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1. |
Cerebral infarction—its pathogenesis and interpretation |
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The Journal of Pathology,
Volume 157,
Issue 4,
1989,
Page 281-282
J. Hume Adams,
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ISSN:0022-3417
DOI:10.1002/path.1711570402
出版商:John Wiley&Sons, Ltd.
年代:1989
数据来源: WILEY
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2. |
Updated Kiel classification for lymphomas |
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The Journal of Pathology,
Volume 157,
Issue 4,
1989,
Page 283-284
D. H. Wright,
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ISSN:0022-3417
DOI:10.1002/path.1711570403
出版商:John Wiley&Sons, Ltd.
年代:1989
数据来源: WILEY
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3. |
Detection of latent virus mRNA in tissues using the polymerase chain reaction |
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The Journal of Pathology,
Volume 157,
Issue 4,
1989,
Page 285-289
Caroline Lynas,
Stuart D. Cook,
Keith A. Laycock,
John W. B. Bradfield,
Norman J. Maitland,
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摘要:
AbstractThe polymerase chain reaction (PCR) has been adapted for use in gene expression studies. Using this technique, we have been able to specifically detectHerpes simplexvirus gene expression in the amount of RNA equivalent to that present in a single mouse ganglion. We have also detected specific transcription of the ras oncogene in biopsies of hepatocellular carcinoma tissue. The single tube RNA PCR reaction should be readily adaptable for use as a rapid screening tool in virus diagnosis; it is capable of detecting several virus infections simultaneously using extremely small tissue biopsies.
ISSN:0022-3417
DOI:10.1002/path.1711570404
出版商:John Wiley&Sons, Ltd.
年代:1989
数据来源: WILEY
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4. |
The identification of cells containing JC papovavirus DNA in progressive multifocal leukoencephalopathy by combinedin situhybridization and immunocytochemistry |
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The Journal of Pathology,
Volume 157,
Issue 4,
1989,
Page 291-297
James W. Ironside,
Fraser A. Lewis,
David Blythe,
Elizabeth A. Wakefield,
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摘要:
AbstractA double‐labelling technique combiningin situhybridization and immunocytochemistry is described which was used to characterize cells in the central nervous system containing JC virus DNA in formalin‐fixed, paraffin‐embedded tissues from four cases of progressive multifocal leukoencephalopathy. All four cases showed positive nuclear labelling for JC virus in both oligodendrocytes and astrocytes. The latter gave a strongly positive cytoplasmic staining reaction using antibodies to glial fibrillary acidic protein and vimentin. No nuclear labelling of neurones or endothelial cells was noted. The results confirm previous suggestions that glia are the main cells infected by JC virus in this disorder and show that the distribution of viral DNA in the brain is more extensive than suggested by routine microscopy alone.In situhybridization for JC virus may be useful in confirming the diagnosis of progressive multifocal leukoencephalopathy in both surgical biopsies and post‐mortem brain
ISSN:0022-3417
DOI:10.1002/path.1711570405
出版商:John Wiley&Sons, Ltd.
年代:1989
数据来源: WILEY
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5. |
Co‐expression of cytokeratin and vimentin intermediate filament proteins in benign and neoplastic breast epithelium |
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The Journal of Pathology,
Volume 157,
Issue 4,
1989,
Page 299-306
Wendy A. Raymond,
Anthony S‐Y. Leong,
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摘要:
AbstractThis paper identifies another neoplasm of epithelial origin which may express vimentin in addition to cytokeratins, thereby adding to the expanding list of tumours which demonstrate intermediate filaments (IFs) other than those of their reputed cell of origin.Twenty examples of benign breast disease and 66 carcinomas were examined for vimentin and cytokeratin IFs using an avidin–biotin–peroxidase complex technique. Co‐expression of these IF proteins was found in 35 per cent of cases of benign breast tissue and in 60 per cent of the carcinomas. In 8 (16 per cent) of 50 cases of infiltrating ductal carcinoma, vimentin and cytokeratin immunostaining was observed in more than 60 per cent of the tumour cells. These carcinomas were predominantly of a high histological grade. In benign breast disease and well‐differentiated carcinoma, vimentin was distributed in the basal and perinuclear regions of the cells, with sparing of the apical portions. In those cases in which large numbers of tumour cells expressed vimentin, cytoplasmic staining was diffuse, and often exhibited distinctive perinuclear and subplasmalemmal accentuation.We propose that a knowledge of the list of carcinomas which may co‐express vimentin and cytokeratin IFs might be helpful in the assessment of undifferentiated tumours and metastatic
ISSN:0022-3417
DOI:10.1002/path.1711570406
出版商:John Wiley&Sons, Ltd.
