Agenesis of the inferior vena cava associated with nephropathy, hypertension, and congenital organ anomalies. Case report of a 12-year-old girl

被引:0
作者
Bedzichowska, Agata [1 ,3 ]
Tomaszewska, Agata [1 ]
Lipinska-Opalka, Agnieszka [1 ]
Rustecka, Agnieszka [1 ]
Przekora, Jedrzej [1 ]
Kozinski, Piotr [2 ]
Kalicki, Boleslaw [1 ]
机构
[1] Panstwowy Inst Badawczy, Wojskowy Inst Med, Klin Pediat Nefrol & Alergol Dzieciecj, Warsaw, Poland
[2] Panstwowy Inst Badawczy, Wojskowy Inst Med, Zaklad Radiol Lekarskiej, Warsaw, Poland
[3] Panstwowy Inst Badawczy, Klin Pediat Nefrol & Alergol Dzieciecej, Wojskowy Inst Med, Ul Szaserow 128, PL-04141 Warsaw, Poland
来源
PEDIATRIA I MEDYCYNA RODZINNA-PAEDIATRICS AND FAMILY MEDICINE | 2023年 / 19卷 / 02期
关键词
children; nephropathy; hypertension; inferior vena cava agenesis; KILT syndrome; DEEP VENOUS THROMBOSIS; SUPRARENAL SEGMENT; VEIN THROMBOSIS; RISK FACTOR; ABSENCE; CONTINUATION; HYPOPLASIA; CT;
D O I
10.15557/PiMR.2023.0017
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Inferior vena cava agenesis is a rare congenital, often asymptomatic vascular anomaly, usually detected accidentally during medical imaging or interventions. In the literature, an association between inferior vena cava malformations and congenital defects of other organs (anomalies of the heart, spleen, kidneys, bowels) has been reported. This results from the concurrent development of these organs in the embryological process. We describe the agenesis of the lower part of the inferior vena cava coexisting with nephropathy, hypertension, unicornuate uterus, lipoma of the lumbar spine, spina bifida, increased activity of factor VIII and von Willebrand factor in a 12-year-old girl. This combination of defects appears to be unique in the medical literature. Exploring and understanding the nature of the link between these conditions could be crucial for avoiding unnecessary surgical interventions, malpractices, and diagnostic errors.
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页码:102 / 106
页数:5
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