominal metastasis (0.92%), 13 of which were asymptomatic. There was a wide variety of DFI and survival noted amongst the case reports. Multiple treatment modalities were used.
The incidence of MT is on the rise with a male predominance. All patients should receive routine imaging to look for extrathoracic metastases as half will not have symptoms. All patients with abdominal metastases should be treated using a multimodal approach. |
doi_str_mv | 10.14740/wjon1057w |
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A National Cancer Institute's Surveillance, Epidemiology and End Results database review was conducted to identify MT cases, followed by a literature review examining cases of metastases to the abdomen. Incidence rates were calculated, and symptoms, treatments, size and location of tumors, disease-free interval (DFI), and survival time were recorded.
From 1973 to 2008, a total of 1,588 MT cases were identified (45.4 cases/year), which were extrapolated to 2,724 over 60 years. Incidence has risen from 17 cases in 1973 to 90 cases in 2008, with a larger incidence in males than females (0.23 vs. 0.17 per 100,000). There were 25 cases of abdominal metastasis (0.92%), 13 of which were asymptomatic. There was a wide variety of DFI and survival noted amongst the case reports. Multiple treatment modalities were used.
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A National Cancer Institute's Surveillance, Epidemiology and End Results database review was conducted to identify MT cases, followed by a literature review examining cases of metastases to the abdomen. Incidence rates were calculated, and symptoms, treatments, size and location of tumors, disease-free interval (DFI), and survival time were recorded.
From 1973 to 2008, a total of 1,588 MT cases were identified (45.4 cases/year), which were extrapolated to 2,724 over 60 years. Incidence has risen from 17 cases in 1973 to 90 cases in 2008, with a larger incidence in males than females (0.23 vs. 0.17 per 100,000). There were 25 cases of abdominal metastasis (0.92%), 13 of which were asymptomatic. There was a wide variety of DFI and survival noted amongst the case reports. Multiple treatment modalities were used.
The incidence of MT is on the rise with a male predominance. All patients should receive routine imaging to look for extrathoracic metastases as half will not have symptoms. All patients with abdominal metastases should be treated using a multimodal approach.</description><subject>Original</subject><issn>1920-4531</issn><issn>1920-454X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpVUNtKw0AQXUSxpfbFD5B9FqK72Vw2PghB6wVahLaCb2GyO2lTmmzJri39e2OrQedlbuecGQ4hl5zd8CAO2O1uZWrOwnh3Qvo88ZkXhMHHaVcL3iNDa1esDSHaIT8nPT_55oa8T1YTdGAduFLRCazLRQ21o_PlvjIVUGeoWyJNc20qrO9oSmej0ZQ-goMcLNIpbkvcUag1Ta1Fa1uUo6ag8wbBHZqZa8DhokR7Qc4KWFsc_uQBeX8azR9evPHb8-tDOvYUD6LAk1GY6JiLkGklQTAd8UJCIRT3c8Zj0FhEDCVPpNJxArniUS51nkQyRF8DiAG5P-puPvMKtWq_aGCdbZqygmafGSiz_5u6XGYLs83CSMYyCVqB66OAaoy1DRYdl7PsYHrWmd6Cr_5e66C_FosvhSt_6Q</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Helm, J Matthew</creator><creator>Lavy, Dan</creator><creator>Figueroa-Bodine, Jazmine</creator><creator>Joseph, Saju</creator><general>Elmer Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20171001</creationdate><title>Metastatic Malignant Thymoma to the Abdomen: A SEER Database Review and Assessment of Treatment Strategies</title><author>Helm, J Matthew ; Lavy, Dan ; Figueroa-Bodine, Jazmine ; Joseph, Saju</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1464-8659d71350dc8a30d61f8af3c12b017adef60e8198cd79abc16b8db9685e2daa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Original</topic><toplevel>online_resources</toplevel><creatorcontrib>Helm, J Matthew</creatorcontrib><creatorcontrib>Lavy, Dan</creatorcontrib><creatorcontrib>Figueroa-Bodine, Jazmine</creatorcontrib><creatorcontrib>Joseph, Saju</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Helm, J Matthew</au><au>Lavy, Dan</au><au>Figueroa-Bodine, Jazmine</au><au>Joseph, Saju</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metastatic Malignant Thymoma to the Abdomen: A SEER Database Review and Assessment of Treatment Strategies</atitle><jtitle>World journal of oncology</jtitle><addtitle>World J Oncol</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>8</volume><issue>5</issue><spage>147</spage><epage>150</epage><pages>147-150</pages><issn>1920-4531</issn><eissn>1920-454X</eissn><abstract>Thymoma is a neoplasm occurring in 0.15 of 100,000 persons/year. Abdominal metastases are rare. We report the incidence of malignant thymoma (MT) and suggest imaging and treatment options for cases of abdominal metastasis.
A National Cancer Institute's Surveillance, Epidemiology and End Results database review was conducted to identify MT cases, followed by a literature review examining cases of metastases to the abdomen. Incidence rates were calculated, and symptoms, treatments, size and location of tumors, disease-free interval (DFI), and survival time were recorded.
From 1973 to 2008, a total of 1,588 MT cases were identified (45.4 cases/year), which were extrapolated to 2,724 over 60 years. Incidence has risen from 17 cases in 1973 to 90 cases in 2008, with a larger incidence in males than females (0.23 vs. 0.17 per 100,000). There were 25 cases of abdominal metastasis (0.92%), 13 of which were asymptomatic. There was a wide variety of DFI and survival noted amongst the case reports. Multiple treatment modalities were used.
The incidence of MT is on the rise with a male predominance. All patients should receive routine imaging to look for extrathoracic metastases as half will not have symptoms. All patients with abdominal metastases should be treated using a multimodal approach.</abstract><cop>Canada</cop><pub>Elmer Press</pub><pmid>29147451</pmid><doi>10.14740/wjon1057w</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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title | Metastatic Malignant Thymoma to the Abdomen: A SEER Database Review and Assessment of Treatment Strategies |
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