THE SYNDROMES of the ARTERIES of the BRAIN AND, SPINAL CORD Part II by LESLIE G
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The Segmentation of the Posterior Cerebral Artery: a Microsurgical Anatomic Study
Neurosurgical Review (2019) 42:155–161 https://doi.org/10.1007/s10143-018-0972-y ORIGINAL ARTICLE The segmentation of the posterior cerebral artery: a microsurgical anatomic study Aysun Uz1,2 Received: 1 November 2017 /Revised: 3 February 2018 /Accepted: 22 March 2018 /Published online: 6 April 2018 # Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract There are still different descriptions of the segmentation of the posterior cerebral artery, although there is a radiological and anatomical consensus on the segmentation of the anterior and the middle cerebral artery. This study aims to define the most appropriate localization for origin and end points of the segments through reviewing the segmentation of the posterior cerebral artery. The segments and the cortical branches originating from those segments of the 40 posterior cerebral arteries of 20 cadaver brains were examined under operating microscope. In this research, the P1,P2,P3,P4,andP5 classification of the segmentation of the posterior cerebral artery is redefined. This redefinition was made to overcome the complexities of previous definitions. The P1 segment in this research takes its origin from the basilar tip and ends at the junction with the posterior communicating artery. The average diameter of this segment at the origin was 2.21 mm (0.9–3.3), and the average length was 6.8 mm (3–12). The P2 segment extends from the junction with the posterior communicating artery to the origin of the lateral temporal trunk. This point usually situates on one level of posterior of the cerebral peduncle. The average diameter of this segment at the origin was 2.32 mm (1.3–3.1), and the average length was 20.1 mm (11–26). -
Endovascular Treatment of Stroke Caused by Carotid Artery Dissection
brain sciences Case Report Endovascular Treatment of Stroke Caused by Carotid Artery Dissection Grzegorz Meder 1,* , Milena Swito´ ´nska 2,3 , Piotr Płeszka 2, Violetta Palacz-Duda 2, Dorota Dzianott-Pabijan 4 and Paweł Sokal 3 1 Department of Interventional Radiology, Jan Biziel University Hospital No. 2, Ujejskiego 75 Street, 85-168 Bydgoszcz, Poland 2 Stroke Intervention Centre, Department of Neurosurgery and Neurology, Jan Biziel University Hospital No. 2, Ujejskiego 75 Street, 85-168 Bydgoszcz, Poland; [email protected] (M.S.);´ [email protected] (P.P.); [email protected] (V.P.-D.) 3 Department of Neurosurgery and Neurology, Faculty of Health Sciences, Nicolaus Copernicus University in Toru´n,Ludwik Rydygier Collegium Medicum, Ujejskiego 75 Street, 85-168 Bydgoszcz, Poland; [email protected] 4 Neurological Rehabilitation Ward Kuyavian-Pomeranian Pulmonology Centre, Meysnera 9 Street, 85-472 Bydgoszcz, Poland; [email protected] * Correspondence: [email protected]; Tel.: +48-52-3655-143; Fax: +48-52-3655-364 Received: 23 September 2020; Accepted: 27 October 2020; Published: 30 October 2020 Abstract: Ischemic stroke due to large vessel occlusion (LVO) is a devastating condition. Most LVOs are embolic in nature. Arterial dissection is responsible for only a small proportion of LVOs, is specific in nature and poses some challenges in treatment. We describe 3 cases where patients with stroke caused by carotid artery dissection were treated with mechanical thrombectomy and extensive stenting with good outcome. We believe that mechanical thrombectomy and stenting is a treatment of choice in these cases. Keywords: stroke; artery dissection; endovascular treatment; stenting; mechanical thrombectomy 1. -
The Cerebellum in Sagittal Plane-Anatomic-MR Correlation: 2
