Congenital Agenesis of the Internal Jugular Vein: An Extremely Rare Anomaly

Joint Authors

Kayiran, Oguz
Calli, Caglar
Emre, Abdulkadir
Soy, Fatih Kemal

Source

Case Reports in Surgery

Issue

Vol. 2015, Issue 2015 (31 Dec. 2015), pp.1-3, 3 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2015-03-03

Country of Publication

Egypt

No. of Pages

3

Main Subjects

Medicine

Abstract EN

Vascular anomalies of major venous vessels are rarely seen.

Moreover, congenital absence of internal jugular vein is extremely uncommon.

In our case, a female patient presented with primary unknown left cervical mass.

Cervical ultrasonography demonstrated absence of right internal jugular vein.

In addition, computed tomography and dynamic magnetic resonance imaging scans confirmed this diagnosis.

Compensatory left internal jugular vein enlargement mimicked sort of cervical mass.

Venous magnetic resonance imaging images revealed the absence of right internal jugular vein with compensatory left internal jugular vein dominance.

In the literature, the agenesis of IJV was mentioned in a case with concomitant multiple problems.

Here, an asymptomatic case is reported with an incident diagnosis.

No interventions were planned upon the patient's request.

It should be kept in mind that any kind of anomalies can be seen during venous access and neck surgery.

American Psychological Association (APA)

Kayiran, Oguz& Calli, Caglar& Emre, Abdulkadir& Soy, Fatih Kemal. 2015. Congenital Agenesis of the Internal Jugular Vein: An Extremely Rare Anomaly. Case Reports in Surgery،Vol. 2015, no. 2015, pp.1-3.
https://search.emarefa.net/detail/BIM-1060104

Modern Language Association (MLA)

Kayiran, Oguz…[et al.]. Congenital Agenesis of the Internal Jugular Vein: An Extremely Rare Anomaly. Case Reports in Surgery No. 2015 (2015), pp.1-3.
https://search.emarefa.net/detail/BIM-1060104

American Medical Association (AMA)

Kayiran, Oguz& Calli, Caglar& Emre, Abdulkadir& Soy, Fatih Kemal. Congenital Agenesis of the Internal Jugular Vein: An Extremely Rare Anomaly. Case Reports in Surgery. 2015. Vol. 2015, no. 2015, pp.1-3.
https://search.emarefa.net/detail/BIM-1060104

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1060104