1. Congenital Intracerebral Pial Arteriovenous Fistula: A Case Report
- Author
-
Qiang Liu, Shun-Bao Xin, Guang-Bin Wang, and Wen-Juan Liu
- Subjects
Intracranial Arteriovenous Malformations ,Male ,congenital, hereditary, and neonatal diseases and abnormalities ,medicine.medical_specialty ,Middle Cerebral Artery ,Arteriovenous fistula ,Magnetic resonance angiography ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,medicine.artery ,medicine ,Humans ,cardiovascular diseases ,Child ,medicine.diagnostic_test ,business.industry ,Angiography, Digital Subtraction ,Magnetic resonance imaging ,Digital subtraction angiography ,medicine.disease ,Magnetic Resonance Imaging ,Cerebral Angiography ,Angiography ,Middle cerebral artery ,Arteriovenous Fistula ,Surgery ,Polyvinyls ,Neurology (clinical) ,Radiology ,business ,Tomography, X-Ray Computed ,030217 neurology & neurosurgery ,Magnetic Resonance Angiography ,Superior sagittal sinus ,Cerebral angiography - Abstract
Pial arteriovenous fistula (AVF) is an extremely rare intracranial vascular lesion. The pediatric type of AVF has a high percentage of varix, leading to mass effect with symptoms. We report a 12-year-old boy who was admitted due to sudden confusion and urinary incontinence. Computed tomography, magnetic resonance imaging, and magnetic resonance angiography (MRA) confirmed the diagnosis of congenital pial AVF. Digital subtraction angiography (DSA) revealed the lesion originating from the left middle cerebral artery and draining into the superior sagittal sinus. The AVF was successfully obliterated with six microcoils and 2.5-mL ethylene vinyl alcohol copolymer using a middle cerebral artery approach. This patient was discharged without neurologic deficits. The AVF became smaller and ultimately disappeared on the DSA and MRA at follow-up.
- Published
- 2017