667 The Cerebellum in Sagittal Plane-Anatomic-MR Correlation: 2. The Cerebellar Hemispheres Gary A. Press 1 Thin (5-mm) sagittal high-field (1 .5-T) MR images of the cerebellar hemispheres James Murakami2 display (1) the superior, middle, and inferior cerebellar peduncles; (2) the primary white Eric Courchesne2 matter branches to the hemispheric lobules including the central, anterior, and posterior Dean P. Berthoty1 quadrangular, superior and inferior semilunar, gracile, biventer, tonsil, and flocculus; Marjorie Grafe3 and (3) several finer secondary white-matter branches to individual folia within the lobules. Surface features of the hemispheres including the deeper fissures (e.g., hori Clayton A. Wiley3 1 zontal, posterolateral, inferior posterior, and inferior anterior) and shallower sulci are John R. Hesselink best delineated on T1-weighted (short TRfshort TE) and T2-weighted (long TR/Iong TE) sequences, which provide greatest contrast between CSF and parenchyma. Correlation of MR studies of three brain specimens and 11 normal volunteers with microtome sections of the anatomic specimens provides criteria for identifying confidently these structures on routine clinical MR. MR should be useful in identifying, localizing, and quantifying cerebellar disease in patients with clinical deficits. The major anatomic structures of the cerebellar vermis are described in a companion article [1). This communication discusses the topographic relationships of the cerebellar hemispheres as seen in the sagittal plane and correlates microtome sections with MR images. Materials, Subjects, and Methods The preparation of the anatomic specimens, MR equipment, specimen and normal volunteer scanning protocols, methods of identifying specific anatomic structures, and system of This article appears in the JulyI August 1989 issue of AJNR and the October 1989 issue of anatomic nomenclature are described in our companion article [1]. -
Basal Ganglia & Cerebellum
1/2/2019 This power point is made available as an educational resource or study aid for your use only. This presentation may not be duplicated for others and should not be redistributed or posted anywhere on the internet or on any personal websites. Your use of this resource is with the acknowledgment and acceptance of those restrictions. Basal Ganglia & Cerebellum – a quick overview MHD-Neuroanatomy – Neuroscience Block Gregory Gruener, MD, MBA, MHPE Vice Dean for Education, SSOM Professor, Department of Neurology LUHS a member of Trinity Health Outcomes you want to accomplish Basal ganglia review Define and identify the major divisions of the basal ganglia List the major basal ganglia functional loops and roles List the components of the basal ganglia functional “circuitry” and associated neurotransmitters Describe the direct and indirect motor pathways and relevance/role of the substantia nigra compacta 1 1/2/2019 Basal Ganglia Terminology Striatum Caudate nucleus Nucleus accumbens Putamen Globus pallidus (pallidum) internal segment (GPi) external segment (GPe) Subthalamic nucleus Substantia nigra compact part (SNc) reticular part (SNr) Basal ganglia “circuitry” • BG have no major outputs to LMNs – Influence LMNs via the cerebral cortex • Input to striatum from cortex is excitatory – Glutamate is the neurotransmitter • Principal output from BG is via GPi + SNr – Output to thalamus, GABA is the neurotransmitter • Thalamocortical projections are excitatory – Concerned with motor “intention” • Balance of excitatory & inhibitory inputs to striatum, determine whether thalamus is suppressed BG circuits are parallel loops • Motor loop – Concerned with learned movements • Cognitive loop – Concerned with motor “intention” • Limbic loop – Emotional aspects of movements • Oculomotor loop – Concerned with voluntary saccades (fast eye-movements) 2 1/2/2019 Basal ganglia “circuitry” Cortex Striatum Thalamus GPi + SNr Nolte. -
