Intramedullary spinal cord metastasis following spontaneous malignant transformation from giant cell tumor of bone 16 years after pulmonary metastasis
Giant cell tumor (GCT) of the bone is a unique bone tumor that can behave in locally aggressive fashion despite its benign histological appearance, and the local recurrence rate is approximately 25-35% following curettage, supplemented with bone grafting, cementation, cryosurgery, or instillation of...
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Veröffentlicht in: | Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association 2011-01, Vol.16 (1), p.119-124 |
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creator | Ozaki, Tomohiko Moriuchi, Shusuke Ueda, Takafumi Wakamatsu, Toru Kakunaga, Shigeki Iwasa, Yoko Konishi, Eiichi Mano, Masayuki |
description | Giant cell tumor (GCT) of the bone is a unique bone tumor that can behave in locally aggressive fashion despite its benign histological appearance, and the local recurrence rate is approximately 25-35% following curettage, supplemented with bone grafting, cementation, cryosurgery, or instillation of phenol or ethanol [1, 2]. Pulmonary metastases, or so-called pulmonary implants, are also a well-documented phenomenon in conventional GCT of the bone, with an incidence of from 1 to 9% of patients with GCT in the literature [3-7]. They have generally self-limited growth potential and a relatively good prognosis; thus, surgical resection of pulmonary metastatic lesions as much as feasible is the treatment of choice. However, approximately 25% of patients with unresectable metastasis eventually die of the disease [1]. Much more unusually, GCT of the bone can metastasize to extrapulmonary sites, including the bone (actually indistinguishable from multicentric GCT of the bone), scalp, prepuce, brain, and mediastinal and regional lymph nodes, especially in the presence of simultaneous pulmonary metastatic lesions [8, 9]. However, intramedullary spinal cord metastasis is an extremely rare event, even in cases of malignant tumors, such as lung and breast cancers [10, 11]. As far as we know, there have been no reports documenting intramedullary spinal cord metastasis from GCT of the bone with or without malignant transformation. The present report describes a patient presenting with an intramedullary spinal cord metastasis following spontaneous malignant transformation from conventional GCT of the bone 16 years after pulmonary metastasis. The patient was informed that data from the case would be submitted for publication and gave her consent during her lifetime. |
doi_str_mv | 10.1007/s00776-010-0002-6 |
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Pulmonary metastases, or so-called pulmonary implants, are also a well-documented phenomenon in conventional GCT of the bone, with an incidence of from 1 to 9% of patients with GCT in the literature [3-7]. They have generally self-limited growth potential and a relatively good prognosis; thus, surgical resection of pulmonary metastatic lesions as much as feasible is the treatment of choice. However, approximately 25% of patients with unresectable metastasis eventually die of the disease [1]. Much more unusually, GCT of the bone can metastasize to extrapulmonary sites, including the bone (actually indistinguishable from multicentric GCT of the bone), scalp, prepuce, brain, and mediastinal and regional lymph nodes, especially in the presence of simultaneous pulmonary metastatic lesions [8, 9]. However, intramedullary spinal cord metastasis is an extremely rare event, even in cases of malignant tumors, such as lung and breast cancers [10, 11]. As far as we know, there have been no reports documenting intramedullary spinal cord metastasis from GCT of the bone with or without malignant transformation. The present report describes a patient presenting with an intramedullary spinal cord metastasis following spontaneous malignant transformation from conventional GCT of the bone 16 years after pulmonary metastasis. The patient was informed that data from the case would be submitted for publication and gave her consent during her lifetime.