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Bilateral internal jugular vein thrombosis in a child with protein S deficiency
S Gunasekaran1, R Anthony, C J Woodhead
1Department of Otolaryngology, Leeds General Infirmary, Leeds, UK. gunasek98@yahoo.com
Insights
Bilateral internal jugular vein thrombosis is rare in children. A 14-year-old girl with protein S deficiency developed this condition with severe complications, a case previously unreported.
Area of Science:
- Vascular Medicine
- Pediatric Thrombosis
- Genetics and Thrombophilia
Background:
- Internal jugular vein thrombosis (IJVT) is a rare condition, predominantly reported in adults.
- Iatrogenic trauma is the most common cause of IJVT, with limited literature on pediatric cases.
Observation:
- A 14-year-old female presented with bilateral internal jugular venous thrombosis.
- The patient had a diagnosed deficiency in protein S, a known risk factor for thrombosis.
Findings:
- The case involved bilateral IJVT, a presentation not previously documented in the pediatric population.
- The patient experienced significant pulmonary and cerebral complications secondary to the thrombosis.
Implications:
- This case highlights the potential for severe IJVT in pediatric patients with thrombophilia, such as protein S deficiency.
- It underscores the need for increased awareness and consideration of IJVT in children presenting with relevant risk factors and symptoms.
- Further research into pediatric IJVT, particularly in the context of inherited thrombophilias, is warranted.
Abstract:
Internal jugular vein thrombosis is a rare but treatable disorder with most of the reports in the literature related to the adult population. The most common reported cause is iatrogenic trauma to the internal jugular vein and only a few cases have been reported in the paediatric population. We present a case of bilateral internal jugular venous thrombosis with pulmonary and cerebral complications in a 14-year-old girl with protein S deficiency. This problem has not been previously reported in the world literature.
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