Thrombosis in a duplicated superficial femoral vein in a patient with haemophilia A

Stewart, Diana; Manson,; Dennis, Saya; Allan,; Ludlam,

doi:10.1046/j.1365-2516.2000.00366.x

Cited by 32 publications

(30 citation statements)

References 6 publications

(6 reference statements)

Supporting

Mentioning

Contrasting

Order By: Relevance

“…17 (2) Venous thrombosis is very rare in these patients. 18 This observation supports a key role for FVIII in venous thrombosis. [7][8][9][10] Partial inhibition of FVIII by mAb-LE2E9 seems to mimic mild hemophilia A.…”

Section: Discussionsupporting

confidence: 62%

Antithrombotic effects of controlled inhibition of factor VIII with a partially inhibitory human monoclonal antibody in a murine vena cava thrombosis model

Singh

Smith

Vanzieleghem

et al. 2002

Blood

View full text Add to dashboard Cite

Section: Discussionsupporting

confidence: 62%

Antithrombotic effects of controlled inhibition of factor VIII with a partially inhibitory human monoclonal antibody in a murine vena cava thrombosis model

Singh

Smith

Vanzieleghem

et al. 2002

Blood

View full text Add to dashboard Cite

“…12 patients with hemophilia A, and 15 patients with hemophilia B were reported to have had a venous thrombotic phenomenon [8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23][24][25].…”

Section: Discussionmentioning

confidence: 99%

“…Non-catheter related venous thrombosis have been occasionally described in patients with major congenital coagul ation disorders and also in hemophilia [8][9][10][11].…”

Section: Introductionmentioning

confidence: 99%

Non-catheter associated venous thrombosis in hemophilia A and B. A critical review of all reported cases

Girolami

Scandellari

Zanon

et al. 2006

J Thromb Thrombolysis

View full text Add to dashboard Cite

All reported cases of non-catheter induced venous thrombosis in patients with hemophilia A or B have been carefully evaluated. A total of 27 cases were reported,12 patients with hemophilia A and 15 patients with hemophilia B. The age of patients varied between 9 and 67 years. There were 10 cases of deep vein thrombosis, 8 patients with pulmonary embolism accompanied or not by deep vein thrombosis, 5 cases of superficial vein thrombosis. In addition, there were 3 cases of thrombosis in unusual sites (1 retinal central vein thrombosis and 2 portal vein thrombosis). Finally, in one case, venous thrombosis was multiple. There was a fatality in a hemophilia B patient with pulmonary embolism. The most frequent risk or triggering factor in hemophilia A was the administration of Feiba or rFVIIa concentrates in patients with inhibitors. Surgery together with Prothrombin Complex concentrates was the most frequent cause in hemophilia B patients. Congenital associated prothrombotic risk factors were present in two patients. No or very few therapeutic procedures were initiated in these patients but for a suspension or reduction of concentrates infusion. In a few instances low molecular weight heparin was given for a few days. The frequent association of venous thrombosis with infusion of concentrates indicates the need for a careful evaluation of patients about to receive such therapy.

show abstract

“…In these cases, however, there is no ambiguity as the duplicate vessels are always quite physically separate from each other (Zucconi et al, 2002;Shaw et al, 2003;Klemm et al, 2005). In contrast, reports pertaining to other regions of the body, particularly the lower limb, use the term duplicated to describe vessels that are fenestrated (Stewart et al, 2000;Wen et al, 2001;Quinlan et al, 2003). In this literature, development of thrombosis, due to reduced blood flow, is the problem of interest.…”

Section: Discussionmentioning

confidence: 99%

Bilateral duplicated internal jugular veins: Case study and literature review

et al. 2006

View full text Add to dashboard Cite

A rare bilateral duplication of the internal jugular vein (IJV) was discovered during cadaveric dissection. From each jugular foramen, a single IJV descended to the level of the hyoid bone then divided into medial and lateral veins. The medial IJVs traveled in the carotid sheath; the lateral IJVs coursed posterolateral to the sheath across the lateral cervical region (posterior triangle) of the neck. On the right side, medial and lateral IJVs entered the subclavian vein separately. C2-C3 anterior rami and the suprascapular artery passed between the medial and lateral IJVs. The right external jugular vein passed aberrantly between the heads of the sternocleidomastoid muscle (SCM) into the subclavian vein anterior to the lateral IJV. On the left side, the medial IJV drained into a large bulbous jugulovertebrosubclavian (JVS) sinus that received six main vessels. The lateral IJV diverged posterolaterally toward the border of the trapezius muscle, received the transverse cervical vein, and then turned sharply anteromedially to drain into the JVS sinus. The lateral IJV also gave an aberrant additional large vein that passed laterally around the omohyoid muscle before entering the JVS sinus. The left external jugular vein paralleled the anterior border of SCM before passing posterolaterally to terminate in the JVS sinus. Jugular vein anomalies of this magnitude are very rare. Determining the frequency of multiple IJVs is hampered by inconsistent terminology. We suggest that IJV duplication differs from fenestration anatomically and, potentially, developmentally. Criteria for characterizing IJV duplication and fenestration are proposed. The mechanism of development and the clinical significance of multiple IJVs are discussed.

show abstract

Thrombosis in a duplicated superficial femoral vein in a patient with haemophilia A

Cited by 32 publications

References 6 publications

Antithrombotic effects of controlled inhibition of factor VIII with a partially inhibitory human monoclonal antibody in a murine vena cava thrombosis model

Antithrombotic effects of controlled inhibition of factor VIII with a partially inhibitory human monoclonal antibody in a murine vena cava thrombosis model

Non-catheter associated venous thrombosis in hemophilia A and B. A critical review of all reported cases

Bilateral duplicated internal jugular veins: Case study and literature review

Contact Info

Product

Resources

About