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Striated muscle-derived intraspinal choristoma: A case report
Choristoma is a mass of tissue that is histologically normal for the organ or part of the body from which it originates, but is located at an abnormal site. Choristoma of the nervous system involves the occurrence of residual dysplastic tissues outside the nervous system and exhibits a low incidence...
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Published in: | Oncology letters 2017-08, Vol.14 (2), p.1787-1789 |
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description | Choristoma is a mass of tissue that is histologically normal for the organ or part of the body from which it originates, but is located at an abnormal site. Choristoma of the nervous system involves the occurrence of residual dysplastic tissues outside the nervous system and exhibits a low incidence. Thus far, there has been no prior report of intraspinal choristoma originating from the striated muscle. The patient in the present case was a young man who was admitted to the hospital wing to intermittent lumbago. A lumbar magnetic resonance imaging examination revealed a cystic-solid lesion in the spinal canal at the S1 level. Preoperatively, the lesion was suspected to be a teratoma and was therefore completely removed. The postoperative pathological report suggested that the mass was an intraspinal choristoma, a benign lesion associated with a good prognosis, which had originated from striated muscle. Early diagnosis and treatment can prevent progression of nerve dysfunction. The patient recovered well postoperatively and the symptoms of lower back pain disappeared. Although intraspinal choristomas are rare, when a lesion in the spinal canal is diagnosed, it should be considered in the differential diagnosis tumors. |
doi_str_mv | 10.3892/ol.2017.6302 |
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Choristoma of the nervous system involves the occurrence of residual dysplastic tissues outside the nervous system and exhibits a low incidence. Thus far, there has been no prior report of intraspinal choristoma originating from the striated muscle. The patient in the present case was a young man who was admitted to the hospital wing to intermittent lumbago. A lumbar magnetic resonance imaging examination revealed a cystic-solid lesion in the spinal canal at the S1 level. Preoperatively, the lesion was suspected to be a teratoma and was therefore completely removed. The postoperative pathological report suggested that the mass was an intraspinal choristoma, a benign lesion associated with a good prognosis, which had originated from striated muscle. Early diagnosis and treatment can prevent progression of nerve dysfunction. The patient recovered well postoperatively and the symptoms of lower back pain disappeared. Although intraspinal choristomas are rare, when a lesion in the spinal canal is diagnosed, it should be considered in the differential diagnosis tumors.</description><identifier>ISSN: 1792-1074</identifier><identifier>EISSN: 1792-1082</identifier><identifier>DOI: 10.3892/ol.2017.6302</identifier><identifier>PMID: 28789410</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>Antigens ; Back pain ; Calcification ; Care and treatment ; Case reports ; Case studies ; choristoma ; Diagnosis ; Hamartoma ; Hypotheses ; intraspinal ; Medical diagnosis ; Nervous system ; NMR ; Nuclear magnetic resonance ; Pathogenesis ; pathology ; Spinal cord</subject><ispartof>Oncology letters, 2017-08, Vol.14 (2), p.1787-1789</ispartof><rights>Copyright © 2017, Spandidos Publications</rights><rights>COPYRIGHT 2017 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2017</rights><rights>Copyright © 2017, Spandidos Publications 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-d83ec38a8988cf03e6e1b28bfe93a992f1d935653b3e080ed4089e33d0b469ac3</citedby><cites>FETCH-LOGICAL-c539t-d83ec38a8988cf03e6e1b28bfe93a992f1d935653b3e080ed4089e33d0b469ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529863/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529863/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28789410$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, Peng-Fei</creatorcontrib><creatorcontrib>Qu, Li-Mei</creatorcontrib><creatorcontrib>Li, Ming</creatorcontrib><creatorcontrib>Qi, Bin</creatorcontrib><title>Striated muscle-derived intraspinal choristoma: A case report</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>Choristoma is a mass of tissue that is histologically normal for the organ or part of the body from which it originates, but is located at an abnormal site. Choristoma of the nervous system involves the occurrence of residual dysplastic tissues outside the nervous system and exhibits a low incidence. Thus far, there has been no prior report of intraspinal choristoma originating from the striated muscle. The patient in the present case was a young man who was admitted to the hospital wing to intermittent lumbago. A lumbar magnetic resonance imaging examination revealed a cystic-solid lesion in the spinal canal at the S1 level. Preoperatively, the lesion was suspected to be a teratoma and was therefore completely removed. The postoperative pathological report suggested that the mass was an intraspinal choristoma, a benign lesion associated with a good prognosis, which had originated from striated muscle. Early diagnosis and treatment can prevent progression of nerve dysfunction. The patient recovered well postoperatively and the symptoms of lower back pain disappeared. Although intraspinal choristomas are rare, when a lesion in the spinal canal is diagnosed, it should be considered in the differential diagnosis tumors.