MovDisordV3, PascalFrancis, Curation, bibRecord, 002526

Distinct Basal Ganglia Hyperechogenicity in Idiopathic Basal Ganglia Calcification

Identifieur interne : 002526 ( PascalFrancis/Curation ); précédent : 002525; suivant : 002527

Distinct Basal Ganglia Hyperechogenicity in Idiopathic Basal Ganglia Calcification

Auteurs : Norbert Brüggemann [Allemagne] ; Susanne A. Schneider [Allemagne] ; Thurid Sander [Allemagne] ; Christine Klein [Allemagne] ; Johann Hagenah [Allemagne]

Source :

Movement disorders [ 0885-3185 ] ; 2010.

RBID : Pascal:10-0512955

Descripteurs français

Pascal (Inist)
- Parkinsonisme, Pathologie du système nerveux, Noyau gris central, Idiopathique, Calcification, Exploration ultrason.

English descriptors

KwdEn :
- Basal ganglion, Calcification, Idiopathic, Nervous system diseases, Parkinsonism, Sonography.

Abstract

We report a 67-year-old patient with idiopathic basal ganglia calcification (IBGC). He presented with progressive cognitive impairment, frontal lobe dysfunction, mild leg spasticity, and levodopa (L-dopa)-responsive parkinsonism. Transcranial sonography (TCS) revealed marked hyperechogenicity of the basal ganglia and periventricular spaces bilaterally. The detected signal alterations showed a fairly symmetric distribution and corresponded to the hyperintense calcifications depicted on the computer tomography brain scan. The combination of symmetric hyperechogenic areas adjacent to the lateral ventricles and of the basal ganglia may serve as an imaging marker characteristic of IBGC. Hyperechogenicity due to extended basal ganglia calcification as presented here is distinct from the pattern of hyperechogenicity caused by heavy metal accumulation, which is described to be less striking. In addition to atypical parkinsonian syndromes such as progressive supranuclear palsy and multiple system atrophy, IBGC is thus another differential diagnosis of parkinsonism with basal ganglia hyperechogenicity.

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A03		`1`		`@0 Mov. disord.`
A05				`@2 25`
A06				`@2 15`
A08	`01`	`1`	`ENG`	`@1 Distinct Basal Ganglia Hyperechogenicity in Idiopathic Basal Ganglia Calcification`
A11	`01`	`1`		`@1 BRÜGGEMANN (Norbert)`
A11	`02`	`1`		`@1 SCHNEIDER (Susanne A.)`
A11	`03`	`1`		`@1 SANDER (Thurid)`
A11	`04`	`1`		`@1 KLEIN (Christine)`
A11	`05`	`1`		`@1 HAGENAH (Johann)`
A14	`01`			`@1 Schilling Section of Clinical and Molecular Neurogenetics, University of Lübeck @2 Lübeck @3 DEU @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut.`
A14	`02`			`@1 Department of Neurology, University of Lübeck @2 Lübeck @3 DEU @Z 1 aut. @Z 2 aut. @Z 4 aut. @Z 5 aut.`
A20				`@1 2661-2664`
A21				`@1 2010`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000191411680270`
A44				`@0 0000 @1 © 2010 INIST-CNRS. All rights reserved.`
A45				`@0 14 ref.`
A47	`01`	`1`		`@0 10-0512955`
A60				`@1 P @3 CC`
A61				`@0 A`
A64	`01`	`1`		`@0 Movement disorders`
A66	`01`			`@0 USA`
C01	`01`		`ENG`	@0 We report a 67-year-old patient with idiopathic basal ganglia calcification (IBGC). He presented with progressive cognitive impairment, frontal lobe dysfunction, mild leg spasticity, and levodopa (L-dopa)-responsive parkinsonism. Transcranial sonography (TCS) revealed marked hyperechogenicity of the basal ganglia and periventricular spaces bilaterally. The detected signal alterations showed a fairly symmetric distribution and corresponded to the hyperintense calcifications depicted on the computer tomography brain scan. The combination of symmetric hyperechogenic areas adjacent to the lateral ventricles and of the basal ganglia may serve as an imaging marker characteristic of IBGC. Hyperechogenicity due to extended basal ganglia calcification as presented here is distinct from the pattern of hyperechogenicity caused by heavy metal accumulation, which is described to be less striking. In addition to atypical parkinsonian syndromes such as progressive supranuclear palsy and multiple system atrophy, IBGC is thus another differential diagnosis of parkinsonism with basal ganglia hyperechogenicity.
C02	`01`	`X`		`@0 002B17`
C02	`02`	`X`		`@0 002A25D01`
C03	`01`	`X`	`FRE`	`@0 Parkinsonisme @2 NM @5 01`
C03	`01`	`X`	`ENG`	`@0 Parkinsonism @2 NM @5 01`
C03	`01`	`X`	`SPA`	`@0 Parkinson síndrome @2 NM @5 01`
C03	`02`	`X`	`FRE`	`@0 Pathologie du système nerveux @5 02`
C03	`02`	`X`	`ENG`	`@0 Nervous system diseases @5 02`
C03	`02`	`X`	`SPA`	`@0 Sistema nervioso patología @5 02`
C03	`03`	`X`	`FRE`	`@0 Noyau gris central @5 09`
C03	`03`	`X`	`ENG`	`@0 Basal ganglion @5 09`
C03	`03`	`X`	`SPA`	`@0 Núcleo basal @5 09`
C03	`04`	`X`	`FRE`	`@0 Idiopathique @5 10`
C03	`04`	`X`	`ENG`	`@0 Idiopathic @5 10`
C03	`04`	`X`	`SPA`	`@0 Idiopático @5 10`
C03	`05`	`X`	`FRE`	`@0 Calcification @5 11`
C03	`05`	`X`	`ENG`	`@0 Calcification @5 11`
C03	`05`	`X`	`SPA`	`@0 Calcificación @5 11`
C03	`06`	`X`	`FRE`	`@0 Exploration ultrason @5 12`
C03	`06`	`X`	`ENG`	`@0 Sonography @5 12`
C03	`06`	`X`	`SPA`	`@0 Exploración ultrasonido @5 12`
C07	`01`	`X`	`FRE`	`@0 Encéphale @5 37`
C07	`01`	`X`	`ENG`	`@0 Encephalon @5 37`
C07	`01`	`X`	`SPA`	`@0 Encéfalo @5 37`
C07	`02`	`X`	`FRE`	`@0 Système nerveux central @5 38`
C07	`02`	`X`	`ENG`	`@0 Central nervous system @5 38`
C07	`02`	`X`	`SPA`	`@0 Sistema nervioso central @5 38`
N21				`@1 347`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

