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Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life

Identifieur interne : 002633 ( Main/Exploration ); précédent : 002632; suivant : 002634

Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life

Auteurs : L. Angelini [Italie] ; N. Nardocci [Italie] ; V. Rumi [Italie] ; C. Zorzi [Italie] ; L. Strada [Italie] ; M. Savoiardo [Italie]

Source :

RBID : ISTEX:5CE0F77B91E7DF548CEE816872A4906EF27202D1

Abstract

Summary: The diagnosis of Hallervorden-Spatz disease (HSD) has usually been made post mortem, although the recent description of characteristic abnormalities in the globus pallidus has suggested the possibility of an in vivo diagnosis. We present the clinical histories, neurological features and MRI findings of 11 patients, diagnosed as having HSD. Generalized dystonia with pre dominance of oromandibular involvement, behavioural changes followed by dementia and retinal degeneration were present in all the patients. MRI pallidal abnormalities consisted of decreased signal intensity in T2-weighted images, compatible with iron deposits, and of a small area of hyperintensity in its internal segment (“eye of the tiger” sign). We propose that the combination of these neurological signs with these MRI findings could be considered as highly suggestive of a diagnosis of HSD in living patients.

Url:
DOI: 10.1007/BF00856805


Affiliations:


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<div type="abstract" xml:lang="en">Summary: The diagnosis of Hallervorden-Spatz disease (HSD) has usually been made post mortem, although the recent description of characteristic abnormalities in the globus pallidus has suggested the possibility of an in vivo diagnosis. We present the clinical histories, neurological features and MRI findings of 11 patients, diagnosed as having HSD. Generalized dystonia with pre dominance of oromandibular involvement, behavioural changes followed by dementia and retinal degeneration were present in all the patients. MRI pallidal abnormalities consisted of decreased signal intensity in T2-weighted images, compatible with iron deposits, and of a small area of hyperintensity in its internal segment (“eye of the tiger” sign). We propose that the combination of these neurological signs with these MRI findings could be considered as highly suggestive of a diagnosis of HSD in living patients.</div>
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