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Literature DB >> 7211206

Pallido-nigro-luysial atrophy with massive appearance of corpora amylacea in the CNS.

K Kosaka, M Matsushita, S Oyanagi, S Uchiyama, S Iwase.

Abstract

A case of pallido-nigro-luysial atrophy, characterized by symptoms typical of progressive supranuclear palsy, presented (1) severe symmetrical abiotrophic degeneration of the globus pallidus, substantia nigra, and subthalamic nucleus and (2) widespread accumulations of corpora amylacea in the CNS. The former is thought to be consistent with pallido-nigro-luysial atrophy and we regard it as a combined system degeneration of both the pallido-nigral and the pallido-luysial systems. The significance of the latter is quite obscure. As far as we know, only three cases of pallido-nigro-luysial atrophy have been reported. However, there is no reported case of this disorder with such widespread and massive accumulations of corpora amylacea as in our case.

Entities: Disease

Mesh：

Year: 1981 PMID： 7211206 DOI： 10.1007/bf00689999

Source DB: PubMed Journal: Acta Neuropathol ISSN： 0001-6322 Impact factor: 17.088

9 in total

1. PROGRESSIVE SUPRANUCLEAR PALSY. A HETEROGENEOUS DEGENERATION INVOLVING THE BRAIN STEM, BASAL GANGLIA AND CEREBELLUM WITH VERTICAL GAZE AND PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA.

Authors: J C STEELE; J C RICHARDSON; J OLSZEWSKI
Journal: Arch Neurol Date: 1964-04

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Authors: H J RAMSEY
Journal: J Neuropathol Exp Neurol Date: 1965-01 Impact factor: 3.685

3. On the nature, origin and distribution of the corpora amylacea of the brain with observations on some new staining reactions.

Authors: N ALDER
Journal: J Ment Sci Date: 1953-10

4. Studies of corpora amylacea. I. Isolation and preliminary characterization by chemical and histochemical techniques.

Authors: M Sakai; J Austin; F Witmer; L Trueb
Journal: Arch Neurol Date: 1969-11

5. Further observations in progressive supranuclear palsy.

Authors: N J David; E A Mackey; J L Smith
Journal: Neurology Date: 1968-04 Impact factor: 9.910

6. [Atrophy of the globus pallidus, substancia nigra, and nucleus subthalamicus. Akinetic syndrome with palilalia, oppositional rigidity and catatonia].

Authors: F Contamin; R Escourolle; J Nick; B Mignot
Journal: Rev Neurol (Paris) Date: 1971-02 Impact factor: 2.607

7. Unusual late-onset type of hallervorden-Spatz disease. Clinico-pathological study of a case presenting as parkinsonism.

Authors: K Jellinger; E Neumayer
Journal: Z Neurol Date: 1972

8. Pallido-nigro-luysial atrophy associated with degeneration of the centrum medianum. A clinicopathologic and electron microscopic study.

Authors: K Takahashi; R Nakashima; T Takao; H Nakamura
Journal: Acta Neuropathol Date: 1977-01-31 Impact factor: 17.088

9. Progressive supranuclear palsy. Clinico-pathological study of four cases.

Authors: S Behrman; J D Carroll; I Janota; W B Matthews
Journal: Brain Date: 1969 Impact factor: 13.501

9 in total

7 in total

1. Peculiar axonal debris with subsequent astrocytic response (foamy spheroid body). A topographic, light microscopic, immunohistochemical and electron microscopic study.

Authors: N Arai; S Yagishita; K Misugi; M Oda; K Kosaka; T Mizutani; Y Morimatsu
Journal: Virchows Arch A Pathol Anat Histopathol Date: 1992

2. Foamy spheroid bodies in the substantia nigra. Report of an unusual case with recurrent attacks of peculiar twilight state.

Authors: N Arai; Y Honda; N Amano; S Yagishita; K Misugi
Journal: J Neurol Date: 1988-07 Impact factor: 4.849