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1. |
Epstein—barr virus latent membrane protein expression by Hodgkin and Reed—Sternberg‐like cells in acute infectious mononucleosis |
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The Journal of Pathology,
Volume 167,
Issue 3,
1992,
Page 267-271
Peter G. Isaacson,
Christina Schmid,
Langxing Pan,
Andrew C. Wotherspoon,
Dennis H. Wright,
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摘要:
AbstractIn the light of reports of latent membrane protein (LMP) expression by Hodgkin and Reed—Sternberg (HRS) cells, paraffin sections of tonsil (two cases), lymph nodes (eight cases; three cervical, one axillary, and four inguinal) and spleen (four cases) from 14 patients with acute infectious mononucleosis (IM) have been examined for the presence of HRS‐like cells and immunostained with an antibody to LMP. Sections of the tonsils and one lymph node were also stained with a panel of antibodies which characterize HRS cells of Hodgkin's disease. The tonsils contained abundant HRS‐like cells, mainly adjacent to the crypts, which were highlighted by strong LMP expression. The immunophenotype of these cells closely, but not completely, resembled that of HRS cells of Hodgkin's disease. The lymph nodes and spleens showed the typical changes of acute IM but only few LMP‐positive HRS‐like cells were present in the cervical lymph nodes and hardly any were present in the inguinal nodes and spleen. These findings suggest that tonsillar crypt squamous epithelium may play a role in the formation of LMP‐positive HRS‐like cells; these cells could be progenitors of Hodgkin's disease HRS cells and, if so, this might explain the restricted sites of presentation of Hodg
ISSN:0022-3417
DOI:10.1002/path.1711670302
出版商:John Wiley&Sons, Ltd.
年代:1992
数据来源: WILEY
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2. |
Mitochondrial and chromosomal DNA alterations in human chromophobe renal cell carcinomas |
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The Journal of Pathology,
Volume 167,
Issue 3,
1992,
Page 273-277
Angela Kovacs,
Stephan Storkel,
Wolfgang Thoenes,
Gyula Kovacs,
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摘要:
AbstractRenal cell tumours are characterized by the loss of chromosome 3p and trisomy of 5q segments (common, nonpapillary renal cell carcinoma), or by trisomy of chromosomes 7 and 17 and loss of the Y chromosome (papillary renal cell carcinoma), or by random karyotype changes and mitochondrial DNA alterations (renal oncocytoma). We have studied by means of RFLP analysis the genomic and mitochondrial DNA in 11 chromophobe renal cell carcinomas, which have a unique morphology among kidney cancers. We found a loss of the constitutional heterozygosity at chromosomal regions 3p, 5q, 17p, and 17q, a combination of allclic losses that has not been found in other types of renal cell tumours. Three of the tumours showed a gross alteration in the restriction pattern of the mitochondrial DNA. A combined morphological and genetic analysis suggests that chromophobe renal cell carcinoma is a distinct entity.
ISSN:0022-3417
DOI:10.1002/path.1711670303
出版商:John Wiley&Sons, Ltd.
年代:1992
数据来源: WILEY
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3. |
A two‐colour technique for chromosomein situhybridization in tissue sections |
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The Journal of Pathology,
Volume 167,
Issue 3,
1992,
Page 279-282
Steffi Lutz,
Cornelius Welter,
Klaus D. Zang,
Gerhard Seitz,
Nikolaus Blin,
Klaus Urbschat,
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摘要:
AbstractBy extending non‐isotopicin situhybridization of DNA probes (targeted to metaphase chromosomes or interphase nuclei) to hybridization using tissue sections, additional topological information on the DNA structure and specific alterations can be obtained. We have established a method for the application of two different, chromosome‐specific probes labelled with two colour dyes allowing simultaneous detection of two‐colour signals. This method was tested in and is applicable to tissue sections of various origins. To demonstrate its sensitivity, prostate carcinomas (either as cryosections or as sections from paraffin blocks) were investigated for the presence or absence of chromosomes 1 and Y. The technique presented here, comparable to immunohistochemical staining, is particularly useful for routine application in diagnostic laboratories and testing of fresh or archival mat
ISSN:0022-3417
DOI:10.1002/path.1711670304
出版商:John Wiley&Sons, Ltd.