A Unique Temporary Collateral Pathway Between Carotid-Vertebrobasilar
Liu et al. BMC Neurology (2020) 20:97 https://doi.org/10.1186/s12883-020-01651-1 CASE REPORT Open Access A unique temporary collateral pathway between carotid-vertebrobasilar arteries in a carotid dissection patient Xiaogang Liu1†, Bing Li2†, Ying Liu3, Hongliang Wu2* , Huilong Zhang2, Lianwei Dou2 and Chuanyu Liu2 Abstract Background: In adults, the anastomosis between carotid and vertebrobasilar arteries is usually the posterior communicating artery, sometimes the primitive trigeminal artery. In this case, the basilar artery fed the internal carotid artery through the pontine-to-tentorial artery anastomosis after severe stenosis from traumatic carotid dissection. Case presentation: A 32-year-old female was diagnosed with ischemic stroke caused by traumatic carotid artery dissection. Aspirin (100 mg/day) and clopidogrel (75 mg/day) were prescribed. Digital subtraction angiography performed 6 days after stroke onset showed a dissection in the cervical segment of left internal carotid artery with severe local stenosis, and a collateral pathway from BA to the cavernous segment of internal carotid artery through the lateral pontine and tentorial artery. Without interventional therapy, clinical symptoms improved significantly within 10 days after onset. At 3-month follow-up, left common carotid artery angiography showed the stenosis had been significantly improved with a residual aneurysm. There was no collateral pathway between carotid-vertebrobasilar arteries, and a residual small artery originated from the posterior vertical segment of cavernous internal carotid artery. The small artery was clearly visualized by 3-dimensional rotational angiography and identified the tentorial artery. Conclusion: To the author’s knowledge, this is the first report of a collateral pathway between carotid vertebrobasilar arteries through the pontine-to-tentorial artery anastomosis. -
Crossed Cerebellar Atrophy in Patients with Precocious Destructive Brain Insults
ORIGINAL CONTRIBUTION Crossed Cerebellar Atrophy in Patients With Precocious Destructive Brain Insults Ricardo A. Teixeira, MD; Li M. Li, MD, PhD; Sergio L. M. Santos, MD; Veronica A. Zanardi, MD, PhD; Carlos A. M. Guerreiro, MD, PhD; Fernando Cendes, MD, PhD Objective: To analyze the frequency and pathogenetic ciated with the extent of the supratentorial lesion (6 from factors of crossed cerebellar atrophy (CCA) in adult pa- group A, 1 from group B, and none from group C; tients with epilepsy secondary to destructive brain in- PϽ.001). Status epilepticus was present in 6 patients from sults of early development. group A and in none from the other groups. There was an association between the antecedent of status epilep- Methods: We studied 51 adult patients with epilepsy ticus and CCA (PϽ.001). All patients had atrophy of the and precocious destructive lesions. Patients were cerebral peduncle ipsilateral to the supratentorial lesion divided into 3 groups according to the topographic dis- and 4 had contralateral atrophy of the middle cerebellar tribution of their lesions on magnetic resonance imag- peduncle. The duration of epilepsy was not associated ing: group A, hemispheric (n=9); group B, main arterial with the presence of CCA (P=.20). territory (n=25); and group C, arterial border zone (n=17). We evaluated the presence of CCA visually and Conclusions: Our data suggest that in patients with epi- with cerebellar volumetric measurement, correlating it lepsy and destructive insults early in life, the extent of with the clinical data. Other features shown on mag- the supratentorial lesion as well as the antecedent of sta- netic resonance imaging, such as the thalamus, brain- tus epilepticus play a major role in the pathogenesis of stem, and middle cerebellar peduncle, were also care- CCA. -