年代:1989
数据来源: WILEY
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6. |
Silver‐binding nucleolar organizer regions (AgNORs) in benign and malignant breast lesions: Correlations with ploidy and growth phase by DNA flow cytometry |
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The Journal of Pathology,
Volume 157,
Issue 4,
1989,
Page 307-313
D. D. Giri,
J. F. Nottingham,
J. Lawry,
S. A. C. Dundas,
J. C. E. Underwood,
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摘要:
AbstractSilver‐binding nucleolar organizer regions (AgNORs) have been counted in sections of routinely processed paraffin‐embedded tissue blocks and have been shown to assist in the distinction between benign and malignant lesions. We have examined 214 benign and malignant breast lesions by this method. The AgNOR counts were fibroadenomas 1.87 + 0.20 (mean + SD; n = 39), papillomas 1.92 + 0.21 (n = 28), sclerosing adenosis 1.96 + 0.24 (n = 23), epitheliosis 2.21 + 0.30 (n = 38), lobular carcinomain situ2.67 + 0.54 (n =9), intraduct carcinoma 3.75 + 1.33 (n = 37), and invasive carcinoma 4.22 + 1.18 (n = 40). However, the counts in 25–30 per cent of epitheliosis lesions and intraduct carcinomas overlapped in the region of 2–3 AgNOR dots per nuclear profile. The AgNOR counts in carcinomas were also compared with ploidy and growth phase fractions (S + G2+ M%) by flow cytometry. Thirty‐three of the 46 cancers with counts over 3 AgNOR dots per nuclear profile contained aneuploid cells (>10 per cent of the total), whereas 8 of the 12 with counts below 3 comprised diploid cells only (P0.10). We conclude that this method alone does not offer a reliable histological discriminant for malignancy in the breast. However, AgNOR counting may provide information on breast cancer prognosis supplementary to that obtained from DNA flow cytometric
ISSN:0022-3417
DOI:10.1002/path.1711570407
出版商:John Wiley&Sons, Ltd.
年代:1989
数据来源: WILEY
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7. |
Interleukin‐2 receptor expression in benign and malignant melanocytic skin lesions |
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The Journal of Pathology,
Volume 157,
Issue 4,
1989,
Page 315-319
N. M. Kernohan,
H. F. Sewell,
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摘要:
AbstractThe immunophenotype of the lymphocytic reaction of melanocytic skin lesions (12 cases of cutaneous malignant melanoma (CMM), three of Hutchinson's melanotic freckle (HMF), and eight naevocellular naevi) has been studied using monoclonal antibodies. CMM was associated with the most intense lymphocytic reaction, the lymphocytes being T cells of both CD‐4 T helper/inducer and CD‐8 suppressor/cytotoxic subsets which were present in varying proportions. Although less marked, the lymphocytic reaction to HMF and benign naevi showed similar features. An antibody to the interleukin‐2 receptor (IL‐2R; Tac, CD‐25) was included in the panel and the earlier findings of positively stained cells in association with CMM were confirmed. In addition, the novel finding of these cells in association with HMF and naevocellular naevi is reported. The number of these CD‐25 positive cells was extremely variable but they appeared most prominent in association with CMM. The findings presented here indicate that it is not possible to infer that CD‐25 positive lymphocytes present in the host response to CMM necessarily indicates tumour specific activation of the cells of the host
ISSN:0022-3417
DOI:10.1002/path.1711570408
出版商:John Wiley&Sons, Ltd.
