TY - JOUR
T1 - The role of percutaneous embolization techniques in the management of dural sinus malformations with atypical angioarchitecture in neonates
T2 - Report of 2 cases
AU - Jagadeesan, Bharathi D.
AU - Grande, Andrew W.
AU - Guillaume, Daniel J.
AU - Nascene, David R.
AU - Tummala, Ramachandra P.
N1 - Publisher Copyright:
© AANS, 2015.
PY - 2015/7
Y1 - 2015/7
N2 - 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.
AB - 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.
KW - Arteriovenous fistula
KW - Dural sinus malformation
KW - Pediatric arteriovenous malformation
KW - Percutaneous embolization
KW - Vascular disorders
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U2 - 10.3171/2014.12.PEDS145
DO - 10.3171/2014.12.PEDS145
M3 - Article
C2 - 25910034
AN - SCOPUS:84964693711
SN - 1933-0707
VL - 16
SP - 74
EP - 79
JO - Journal of Neurosurgery: Pediatrics
JF - Journal of Neurosurgery: Pediatrics
IS - 1
ER -