ULTRASTRUCTURAL PATHOLOGY OF GERSTMANN-STRAUSSLER-SCHEINKER DISEASE

被引:20
作者
LIBERSKI, PP
BUDKA, H
机构
[1] POLISH MOTHER MEM HOSP,DEPT PATHOL,ELECTRON MICROSCOP LAB,LODZ,POLAND
[2] UNIV VIENNA,INST NEUROL,VIENNA,AUSTRIA
关键词
CREUTZFELDT-JAKOB DISEASE; GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; PRION DISEASES;
D O I
10.3109/01913129509014600
中图分类号
TH742 [显微镜];
学科分类号
摘要
We report a detailed ultrastructural study based on a large series of samples from a recent case of Gerstmann-Straussler-Scheinker disease from the original Austrian family. Numerous PrP-immunopositive plaques dominated light microscopic neuropathology. Ultrastructurally, several types of plaques were observed: unicentric ''kuru,'' multicentric, and neuritic. Dystrophic neurites accompanied amyloid plaques to differing degrees. Plaques were enveloped by astrocytic processes and invaded by microglial cells. A prominent astrocytic reaction accompanied abundant spongiform change. Unusual crystalloids were observed in mitochondria while another type of crystalloid was seen within lysosomes. We conclude that Gerstmann-Straussler-Scheinker disease is distinct also at the ultrastructural level.
引用
收藏
页码:23 / 36
页数:14
相关论文
共 47 条
[1]   GERSTMANN-STRAUSSLER SYNDROME - A VARIANT TYPE - AMYLOID PLAQUES AND ALZHEIMERS NEUROFIBRILLARY TANGLES IN CEREBRAL-CORTEX [J].
AMANO, N ;
YAGISHITA, S ;
YOKOI, S ;
ITOH, Y ;
KINOSHITA, J ;
MIZUTANI, T ;
MATSUISHI, T .
ACTA NEUROPATHOLOGICA, 1992, 84 (01) :15-23
[2]   MICROGLIA IS A COMPONENT OF THE PRION PROTEIN AMYLOID PLAQUE IN THE GERSTMANN-STRAUSSLER-SCHEINKER SYNDROME [J].
BARCIKOWSKA, M ;
LIBERSKI, PP ;
BOELLAARD, JW ;
BROWN, P ;
GAJDUSEK, DC ;
BUDKA, H .
ACTA NEUROPATHOLOGICA, 1993, 85 (06) :623-627
[3]   GLIAL PLAQUES - AMYLOID DEPOSITS CHARACTERISTIC OF SLOW TRANSMISSIBLE ENCEPHALOPATHIES [J].
BOELLAARD, JW ;
SCHLOTE, W .
VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1981, 37 (03) :337-341
[4]  
BROWN P, 1992, LIGHT ELECTRON MICRO, P63
[5]  
BURGER D, 1964, REPORT SCRAPIE SEMIN, P225
[6]   KURU-PLAQUES IN A CASE OF CREUTZFELDT-JAKOB DISEASE [J].
CHOU, SM ;
MARTIN, JD .
ACTA NEUROPATHOLOGICA, 1971, 17 (02) :150-&
[7]  
CUILLE L, 1938, CR HEBD ACAD SCI, V206, P1687
[8]   LINKAGE OF THE INDIANA KINDRED OF GERSTMANN-STRAUSSLER-SCHEINKER DISEASE TO THE PRION PROTEIN GENE [J].
DLOUHY, SR ;
HSIAO, K ;
FARLOW, MR ;
FOROUD, T ;
CONNEALLY, PM ;
JOHNSON, P ;
PRUSINER, SB ;
HODES, ME ;
GHETTI, B .
NATURE GENETICS, 1992, 1 (01) :64-67
[9]   PRO-]LEU CHANGE AT POSITION-102 OF PRION PROTEIN IS THE MOST COMMON BUT NOT THE SOLE MUTATION RELATED TO GERSTMANN-STRAUSSLER SYNDROME [J].
DOHURA, K ;
TATEISHI, J ;
SASAKI, H ;
KITAMOTO, T ;
SAKAKI, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 163 (02) :974-979
[10]  
FRASER H, 1979, SLOW TRANSMISSIBLE D, V1, P387