Cerebellar Ataxia
CEREBELLAR ATAXIA Dr. Waqar Saeed Ziauddin Medical University, Karachi, Pakistan What is Ataxia? ■ Derived from a Greek word, ‘A’ : not, ‘Taxis’ : orderly Ataxia is defined as an inability to maintain normal posture and smoothness of movement. Types of Ataxia ■ Cerebellar Ataxia ■ Sensory Ataxia ■ Vestibular Ataxia Cerebellar Ataxia Cerebrocerebellum Spinocerebellum Vestibulocerebellum Vermis Planning and Equilibrium balance Posture, limb and initiating and posture eye movements movements Limb position, touch and pressure sensation Limb ataxia, Eye movement dysdiadochokinesia, disorders, Truncal and gait Dysmetria dysarthria nystagmus, VOR, ataxia hypotonia postural and gait. Gait ataxia Types of Cerebellar Ataxia • Vascular Acute Ataxia • Medications and toxins • Infectious etiologies • Atypical Infectious agents • Autoimmune disorders • Primary or metastatic tumors Subacute Ataxia • Paraneoplastic cerebellar degeneration • Alcohol abuse and Vitamin deficiencies • Systemic disorders • Autosomal Dominant Chronic • Autosomal recessive Progressive • X linked ataxias • Mitochondrial • Sporadic neurodegenerative diseases Vascular Ataxia ▪ Benedikt Syndrome It is a rare form of posterior circulation stroke of the brain. A lesion within the tegmentum of the midbrain can produce Benedikt Syndrome. Disease is characterized by ipsilateral third nerve palsy with contralateral hemitremor. Superior cerebellar peduncle and/or red nucleus damage in Benedikt Syndrome can further lead in to contralateral cerebellar hemiataxia. ▪ Wallenberg Syndrome In -
Stroke and Aphasia Aphasia Is a Language Disorder That Affects the Ability to Communicate
Recovery Primary motor cortex Primary sensory cortex let’s talk about Broca’s area Stroke and Aphasia Aphasia is a language disorder that affects the ability to communicate. It’s most often caused by strokes that occur in areas of the brain that control Primary auditory area Primary speech and language. Wernicke’s area visual cortex Certain areas of the brain (usually in the left side of the brain) influence one’s ability to communicate and understand language. When a stroke occurs in one of these areas, it may result in aphasia. What are the effects of aphasia? sender plissen.” Thousands of alert, intelligent men and Aphasia does not affect intelligence. Stroke survivors women are suddenly plunged into a world of jumbled remain mentally alert, even though their speech may communication because of aphasia. be jumbled, fragmented or impossible to understand. Are there different types of aphasia? Some survivors continue to have: Yes, there are several forms of aphasia. They include: • Trouble speaking, like “getting the words out” • Global aphasia — People with this aphasia may • Trouble finding words be completely unable to speak, name objects, repeat • Problems understanding what others say phrases or follow commands. • Problems with reading, writing or math • Broca’s aphasia — The person knows what they • Inability to process long words and infrequently want to say, but can’t find the right words (can’t get used words the words out). • Wernicke’s aphasia — A person with this aphasia How does it feel to have aphasia? can seldom understand what’s being said or control People with aphasia are often frustrated and confused what they’re saying. -
Spinocerebellar Ataxia Type 29 Due to Mutations in ITPR1: a Case Series and Review of This Emerging Congenital Ataxia Jessica L
