Journal of Pediatric Neurology 2006; 04(02): 139-142
DOI: 10.1055/s-0035-1557317
Case Report
Georg Thieme Verlag KG Stuttgart – New York

Behçet’s disease as cause of sinovenous thrombosis in a pediatric patient

Serap Teber
a   Department of Pediatric Neurology, Ankara University School of Medicine, Ankara, Turkiye
,
Ozlem Unal
a   Department of Pediatric Neurology, Ankara University School of Medicine, Ankara, Turkiye
,
Gulhis Deda
a   Department of Pediatric Neurology, Ankara University School of Medicine, Ankara, Turkiye
,
Suat Fitoz
b   Department of Radiology, Ankara University School of Medicine, Ankara, Turkiye
,
Zumrut Uysal
c   Department of Pediatric Hematology, Ankara University School of Medicine, Ankara, Turkiye
,
Nejat Akar
d   Department of Pediatric Molecular Pathology, Ankara University School of Medicine, Ankara, Turkiye
› Author Affiliations

Subject Editor:
Further Information

Publication History

29 March 2005

28 September 2005

Publication Date:
29 July 2015 (online)

Abstract

Sinovenous thrombosis is very rare in the pediatric population especially beyond neonatal period. This condition can be related to various etiologies depending upon patient’s age. In this case report, we present a child with sinovenous thrombosis secondary to Behçet’s disease. This 15-year-old male was admitted to our hospital with headache after he was followed for uveitis and recurrent oral aphthous ulceration. Since the cerebrospinal fluid pressure was 58 cm H2O and there was no lesion on cranial computed tomography and magnetic resonance imaging, he was first diagnosed as pseudotumor cerebri. In spite of acetazolamide therapy and intermittent lumber punctures, his symptoms and high cerebrospinal fluid pressure persisted. Three weeks later cranial computed tomography with contrast was performed again and thrombosis was seen in the transverse and sagittal sinuses. He was treated successfully with heparin and steroid therapy.