In cerebral embolism, recanaiization occurs very

Similar documents
Diagnosis of Middle Cerebral Artery Occlusion with Transcranial Color-Coded Real-Time Sonography

Occlusion of All Four Extracranial Vessels With Minimal Clinical Symptomatology. Case Report

Hemorrhagic Transformation in Cerebral Embolism

ACUTE ISCHEMIC STROKE. Current Treatment Approaches for Acute Ischemic Stroke

Redgrave JN, Coutts SB, Schulz UG et al. Systematic review of associations between the presence of acute ischemic lesions on

Clinical Features and Subtypes of Ischemic Stroke Associated with Peripheral Arterial Disease

Brain Attack. Strategies in the Management of Acute Ischemic Stroke: Neuroscience Clerkship. Case Medical Center

WHI Form Report of Cardiovascular Outcome Ver (For items 1-11, each question specifies mark one or mark all that apply.

HEART AND SOUL STUDY OUTCOME EVENT - MORBIDITY REVIEW FORM


Asymptomatic Occlusion of an Internal Carotid Artery in a Hospital Population: Determined by Directional Doppler Ophthalmosonometry

Early Angiographic and CT Findings in Patients with Hemorrhagic Infarction in the Distribution of the Middle Cerebral Artery

Subclavian artery Stenting

/ / / / / / Hospital Abstraction: Stroke/TIA. Participant ID: Hospital Code: Multi-Ethnic Study of Atherosclerosis

Comparison of Five Major Recent Endovascular Treatment Trials

Cerebrovascular Disorders. Blood, Brain, and Energy. Blood Supply to the Brain 2/14/11

CEREBRO VASCULAR ACCIDENTS

Carotid Embolectomy and Endarterectomy for Symptomatic Complete Occlusion of the Carotid Artery as a Rescue Therapy in Acute Ischemic Stroke

Cryptogenic Strokes: Evaluation and Management

Original Contributions. Brain Damage After Open Heart Surgery in Patients With Acute Cardioembolic Stroke

Nonembolic Occlusion of the Middle Cerebral and Carotid Arteries- A Comparison of Predisposing Factors

Recurring Extracranial Internal Carotid Artery Vasospasm Detected by Intravascular Ultrasound

Supplementary material 1. Definitions of study endpoints (extracted from the Endpoint Validation Committee Charter) 1.

Stroke 101. Maine Cardiovascular Health Summit. Eileen Hawkins, RN, MSN, CNRN Pen Bay Stroke Program Coordinator November 7, 2013

TIA AND STROKE. Topics/Order of the day 1. Topics/Order of the day 2 01/08/2012

TIA: Updates and Management 2008

Imaging of Moya Moya Disease

Amaurosis fugax: some aspects of management

Cerebral hyperperfusion syndrome after carotid angioplasty

Spontaneous Recanalization after Complete Occlusion of the Common Carotid Artery with Subsequent Embolic Ischemic Stroke

IMAGING IN ACUTE ISCHEMIC STROKE

Basilar artery stenosis with bilateral cerebellar strokes on coumadin

Distal anterior cerebral artery (DACA) aneurysms are. Case Report

Raluca Pavaloiu et al. - Clinical, Epidemiological and Etiopathogenic Study of Ischemic Stroke

Occlusio Supra Occlusionem: Intracranial Occlusions Following Carotid Thrombosis as Diagnosed by Cerebral Angiography

Does ABCD 2 Score Below 4 Allow More Time to Evaluate Patients With a Transient Ischemic Attack?

Transorbital blood flow sound recordings have the

Stroke/TIA. Tom Bedwell

Introduction. Abstract. Michael Yannes 1, Jennifer V. Frabizzio, MD 1, and Qaisar A. Shah, MD 1 1

Although moyamoya disease, a rare cerebrovascular occlusive

Early neurological worsening in acute ischaemic stroke patients

Hyperperfusion syndrome after MCA embolectomy a rare complication?

Michael Horowitz, MD Pittsburgh, PA

Bilateral traumatic internal carotid artery dissections: Case report

SWISS SOCIETY OF NEONATOLOGY. Neonatal cerebral infarction

ACUTE STROKE TREATMENT IN LARGE NIHSS PATIENTS. Justin Nolte, MD Assistant Profession Marshall University School of Medicine

Carotid artery stenting for long CTO and pseudo occlusion of carotid artery -2 case reports-

INSTITUTE OF NEUROSURGERY & DEPARTMENT OF PICU

Transient Ischemic Attacks and Risk of Stroke in an Elderly Poor Population

Neuroanatomy of a Stroke. Joni Clark, MD Professor of Neurology Barrow Neurologic Institute

Vascular Disorders. Nervous System Disorders (Part B-1) Module 8 -Chapter 14. Cerebrovascular disease S/S 1/9/2013

Moyamoya disease in the midwestern United States

Treatment of Unruptured Vertebral Artery Dissecting Aneurysms

Non-commercial use only

Evaluation of Carotid Vessels and Vertebral Artery in Stroke Patients with Color Doppler Ultrasound and MR Angiography

Endovascular Neurointervention in Cerebral Ischemia

Transcranial Doppler ultrasonography (TCD)

THE FRAMINGHAM STUDY Protocol for data set vr_soe_2009_m_0522 CRITERIA FOR EVENTS. 1. Cardiovascular Disease

Endovascular Treatment Updates in Stroke Care

The phenomenon of unilateral loss of vision in

Reduction of flow velocities in patients with ischemic events in the middle cerebral artery long-term follow-up with ultrasound

Disclosures. Anesthesia for Endovascular Treatment of Acute Ischemic Stroke. Acute Ischemic Stroke. Acute Stroke = Medical Emergency!

