| Literature DB >> 9008537 |
T Matsushima1, K Nakamura, T Oka, N Tachikawa, T Sata, S Murayama, N Nukina, I Kanazawa.
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.Entities:
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Year: 1997 PMID: 9008537 DOI: 10.1212/wnl.48.1.279
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910