ABSTRACT
Spinal vascular malformations are rare diseases with a wide variety of neurological presentations. In this article, arteriovenous malformations (both from the fistulous and glomerular type) and spinal dural arteriovenous fistulae are described and an overview about their imaging features on magnetic resonance imaging (MRI) and digital subtraction angiography is given. Clinical differential diagnoses, the neurological symptomatology and the potential therapeutic approaches of these diseases which vary depending on the underlying pathology are given. Although MRI constitutes the diagnostic modality of first choice in suspected spinal vascular malformation, a definite diagnosis of the disease and therefore the choice of suited therapeutic approach rests on selective spinal angiography. Treatment in symptomatic patients offers an improvement in the prognosis. In most spinal vascular malformations, the endovascular approach is the method of first choice; in selected cases, a combined or surgical therapy may be considered.
Subject(s)
Central Nervous System Vascular Malformations/surgery , Neurosurgical Procedures , Spinal Diseases/surgery , Spine/blood supply , Animals , Arteriovenous Fistula/classification , Arteriovenous Fistula/surgery , Central Nervous System Vascular Malformations/classification , Central Nervous System Vascular Malformations/pathology , Humans , Regional Blood Flow/physiology , Spinal Diseases/pathology , Spine/anatomy & histology , Spine/pathologyABSTRACT
BACKGROUND AND PURPOSE: Although it is generally accepted that developmental venous anomalies (DVAs) are benign vascular malformations, over the past years, we have seen patients with symptomatic DVAs. Therefore, we performed a retrospective study and a literature study to review how, when, and why DVAs can become clinically significant. METHODS: Charts and angiographic films of 17 patients with DVAs whose 18 vascular symptoms could be attributed to a DVA were selected from a neurovascular databank of our hospital. MRI had to be available to rule out any other associated disease. In the literature, 51 cases of well-documented symptomatic DVAs were found. Pathomechanisms were divided into mechanical and flow-related causes. RESULTS: Mechanical (obstructive or compressive) pathomechanisms accounted for 14 of 69 symptomatic patients resulting in hydrocephalus or nerve compression syndromes. Flow-related pathomechanisms (49 of 69 patients) could be subdivided into complications resulting from an increase of flow into the DVA (owing to an arteriovenous shunt using the DVA as the drainage route; n=19) or a decrease of outflow (n=26) or a remote shunt with increased venous pressure (n=4) leading to symptoms of venous congestion. In 6 cases, no specific pathomechanisms were detected. CONCLUSIONS: Although DVAs should be considered benign, under rare circumstances, they can be symptomatic. DVAs, as extreme variations of normal venous drainage, may represent a more fragile venous drainage system that can be more easily affected by in- and outflow alterations. The integrity of the DVA needs to be preserved irrespective of the treatment that should be tailored to the specific pathomechanism.
Subject(s)
Central Nervous System Venous Angioma/physiopathology , Adolescent , Adult , Arteriovenous Fistula/etiology , Blood Pressure , Central Nervous System Venous Angioma/complications , Central Nervous System Venous Angioma/therapy , Child , Child, Preschool , Embolization, Therapeutic , Female , Hemorheology , Humans , Hydrocephalus/etiology , Infant , Infant, Newborn , Intracranial Arteriovenous Malformations/complications , Intracranial Arteriovenous Malformations/physiopathology , Male , Middle Aged , Nerve Compression Syndromes/etiology , Paresis/etiology , Radiosurgery , Seizures/etiology , Stress, Mechanical , Stroke/etiologyABSTRACT
Vascular injury of the head and neck region is a rare and often life-threatening complication of head or neck trauma and is due to two major pathomechanisms: penetrating or blunt trauma. Both the arterial and the venous site of the CNS vasculature can be involved, the latter one being often overlooked. Concerning arterial lesions, depending on how many layers of the arterial vessel are affected and on the spatial relationship to adjacent structures, dissections, false aneurysms or arteriovenous fistulae may develop. On the venous side, dural tears, compressive effects on pial veins and a deranged clotting system may lead to delayed venous thrombosis. In this review we describe clinical and imaging findings, as well as diagnostic and treatment strategies in these lesions.