</description><identifier>ISSN: 0949-2658</identifier><identifier>EISSN: 1436-2023</identifier><identifier>DOI: 10.1007/s00776-010-0002-6</identifier><identifier>PMID: 21249405</identifier><language>eng</language><publisher>Japan: Elsevier B.V</publisher><subject>Adult ; Bone Neoplasms - pathology ; Case Report ; Cell Transformation, Neoplastic ; Diagnosis, Differential ; Fatal Outcome ; Female ; Finger Phalanges ; Follow-Up Studies ; Giant Cell Tumor of Bone - diagnosis ; Giant Cell Tumor of Bone - secondary ; Humans ; Lung Neoplasms - diagnosis ; Lung Neoplasms - secondary ; Medicine ; Medicine & Public Health ; Orthopedics ; Rheumatology ; Spinal Cord Neoplasms - diagnosis ; Spinal Cord Neoplasms - secondary ; Thoracic Vertebrae ; Time Factors</subject><ispartof>Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association, 2011-01, Vol.16 (1), p.119-124</ispartof><rights>2011 The Japanese Orthopaedic Association</rights><rights>The Japanese Orthopaedic Association 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-aad0119c37d73fa4b0fccba0d8904b7828ed50cfe9d03e8672c2bc7193e728dc3</citedby><cites>FETCH-LOGICAL-c475t-aad0119c37d73fa4b0fccba0d8904b7828ed50cfe9d03e8672c2bc7193e728dc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00776-010-0002-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00776-010-0002-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21249405$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ozaki, Tomohiko</creatorcontrib><creatorcontrib>Moriuchi, Shusuke</creatorcontrib><creatorcontrib>Ueda, Takafumi</creatorcontrib><creatorcontrib>Wakamatsu, Toru</creatorcontrib><creatorcontrib>Kakunaga, Shigeki</creatorcontrib><creatorcontrib>Iwasa, Yoko</creatorcontrib><creatorcontrib>Konishi, Eiichi</creatorcontrib><creatorcontrib>Mano, Masayuki</creatorcontrib><title>Intramedullary spinal cord metastasis following spontaneous malignant transformation from giant cell tumor of bone 16 years after pulmonary metastasis</title><title>Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association</title><addtitle>J Orthop Sci</addtitle><addtitle>J Orthop Sci</addtitle><description>Giant cell tumor (GCT) of the bone is a unique bone tumor that can behave in locally aggressive fashion despite its benign histological appearance, and the local recurrence rate is approximately 25-35% following curettage, supplemented with bone grafting, cementation, cryosurgery, or instillation of phenol or ethanol [1, 2]. Pulmonary metastases, or so-called pulmonary implants, are also a well-documented phenomenon in conventional GCT of the bone, with an incidence of from 1 to 9% of patients with GCT in the literature [3-7]. They have generally self-limited growth potential and a relatively good prognosis; thus, surgical resection of pulmonary metastatic lesions as much as feasible is the treatment of choice. However, approximately 25% of patients with unresectable metastasis eventually die of the disease [1]. Much more unusually, GCT of the bone can metastasize to extrapulmonary sites, including the bone (actually indistinguishable from multicentric GCT of the bone), scalp, prepuce, brain, and mediastinal and regional lymph nodes, especially in the presence of simultaneous pulmonary metastatic lesions [8, 9]. However, intramedullary spinal cord metastasis is an extremely rare event, even in cases of malignant tumors, such as lung and breast cancers [10, 11]. As far as we know, there have been no reports documenting intramedullary spinal cord metastasis from GCT of the bone with or without malignant transformation. The present report describes a patient presenting with an intramedullary spinal cord metastasis following spontaneous malignant transformation from conventional GCT of the bone 16 years after pulmonary metastasis. The patient was informed that data from the case would be submitted for publication and gave her consent during her lifetime.