PubMed · 13582992
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L S RALSTON, W A WASDAHL. 1958. Chiari's network.. https://doi.org/10.1016/0002-9343(58)90020-2
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Retrocaval ureter is a relatively rare anomaly that usually manifests in the third or fourth decades. Symptoms are due to ureteric obstruction, either extrinsic by the abnormal inferior vena cava (IVC), or intrinsic ureteric hypoplasia. Surgery is needed for symptomatic cases and involves transection and relocation of the ureter anterior to the IVC. We report our experience with two such children who needed surgery because of increasing hydronephrosis and who have done well since.
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This article describes an approach to imaging of fetal head and neck anomalies. Topics include cleft lip and palate, facial clefts, amniotic band sequence, micrognathia and retrognathia, ocular and orbital abnormalities, craniosynostosis, posterior nuchal translucency, cephaloceles, vascular anomalies, and tumors. Some of the more common syndromes are also described.