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Sacral Chordoma with Bilateral Inguinal Lymph Node Metastasis and Metachronous Tumor of the Clivus: A Case Report
Chordoma is a malignant neoplasm that arises from notochord remnants. Its incidence is highest above the age of 50 and behaves as a locally aggressive tumor with a slow growth rate. In most cases, complete surgical resection followed by radiotherapy offers the best chance of control. Developing meta...
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Published in: | Journal of orthopaedic case reports 2021-05, Vol.11 (5), p.1-3 |
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container_title | Journal of orthopaedic case reports |
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creator | Elghareeb, Manal Ms Allah, Mona Yy Abd Abdallah, Sieza S Eldesoky, Ahmed R Halim, Amal Af |
description | Chordoma is a malignant neoplasm that arises from notochord remnants. Its incidence is highest above the age of 50 and behaves as a locally aggressive tumor with a slow growth rate. In most cases, complete surgical resection followed by radiotherapy offers the best chance of control. Developing metachronous tumors or distant metastasis is uncommon.
A 56-year-old male patient of sacral chordoma was treated by surgery and radiotherapy. He developed later bilateral inguinal lymph node metastasis and metachronous clivus chordoma.
Chordomas are rare. Multiplicity of primary disease and distant metastasis could happen, so regular follow-up is warranted and more effective therapeutic modalities are needed. |
doi_str_mv | 10.13107/jocr.2021.v11.i05.2180 |
format | article |
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A 56-year-old male patient of sacral chordoma was treated by surgery and radiotherapy. He developed later bilateral inguinal lymph node metastasis and metachronous clivus chordoma.
Chordomas are rare. Multiplicity of primary disease and distant metastasis could happen, so regular follow-up is warranted and more effective therapeutic modalities are needed.</description><identifier>ISSN: 2250-0685</identifier><identifier>EISSN: 2321-3817</identifier><identifier>DOI: 10.13107/jocr.2021.v11.i05.2180</identifier><identifier>PMID: 34557428</identifier><language>eng</language><publisher>India: Indian Orthopaedic Research Group</publisher><subject>Case Report</subject><ispartof>Journal of orthopaedic case reports, 2021-05, Vol.11 (5), p.1-3</ispartof><rights>Copyright: © Indian Orthopaedic Research Group.</rights><rights>Copyright: © Indian Orthopaedic Research Group 2021</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422020/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422020/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34557428$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Elghareeb, Manal Ms</creatorcontrib><creatorcontrib>Allah, Mona Yy Abd</creatorcontrib><creatorcontrib>Abdallah, Sieza S</creatorcontrib><creatorcontrib>Eldesoky, Ahmed R</creatorcontrib><creatorcontrib>Halim, Amal Af</creatorcontrib><title>Sacral Chordoma with Bilateral Inguinal Lymph Node Metastasis and Metachronous Tumor of the Clivus: A Case Report</title><title>Journal of orthopaedic case reports</title><addtitle>J Orthop Case Rep</addtitle><description>Chordoma is a malignant neoplasm that arises from notochord remnants. Its incidence is highest above the age of 50 and behaves as a locally aggressive tumor with a slow growth rate. In most cases, complete surgical resection followed by radiotherapy offers the best chance of control. Developing metachronous tumors or distant metastasis is uncommon.
A 56-year-old male patient of sacral chordoma was treated by surgery and radiotherapy. He developed later bilateral inguinal lymph node metastasis and metachronous clivus chordoma.
Chordomas are rare. Multiplicity of primary disease and distant metastasis could happen, so regular follow-up is warranted and more effective therapeutic modalities are needed.</description><subject>Case Report</subject><issn>2250-0685</issn><issn>2321-3817</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpVkW9L5DAQxoN4nOL5Fc58ge3NJE3T-kLQ4qmwKnje65BNUxvZNmvSruy3N-s_FAYyk-F5JpkfIUcIGXIE-efRm5AxYJitETMHImNYwg7ZZ5zhjJcod1POBMygKMUeOYzxEQCQ5wwq_En2eC6EzFm5T57-aRP0ktadD43vNX12Y0fP3FKPdnt_NTxMbkjJfNOvOnrjG0uv7ahjChepHprX0nTBD36K9H7qfaC-pWNnab106yke01Na62jpnV35MP4iP1q9jPbw_Twg__-e39eXs_ntxVV9Op8ZlOnl3AhsobBywQtbYFHavDJSg1xUpZS8qlpR5VA2WgqG7aKVFTIQrNG81VWhDT8gJ2--q2nR28bYYUwfUqvgeh02ymunvncG16kHv1ZlztJuIRnINwMTfIzBtp9aBPUKQm1BqC0IlUCoBEJtQSTl76-jP3Ufa-cvMxCHYA</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Elghareeb, Manal Ms</creator><creator>Allah, Mona Yy Abd</creator><creator>Abdallah, Sieza S</creator><creator>Eldesoky, Ahmed R</creator><creator>Halim, Amal Af</creator><general>Indian Orthopaedic Research Group</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20210501</creationdate><title>Sacral Chordoma with Bilateral Inguinal Lymph Node Metastasis and Metachronous Tumor of the Clivus: A Case Report</title><author>Elghareeb, Manal Ms ; Allah, Mona Yy Abd ; Abdallah, Sieza S ; Eldesoky, Ahmed R ; Halim, Amal Af</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1750-3c51f06e7b36e6168e49c7a07b9877399f59408da7521fbf7912052da3fa96ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Case Report</topic><toplevel>online_resources</toplevel><creatorcontrib>Elghareeb, Manal Ms</creatorcontrib><creatorcontrib>Allah, Mona Yy Abd</creatorcontrib><creatorcontrib>Abdallah, Sieza S</creatorcontrib><creatorcontrib>Eldesoky, Ahmed R</creatorcontrib><creatorcontrib>Halim, Amal Af</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of orthopaedic case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elghareeb, Manal Ms</au><au>Allah, Mona Yy Abd</au><au>Abdallah, Sieza S</au><au>Eldesoky, Ahmed R</au><au>Halim, Amal Af</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sacral Chordoma with Bilateral Inguinal Lymph Node Metastasis and Metachronous Tumor of the Clivus: A Case Report</atitle><jtitle>Journal of orthopaedic case reports</jtitle><addtitle>J Orthop Case Rep</addtitle><date>2021-05-01</date><risdate>2021</risdate><volume>11</volume><issue>5</issue><spage>1</spage><epage>3</epage><pages>1-3</pages><issn>2250-0685</issn><eissn>2321-3817</eissn><abstract>Chordoma is a malignant neoplasm that arises from notochord remnants. Its incidence is highest above the age of 50 and behaves as a locally aggressive tumor with a slow growth rate. In most cases, complete surgical resection followed by radiotherapy offers the best chance of control. Developing metachronous tumors or distant metastasis is uncommon.
A 56-year-old male patient of sacral chordoma was treated by surgery and radiotherapy. He developed later bilateral inguinal lymph node metastasis and metachronous clivus chordoma.
Chordomas are rare. Multiplicity of primary disease and distant metastasis could happen, so regular follow-up is warranted and more effective therapeutic modalities are needed.</abstract><cop>India</cop><pub>Indian Orthopaedic Research Group</pub><pmid>34557428</pmid><doi>10.13107/jocr.2021.v11.i05.2180</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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title | Sacral Chordoma with Bilateral Inguinal Lymph Node Metastasis and Metachronous Tumor of the Clivus: A Case Report |
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