Characteristic signal changes in the pontine base on T2- and multishot diffusion-weighted images in spinocerebellar ataxia type 1
Creators
- 1. Department of Radiology of Ohshima Clinic, Yamagata (Japan)
- 2. Yamagata University School of Medicine, Department of Internal Medicine, Yamagata (Japan)
- 3. Department of Neurology of Ohshima Clinic, Yamagata (Japan)
- 4. Yamagata University School of Medicine, Department of Radiology, Yamagata (Japan)
Description
The aim of the present study was to demonstrate characteristic signal changes of the pontine base on T2-weighted images of patients with SCA 1, and to elucidate the relationship between abnormal high-intensities of the pontine base on T2-weighted images and the findings on multishot diffusion-weighted images. We assessed abnormal signals of the pontine base on T2-weighted images from 50 controls and six patients with SCA 1 diagnosed by genetic analysis. At the same time, we evaluated the degeneration of the transverse pontine fibers in the pontine base by multishot diffusion-weighted imaging. A midline high-intensity was seen in the pontine base on T2-weighted images in two of the 50 controls and five of the six patients with SCA 1. The midline high-intensity had a sensitivity of 83.3% for patients and a specificity of 96.0% for controls. Multishot diffusion-weighted imaging demonstrated the degeneration - the amorphous-pattern signal - of the transverse pontine fibers in four (66.7%) of the six patients. In the other two patients, the zebra-pattern signal was seen in the pontine base. The midline high-intensity on T2-weighted images appears to be one of characteristic MRI findings of SCA 1. Multishot diffusion-weighted imaging suggested that the midline high-intensity should reflect the degeneration of the transverse pontine fibers. (orig.)
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00234-005-0002-yAdditional details
Identifiers
Publishing Information
- Journal Title
- Neuroradiology
- Journal Volume
- 48
- Journal Issue
- 1
- Journal Page Range
- p. 8-13
- ISSN
- 0028-3940
- CODEN
- NRDYAB
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 37022357
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CONGENITAL MALFORMATIONS; GENETICS; IMAGES; NEUROLOGY; NMR IMAGING; SIGNALS
- Descriptors DEC
- BIOLOGY; DIAGNOSTIC TECHNIQUES; MALFORMATIONS; MEDICINE; PATHOLOGICAL CHANGES