Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/13231
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dc.contributor.authorKirovski, Ien_US
dc.contributor.authorGucev, Zen_US
dc.contributor.authorTasic, Ven_US
dc.contributor.authorPop Jordanova, Nadaen_US
dc.date.accessioned2021-06-08T10:32:44Z-
dc.date.available2021-06-08T10:32:44Z-
dc.date.issued2011-
dc.identifier.issn0351-3254-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/13231-
dc.description.abstractHereditary multiple exostoses (HME) is an inherited autosomal dominant disorder characterised by the presence of multiple exostoses, in fact benign cartilaginous tumors (enchondromata on the long bones). A six-year-old boy was found to have multiple osteochondromas on the legs, arms and ribs. Unusually, one of the osteochondromas on the right arm was huge (5 x 6 cm) and painful. X ray confirmed the benign nature of the osteochondromas. The family history was uneventful as well as the pregnancy and delivery. His intelligence is normal, and ultrasound did not detect any anomalies of the heart or kidneys. The occurrence of a large osteochondroma in a young boy is rare. In spite of its size and growth the lesion is so far benign. Frequent follow-up is recommended for the timely detection of eventual malignant transformation.en_US
dc.language.isoenen_US
dc.publisherMacedonian Academy of Sciences and Artsen_US
dc.relation.ispartofPrilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)en_US
dc.titleA giant osteochondroma in a boy with multiple exostosesen_US
dc.typeArticleen_US
dc.identifier.volume32-
dc.identifier.issue2-
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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