1.White matter pattern of Leigh's syndrome, a case report.
Xiao-na YANG ; Wan-liang DU ; Wei ZHANG ; Wei YANG ; Jiong QIN ; Yun YUAN
Chinese Journal of Pediatrics 2004;42(10):792-792
8.Primary agiitis of central nervous system.
Zhi LIU ; Lin CHEN ; Yu-Pu GUO
Acta Academiae Medicinae Sinicae 2006;28(3):453-456
The common clinical manifestations of the primary agiitis of the central nervous system include burst of headache, dementia, change of aptitude, paralysis of cranial nerves, and recurrent focal depletion of the neural function. Lptomeningeal and brain biopsy are still the gold criteria for diagnosis. The prognosis may be improved after cortin and immunosuppressant therapy.
Humans
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Vasculitis, Central Nervous System
;
diagnosis
;
pathology
;
therapy
10.Sporadic Creutzfeldt-Jakob Disease With Slow Progression:Report of One Case.
Jia-Hua ZHAO ; Lei WU ; Wei JIN ; Qiu-Ping GUI ; Jia-Tang ZHANG ; De-Hui HUANG
Acta Academiae Medicinae Sinicae 2023;45(5):859-862
Sporadic Creutzfeldt-Jakob disease(sCJD)is a prion-caused degenerative disease of the central nervous system,with the typical clinical manifestation of rapidly progressive dementia.The course of disease is less than 1 year in most patients and more than 2 years in only 2% to 3% patients.We reported a case of sCJD with expressive language disorder and slow progression in this paper.By summarizing the clinical manifestations and the electroencephalograhpy,MRI,and pathological features,we aimed to enrich the knowledge about the sCJD with slow progression.
Humans
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Creutzfeldt-Jakob Syndrome/pathology*
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Brain/pathology*
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Magnetic Resonance Imaging
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Central Nervous System/pathology*
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