</description><subject>Antigens</subject><subject>Back pain</subject><subject>Calcification</subject><subject>Care and treatment</subject><subject>Case reports</subject><subject>Case studies</subject><subject>choristoma</subject><subject>Diagnosis</subject><subject>Hamartoma</subject><subject>Hypotheses</subject><subject>intraspinal</subject><subject>Medical diagnosis</subject><subject>Nervous system</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Pathogenesis</subject><subject>pathology</subject><subject>Spinal cord</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNptkt1rFDEUxQdRbGn75rMMKOKDs-ZjMpMUFJaitbDQB_U5ZJI73ZTMZEwyBf97M926dqW5D_n63ZNwOEXxCqMV5YJ89G5FEG5XDUXkWXGMW0EqjDh5vl-39VFxFuMtyoM1mPPmZXFEeMtFjdFx8el7ClYlMOUwR-2gMhDsXd7aMQUVJzsqV-qtDzYmP6jzcl1qFaEMMPmQTosXvXIRzh7mk-Ln1y8_Lr5Vm-vLq4v1ptKMilQZTkFTrrjgXPeIQgO4I7zrQVAlBOmxEZQ1jHYUEEdgasQFUGpQVzdCaXpSfN7pTnM3gNGwfM7JKdhBhd_SKysPb0a7lTf-TjJGBG9oFnj_IBD8rxlikoONGpxTI_g5SixIywRD9-ib_9BbP4dsw0K1omZNK5p_1I1yIO3Y-_yuXkTlmqE6m18TnKnVE1QuA4PVfoTe5vODhnePGragXNpG7-Zk_RgPwQ87UAcfY4B-bwZGcomG9E4u0ZBLNDL--rGBe_hvEDLwdgfESY3GGh_3zPWmQrnudf4AcLi9Rw</recordid><startdate>20170801</startdate><enddate>20170801</enddate><creator>Chang, Peng-Fei</creator><creator>Qu, Li-Mei</creator><creator>Li, Ming</creator><creator>Qi, Bin</creator><general>D.A. Spandidos</general><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170801</creationdate><title>Striated muscle-derived intraspinal choristoma: A case report</title><author>Chang, Peng-Fei ; Qu, Li-Mei ; Li, Ming ; Qi, Bin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-d83ec38a8988cf03e6e1b28bfe93a992f1d935653b3e080ed4089e33d0b469ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antigens</topic><topic>Back pain</topic><topic>Calcification</topic><topic>Care and treatment</topic><topic>Case reports</topic><topic>Case studies</topic><topic>choristoma</topic><topic>Diagnosis</topic><topic>Hamartoma</topic><topic>Hypotheses</topic><topic>intraspinal</topic><topic>Medical diagnosis</topic><topic>Nervous system</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Pathogenesis</topic><topic>pathology</topic><topic>Spinal cord</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chang, Peng-Fei</creatorcontrib><creatorcontrib>Qu, Li-Mei</creatorcontrib><creatorcontrib>Li, Ming</creatorcontrib><creatorcontrib>Qi, Bin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</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)</collection><collection>ProQuest Central</collection><collection>British Nursing Database</collection><collection>ProQuest Central</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>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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, Peng-Fei</au><au>Qu, Li-Mei</au><au>Li, Ming</au><au>Qi, Bin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Striated muscle-derived intraspinal choristoma: A case report</atitle><jtitle>Oncology letters</jtitle><addtitle>Oncol Lett</addtitle><date>2017-08-01</date><risdate>2017</risdate><volume>14</volume><issue>2</issue><spage>1787</spage><epage>1789</epage><pages>1787-1789</pages><issn>1792-1074</issn><eissn>1792-1082</eissn><abstract>Choristoma is a mass of tissue that is histologically normal for the organ or part of the body from which it originates, but is located at an abnormal site. Choristoma of the nervous system involves the occurrence of residual dysplastic tissues outside the nervous system and exhibits a low incidence. Thus far, there has been no prior report of intraspinal choristoma originating from the striated muscle. The patient in the present case was a young man who was admitted to the hospital wing to intermittent lumbago. A lumbar magnetic resonance imaging examination revealed a cystic-solid lesion in the spinal canal at the S1 level. Preoperatively, the lesion was suspected to be a teratoma and was therefore completely removed. The postoperative pathological report suggested that the mass was an intraspinal choristoma, a benign lesion associated with a good prognosis, which had originated from striated muscle. Early diagnosis and treatment can prevent progression of nerve dysfunction. The patient recovered well postoperatively and the symptoms of lower back pain disappeared. Although intraspinal choristomas are rare, when a lesion in the spinal canal is diagnosed, it should be considered in the differential diagnosis tumors.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>28789410</pmid><doi>10.3892/ol.2017.6302</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Back pain Calcification Care and treatment Case reports Case studies choristoma Diagnosis Hamartoma Hypotheses intraspinal Medical diagnosis Nervous system NMR Nuclear magnetic resonance Pathogenesis pathology Spinal cord |
title | Striated muscle-derived intraspinal choristoma: A case report |
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