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Clinical Profile and Long-Term Outcomes in Pediatric Cavernous Sinus Thrombosis
Cemal Karakas1, Yusif Hajiyev2, Henry C Skrehot3
1Division of Pediatric Neurology, Department of Neurology, University of Louisville, Norton Children's Medical Group, Louisville, Kentucky.
Insights
Pediatric cavernous sinus thrombosis (CST) is rare, but most children experience good outcomes. This study found no specific clinical factors predicted the resolution of CST in pediatric patients.
Area of Science:
- Pediatric Neurology
- Vascular Neurology
- Ophthalmology
Background:
- Pediatric cavernous sinus thrombosis (CST) is a rare condition with limited clinical and long-term outcome data.
- Understanding CST's characteristics is crucial for improving patient management and prognosis.
Purpose of the Study:
- To describe clinical and radiologic features of pediatric CST.
- To evaluate diagnostic methods, management strategies, and long-term prognosis.
- To identify clinical variables associated with long-term outcomes in pediatric CST.
Main Methods:
- Retrospective chart review of pediatric patients (<18 years) diagnosed with CST.
- Data collected from 2004 to 2018 at a single institution.
- Analysis of clinical variables, treatments, and follow-up neuroimaging outcomes.
Main Results:
- 16 pediatric patients (mean age 7.6 years) were identified with a mean follow-up of 29 months.
- Common symptoms included eyelid swelling; common etiologies were sinusitis and orbital cellulitis.
- Most patients received antibiotics and anticoagulation; one patient died. Twelve patients had normal follow-up examinations.
- No clinical variables significantly predicted thrombosis resolution on follow-up neuroimaging.
Conclusions:
- This study represents one of the largest cohorts with the longest follow-up for pediatric CST.
- The majority of pediatric patients with CST experienced favorable outcomes.
- No specific clinical variables were found to be statistically significant in predicting the resolution of CST.
Background:
Pediatric cavernous sinus thrombosis (CST) is a rare condition with limited data regarding its clinical characteristics and long-term outcomes. The objective of this study was to describe the clinical and radiologic features, diagnostic evaluation, management, and long-term prognosis and to identify clinical variables associated with long-term outcomes in pediatric CST.
Methods:
A retrospective chart review of patients younger than 18 years diagnosed with a CST between 2004 and 2018 at a single center was conducted.
Results:
We identified 16 (M:F = 10:6) children with CST with a mean age of 7.6 years (10 days to 15 years) and average follow-up duration of 29 months (3 weeks to 144 months). The most common symptom and examination finding at presentation was eyelid swelling (n = 8). Six patients had bilateral CST. The most common etiologies were sinusitis (n = 5) and orbital cellulitis (n = 5). Treatments included antibiotics (n = 14), anticoagulation (n = 11), and surgery (n = 5). Only one patient died due to intracranial complications. Twelve patients had a normal examination at follow-up. None of the clinical variables including age (P = 0.14), gender (P = 0.09), use of antibiotics (P = 1.00) or anticoagulation (P = 1.00), surgery (P = 0.28), parenchymal abnormalities (P = 0.30), additional cerebral venous thrombosis (P = 0.28), and early versus late commencing of anticoagulation (P = 1.00) were significant when comparing patients with full/partial resolution versus those with no resolution of thrombosis on follow-up neuroimaging.
Conclusions:
Our study is one of the largest cohorts with the longest follow-up data for the pediatric CST. Most of our patients had favorable outcomes at follow-up. We found no statistical difference between clinical variables when comparing patients with full/partial resolution versus those with no resolution of thrombosis on follow-up neuroimaging.
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