年代:1989
数据来源: WILEY
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8. |
IgA nephropathy associated with chronic hepatitis B virus infection in adults: The pathogenetic role of HBsAG |
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The Journal of Pathology,
Volume 157,
Issue 4,
1989,
Page 321-327
Kar Neng Lai,
Fernand Mac‐Moune Lai,
John S. Tam,
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摘要:
AbstractFive adult cases of IgA nephropathy associated with chronic hepatitis B virus infection were studied. Serum HBsAg and anti‐HBc were present in five patients and HBeAg in four patients. Glomerular changes were typical of primary IgA nephropathy in four patients, and a mixed picture of IgA and membranous nephropathy was demonstrated in one patient. Immunofluorescence microscopy using polyclonal and monoclonal antibodies against HBsAg, HBcAg, and HBcAg revealed mesangial deposits of HBsAg in renal biopsies from four patients. One renal biopsy showed only mesangial and capillary HBcAg by polyclonal antiserum, and virus‐like particles were demonstrated in the intramembranous electron‐dense deposits on ultrastructural examination. Mesangial HBeAg was not detected in the renal biopsies from these patients with IgA nephropathy. As for the single patient with a mixed picture of IgA and membranous nephropathy, granular deposits of HBeAg with a distribution similar to IgG were detected in the glomerular capillary walls in addition to the mesangial deposition of HBsAg. These findings suggest that HBsAg rather than HBeAg may play a role of the pathogenesis in some of the adult patients with IgA nephropathy associated with chronic hepatitis B virus infe
ISSN:0022-3417
DOI:10.1002/path.1711570409
出版商:John Wiley&Sons, Ltd.
年代:1989
数据来源: WILEY
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9. |
Type 4 chain H expression by bile ductules and hepatocytes in cirrhosis |
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The Journal of Pathology,
Volume 157,
Issue 4,
1989,
Page 329-338
Yoshio Okada,
Maria I. Colnaghi,
Takao Tsuji,
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摘要:
AbstractThe monoclonal antibody MBrl defines the blood group H determinant with β 1 → 3N‐acetylgalactosamine linkage (Fucα 1 → 2Galβ 1 → 3GalNAc → R) carried by type 3 or 4 backbone. The distribution of the antigen detected by this antibody was studied immunohistochemically in liver tissues. Although bile ducts with a diameter of more than about 100 μm normally expressed the MBrl‐reactive antigen supranuclearly, smaller bile ducts and bile ductules did not express the antigen. In cirrhotic liver, proliferated bile ductules extensively expressed the MBrl‐reactive antigen. In spite of the absence in normal liver cells, the antigen was expressed membranously in some cirrhotic liver cells. Under subcellular fractionation, MBrl reactivity was almost exclusively recovered in the microsomal fraction. By HPTLC immunostaining, the major MBrl‐reactive antigen was shown to be carried by type 4 chain H glycolipid (globo‐H, Fuca 1 → 2Galβ 1 → 3GalNAcβ 1 → 3Galα 1 → 4Galβ 1 → 4Glcβ 1 → 1Cer). MBrl reactive glycoprotein was not found. In conclusion, although type 4 chain H glycolipid is not expressed by normal bile ductules and liver cells, it is actively synthesized and expressed by proliferated bile ductules and some of the liver cells in cirrhosis i
ISSN:0022-3417
DOI:10.1002/path.1711570410
出版商:John Wiley&Sons, Ltd.
年代:1989
数据来源: WILEY
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10. |
Platelet participation in the increased severity of endotoxin‐induced pulmonary injury in aged rats |
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The Journal of Pathology,
Volume 157,
Issue 4,
1989,
Page 339-345
Stephen K. Durham,
Michael A. Horan,
Adriaan Brouwer,
Roel J. Barelds,
Dick L. Knook,
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摘要:
AbstractRecent studies have demonstrated that aged rats are more susceptible to the lethal effects of endotoxin as compared with young rats. The morphogenesis of early endotoxin‐induced pulmonary injury in young (6 months) and aged (24 months) rats was examined by combined light and transmission electron microscopy to elucidate cell populations that may be responsible for these effects. Pulmonary endothelial cell injury was of greater severity and occurred at earlier time periods in aged rats as compared with young rats. Platelet sequestration and aggregation were observed only in aged rats in this study, and occurred in conjunction with the initial degenerative changes in the endothelium. Morphological evidence of granulocyte degranulation and fragmentation was also observed only in aged rats. These results suggest that pulmonary endothelial cells of aged rats are more susceptible to endotoxin‐induced injury and that platelets may play an important role in the enhancement of initial endothelial damage. Furthermore, the extent of injury to the endothelial cell population may play an important role in accounting for differences in endotoxin‐induced mortality between young and aged
ISSN:0022-3417
DOI:10.1002/path.1711570411
出版商:John Wiley&Sons, Ltd.
年代:1989
数据来源: WILEY
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