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Objective To analyse the ability of systematic core biopsy mapping to provide prognostic information in patients with prostatic cancer. Materials and methods The prostates of 60 men with prostatic cancer, stages TOd-T2, who had undergone total retropubic prostatectomy were studied. The average age of the patients was 63 years (range 49-72). Ten core biopsies (1.2 times 35 mm) were taken from the fresh specimens according to a standardized procedure. The total prostatectomy specimens were serially stepsectioned at 5 mm intervals and were assessed regarding tumour volume, grade and pT-stage. The World Health Organization (WHO) grade obtained in the mapping biopsies was compared with that in the operative specimens. Undergrading (WHO) decreased substantially by mapping biopsies, but was still present with the Gleason system. Results The volume of extracapsular tumours with extensively positive margins was significantly larger than that of intracapsular tumours (P<0.01). In addition, the fraction of cancer obtained in the biopsies from tumours with grossly positive margins was significantly smaller than that observed in biopsies from pT2 tumours (P<0.01). The cancer volume calculated from the result of the mapping correlated positively with the tumour volume determined by planimetry (R=0.83). A weaker correlation was found when only the six dorsal mapping biopsies were taken into consideration (R=0.68), but the correlation increased to R=0.75 when the six most significant biopsies were selected with the help of a correlation matrix. Biopsies from the ventral part of the prostate were also important, to obtain an accurate assessment of the tumour fraction within the whole gland. Conclusion Mapping of the prostate gland with multiple (six or more) core biopsies is necessary for preoperative assessment of tumour volume, grade and pT stage; these are all of importance when assigning patients with clinically localized prostatic cancer to prognostic classes. [ABSTRACT FROM AUTHOR]

In an attempt to define the pathogenesis of congenital malformations in diabetic pregnancy, a number of serum factors were determined in normal and diabetic pregnant rats and correlated to the outcome of gestation with the aid of multivariate linear regression analysis. The animals were from two different lines of Sprague-Dawley rats with documented differences in rates of fetal dysmorphogenesis in diabetic pregnancy. The diabetic rats increased less in body weight than the normal rats, yet displayed increased liver and kidney weights. The serum concentrations of glucose, beta-hydroxybutyrate, triglycerides, the branched-chain amino acids, and asparagine, proline, alanine, citrulline, tyrosine, and ornithine were increased by diabetes. In contrast, IGF-I, glutamic acid, glutamine, cystine, and lysine were decreased in the serum of the diabetic pregnant rats. The maternal metabolic imbalance exerted profound effects on embryonic development. Thus, the embryos of the diabetic rats were smaller, had fewer somites, and contained less DNA and protein than the control embryos. In addition, the resorption and malformation rates were increased in the embryos of the diabetic rats. The regression analysis of the data revealed significant interrelationships between adverse embryonic outcome (rates of malformations and resorptions) and the maternal serum concentrations of glucose, triglycerides, beta-hydroxybutyrate, branched-chain amino acids, and creatinine. This suggests that the maternal metabolism of the three major classes of nutrients covariates with the embryonic development in diabetic rat pregnancy. The monitoring of only one of these maternal parameters, e.g. the serum glucose concentration, may therefore not adequately predict the developmental status of the offspring. Our results suggest that the pathogenesis of fetal malformations in diabetic pregnancy is multifactorial. Thus, maintaining metabolites from all nutrient classes at a normal level may be important in preventing adverse fetal outcome.

The sources and routes of postoperative wound infections were prospectively studied in 440 patients undergoing biliary tract surgery. The overall infection rate was 7.3%. Specimens for culture were taken peroperatively from bile, liver bed and subcutaneous fat in 402 patients and also from skin in 64. Of the 126 patients with positive bile culture (31%), all but one had bacteria in the other intraoperative cultures, with high counts of bile bacteria in liver bed and transfer of such bacteria to subcutaneous fat in 81.2%. The wound infection rate in this group was 12.8%. Of the 276 patients with sterile bile, more than 90% had bacteria in the other intraoperative cultures. The degree of contamination was low, with dominance of typical skin bacteria, and the group wound infection rate was 3.2%. In 19 postoperative wound infections intraoperative cultures were available for comparison. Eleven of these infections were classified as endogenous, six as exogenous and two as of uncertain origin. S. aureus was uncommon in bile and intraoperative wound cultures, but was almost as common as E. coli in the etiology of postoperative wound infections, indicating high pathogenicity.