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先天性下腔静脉缺如所致深静脉血栓形成：一例报告

Deep venous thrombosis caused by congenital absence of the inferior vena cava: report of a case.

作者信息

Kondo Yuka, Koizumi Jun, Nishibe Masayasu, Muto Akihito, Dardik Alan, Nishibe Toshiya

机构信息

Division of Cardiovascular Surgery, Department of Surgery, Fujita Health University, Aichi, Japan.

出版信息

Surg Today. 2009;39(3):231-4. doi: 10.1007/s00595-008-3830-7. Epub 2009 Mar 12.

DOI:10.1007/s00595-008-3830-7
PMID:19280283
Abstract

Although anomalies of the inferior vena cava (IVC) are seen frequently in a clinical setting, congenital absence of the IVC (AIVC) is rare. However, anomalies of the IVC should be considered in young patients suffering from recurrent and idiopathic DVT. We report a case of DVT possibly caused by AIVC in a 27-year-old man, and discuss the clinical features, diagnosis, and treatment of this unusual entity.

摘要

尽管下腔静脉（IVC）异常在临床环境中较为常见，但先天性下腔静脉缺如（AIVC）却很罕见。然而，对于患有复发性特发性深静脉血栓形成（DVT）的年轻患者，应考虑下腔静脉异常情况。我们报告一例27岁男性可能由先天性下腔静脉缺如导致的深静脉血栓形成病例，并讨论这一罕见病症的临床特征、诊断及治疗方法。

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本文引用的文献

1
Pulmonary and deep vein thrombosis in a young patient with protein S deficiency: report of a case.
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Congenital hypoplasia of the inferior vena cava: an underappreciated cause of deep venous thromboses among young adults.
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Absence of the retrohepatic inferior vena cava: what the surgeon should know.肝后下腔静脉缺如：外科医生应了解的情况。
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Massive gangrene of the stomach due to primary antiphospholipid syndrome: report of two cases.原发性抗磷脂综合征致胃大片状坏疽 2 例报告
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A case of deep venous thrombosis with a double inferior vena cava effectively treated by suprarenal filter implantation.1例双下腔静脉合并深静脉血栓形成经肾上极滤器植入治疗效果良好。
Jpn Heart J. 2004 Nov;45(6):1063-9. doi: 10.1536/jhj.45.1063.
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