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Dural Sinus Thrombosis with Nonsymptomatic Persistent Falcine Sinus: A Case Report.
Ayako Shioya1, Ryota Mashiko2, Masanari Shiigai3
1Department of Neurology, Mito Kyodo General Hospital, Tsukuba University Hospital Mito Area Medical Education Center, Ibaraki, Japan; Address correspondence to Ayako Shioya, MD, PhD, Department of Neurology, Mito Kyodo General Hospital, Tsukuba University Hospital Mito Area Medical Education Center, 3-2-7, Miyamachi, Mito, Ibaraki 310-0015, Japan.
A rare congenital venous anomaly, persistent fetal falcine sinus, was linked to sinus thrombosis and convulsive status epilepticus in a young woman. Treatment with heparin and antiepileptics led to a full neurological recovery.
Area of Science:
- Neurology
- Radiology
- Vascular Anatomy
Background:
- Congenital venous anomalies can predispose individuals to cerebrovascular complications.
- Persistent fetal falcine sinus is a rare anatomical variation of cerebral venous drainage.
Observation:
- A 24-year-old woman presented with convulsive status epilepticus.
- Cerebral magnetic resonance venography revealed a persistent fetal falcine sinus and a hypoplastic posterior superior sagittal sinus with abnormal deep venous drainage.
- Sinus thrombosis was identified in the hypoplastic superior sagittal sinus.
Findings:
- Cerebral angiography demonstrated delayed venous return in the left parieto-occipital lobe, suggesting cerebral venous stasis.
- The patient received heparin and antiepileptic drugs, resulting in complete neurological recovery.
Implications:
- This case highlights the potential link between congenital venous anomalies, specifically persistent fetal falcine sinus and superior sagittal sinus hypoplasia, and the development of sinus thrombosis.
- Cerebral venous stasis secondary to thrombosis in a hypoplastic superior sagittal sinus may precipitate convulsive status epilepticus.
- The persistent falcine sinus may act as an alternative drainage pathway, but hypoplasia of the superior sagittal sinus remains a critical factor.
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