A Case Report of Zinner Syndrome Combined with Double Inferior Vena Cava Malformation and Sigmoid Colon Prolongation with a Literature Review
Abstract：Zinner syndrome is a rare congenital developmental anomaly involving the urinary and reproductive systems caused by failure of mesonephric duct development and obstruction of ureteric bud ascent during embryonic development. Its incidence is low, and the coexistence of other system developmental anomalies is even rarer. To date, only two cases of Zinner syndrome in children with vertebral developmental abnormalities have been reported in domestic and foreign literature [1], and there are no reports of Zinner syndrome combined with cardiovascular or gastrointestinal system developmental malformations. This article reports the case data of one patient diagnosed with Zinner syndrome combined with double inferior vena cava malformation and sigmoid colon prolongation in our hospital.
Keywords：Urogenital System Malformations%Zinner Syndrome%Tomography%X-ray Computed
Publication Date：2025-01-19
Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)
Pages：3( 93-95 )