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KERD
논문KCI 등재

가역적인 전두엽 기능 이상을 보인 교뇌외 수초융해증

Reversible Frontal Lobe Dysfunction in a Patient with Extrapontine Myelinolysis

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초록

Extrapontine myelinolysis (EPM) is an acute demyelinating disease caused by rapidly fluctuating serum osmolality. EPM mainly affects the bilateral basal ganglia, such as the caudate nucleus, putamen, and globus pallidus. Its major clinical symptoms are movement disorders such as parkinsonism, dystonia, and catatonia. However, frontal lobe dysfunction, such as executive dysfunction, personality changes, and apathy, is rare. We report a patient with EPM with reversible frontal lobe dysfunction without any definite movement symptoms. EPM should be included in the differential diagnosis when a patient shows acute behavioral changes following correction of electrolyte imbalance.

Abstract

Extrapontine myelinolysis (EPM) is an acute demyelinating disease caused by rapidly fluctuating serum osmolality. EPM mainly affects the bilateral basal ganglia, such as the caudate nucleus, putamen, and globus pallidus. Its major clinical symptoms are movement disorders such as parkinsonism, dystonia, and catatonia. However, frontal lobe dysfunction, such as executive dysfunction, personality changes, and apathy, is rare. We report a patient with EPM with reversible frontal lobe dysfunction without any definite movement symptoms. EPM should be included in the differential diagnosis when a patient shows acute behavioral changes following correction of electrolyte imbalance.

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