</description><subject>Adult</subject><subject>Bone Neoplasms - pathology</subject><subject>Case Report</subject><subject>Cell Transformation, Neoplastic</subject><subject>Diagnosis, Differential</subject><subject>Fatal Outcome</subject><subject>Female</subject><subject>Finger Phalanges</subject><subject>Follow-Up Studies</subject><subject>Giant Cell Tumor of Bone - diagnosis</subject><subject>Giant Cell Tumor of Bone - secondary</subject><subject>Humans</subject><subject>Lung Neoplasms - diagnosis</subject><subject>Lung Neoplasms - secondary</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Orthopedics</subject><subject>Rheumatology</subject><subject>Spinal Cord Neoplasms - diagnosis</subject><subject>Spinal Cord Neoplasms - secondary</subject><subject>Thoracic Vertebrae</subject><subject>Time Factors</subject><issn>0949-2658</issn><issn>1436-2023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kc2OFSEQhYnRONfRB3BjiBtXrQX9Q3dcmYk_k0ziRteEhuKGCQ1XoDXzIvO80vboJC4mIbCo75yi6hDyksFbBiDe5XqJoQEGDQDwZnhEDqxrh4YDbx-TA0zd1PChH8_Is5yvAZjop_4pOeOMd1MH_YHcXoaS1IJm9V6lG5pPLihPdUyGLlhUrsdlaqP38ZcLxwrEUFTAuGa6KO-OQYVCq0fINqZFFRcDtSku9Oi2ikbvaVmXmGi0dI4BKRvoDaqUqbIFEz2tfolha37f8Dl5YpXP-OLuPSffP338dvGlufr6-fLiw1WjO9GXRikDjE26FUa0VnUzWK1nBWacoJvFyEc0PWiLk4EWx0FwzWct2NSi4KPR7Tl5s_ueUvyxYi5ycXn78j6hHPtBjGxooZKv_yOv45rqrv5AXTv1Y1chtkM6xZwTWnlKbqmjSQZyi0zukckamdwik0PVvLozXueawz_F34wqwHcg11I4Yrrv_JDr-12EdXs_XRVl7TBoNC6hLtJE94D6NzQ6uMs</recordid><startdate>201101</startdate><enddate>201101</enddate><creator>Ozaki, Tomohiko</creator><creator>Moriuchi, Shusuke</creator><creator>Ueda, Takafumi</creator><creator>Wakamatsu, Toru</creator><creator>Kakunaga, Shigeki</creator><creator>Iwasa, Yoko</creator><creator>Konishi, Eiichi</creator><creator>Mano, Masayuki</creator><general>Elsevier B.V</general><general>Springer Japan</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>201101</creationdate><title>Intramedullary spinal cord metastasis following spontaneous malignant transformation from giant cell tumor of bone 16 years after pulmonary metastasis</title><author>Ozaki, Tomohiko ; 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Pulmonary metastases, or so-called pulmonary implants, are also a well-documented phenomenon in conventional GCT of the bone, with an incidence of from 1 to 9% of patients with GCT in the literature [3-7]. They have generally self-limited growth potential and a relatively good prognosis; thus, surgical resection of pulmonary metastatic lesions as much as feasible is the treatment of choice. However, approximately 25% of patients with unresectable metastasis eventually die of the disease [1]. Much more unusually, GCT of the bone can metastasize to extrapulmonary sites, including the bone (actually indistinguishable from multicentric GCT of the bone), scalp, prepuce, brain, and mediastinal and regional lymph nodes, especially in the presence of simultaneous pulmonary metastatic lesions [8, 9]. However, intramedullary spinal cord metastasis is an extremely rare event, even in cases of malignant tumors, such as lung and breast cancers [10, 11]. As far as we know, there have been no reports documenting intramedullary spinal cord metastasis from GCT of the bone with or without malignant transformation. The present report describes a patient presenting with an intramedullary spinal cord metastasis following spontaneous malignant transformation from conventional GCT of the bone 16 years after pulmonary metastasis. The patient was informed that data from the case would be submitted for publication and gave her consent during her lifetime.</abstract><cop>Japan</cop><pub>Elsevier B.V</pub><pmid>21249405</pmid><doi>10.1007/s00776-010-0002-6</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Bone Neoplasms - pathology Case Report Cell Transformation, Neoplastic Diagnosis, Differential Fatal Outcome Female Finger Phalanges Follow-Up Studies Giant Cell Tumor of Bone - diagnosis Giant Cell Tumor of Bone - secondary Humans Lung Neoplasms - diagnosis Lung Neoplasms - secondary Medicine Medicine & Public Health Orthopedics Rheumatology Spinal Cord Neoplasms - diagnosis Spinal Cord Neoplasms - secondary Thoracic Vertebrae Time Factors |
title | Intramedullary spinal cord metastasis following spontaneous malignant transformation from giant cell tumor of bone 16 years after pulmonary metastasis |
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