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Biomedical subjects

K Streitman

Publications and source records attributed to K Streitman.

12 recordsLinked to original sources

Fetal renal hyperechogenicity in pathological pregnancies.

A relationship was sought between renal hyperechogenicity and the hypoxic state of fetuses. 120 pathological pregnancies were examined between the 28th and 36th week. All of these women exhibited moderately increased levels of hepatic enzymes, 3 of them had a pathological kidney function, and 4 of them displayed hyperuricemia during the examination period. The echogenicity of the fetal kidneys was examined with Hitachi EUB-450 ultrasound equipment with a 3.5 MHz transducer. The kidney (creatinine, urea-N, uric acid, triglyceride, cholsterin) and liver (SGOT, SGPT, GGT, bilirubin) functions and plasma electrolytes (Na, K, Ca, Cl) of the mothers were also examined and blood was collected from the pulsating umbilical artery for determination of the same parameters. After delivery, the physical condition of the neonates was followed and their kidneys were examined with the same ultrasound equipment within the first 5 days. There was a significant correlation between a pathological neonatal clinical outcome and the frequency of fetal and hyperechogenicity (chi-square test with Yates correction, p < 0.01). The results demonstrate that fetuses exhibiting renal hyperechogenicity in pathological pregnancies require particularly careful obstetric control and neonatological consultation. It is important that hyperechogenic cases be admitted to a perinatal intensive care unit. Fetal renal hyperechogenicity is considered to be associated with an enhanced risk of an adverse perinatal outcome.

Female

The possible role of uric acid in renal hyper-echogenicity in neonatal hypoxic acute shock.

Sonographic examinations as well as blood and urine chemistry tests were carried out in 4 neonates (3 mature, 1 premature) with transient renal failure, who were suffering from the effects of neonatal asphyxia of varying etiology. The first ultrasound examinations of the kidneys were performed within 24 hours after the hypoxic event. Simultaneously, blood and urine tests for parameters of renal function and purine metabolites were also carried out. Transient insufficiency of renal function could be detected in all cases with hyper-uricemia and hyper-uricosuria with no hypercalciuria. Ultrasonographic examinations showed hyper-echogenicity of the renal pyramids in all of the cases and hyper-reflectivity of the renal cortex in cases 2 and 4. In 3 cases, hyper-echogenicity appeared within 24 hours and disappeared in a short time, while in case 3 it could be detected from day 4 until day 14. These findings demonstrate, that the neonatal kidney is very sensitive to hypoxia and that hypoxic renal failure is accompanied by hyper-echogenicity of the kidneys. Uric acid is a possible cause of the renal hyper-echogenicity.

Asphyxia Neonatorum

Herpesnephropathy.

Two cases of acute renal insufficiency occurred in association with episodes of severe encephalitis due to herpes simplex type I. The possibility was considered that the renal failure was due to viral infection of the kidneys, and animal experiments were carried out in an attempt to confirm this. Young New Zealand albino rabbits were infected i. v. with HSV type I; the virus antigen was detected in the kidney of 8 of 10 animals, and IgG was found on the GBM in 9 of 19 animals. Viruria was observed in 12 of the 29 infected animals, and electronmicroscopic examination confirmed the presence of immune complexes in the glomeruli.

Animals