Zambonin et al. Orphanet Journal of Rare Diseases (2017) 12:121 DOI 10.1186/s13023-017-0672-7 RESEARCH Open Access Spinocerebellar ataxia type 29 due to mutations in ITPR1: a case series and review of this emerging congenital ataxia Jessica L. Zambonin1*, Allison Bellomo2, Hilla Ben-Pazi3, David B. Everman2, Lee M. Frazer2, Michael T. Geraghty4, Amy D. Harper5, Julie R. Jones2, Benjamin Kamien6, Kristin Kernohan1,4, Mary Kay Koenig7, Matthew Lines4, Elizabeth Emma Palmer8,9, Randal Richardson10, Reeval Segel11, Mark Tarnopolsky12, Jason R. Vanstone4, Melissa Gibbons13, Abigail Collins14, Brent L. Fogel15, Care4Rare Canada Consortium, Tracy Dudding-Byth16 and Kym M. Boycott1,4 Abstract Background: Spinocerebellar ataxia type 29 (SCA29) is an autosomal dominant, non-progressive cerebellar ataxia characterized by infantile-onset hypotonia, gross motor delay and cognitive impairment. Affected individuals exhibit cerebellar dysfunction and often have cerebellar atrophy on neuroimaging. Recently, missense mutations in ITPR1 were determined to be responsible. Results: Clinical information on 21 individuals from 15 unrelated families with ITPR1 mutations was retrospectively collected using standardized questionnaires, including 11 previously unreported singletons and 2 new patients from a previously reported family. We describe the genetic, clinical and neuroimaging features of these patients to further characterize the clinical features of this rare condition and assess for any genotype-phenotype correlation for this disorder. Our cohort consisted of 9 males and 12 females, with ages ranging from 28 months to 49 years. Disease course was non-progressive with infantile-onset hypotonia and delays in motor and speech development. Gait ataxia was present in all individuals and 10 (48%) were not ambulating independently between the ages of 3–12 years of age. -
Diagnostic Clues in Multiple System Atrophy
DO I:10.4274/Tnd.82905 Case Report / Olgu Sunumu Diagnostic Clues in Multiple System Atrophy: A Case Report and Literature Review Multisistem Atrofi Tanısında İpuçları: Bir Olgu Sunumu ve Literatürün Gözden Geçirilmesi Mehmet Yücel, Oğuzhan Öz, Hakan Akgün, Semai Bek, Tayfun Kaşıkçı, İlter Uysal, Yaşar Kütükçü, Zeki Odabaşı Gülhane Military Medical Academy, Ankara, Turkey Sum mary Multiple system atrophy (MSA) is an adult-onset, sporadic, progressive neurodegenerative disease. Based on the consensus criteria, patients with MSA are clinically classified into cerebellar (MSA-C) and parkinsonian (MSA-P) subtypes. In addition to major diagnostic criteria including poor response to levodopa, and presence of pyramidal or cerebellar signs (ataxia) or autonomic failure, certain clinical features or ‘‘red flags’’ may raise the clinical suspicion for MSA. In our case report we present a 67-year-old female patient admitted to our hospital due to inability to walk, with poor response to levodopa therapy, whose neurological examination revealed severe Parkinsonism, ataxia and who fulfilled all criteria for MSA, as rarely seen in clinical practice.(Turkish Journal of Neurology 2013; 19:28-30) Key Words: Multiple system atrophy, autonomic failure, diagnostic criteria Özet Multisistem atrofi (MSA) erişkin dönemde başlayan, ilerleyici, nedeni bilinmeyen sporadik nörodejeneratif bir hastalıktır. MSA kabul görmüş tanı kriterlerine göre klinik olarak serebellar (MSA-C) ve parkinsoniyen (MSA-P) alt tiplerine ayrılmaktadır. Düşük levadopa yanıtı, piramidal, serebellar bulguların (ataksi) ya da otonomik bozukluk olması gibi majör tanı kriterlerininin yanında “red flags” olarak isimlendirilen belirgin klinik bulgular ya da uyarı işaretlerinin olması MSA tanısı için klinik şüpheyi oluşturmalıdır. Olgu sunumunda 67 yaşında yürüyememe şikayeti ile polikliniğimize müracaat eden ve levadopa tedavisine düşük yanıt gösteren ciddi parkinsonizm bulguları ile ataksi bulunan kadın hasta MSA tanı kriterlerini tam olarak karşıladığı ve klinik pratikte nadir görüldüğü için sunduk. -