Subject(s)
Cerebral Arteries/injuries , Cerebral Veins/injuries , Craniocerebral Trauma/diagnosis , Craniocerebral Trauma/therapy , Magnetic Resonance Imaging/methods , Tomography, X-Ray Computed/methods , Cerebral Arteries/diagnostic imaging , Cerebral Arteries/pathology , Cerebral Veins/diagnostic imaging , Cerebral Veins/pathology , HumansABSTRACT
BACKGROUND AND PURPOSE: The purpose of this article is to describe "cerebral proliferative angiopathy" (CPA) as a clinical entity, which may be regarded as separate from "classical" brain AVMs in angioarchitecture, natural history, clinical presentation, and, therefore, treatment and which can be discerned from other cerebral AVMs by characteristic imaging features. METHODS: In a prospectively entered databank encompassing 1434 patients with brain AVMs, a subgroup of 49 patients harboring specific angiographic characteristics were identified. Their charts and imaging films were retrospectively reviewed. RESULTS: We found a preponderance of CPA in young (mean age: 22) females (67%). Clinical symptoms were seizures, disabling headaches, and stroke-like symptoms; hemorrhagic presentations were exceptional. On cross-sectional imaging, CPA demonstrated as a diffuse network of densely enhancing vascular spaces with intermingled normal brain parenchyma. The discrepancy between the large size of the nidus and the small shunting volume, the absence of flow-related aneurysms, the presence of diffuse angiogenesis (eg, transdural supply, progressive arterial occlusion), and the small calibre of a multitude of feeding arteries and draining veins were the angiographic hallmarks of this disease. CONCLUSIONS: The diffuse angiogenetic activity is presumably related to reduced perinidal perfusion and subsequent chronic cortical ischemia. Natural history demonstrates a low risk of hemorrhage. CPA may be regarded as a separate clinical entity different to "classical" cerebral AVMs, because normal brain is interspersed with the abnormal vascular channels increasing the risk of neurological deficit in aggressive treatments, which in the light of the natural history does not seem to be indicated.
Subject(s)
Cerebral Angiography , Intracranial Arteriovenous Malformations/classification , Intracranial Arteriovenous Malformations/diagnosis , Adolescent , Adult , Aged , Central Nervous System Diseases/etiology , Child , Databases, Factual , Female , Headache/etiology , Humans , Intracranial Arteriovenous Malformations/complications , Intracranial Arteriovenous Malformations/therapy , Magnetic Resonance Imaging , Male , Middle Aged , Neovascularization, Pathologic/etiology , Retrospective Studies , Tomography, X-Ray ComputedABSTRACT
Spinal vascular diseases are rare and constitute only 1% to 2% of all vascular neurologic pathologies. In this article, the following vascular pathologies of the spine are described: spinal arterial infarcts, spinal cavernomas, and arteriovenous malformations (including perimedullary fistulae and glomerular arterivenous malformations), and spinal dural arteriovenous fistulae. This article gives an overview about their imaging features on MRI, MR angiography, and digital subtraction angiography. Clinical differential diagnoses, the neurologic symptomatology, and the potential therapeutic approaches of these diseases, which might vary depending on the underlying pathologic condition, are given.
Subject(s)
Angiography, Digital Subtraction/methods , Magnetic Resonance Imaging/methods , Spinal Cord Vascular Diseases/diagnosis , Spinal Cord/blood supply , Arteriovenous Fistula/diagnosis , Arteriovenous Malformations/diagnosis , Female , Humans , Male , Neovascularization, Pathologic/diagnosis , Rare Diseases , Spinal Cord/diagnostic imaging , Spinal Cord/pathologyABSTRACT
BACKGROUND: We describe two previously unreported cases with complete or incomplete expression of PHACES syndrome, a rare congenital syndromal pediatric disorder, which is characterized by posterior cranial fossa malformations, large facial hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, abnormalities of the eye, sternal and supraabdominal raphe defects. CASE REPORTS: These two children exhibited a feature not reviewed extensively in the literature, namely, segmental elongation and dilatation of intracranial arteries associated with intracranial occlusive arterial disease, predominantly on the anterior division of the internal carotid artery (ICA) and on the P2 segment of the posterior cerebral artery. This dolichoectasia was found at the distal cervical internal carotid artery, the intradural segment of the ICA before the division, the trigeminal artery, and the posterior division of the ICA. We presume that the different forms of arterial involvement in PHACES syndrome (arterial stenoses, segmental agenesis of vessels, and the dolichoectasia described in this study) constitute a spectrum of angiogenetic dysfunctions related to an embryonic event involving several cephalic neural crest segments of the dorsal aorta.
