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Unusual MRI and pathologic findings of progressive multifocal leukoencephalopathy complicating adult Wiskott-Aldrich syndrome.

作者信息

Matsushima T, Nakamura K, Oka T, Tachikawa N, Sata T, Murayama S, Nukina N, Kanazawa I

机构信息

Department of Neurology, Institute for Brain Research, Tokyo, Japan.

出版信息

Neurology. 1997 Jan;48(1):279-82. doi: 10.1212/wnl.48.1.279.

Abstract

We present a long-surviving patient with Wiskott-Aldrich syndrome complicated by atypical progressive multifocal leukoencephalopathy (PML). MRI showed multiple tiny spots of Gd-DTPA-enhanced lesions on the T1-weighted image. Pathologic findings for brain biopsy were patchy demyelinated vascularized lesions infiltrated by a surprising number of eosinophils. The presence of polyomavirus JC was confirmed by in situ hybridization and polymerase chain reaction. PML should be included in the differential diagnosis when Gd-DTPA-enhanced spotty lesions are present in the white matter, especially in patients who have a mild immunologic defect.

摘要

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