Dual Pathologies: Pial Arteriovenous Fistula in Combination with an Arteriovenous Malformation

被引:2
作者
Jannelli, Gianpaolo [1 ,2 ]
Joswig, Holger [1 ,2 ]
Bernava, Gianmarco [1 ,2 ]
Meling, Torstein R. [1 ,2 ]
Bijlenga, Philippe [1 ,2 ]
机构
[1] Geneva Univ Hosp, Dept Clin Neurosci, Div Neurosurg, Rue Gabrielle Perret Gentil 4, CH-1205 Geneva, Switzerland
[2] Fac Med, Rue Gabrielle Perret Gentil 4, CH-1205 Geneva, Switzerland
关键词
arteriovenous malformation; augmented reality; hybrid operating room; pial arteriovenous fistula; VASCULAR MALFORMATIONS; ENDOVASCULAR TREATMENT; CLINICAL PRESENTATION; BRAIN;
D O I
10.1055/s-0039-1698398
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background A pial arteriovenous fistula (PAVF) is a rare neurovascular pathology consisting of a direct connection between one or more arterial feeders and a single venous channel. A PAVF was previously considered a subtype of an arteriovenous malformation (AVM). In the current literature these are distinguished as two independent entities with different clinical, physiopathologic, and structural characteristics. We report a case of a surgically treated 37-year-old woman with an extremely rare combination of an unruptured PAVF and AVM. Patient The AVM was mainly supplied by feeders of the middle cerebral artery and drained into the sigmoid sinus via an abnormally dilated and tortuous vein. Following its resection, intraoperative digital subtraction angiography (DSA) in the hybrid operating room revealed the presence of a PAVF that had not been noted during the preoperative planning. Hence the PAVF was completely disconnected as confirmed by DSA again. Conclusion This is the second reported case of an AVM-associated PAVF. Without the intraoperative DSA in the hybrid operating room, this unusual complex cerebrovascular entity would likely have been missed.
引用
收藏
页码:185 / 187
页数:3
相关论文
共 17 条
[1]   Augmented reality in the surgery of cerebral arteriovenous malformations: technique assessment and considerations [J].
Cabrilo, Ivan ;
Bijlenga, Philippe ;
Schaller, Karl .
ACTA NEUROCHIRURGICA, 2014, 156 (09) :1769-1774
[2]   Pial Arteriovenous Fistulas Associated with Multiple Aneurysms Presenting as Intracerebral Hemorrhage: A Case Report [J].
Cai, Wu ;
Gong, Jianping ;
Cheng, Bochao ;
Qiao, Fang ;
Zhang, Wei ;
Zhu, Qing ;
Lan, Qing .
TURKISH NEUROSURGERY, 2014, 24 (05) :778-781
[3]  
da Silva Martins Warley Carvalho, 2015, Surg Neurol Int, V6, P102, DOI 10.4103/2152-7806.158518
[4]   Treatment of complex neurovascular lesions: an interdisciplinary angio suite approach [J].
Dammann, Philipp ;
Breyer, Tobias ;
Wrede, Karsten H. ;
Stein, Klaus-Peter ;
Wanke, Isabel ;
Grams, Astrid E. ;
Gizewski, Elke R. ;
Schlamann, Marc ;
Forsting, Michael ;
Sandalcioglu, I. Erol ;
Sure, Ulrich .
THERAPEUTIC ADVANCES IN NEUROLOGICAL DISORDERS, 2014, 7 (01) :60-70
[5]   The validity of classification for the clinical presentation of intracranial dural arteriovenous fistulas [J].
Davies, MA ;
TerBrugge, K ;
Willinsky, R ;
Coyne, T ;
Saleh, J ;
Wallace, MC .
JOURNAL OF NEUROSURGERY, 1996, 85 (05) :830-837
[6]   Dural and Pial Arteriovenous Fistulas Connected to the Same Drainer in the Middle Cranial Fossa: A Case Report [J].
Funakoshi, Yusuke ;
Hatano, Taketo ;
Saka, Makoto ;
Ando, Mitsushige ;
Chihara, Hideo ;
Takita, Wataru ;
Tokunaga, Keisuke ;
Hashikawa, Takuro ;
Kamata, Takahiko ;
Higashi, Eiji ;
Nagata, Izumi .
WORLD NEUROSURGERY, 2018, 118 :47-52
[7]   Pial Arteriovenous Fistula: A Brief Review and Report of 14 Surgically Treated Cases [J].
Goel, Atul ;
Jain, Sonal ;
Shah, Abhidha ;
Rai, Survendra ;
Gore, Sandeep ;
Dharurkar, Pralhad .
WORLD NEUROSURGERY, 2018, 110 :E873-E881
[8]   Surgical and endovascular flow disconnection of intracranial pial single-channel arteriovenous fistulae [J].
Hoh, BL ;
Putman, CM ;
Budzik, RF ;
Ogilvy, CS .
NEUROSURGERY, 2001, 49 (06) :1351-1363
[9]   Endovascular Treatment of Cerebral Dural and Pial Arteriovenous Fistulas [J].
Jabbour, Pascal ;
Tjoumakaris, Stavropoula ;
Chalouhi, Nohra ;
Randazzo, Ciro ;
Gonzalez, Luis Fernando ;
Dumont, Aaron ;
Rosenwasser, Robert .
NEUROIMAGING CLINICS OF NORTH AMERICA, 2013, 23 (04) :625-+
[10]   VASCULAR MALFORMATIONS OF THE BRAIN IN HEREDITARY HEMORRHAGIC TELANGIECTASIA (RENDU-OSLER-WEBER DISEASE) [J].
KIKUCHI, K ;
KOWADA, M ;
SASAJIMA, H .
SURGICAL NEUROLOGY, 1994, 41 (05) :374-380