Published January 2006 | Version v1
Journal article

Characteristic signal changes in the pontine base on T2- and multishot diffusion-weighted images in spinocerebellar ataxia type 1

  • 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-y

Additional 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