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2.
J Belge Radiol ; 75(2): 99-103, 1992 Apr.
Article in French | MEDLINE | ID: mdl-1618728

ABSTRACT

An extensive case of undifferentiated neuroendocrine carcinoma with small cells of the anorectal region is reported. The carcinoma is related to pulmonary anaplasia and quite rare in the colonic and rectal region. Its aggressivity is considerable with a strong propensity for hematogenous and lymphatic metastases and with a disastrous prognosis: 0% survival over 1 year. The incidence, the characteristic features, the histogenesis, and the anatomical pathology of this rare neoplasm are mentioned. Furthermore, the case illustrates a radiological pattern typical for major lymphatic dissemination with an intra- and extraparietal component. The mechanism of dissemination is explained by the "lymphatic block" theory. The absolute necessity of obtaining an histology in radiologically unusual and/or extensive cases is mentioned.


Subject(s)
Anus Neoplasms/diagnostic imaging , Carcinoma/diagnostic imaging , Adult , Anus Neoplasms/pathology , Anus Neoplasms/therapy , Barium Sulfate , Carcinoma/pathology , Carcinoma/therapy , Combined Modality Therapy , Enema , Humans , Male , Prognosis , Tomography, X-Ray Computed
5.
Eur J Clin Pharmacol ; 21(5): 409-15, 1982.
Article in English | MEDLINE | ID: mdl-7075646

ABSTRACT

The pharmacokinetics of the fixed combination trimethoprim sulfamethoxazole (TMP--SMZ), including peritoneal transfer, has been studied in patients with end-stage renal disease treated by peritoneal dialysis, intermittent in 18 cases and continuous ambulatory dialysis in 6 cases. After a single oral dose of TMP 4 mg and SMZ 20 mg per kg, peak serum levels of approximately 2.0 micrograms/ml TMP and 28 micrograms/ml SMZ were achieved at 4 hours for TMP, and at 6 hours for SMZ. The protein binding of TMP was 34.7 +/- 1.1% and its distribution volume was 2.2 +/- 0.51/kg. Total plasma clearance of TMP was 66.2 +/- 11.5 ml/min, peritoneal dialysance was 5.1 +/- 0.5 ml/min, and renal clearance was negligible. The protein binding of SMZ was 48.0 +/- 1.4% and the distribution volume was 0.55 +/- 0.071/kg. Total plasma clearance of SMZ was 26.2 +/- 5.7 ml/min, peritoneal dialysance was 1.2 +/- 0.2 ml/min, and renal clearance was negligible. The half lives of TMP and SMZ were 23.7 +/- 4.0 h and 18.1 +/- 3.5 h, respectively. The peritoneal dialysance both of TMP and SMZ after oral administration was very low. In contrast the absorption after intra-peritoneal administration is high. Peritoneal absorption was increased during peritonitis. In patients with peritonitis, the intra-peritoneal administration of TMP-SMZ resulted in an immediate high local concentration, and a serum concentration of both drugs in the therapeutic range within 6 to 12 h.


Subject(s)
Kidney Failure, Chronic/metabolism , Peritonitis/metabolism , Sulfamethoxazole/metabolism , Trimethoprim/metabolism , Administration, Oral , Adolescent , Adult , Aged , Drug Combinations , Female , Humans , Kinetics , Male , Middle Aged , Peritoneal Dialysis , Peritonitis/drug therapy , Sulfamethoxazole/therapeutic use , Trimethoprim/therapeutic use
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