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Article: Costal osteochondroma: A rare cause of spinal cord compression

TitleCostal osteochondroma: A rare cause of spinal cord compression
Authors
KeywordsBone tissue
Exostoses
Multiple hereditary
Neoplasms
Osteochondroma
Ribs
Spinal cord compression
Issue Date1998
PublisherLippincott, Williams & Wilkins. The Journal's web site is located at http://www.spinejournal.com
Citation
Spine, 1998, v. 23 n. 17, p. 1900-1903 How to Cite?
AbstractStudy Design. Report of a rare cause of spinal cord compression: costal osteochondroma. Objective. To describe a very rare cause of spinal cord compression, costal osteochondroma, which was present in a 16-year-old girl with a history of hereditary multiple exostoses. Summary of Background Data. Only four cases of expansion of costal osteochondroma into the spinal canal through an intervertebral foramen have been reported previously. Methods and Results. The origin of the osteochondroma at the head of the right 12th rib, the invasion of the spinal canal through the right T12-L1 intervertebral foramen, and the compression of the spinal cord were shown on computed tomography and magnetic resonance imaging. The exact extent of the osteochondroma, particularly the cartilage cap, was delineated accurately by magnetic resonance imaging. Complete excision followed by full recovery occurred 19 months after surgery. Conclusion. Magnetic resonance imaging is the preferred method of investigation in cases of osteochondroma related to spine, because it allows for better preoperative planning and helps to prevent incomplete excision of the tumor.
Persistent Identifierhttp://hdl.handle.net/10722/79665
ISSN
2023 Impact Factor: 2.6
2023 SCImago Journal Rankings: 1.221
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorTang, WMen_HK
dc.contributor.authorLuk, KDKen_HK
dc.contributor.authorLeong, JCYen_HK
dc.date.accessioned2010-09-06T07:57:12Z-
dc.date.available2010-09-06T07:57:12Z-
dc.date.issued1998en_HK
dc.identifier.citationSpine, 1998, v. 23 n. 17, p. 1900-1903en_HK
dc.identifier.issn0362-2436en_HK
dc.identifier.urihttp://hdl.handle.net/10722/79665-
dc.description.abstractStudy Design. Report of a rare cause of spinal cord compression: costal osteochondroma. Objective. To describe a very rare cause of spinal cord compression, costal osteochondroma, which was present in a 16-year-old girl with a history of hereditary multiple exostoses. Summary of Background Data. Only four cases of expansion of costal osteochondroma into the spinal canal through an intervertebral foramen have been reported previously. Methods and Results. The origin of the osteochondroma at the head of the right 12th rib, the invasion of the spinal canal through the right T12-L1 intervertebral foramen, and the compression of the spinal cord were shown on computed tomography and magnetic resonance imaging. The exact extent of the osteochondroma, particularly the cartilage cap, was delineated accurately by magnetic resonance imaging. Complete excision followed by full recovery occurred 19 months after surgery. Conclusion. Magnetic resonance imaging is the preferred method of investigation in cases of osteochondroma related to spine, because it allows for better preoperative planning and helps to prevent incomplete excision of the tumor.en_HK
dc.languageengen_HK
dc.publisherLippincott, Williams & Wilkins. The Journal's web site is located at http://www.spinejournal.comen_HK
dc.relation.ispartofSpineen_HK
dc.subjectBone tissueen_HK
dc.subjectExostosesen_HK
dc.subjectMultiple hereditaryen_HK
dc.subjectNeoplasmsen_HK
dc.subjectOsteochondromaen_HK
dc.subjectRibsen_HK
dc.subjectSpinal cord compressionen_HK
dc.titleCostal osteochondroma: A rare cause of spinal cord compressionen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0887-9869&volume=23 &issue=17&spage=1900&epage=1903&date=1998&atitle=Costal+osteochondroma:+a+rare+cause+of+spinal+cord+compressionen_HK
dc.identifier.emailLuk, KDK:hcm21000@hku.hken_HK
dc.identifier.authorityLuk, KDK=rp00333en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1097/00007632-199809010-00021en_HK
dc.identifier.pmid9762749en_HK
dc.identifier.scopuseid_2-s2.0-0032167576en_HK
dc.identifier.hkuros39442en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0032167576&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume23en_HK
dc.identifier.issue17en_HK
dc.identifier.spage1900en_HK
dc.identifier.epage1903en_HK
dc.identifier.isiWOS:000075835500020-
dc.publisher.placeUnited Statesen_HK
dc.identifier.scopusauthoridTang, WM=7403430820en_HK
dc.identifier.scopusauthoridLuk, KDK=7201921573en_HK
dc.identifier.scopusauthoridLeong, JCY=35560782200en_HK
dc.identifier.issnl0362-2436-

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