Corticobasal degeneration with deep white matter lesion diagnosed by brain biopsy.

Autor: Arakawa A; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan., Saito Y; Department of Pathology and Laboratory Medicine, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan., Seki T; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan., Mitsutake A; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan., Sato T; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan., Katsumata J; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan., Maekawa R; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan., Hideyama T; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan., Tamura K; Department of Pathology, Tokyo Teishin Hospital, Tokyo, Japan., Hasegawa M; Department of Dementia and Higher Brain Function, Metropolitan Institute of Medical Science, Tokyo, Japan., Shiio Y; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan.
Jazyk: angličtina
Zdroj: Neuropathology : official journal of the Japanese Society of Neuropathology [Neuropathology] 2020 Jun; Vol. 40 (3), pp. 287-294. Date of Electronic Publication: 2020 Jan 10.
DOI: 10.1111/neup.12638
Abstrakt: Corticobasal degeneration (CBD) is a rare progressive neurodegenerative disorder characterized by asymmetric presentation of cerebral cortex signs, cortical sensory disturbance and extrapyramidal signs. Herein, we report a case of a 66-year-old Japanese woman who presented with apraxia of the right hand. She subsequently developed postural instability and cognitive impairments that rapidly worsened. One and a half years later, the patient was wheelchair-bound and severely demented. Brain magnetic resonance imaging revealed left dominant atrophy of the frontoparietal lobe. There was a hyperintense lesion in the deep white matter expanding toward the subcortical area on fluid-attenuated inversion recovery (FLAIR) images. In order to rule out the possibility of an intracranial tumor such as an astrocytoma or malignant lymphoma, we performed a brain biopsy of the left frontal middle gyrus. The patient became bedridden and showed akinetic mutism 1 year after biopsy. Pathological examination revealed a large amount of 4-repeat tau-immunoreactive neuropil threads scattered predominantly in the corticomedullary junction and tau-immunoreactive structures, consistent with CBD. Immunostaining for p53 showed no positive cells, and there were very few Ki-67-positive cells. On immunoblots of sarkosyl-insoluble brain extracts, a major doublet of 64 and 68 kDa full-length tau with two closely related fragments of approximately 37 kDa were detected. Based on these results, the patient was pathologically diagnosed as having CBD, excluding the possibility of tumor. Taken together with previous similar case reports, our findings indicate that a deep white matter hyperintense lesion on FLAIR images may be a useful clue to CBD, predicting rapid clinical progression with severe dementia based on severe white matter degeneration with a large amount of tau accumulation on pathological examination.
(© 2020 Japanese Society of Neuropathology.)
Databáze: MEDLINE
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