Multiple and recurrent systemic thrombotic events associated with congenital anomaly of inferior vena cava

Journal of Thrombosis and Thrombolysis

Volumn 19, Issue 2, 2005, Pages 101-103

  Takehara, Naohumi ^a   Hasebe, Naoyuki ^a   Enomoto, Setsu ^b   Takeuchi, Toshiharu ^a   Takahashi, Fumihiko ^a   Ota, Takahumi ^a   Kawamura, Yuichiro ^a   Kikuchi, Kenjiro ^a  

^a ASAHIKAWA MEDICAL COLLEGE   (Japan)

^b Department of Respiratory Medicine   (Japan)

Author keywords

AMI; Anomaly; Cerebral infarction; Deep venous thrombosis; Inferior vena cava

Indexed keywords

BLOOD CLOTTING FACTOR 8; D DIMER; HEPARIN; ISOSORBIDE DINITRATE; PLASMINOGEN ACTIVATOR INHIBITOR 1; THROMBIN ANTITHROMBIN COMPLEX; THROMBOMODULIN; VON WILLEBRAND FACTOR; WARFARIN;

ACUTE HEART INFARCTION; AGED; ANGINA PECTORIS; ANGIOCARDIOGRAPHY; ARTICLE; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; CORONARY ARTERY DILATATION; DEEP VEIN THROMBOSIS; DISEASE ASSOCIATION; ELECTROCARDIOGRAM; FEMALE; FEMORAL VEIN; FOLLOW UP; HEART LEFT VENTRICLE WALL MOTION; HUMAN; HYPERLIPIDEMIA; INFERIOR CAVA VEIN; KIDNEY VEIN; LABORATORY TEST; LEG BLOOD FLOW; PHLEBOGRAPHY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; RECURRENT DISEASE; THROMBOSIS; VEIN BLOOD FLOW; VEIN MALFORMATION;

AGED; BLOOD CIRCULATION; CEREBROVASCULAR ACCIDENT; CHEST PAIN; FEMALE; HUMANS; PULMONARY EMBOLISM; RECURRENCE; THROMBOSIS; VENA CAVA, INFERIOR;

EID: 23644459215     PISSN: 09295305     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11239-005-1380-z     Document Type: Article

References (13)

1. Rosendaal FR. Venous thrombosis: A multicausal disease. Lancet 1999;353:1167-1173. 10.1016/S0140-6736(98)10266-0
2. Castaman G, Ruggeri M, Tosetto AFR. Heterogeneity of activated protein C resistance phenotype in subjects with compound heterozygosity for HR2 haplotype and FV Leiden mutation (R506Q) in factor V gene. Thromb Haemost 2000;84:357-358. 10959717
3. Tosetto A, Rodeghiero F, Martinelli I, et al. Additional genetic risk factors for venous thromboembolism in carriers of the factor V Leiden mutation. Br J Haematol 1998;103:871-876. 10.1046/ j.1365-2141.1998.01028.x
4. van Boven HH, Vandenbroucke JP, Briet E, Rosendaal FR. Gene-Gene and Gene-Enviroment interactions determine risk of thrombosis in families with inherited antithrombin deficiency. Blood 1999;94:2590-2594. 10515862
5. Ruggeri M, Tosetto A, Castaman G, Rodeghiero F. Congenital absence of the inferior vena cava: A rare risk factor for idiopathic deep-vein thrombosis. The Lancet 2001;357:441. 10.1016/S0140-6736(00)04010-1
6. Chee YL, Culligan DJ, Watson HG. Inferior vena cava malformation as a risk factor for deep venous thrombosis in the young. British Journal of Haematology. 2001;114:878-880. 10.1046/j.1365-2141.2001.03025.x
7. Obemosterer A, Aschauer M, Schnedl W, W.Lipp R. Anomalies of the inferior vena cava in patients with iliac venous thrombosis. Annals of Internal Medicine 2002;136:37-41. 11777362
8. Shah NL, Shanley CJ, Prince MR, Wakwfield TW. Deep venous thrombosis complicating a congenital absence of the inferior vena cava. Surgery 1996;120:891-896. 8909527
9. Bass JE, Redwine MD, Kramer LA, Huynh PT, Harris JH. Spectrum of congenital anomalies of the inferior vena cava: Cross-sectional imaging findings. Radio Graphics 2000;20:639-652.
10. Chuang VP, Mena CE, Hoskins PA. Congenital anomalies of the inferior vena cava. Review of embryogenesis and presentation of a simplified classification. 3Br J Radiol 1974;47:206-213. 4824552
11. Fukuzawa J, Haneda T, Tobise K, Onodera S. A case report of isolated levocardia without intracardiac anomalies associated with sick sinus syndrome. Japanese Circulation Journal 1993;57:245-250. 8464143
12. Debing E, Tielemans Y, Jolie E, Van den Brande P. Congenital absence of inferior vena cava. Eur J Vasc Surg 1993;7:201-203. 10.1016/ S0950-821X(05)80763-7
13. Bass JE, Redwine MD, Kramer LA, Harris JH. Absence of the infrarenal inferior vena cava with preservation of the suprarenal segment as revealed by CT and MR venography. Am J Roentgenol 1999;172:1610-1612.