Subject(s)
Cerebral Arteries/pathology , Cranial Fossa, Posterior/abnormalities , Craniofacial Abnormalities/pathology , Eye Abnormalities/complications , Eye Abnormalities/pathology , Hemangioma/pathology , Brain/pathology , Carotid Artery, Internal/abnormalities , Carotid Artery, Internal/pathology , Child, Preschool , Female , Heart Septal Defects, Ventricular/complications , Heart Septal Defects, Ventricular/pathology , Humans , Infant , Magnetic Resonance Imaging , Maxillofacial Abnormalities/pathology , Middle Cerebral Artery/pathology , Raphe Nuclei/abnormalities , Seizures/complications , Seizures/drug therapy , Stroke/etiology , Syndrome , Tomography, X-Ray ComputedABSTRACT
OBJECTIVE: The vein of Galen aneurysmal malformation (VGAM) is a choroidal type of arteriovenous malformation involving the vein of Galen forerunner. This is distinct from an arteriovenous malformation with venous drainage into a dilated, but already formed, vein of Galen. Reports of endovascular treatment of VGAM in the literature approach the disease from a purely technical viewpoint and often fail to provide satisfactory midterm results. To focus the therapeutic challenge to a strictly morphological goal overlooks the fundamental aspects of neonatal and infant anatomy and fluid physiology. During the past 20 years, our approach to VGAM has remained the same. Our experience, based on 317 patients with VGAM who were studied in Hospital Bicêtre between October 1981 and October 2002, allows us to describe the angioarchitecture, natural history, and management of VGAM in neonates, infants, and children. METHODS: Of our cohort of 317 patients, 233 patients were treated with endovascular embolization; of these, 216 patients were treated in our hospital. The treatment method of choice was a transfemoral arterial approach to deliver glue at the fistulous zone. RESULTS: Of 216 patients, 23 died despite or because of the embolization (10.6%). Twenty out of the 193 (10.4%) surviving patients were severely retarded, 30 (15.6%) were moderately retarded, and 143 (74%) were neurologically normal on follow-up. CONCLUSION: Our data demonstrate that most treated children survive and undergo normal neurological development; an understanding of the clinical, anatomical, and pathophysiological features of VGAM has, therefore, reversed the former poor prognosis. Our level of understanding about the lesion allows us to predict most situations and remedy them by applying a strict evaluation protocol and working within an optimal therapeutic window. Patient selection and timing remain the keys in the management of this condition. It is more important to restore normal growth conditions than a normal morphological appearance, with the primary therapeutic objective being normal development in a child without neurological deficit.
Subject(s)
Cerebral Veins/abnormalities , Cerebral Veins/drug effects , Cyanoacrylates/administration & dosage , Embolization, Therapeutic/methods , Intracranial Aneurysm/therapy , Intracranial Arteriovenous Malformations/therapy , Tissue Adhesives/therapeutic use , Child , Child, Preschool , Humans , Infant , Infant, Newborn , Treatment OutcomeSubject(s)
Carotid Artery, Internal/abnormalities , Carotid Artery, Internal/embryology , Cerebral Angiography , Cerebral Arteries/embryology , Posterior Cerebral Artery/embryology , Carotid Artery, Internal/diagnostic imaging , Cerebral Arteries/diagnostic imaging , Humans , Posterior Cerebral Artery/diagnostic imagingABSTRACT
The pathogenesis of intracranial arterial aneurysms (AA) remains unclear, despite their clinical importance. An improved understanding of this disease is important in choosing therapeutic options. In addition to the "classical" berry-type aneurysm, there are various other types of intracranial AA such as infectious, dissecting or giant, partially-thrombosed aneurysms. From the clinician's perspective, the hypothesis that some of these intracranial AA might be due to abluminal factors has been proposed for several years. Indeed, this hypothesis and the empirical use of anti-inflammatory drugs in giant intracranial aneurysms have been confirmed by recent studies reporting that an enzyme involved in the inflammatory cascade (5-lipoxygenase or 5-LO) promotes the pathogenesis of specific aneurysms in humans. 5-LO generates different forms of leukotrienes which are potent mediators of inflammation. Adventitial inflammation leads to a weakening of the media from the abluminal part of the vessel wall due to the release of proinflammatory factors that invade the media, thereby degrading the extracellular matrix, the elastic lamina of the vascular wall, and, finally, the integrity of the vessel lumen. This in turn results in a dilation of the vessel and aneurysm formation. Moreover, neoangiogenesis of vasa vasorum is found in close proximity to 5-LO activated macrophages. In addition to this biological cascade, we argue that repeated subadventitial haemorrhages from the new vasa vasorum play an important role in aneurysm pathogenesis, due to a progressive increase in size mediated by the apposition of new layers of intramural haematoma within the vessel wall. Intracranial giant AA can therefore be regarded as a proliferative disease of the vessel wall induced by extravascular activity. Considering certain aneurysmal vasculopathies as an abluminal disease might alter current therapeutic strategies. Therapy should not only be aimed at the intraluminal repair of the artery, but also cross the vessel wall to reach the vasa vasorum. Drug-eluting stents placed proximal to the lesion and targeted to the origin of the vasa vasorum could be considered as a potential future option. "Intelligent" MRI contrast agents (i.e., macrophage marking) could be used to detect vasa vasorum proliferation and weakening of the vessel wall in vivo.