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Clinico-radiological spectrum of reversible splenial lesions in children.

Identifieur interne : 001D16 ( Main/Exploration ); précédent : 001D15; suivant : 001D17

Clinico-radiological spectrum of reversible splenial lesions in children.

Auteurs : Mitsuru Kashiwagi [Japon] ; Takuya Tanabe [Japon] ; Shuichi Shimakawa [Japon] ; Michiko Nakamura [Japon] ; Shinya Murata [Japon] ; Kousuke Shabana [Japon] ; Jun Shinohara [Japon] ; Yutaka Odanaka [Japon] ; Hideki Matsumura [Japon] ; Koh Maki [Japon] ; Kenichi Okumura [Japon] ; Keisuke Okasora [Japon] ; Hiroshi Tamai [Japon]

Source :

RBID : pubmed:23790266

Descripteurs français

English descriptors

Abstract

Recently, many cases of children presenting reversible splenial lesions during febrile illness (RESLEF) have been reported; however, their overall clinico-radiological features are unclear. To describe the clinico-radiological features, we retrospectively reviewed the etiology (pathogen), clinical course, laboratory data, magnetic resonance imaging and electroencephalography (EEG) findings, therapy, and prognosis of 23 episodes in 22 children (1 child recurred) who presented neurological symptoms, with RESLEF. The etiologies (pathogens) varied. Seizure occurred in 7 episodes, disturbance of consciousness (DC) in 13, and delirious behavior in 18. Serum sodium levels <136 mEq/L were observed in 18 episodes. Lesions outside the splenium were found in 4 cases. Slow waves were observed on EEG in 10 episodes. Methylprednisolone pulse therapy was given in 7 cases. No case resulted in neurological sequelae. Among 23 episodes, clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) was diagnosed in 6 episodes, whereas non-MERS was observed in 17 episodes. No difference was observed in almost all the clinico-radiological features' data between the 2 groups. The largest differences were observed in the rate of purposeless movement, DC, extension of the abnormal lesions outside the splenium, and marked slowing of background activity on EEG. RESLEF exhibit a spectrum of clinico-radiological features. These results suggest that non-MERS and MERS both are a part of a larger pathological condition, which we have termed as RESLEF spectrum syndrome. Given the view that such a syndrome exists, the clinical characteristics and position of non-MERS and MERS become clear.

DOI: 10.1016/j.braindev.2013.05.007
PubMed: 23790266


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Le document en format XML

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<div type="abstract" xml:lang="en">Recently, many cases of children presenting reversible splenial lesions during febrile illness (RESLEF) have been reported; however, their overall clinico-radiological features are unclear. To describe the clinico-radiological features, we retrospectively reviewed the etiology (pathogen), clinical course, laboratory data, magnetic resonance imaging and electroencephalography (EEG) findings, therapy, and prognosis of 23 episodes in 22 children (1 child recurred) who presented neurological symptoms, with RESLEF. The etiologies (pathogens) varied. Seizure occurred in 7 episodes, disturbance of consciousness (DC) in 13, and delirious behavior in 18. Serum sodium levels <136 mEq/L were observed in 18 episodes. Lesions outside the splenium were found in 4 cases. Slow waves were observed on EEG in 10 episodes. Methylprednisolone pulse therapy was given in 7 cases. No case resulted in neurological sequelae. Among 23 episodes, clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) was diagnosed in 6 episodes, whereas non-MERS was observed in 17 episodes. No difference was observed in almost all the clinico-radiological features' data between the 2 groups. The largest differences were observed in the rate of purposeless movement, DC, extension of the abnormal lesions outside the splenium, and marked slowing of background activity on EEG. RESLEF exhibit a spectrum of clinico-radiological features. These results suggest that non-MERS and MERS both are a part of a larger pathological condition, which we have termed as RESLEF spectrum syndrome. Given the view that such a syndrome exists, the clinical characteristics and position of non-MERS and MERS become clear.</div>
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<country name="Japon">
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<name sortKey="Kashiwagi, Mitsuru" sort="Kashiwagi, Mitsuru" uniqKey="Kashiwagi M" first="Mitsuru" last="Kashiwagi">Mitsuru Kashiwagi</name>
</noRegion>
<name sortKey="Maki, Koh" sort="Maki, Koh" uniqKey="Maki K" first="Koh" last="Maki">Koh Maki</name>
<name sortKey="Matsumura, Hideki" sort="Matsumura, Hideki" uniqKey="Matsumura H" first="Hideki" last="Matsumura">Hideki Matsumura</name>
<name sortKey="Murata, Shinya" sort="Murata, Shinya" uniqKey="Murata S" first="Shinya" last="Murata">Shinya Murata</name>
<name sortKey="Nakamura, Michiko" sort="Nakamura, Michiko" uniqKey="Nakamura M" first="Michiko" last="Nakamura">Michiko Nakamura</name>
<name sortKey="Odanaka, Yutaka" sort="Odanaka, Yutaka" uniqKey="Odanaka Y" first="Yutaka" last="Odanaka">Yutaka Odanaka</name>
<name sortKey="Okasora, Keisuke" sort="Okasora, Keisuke" uniqKey="Okasora K" first="Keisuke" last="Okasora">Keisuke Okasora</name>
<name sortKey="Okumura, Kenichi" sort="Okumura, Kenichi" uniqKey="Okumura K" first="Kenichi" last="Okumura">Kenichi Okumura</name>
<name sortKey="Shabana, Kousuke" sort="Shabana, Kousuke" uniqKey="Shabana K" first="Kousuke" last="Shabana">Kousuke Shabana</name>
<name sortKey="Shimakawa, Shuichi" sort="Shimakawa, Shuichi" uniqKey="Shimakawa S" first="Shuichi" last="Shimakawa">Shuichi Shimakawa</name>
<name sortKey="Shinohara, Jun" sort="Shinohara, Jun" uniqKey="Shinohara J" first="Jun" last="Shinohara">Jun Shinohara</name>
<name sortKey="Tamai, Hiroshi" sort="Tamai, Hiroshi" uniqKey="Tamai H" first="Hiroshi" last="Tamai">Hiroshi Tamai</name>
<name sortKey="Tanabe, Takuya" sort="Tanabe, Takuya" uniqKey="Tanabe T" first="Takuya" last="Tanabe">Takuya Tanabe</name>
</country>
</tree>
</affiliations>
</record>

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