年代:1992
数据来源: WILEY
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4. |
Parathyroid glands in primary hyperparathyroidism: An ultrastructural morphometric study of 25 cases |
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The Journal of Pathology,
Volume 167,
Issue 3,
1992,
Page 283-290
Saverio Cinti,
Andrea Sbarbati,
Manrico Morroni,
Vittorio Carboni,
Carlo Zancanaro,
Vincenzo Lo Cascio,
G. Richard Dickersin,
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摘要:
AbstractIn parathyroid glands removed from patients with primary hyperparathyroidism (pHPT). hyperplasias and adenomas cannot be distinguished from one another by light microscopy when only one gland is available for examination. When a second gland is available, it is necessary to establish whether it is normal, suppressed, or hyperplastic. This distinction may be difficult, and the main criterion is the amount of cytoplasmic lipid in the parenchymal cells. If the lipid is abundant, the gland is considered normal or suppressed, and if it is scanty, the gland is interpreted as hyperplastic. We have performed a morphometric ultrastructural study to test the reliability of this criterion. Twentyfive adenomatous glands removed from patients with pHPT, when compared with glands of normal size from euparathyroid patients, showed a significant increase in the parameters indicative of metabolic activity, namely the size of the Golgi apparatus, the amount of rough endoplasmic reticulum, and the length of plasmalemmas. In addition, the amount of cytoplasmic lipid was significantly reduced. Furthermore, 25 glands of normal size removed from the same patients with pHPT showed an amount of lipid similar to that of normal glands from euparathyroid patients. However, all the parameters indicative of metabolic activity were significantly higher than those in glands from euparathyroid patients and comparable to those found in adenomatous glands. These results suggest that in pHPT, normal‐size glands are as active as adenomatous glands, regardless of a higher lipid conten
ISSN:0022-3417
DOI:10.1002/path.1711670305
出版商:John Wiley&Sons, Ltd.
年代:1992
数据来源: WILEY
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5. |
Parathyroid hormone‐related peptide: Expression in fetal and neonatal development |
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The Journal of Pathology,
Volume 167,
Issue 3,
1992,
Page 291-296
P. B. J. Burton,
C. Moniz,
P. Quirke,
A. Malik,
T. D. Bui,
H. Juppner,
G. V. Segre,
D. E. Knight,
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摘要:
AbstractHypercalcaemia frequently complicates the clinical management of cancer. Many factors have been implicated in the pathogenesis of this humoral hypercalcaemia of malignancy, the most recent candidate being parathyroid hormonerelated peptide (PTHrP). Until now, this peptide has been detected only in some normal and transformed adult tissues. In recent years, it has become apparent that tumours are capable of expressing and secreting factors previously elaborated only during fetal life. Many of these factors act to stimulate the growth of both tumour and fetal cells in an autocrine manner. The data presented here demonstrate that PTHrP is expressed in the human and rat fetus throughout gestation. Immunocytochemistry reveals a gestationally related, changing pattern of expression which is paralleled by changes in mRNA transcription. These data sunport the hypothesis that PTHrP may function as a fetal growth factor.
ISSN:0022-3417
DOI:10.1002/path.1711670306
出版商:John Wiley&Sons, Ltd.
年代:1992
数据来源: WILEY
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6. |
Seminal vesicle amyloid: The first example of exocrine cell origin of an amyloid fibril precursor |
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The Journal of Pathology,
Volume 167,
Issue 3,
1992,
Page 297-303
Gibbons G. Cornwell,
Gunilla T. Westermark,
Peter Pitkanen,
Per Westermark,
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摘要:
AbstractAmyloid fibrils have been extracted from seminal vesicles, and a dominant 14 kD amyloid fibril protein has been identified. An antiserum to this protein reacted both with amyloid and with epithelial cells in some normal seminal vesicles. These reactions were blocked with seminal vesicle secretion and seminal vesicle amyloid fibril protein, but not by degraded amyloid fibrils or fibril protein from other types of amyloid. It is concluded that seminal vesicle amyloid is derived from secretory proteins of the seminal vesicles. As such, it is the first amyloid described which appears to be the product of an exocrine secretory cell.
ISSN:0022-3417
DOI:10.1002/path.1711670307
出版商:John Wiley&Sons, Ltd.