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ONLINE FIRST This is a provisional PDF only. Copyedited and fully formatted version will be made available soon. ISSN: 0015-5659 e-ISSN: 1644-3284 Two cases of combined anatomical variations: maxillofacial trunk, vertebral, posterior communicating and anterior cerebral atresia, linguofacial and labiomental trunks Authors: M. C. Rusu, A. M. Jianu, M. D. Monea, A. C. Ilie DOI: 10.5603/FM.a2021.0007 Article type: Case report Submitted: 2020-11-28 Accepted: 2021-01-08 Published online: 2021-01-29 This article has been peer reviewed and published immediately upon acceptance. It is an open access article, which means that it can be downloaded, printed, and distributed freely, provided the work is properly cited. Articles in "Folia Morphologica" are listed in PubMed. Powered by TCPDF (www.tcpdf.org) Two cases of combined anatomical variations: maxillofacial trunk, vertebral, posterior communicating and anterior cerebral atresia, linguofacial and labiomental trunks M.C. Rusu et al., The maxillofacial trunk M.C. Rusu1, A.M. Jianu2, M.D. Monea2, A.C. Ilie3 1Division of Anatomy, Faculty of Dental Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania 2Department of Anatomy, Faculty of Medicine, “Victor Babeş” University of Medicine and Pharmacy, Timişoara, Romania 3Department of Functional Sciences, Discipline of Public Health, Faculty of Medicine, “Victor Babes” University of Medicine and Pharmacy, Timisoara, Romania Address for correspondence: M.C. Rusu, MD, PhD (Med.), PhD (Biol.), Dr. Hab., Prof., Division of Anatomy, Faculty of Dental Medicine, “Carol Davila” University of Medicine and Pharmacy, 8 Eroilor Sanitari Blvd., RO-76241, Bucharest, Romania, , tel: +40722363705 e-mail: [email protected] ABSTRACT Background: Commonly, arterial anatomic variants are reported as single entities. -
Mechanical Thrombectomy in Basilar Artery Occlusion Presence of Bilateral Posterior Communicating Arteries Is a Predictor of Favorable Clinical Outcome
Clin Neuroradiol (2019) 29:153–160 https://doi.org/10.1007/s00062-017-0651-3 ORIGINAL ARTICLE Mechanical Thrombectomy in Basilar Artery Occlusion Presence of Bilateral Posterior Communicating Arteries is a Predictor of Favorable Clinical Outcome Volker Maus 1 ·AlevKalkan1 · Christoph Kabbasch1 · Nuran Abdullayev1 · Henning Stetefeld2 · Utako Birgit Barnikol3 · Thomas Liebig4 · Christian Dohmen2 · Gereon Rudolf Fink2,5 · Jan Borggrefe1 · Anastasios Mpotsaris6 Received: 17 August 2017 / Accepted: 21 November 2017 / Published online: 19 December 2017 © Springer-Verlag GmbH Germany, part of Springer Nature 2017 Abstract Results The favorable clinical outcome at 90 days was 25% Background Mechanical thrombectomy (MT) of basilar and mortality was 43%. The rate of successful reperfusion, artery occlusions (BAO) is a subject of debate. We inves- i.e. modified thrombolysis in cerebral infarction (mTICI) ≥ tigated the clinical outcome of MT in BAO and predictors 2b was 82%. Presence of bilateral PcoAs (area under the of a favorable outcome. curve, AUC: 0.81, odds ratio, OR: 4.2, 2.2–8.2; p < 0.0001), Material and Methods A total of 104 MTs of BAO (carried lower National Institute of Health Stroke Scale (NIHSS) out between 2010 and 2016) were analyzed. Favorable out- on admission (AUC: 0.74, OR: 2.6, 1.3–5.2; p < 0.01), PC- come as a modified Rankin scale (mRS) Ä 2at90days ASPECTS ≥ 9 (AUC: 0.72, OR: 4.2, 1.5–11.9; p < 0.01), was the primary endpoint. The influence of the follow- incomplete BAO (AUC: 0.66, OR: 2.6, 1.4–4.8; p < 0.001), ing variables on outcome was investigated: number of de- and basilar tip patency (AUC: 0.66, OR: 2.5, 1.3–4.8; p < tectable posterior communicating arteries (PcoAs), patency 0.01) were associated with a favorable outcome.