MRI-visible pericochlear lesions in osteogenesis imperfecta type I
Osteogenesis imperfecta (OI) is an inherited generalized disorder of type-I collagen synthesis often associated with hearing loss. We present a case of OI type I in which hearing loss led to examination of the temporal bone with MRI. In the osseous otic capsule MRI demonstrated pericochlear lesions...
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Veröffentlicht in: | European radiology 2000-01, Vol.10 (10), p.1675-1677 |
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description | Osteogenesis imperfecta (OI) is an inherited generalized disorder of type-I collagen synthesis often associated with hearing loss. We present a case of OI type I in which hearing loss led to examination of the temporal bone with MRI. In the osseous otic capsule MRI demonstrated pericochlear lesions with soft tissue signal intensity and contrast enhancement. Changes similar to otosclerosis have been described in the temporal bone of OI patients when applying CT, but reports on MRI findings do not yet exist. |
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We present a case of OI type I in which hearing loss led to examination of the temporal bone with MRI. In the osseous otic capsule MRI demonstrated pericochlear lesions with soft tissue signal intensity and contrast enhancement. 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subjects | Bones Cochlea - pathology Deafness - diagnosis Deafness - etiology Diagnosis, Differential Female Humans Magnetic Resonance Imaging Middle Aged Osteogenesis Imperfecta - complications Osteogenesis Imperfecta - diagnosis Otosclerosis - complications Otosclerosis - diagnosis Temporal Bone - pathology |
title | MRI-visible pericochlear lesions in osteogenesis imperfecta type I |
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