年代:1992
数据来源: WILEY
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7. |
‘Pleural’ and pulmonary carcinosarcomas |
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The Journal of Pathology,
Volume 167,
Issue 3,
1992,
Page 305-311
Frederick G. Mayall,
Allen R. Gibbs,
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摘要:
AbstractThe histological distinction between carcinosarcoma and mesothelioma has received little attention. The object of this study was to describe the histology and immunohistochemistry of two carcinosarcomas presenting as pleural tumours. These were compared with 12 carcinosarcomas from sites within the lung, and with the established features of mesothelioma. Histologically and immunohistochemically, these ‘pleural’ carcinosarcomas are similar to conventional pulmonary carcinosarcomas but accurate recognition is hindered by their gross appearance and biphasic histology which closely mimic mesothelioma. They may exhibit features such as neutral mucin, expression of carcinoembryonic antigen, squamous differentiation, and neuroendocrine differentiation which, when present, are evidence against mesothelioma. These tumours are rare and have passed unnoticed until
ISSN:0022-3417
DOI:10.1002/path.1711670308
出版商:John Wiley&Sons, Ltd.
年代:1992
数据来源: WILEY
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8. |
Immunopathological changes in the skin following recombinant interleukin‐2 treatment |
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The Journal of Pathology,
Volume 167,
Issue 3,
1992,
Page 313-319
Karen Blessing,
Kenneth G. M. Park,
Steven D. Heys,
George King,
Oleg Eremin,
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摘要:
AbstractThe systemic administration of the cytokine recombinant interleukin‐2 (rIL‐2) is associated with a number of toxic effects, including dermatological complications. The clinical, histological, and immunopathological changes occurring in the skin of six patients receiving rIL‐2 for metastatic colorectal carcinoma have been studied. All of the patients developed a diffuse erythema shortly after initiation of the treatment. In one patient, generalized erythroderma and photosensitivity developed. The initial biopsy revealed patchy spongiosis, focal exocytosis, and focal basal layer damage with a perivascular chronic inflammatory cell infiltrate. With further treatment there was progressive thickening of the epidermis, Immunohistochemistry revealed changes in the expression of CD1, CD3, CD4, and CD25, particularly on perivascular cells. Additionally, there was an increase in the expression of intercellular adhesion molecule‐1 (ICAM‐1) on keratinocytes in the basal and mid‐layers of the epidermis, endothelial cells, and perivascular cells. It is hypothesized that the expression of ICAM‐1 by the epidermal keratinocytes may be the important event in initiating the cutaneous manifestations associated with rIL‐2
ISSN:0022-3417
DOI:10.1002/path.1711670309
出版商:John Wiley&Sons, Ltd.
年代:1992
数据来源: WILEY
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9. |
Flow cytometry of oesophageal mucosal biopsies; epidermal growth factor receptor, and CD15 |
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The Journal of Pathology,
Volume 167,
Issue 3,
1992,
Page 321-326
D. Hopwood,
J. Jankowski,
G. Milne,
K. G. Wormsley,
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摘要:
AbstractFlow cytometry may be used to examine the properties of single or isolated cells. We have shown that it is possible to disaggregate and label oesophageal epithelial cells for two surface markers, CD15 and epidermal growth factor receptor. We have previously demonstrated these markers, in oesophageal squamous cells using immunoperoxidase techniques. These labelled disaggregated cells could then be measured by flow cytometry.
ISSN:0022-3417
DOI:10.1002/path.1711670310
出版商:John Wiley&Sons, Ltd.
年代:1992
数据来源: WILEY
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10. |
Differential expression of integrin alpha chains by renal epithelial cells |
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The Journal of Pathology,
Volume 167,
Issue 3,
1992,
Page 327-334
Maeve A. Rahilly,
Stewart Fleming,
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摘要:
AbstractWe have investigated the expression of integrin chains by human renal epithelial cells duringin vivorenal differentiation andin vitrocell culture on different extracellular matrices. Using the immunoperoxidase technique to visualize the binding of monoclonal antibodies to different integrin chains in fetal and adult kidneys, we found a change during development from α1β1, α3β1, and α4β1 ‐positive blastemal cells to α2β1, α3β1, and α6β1 ‐positive epithelial cells. The pattern of integrin expression correlates with the presence in the extracellular matrix of the appropriate ligands. Inin vitrocell culture experiments, renal epithelium expressed α3 and α5 integrins on all extracellular matrices. Integrins α2 and α6 were found only in cells grown on a laminin‐containing substratum. Fibronectin and α5 integrin co‐localized on the ventral surface of cells grown on a laminin substratum and at the periphery of cells on glass coverslips. These results suggest that there is a close relationship between integrin α chain usage and the presence of appropriate ligands in
ISSN:0022-3417
DOI:10.1002/path.1711670311
出版商:John Wiley&Sons, Ltd.
年代:1992
数据来源: WILEY
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