1982
DOI: 10.1148/radiology.143.2.7071349
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Ossification of the thoracic posterior longitudinal ligament in a fixed population. Radiological and neurological manifestations.

Abstract: Reportedly, ossification of the posterior longitudinal ligament (OPLL) usually involves the cervical spine and often accompanies other ligamentous ossification such as diffuse idiopathic skeletal hyperostosis (DISH). It is considered serious because it sometimes causes severe radiculomyelopathy; however, the present study, based on a fixed population sample, revealed that OPLL of the thoracic spine is nearly always asymptomatic. The prevalence of thoracic OPLL was 0.6%, with three times as many women as men be… Show more

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Cited by 50 publications
(29 citation statements)
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“…A Japanese study, based on a ®xed population sample, revealed that the prevalence of thoracic OPLL was 0.6%, and that patients were nearly always asymptomatic. 17 In OPLL, proton density MR imaging demonstrated ossi®ed lesions with high sensitivity. 18 High signal intensity seen on T1 weighted images within ossi®ed lesions indicates the presence of fatty marrow and corresponds with a radiolucent area within the ossi®ed lesions seen on conventional tomograms.…”
Section: Radiological ®Ndingsmentioning
confidence: 99%
“…A Japanese study, based on a ®xed population sample, revealed that the prevalence of thoracic OPLL was 0.6%, and that patients were nearly always asymptomatic. 17 In OPLL, proton density MR imaging demonstrated ossi®ed lesions with high sensitivity. 18 High signal intensity seen on T1 weighted images within ossi®ed lesions indicates the presence of fatty marrow and corresponds with a radiolucent area within the ossi®ed lesions seen on conventional tomograms.…”
Section: Radiological ®Ndingsmentioning
confidence: 99%
“…Although OPLL is considered a rare disease in Western countries [2], it is a major disorder in Asia and often causes severe myelopathy or spinal cord injury. The prevalence of OPLL in Japanese populations has been reported to range from 1.9% to 4.3% [3], compared with only 0.1% to 1.3% in the United States [4–6].…”
Section: Introductionmentioning
confidence: 99%
“…Mice deficient in TNALP (Akp2 À/À ) display poor mineralization, primarily from the inability of the initial mineral crystal to form within the matrix-vesicle membrane, leading to severe hypophosphatasia [93], similar to the deactivating mutations seen in human hypophosphatasia (OMIM #146300) [94]. The NPP1-knockout mice (Enpp1 À/À ; tip-toe walking mouse, or tww/tww) [95,96] exhibit soft-tissue calcification and mineralization leading to progressive postnatal ankylosis of intervertebral disc, peripheral joint hyperostosis, arterial and cartilage calcification and increase bone formation due to deficiency of ePPi similar to the human mutations seen in the posterior longitudinal ligament [97]. Despite the different mechanism of supplying ePPi, the mutant ank mice (ank/ank), due to truncation mutation of the C-terminal domain leading to loss of function of the pyrophosphate transporter, exhibit a similar hypermineralized phenotype to the Enpp1 À/À mice.…”
Section: Normal and Pathological Mineralizationmentioning
confidence: 87%