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
Hauptverfasser: Ziyeh, S, Berger, R, Reisner, K
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Berger, R
Reisner, K
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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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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