Links toward previous steps (curation, corpus...)

to stream PascalFrancis, to step Corpus: Pour aller vers cette notice dans l'étape Curation :000793

Links to Exploration step

Pascal:10-0512955

Le document en format XML

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<front><div type="abstract" xml:lang="en">We report a 67-year-old patient with idiopathic  basal ganglia calcification (IBGC). He presented with progressive cognitive impairment, frontal lobe dysfunction, mild leg spasticity, and levodopa (L-dopa)-responsive parkinsonism. Transcranial sonography (TCS) revealed marked hyperechogenicity of the basal ganglia and periventricular spaces bilaterally. The detected signal alterations showed a fairly symmetric distribution and corresponded to the hyperintense calcifications depicted on the computer tomography brain scan. The combination of symmetric hyperechogenic areas adjacent to the lateral ventricles and of the basal ganglia may serve as an imaging marker characteristic of IBGC. Hyperechogenicity due to extended basal ganglia calcification as presented here is distinct from the pattern of hyperechogenicity caused by heavy metal accumulation, which is described to be less striking. In addition to atypical parkinsonian syndromes such as progressive supranuclear palsy and multiple system atrophy, IBGC is thus another differential diagnosis of parkinsonism with basal ganglia hyperechogenicity.</div>
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<fC01 i1="01" l="ENG"><s0>We report a 67-year-old patient with idiopathic  basal ganglia calcification (IBGC). He presented with progressive cognitive impairment, frontal lobe dysfunction, mild leg spasticity, and levodopa (L-dopa)-responsive parkinsonism. Transcranial sonography (TCS) revealed marked hyperechogenicity of the basal ganglia and periventricular spaces bilaterally. The detected signal alterations showed a fairly symmetric distribution and corresponded to the hyperintense calcifications depicted on the computer tomography brain scan. The combination of symmetric hyperechogenic areas adjacent to the lateral ventricles and of the basal ganglia may serve as an imaging marker characteristic of IBGC. Hyperechogenicity due to extended basal ganglia calcification as presented here is distinct from the pattern of hyperechogenicity caused by heavy metal accumulation, which is described to be less striking. In addition to atypical parkinsonian syndromes such as progressive supranuclear palsy and multiple system atrophy, IBGC is thus another differential diagnosis of parkinsonism with basal ganglia hyperechogenicity.</s0>
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<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Idiopático</s0>
<s5>10</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Calcification</s0>
<s5>11</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Calcification</s0>
<s5>11</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Calcificación</s0>
<s5>11</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Exploration ultrason</s0>
<s5>12</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Sonography</s0>
<s5>12</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Exploración ultrasonido</s0>
<s5>12</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Encéphale</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Encephalon</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Encéfalo</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Système nerveux central</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Central nervous system</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Sistema nervioso central</s0>
<s5>38</s5>
</fC07>
<fN21><s1>347</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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   |area=    MovDisordV3
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   |texte=   Distinct Basal Ganglia Hyperechogenicity in Idiopathic Basal Ganglia Calcification
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	Movement Disorders (revue)
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Movement Disorders (revue)

Distinct Basal Ganglia Hyperechogenicity in Idiopathic Basal Ganglia Calcification

Distinct Basal Ganglia Hyperechogenicity in Idiopathic Basal Ganglia Calcification

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Descripteurs français

English descriptors

Abstract

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