2003
DOI: 10.1016/s0967-5868(02)00281-3
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Convexity dural chondroma: a case report and review of the literature

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Cited by 48 publications
(61 citation statements)
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“…They develop due to heterotrophic chondrocytes, metaplasia of perivascular mezenchymal cells or meningeal fibroblasts or migration caused by trauma or inflammatory process [18,20,21]. Heterotypically located embryonal cartilaginous remanants are most likely the origin of falx chondromas [8]. Without a head trauma history, we can support the idea that the chondroma in our report had its origin in intradurally located embryonal cartilaginous rests in the falx cerebri.…”
Section: Discussionsupporting
confidence: 66%
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“…They develop due to heterotrophic chondrocytes, metaplasia of perivascular mezenchymal cells or meningeal fibroblasts or migration caused by trauma or inflammatory process [18,20,21]. Heterotypically located embryonal cartilaginous remanants are most likely the origin of falx chondromas [8]. Without a head trauma history, we can support the idea that the chondroma in our report had its origin in intradurally located embryonal cartilaginous rests in the falx cerebri.…”
Section: Discussionsupporting
confidence: 66%
“…The majority of patients are between 20 and 60 years of age with a high frequency around the third decade [1,8]. Although a slight female preference has been reported, there is no gender predominance [9].…”
Section: Discussionmentioning
confidence: 99%
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“…There are 127 reports of intracranial chondroma in the English-language literature (3,4,8). Among them, 19 cases were reported as having originated from the falx and dural convexities (3).…”
Section: Discussionmentioning
confidence: 99%
“…In particular, the mass showed a peripheral enhancement that extended along the neural foramen, and this mimicked a nerve sheath tumor. Some published papers have confusingly used the terms "chondroma of a dural origin" (3), "intracranial chondroma" (4) and "dural chondroma" (8), and they failed to distinguish whether the tumor was categorized as a soft tissue tumor or a bony tumor. The distinctions were based on the pathological findings.…”
Section: Discussionmentioning
confidence: 99%