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首页> 外文期刊>BMC Pediatrics >Thrombophlebitis hiding under a KILT – case report on 40?years long-term follow-up of neonatal renal vein thrombosis
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Thrombophlebitis hiding under a KILT – case report on 40?years long-term follow-up of neonatal renal vein thrombosis

机译:妊娠期妊娠病例的血栓性炎 - 案例报告40?年的新生儿肾静脉血栓形成的长期随访

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Neonatal renal vein thrombosis is a recognised cause of renal and inferior caval vein atresia (IVCA). However, the long-term impact of the condition is underrecognized with a high burden of morbidity for the patient, especially in adulthood. IVCA has been shown to be an independent risk factor for deep venous thrombosis (DVT) with a high risk of recurrence. The acronym KILT for kidney and inferior vena cava anomaly with leg thrombosis summarizes the pathological situation. We present the case of a 40-year-old patient with pain in the right lower limb resulting from acute thrombophlebitis. No risk factors could be identified. His history was remarkable with two episodes of deep venous thrombosis first of the left, then the right leg 22?years earlier; at that time also, no risk factor was identified. Because of the idiopathic character of that thrombosis, the patient remained on long-term anticoagulation with phenprocoumon. The present thrombophlebitis occurred while the INR was not therapeutic in the preceding weeks. A CT with contrast showed atresia of the inferior vena cava and of the right kidney, and presence of numerous collaterals. A thorough medical history revealed a renal vein thrombosis as a neonate. Anticoagulation was intensified, and stent placement became necessary after a further 2?years. KILT syndrome is a rare but underrecognized condition. Complications may arise in young adulthood only, and it is of prime importance to instruct parents of the pediatric patient of the possible consequences of renal vein thrombosis and to assure guidance from the treating physicians throughout adulthood. Diagnosis of IVCA is by CT with contrast or by MRI, and lifelong anticoagulation may be necessary. Since the KILT syndrome is widely underdiagnosed, we challenge the clinicians to keep it in mind when confronted with thrombophlebitis or thrombosis of the young, male and with no other identifiable risk factors for deep vein thrombosis.
机译:新生儿肾静脉血栓形成是肾病和较差脉静脉Atresia(IVCA)的公认原因。然而,该病症的长期影响是患者的发病率高,特别是在成年期。 IVCA已被证明是深静脉血栓形成(DVT)的独立危险因素,具有很高的复发风险。肾脏和较差腔静脉异常具有腿血栓形成的缩略差术语总结了病理情况。我们展示了一个40岁的患者,患有急性血栓性血栓炎导致的右下肢疼痛。无法确定风险因素。他的历史与左边的两个深静脉血栓形成发作出色,然后右腿22?年前;此时,没有确定危险因素。由于这种血栓形成的特发性特征,患者保持与苯处理的长期抗凝。目前的血栓性炎发生,而INR在前几周内没有治疗。对比度的CT显示出下腔静脉和右肾的休息,以及许多侧面的存在。彻底的病程揭示了肾静脉血栓形成作为新生儿。抗凝加剧,在进一步的2年后,突击部门的展示率变得必要。凯尔综合征是一种罕见但低于识别的病情。仅在年轻的成年期中可能出现并发症,并且指导肾静脉血栓形成可能后果的儿科患者的父母并向在成年期间治疗医师的指导来指导儿科患者的素质是最重要的。 IVCA的诊断是CT,具有对比度或MRI,并且可能需要终身抗凝。由于综合征综合征被广泛补贴,我们挑战临床医生在遇到血栓形成或幼小血栓形成或没有其他可识别的危险因素的深静脉血栓形成的情况下,请记住它。

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