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  • 2000-2004  (1)
  • 1995-1999
  • 1980-1984  (1)
  • Chronic renal failure  (1)
  • Immunhistochemie  (1)
  • 1
    ISSN: 1437-7799
    Keywords: Key words Hemodialysis ; Chronic renal failure ; Renal osteodystrophy ; Parathyroid hormone ; Intact osteocalcin ; Serum calcium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background. This study was carried out to evaluate potential factors affecting long-term parathyroid function in patients on maintenance hemodialysis. Methods. Biochemical parameters, including intact parathyroid hormone (i-PTH) and intact osteocalcin (i-OC) were analyzed retrospectively in 120 outpatients receiving hemodialysis, for the 4 years between 1992 and 1996. Patients were classified into the following three groups according to their serum i-PTH levels in 1996: low PTH (〈100 pg/ml), normal PTH (100–450 pg/ml), and high PTH (≧450 pg/ml). Results. Among the three PTH groups, no differences were found in age, sex, duration of dialysis, and laboratory parameters, except for serum levels of alkaline phosphatase (ALP), i-PTH, and i-OC. The percentage of diabetic patients was higher in the low PTH group than in the other two PTH groups. Both serum ALP and i-PTH levels increased in the high PTH group, and serum i-PTH level decreased in the low PTH group during the 4 years. The change in serum calcium (Ca) level was negatively correlated with that in serum i-PTH level (1994–1996, r = −0.623, 1992–1996, r = −0.565; P 〈0.0001). A higher correlation coefficient was observed in the low PTH group than in the other PTH groups, although the difference was not significant. A weak positive correlation of the changes in serum inorganic phosphorus (IP) level (1994–1996) and i-PTH level (1994–1996) was found in the high PTH group (r = 0.379, P 〈 0.05). Conclusion. Serum Ca level may play a determinant role in suppressing serum i-PTH level in hemodialysis patients. Serum IP level may stimulate serum i-PTH level in patients with hyperparathyroidism, although the physiological role of serum IP is yet to be established.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1335
    Keywords: Gastric endocrine cells ; Endocrine cell carcinoma ; Early gastric cancer ; Scirrhous carcinoma ; Immunohistochemistry ; Schlüsselwörter ; Gastrische Endokrinzellen ; Endokrine Carcinome ; Frühcarcinom des Magens ; Scirrhöses Carcinom ; Immunhistochemie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung 18 Argyrophilzellencarcinome aus insgesamt 101 Frühcarcinomen des Magens wurden lichtmikroskopisch, elektronenmikroskopisch sowie immunhistochemisch mit Antiseren gegen Polypeptide, CEA, Lysozyme und hCG untersucht. 7 dieser Tumoren enthielten Gastrin und 2 unter ihnen außerdem Somatostatin. In allen 18 Tumoren wurde CEA nachgewiesen, 7 von diesen 18 Tumoren zeigten Lysozyme, darunter 5 auch noch Gastrin. In 4 Tumoren wurde hCG beobachtet, und in 2 aus dieser Reihe von 4 fand sich gleichzeitig Gastrin, CEA, Mucin sowie Lysozyme. Argentaffine Zellen wurden in 7 von 18 Tumoren beobachtet. Drei von 7 Gastrin enthaltende Tumoren hatten mehr oder weniger argentaffine Zellen. Elektronmikroskopisch wurden unterschiedliche Sekretgranula beobachtet und 9 von 18 Tumoren waren D1 oder P Zellen ähnlich. Makroskopisch entsprach die Mehrzahl der Tumoren dem IIc oder IIc+III Typ. Histologisch waren von diesen 18 Tumoren 6 gut differenzierte und 12 wenig differenzierte Adenocarcinome, einschließlich Siegelring-zellencarcinomen. Sie waren öfters im Fundusbereich jüngerer Frauen lokalisiert. Unter Heranziehung unserer schon publizierten Untersuchungsbefunde wird vermutet, daß IIc-Typ Argyrophilzellencarcinome mit dem histologischen Bild des wenig differenzierten Adenocarcinoms dem scirrhösen Carcinom zugeordnet werden kann.
    Notes: Summary Eighteen argyrophil cell carcinomas in 101 early gastric carcinomas were examined histologically, ultrastructurally, and immunohistochemically for polypeptides, carcinoembryonic antigen (CEA), lysozyme, and human chorionic gonadotrophin (hCG). Seven of these 18 tumors had gastrin, and two of seven tumors also contained somatostatin. In all of these 18 tumors CEA were demonstrated. Seven had lysozyme and five of seven tumors also contained gastrin; hCG were present in four of 18 tumors and two of four tumors had gastrin, CEA, mucin, and lysozyme simultaneously. Argentaffin cells were found in seven of 18 tumors. Of the above seven tumors containing gastrin, three had argentaffin cells. Ultrastructurally, several types of secretory granules were noted and tumor cells resembling D1-or P cells were present in nine of the 18 tumors. Macroscopically, many of the tumors showed IIc or IIc+III type. Histologically, the 18 tumors consisted of six well differentiated adenocarcinomas and 12 poorly differentiated adenocarcinomas including signet-ring cell carcinoma. These 12 tumors frequently developed in the stomach of young females. In view of our previous investigations, it was suggested that the IIc-type argyrophil cell carcinoma histologically showing poorly differentiated adenocarcinoma may be related to scirrhous carcinoma of the stomach.
    Type of Medium: Electronic Resource
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