Abstract
Dural sinus malformations (DSMs) are rare congenital malformations that can be midline or lateral in location. Midline DSMs have been reported to have a worse prognosis than lateral DSMs and have traditionally been more difficult to manage. The authors report 2 unusual manifestations of midline DSMs and their management with percutaneous trans-fontanelle embolization. The first patient (Case 1) presented at 21 days of life with a large midline DSM and multiple high-flow dural and pial arteriovenous shunts. The child developed congestive cardiac failure and venous congestion with intracranial hemorrhage and seizures within a few weeks. The second patient (Case 2) presented with a large midline DSM found on prenatal imaging that was determined to be a purely venous malformation on postnatal evaluation. This large malformation resulted in consumptive coagulopathy and apneic episodes from brainstem compression. The patient in Case 1 was treated initially with endovascular embolization and eventually with curative percutaneous-transfontanelle embolization. The patient in Case 2 was treated with percutaneous transfontanelle embolization in combination with posterior fossa decompression and cranial expansion surgery.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 74-79 |
| Number of pages | 6 |
| Journal | Journal of Neurosurgery: Pediatrics |
| Volume | 16 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jul 2015 |
Bibliographical note
Publisher Copyright:© AANS, 2015.
Keywords
- Arteriovenous fistula
- Dural sinus malformation
- Pediatric arteriovenous malformation
- Percutaneous embolization
- Vascular disorders
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