Carotid Endarterectomy for Symptomatic Complete Occlusion of the Internal Carotid Artery

Moyamoya Disease A Vasculopathy and an Uncommon Cause of Recurrent Cerebrovascular Accidents

NEURORADIOLOGY DIL part 4

IDPH EMS Region Five. Stroke Education

ESM 1. Survey questionnaire sent to French GPs. Correct answers are in bold. Part 2: Clinical cases: (Good answer are in bold) Clinical Case 1:

Int J Clin Exp Med 2018;11(9): /ISSN: /IJCEM

Case Report 1. CTA head. (c) Tele3D Advantage, LLC

Effect of Intracranial Stenosis Revascularization on Dynamic and Static Cerebral Autoregulation

Moyamoya Syndrome with contra lateral DACA aneurysm: First Case report with review of literature

From the Cerebrovascular Imaging and Intervention Committee of the American Heart Association Cardiovascular Council

Ruptured aberrant internal carotid artery pseudoaneurysm presenting with spontaneous massive ear bleeding following a single sneeze: a case report

Cryptogenic Stroke: What Don t We Know. Siddharth Sehgal, MD Medical Director, TMH Stroke Center Tallahassee Memorial Healthcare

Carotid Revascularization

Concurrent Subarachnoid Hemorrhage and Acute Myocardial Infarction: A Case Report

Coronary Spasm as a Cause of Coronary Thrombosis and Myocardial Infarction

Practical Considerations in the Early Treatment of Acute Stroke

Alan Barber. Professor of Clinical Neurology University of Auckland

(For items 1-12, each question specifies mark one or mark all that apply.)

Case 1 5/26/2017 ENDOVASCULAR MECHANICAL THROMBECTOMY IN PATIENTS WITH ACUTE ISCHEMIC STROKE

Emergently? Michigan Institute for Neurological Disorders. Garden City Hospital, Garden City, Michigan

Recent Advances in Neurology Difficult Cases

Stroke is the third-leading cause of death and a major

Vivek R. Deshmukh, MD Director, Cerebrovascular and Endovascular Neurosurgery Chairman, Department of Neurosurgery Providence Brain and Spine

The severity of neurologic deficits associated with

9 : , Fogarty 89% 9 : , Table 1. (Tel : )

PFO Management update

Spontaneous cervicocephalic arterial dissection with headache and neck pain as the only symptom

framework for flow Objectives Acute Stroke Treatment Collaterals in Acute Ischemic Stroke framework & basis for flow

Dr Julia Hopyan Stroke Neurologist Sunnybrook Health Sciences Centre

EMBOLIC OCCLUSION OF THE SUPERIOR AND IN- FERIOR DIVISIONS OF THE MIDDLE CEREBRAL ARTERY WITH ANGIOGRAPHIC-CLINICAL CORRELATION*

A CASE OF RECURRENT ALTERNATING TRANSIENT HEMIPARESIS Dr. Shunmuga Arumugasamy.S DNB Resident Railway Hospital, Perambur.

Subclavian and Vertebral Artery Angioplasty - Vertebro-basilar Insufficiency: Clinical Aspects and Diagnosis

TRAUMATIC CAROTID &VERTEBRAL ARTERY INJURIES

Advances in Neuro-Endovascular Care for Acute Stroke

Is Stroke a Paradoxical Embolism in Patients with Patent Foramen Ovale?

Endovascular Treatment for Acute Ischemic Stroke

Advances in Prevention and Treatment of Stroke: What Every Primary Care Physician Needs to Know. Case 1 4/5/11. What treatment should you initiate?

Transcription:

680 Case Reports Recanaiization of Intracranial Carotid Occlusion Detected by Duplex Carotid Sonography Haruhiko Hoshino, MD, Makoto Takagi, MD, Ikuo Takeuchi, MD, Tsugio Akutsu, MD, Yasuyuki Takagi, MD, and Shinichirou Ebihara, MD We studied three patients with internal carotid artery occlusion at the siphon who had recanaiization during 1 month of close observation. Angiography and duplex carotid sonography (DCS) were repeated serially in each patient. Blood flow patterns detected by DCS were classified into three patterns by specific angiographic changes. The distal occiusive flow pattern on DCS corresponds to internal carotid artery occlusion at the siphon angiographically, the median flow pattern on DCS corresponds to partial recanaiization, and a normal flow pattern on DCS indicates almost complete recanaiization. Since DCS can be easily repeated, the exact time of recanaiization can be determined noninvasively. In all three patients, hemorrhagic infarction observed on computed tomograms occurred at the time of recanaiization detected by DCS. DCS demonstrates that recanaiization is one of the mechanisms of hemorrhagic infarction. (Stroke 1989;20:680-686) In cerebral embolism, recanaiization occurs very commonly, ranging from 40% to 75%. '- 5 When recanaiization occurs, cerebral infarction may become hemorrhagic and clinical conditions may be aggravated. Recanaiization can be diagnosed on serial angiograms, but repeated angiography is impractical and not without risk during the acute illness. For this reason, it is difficult to tell the exact time of recanaiization by the limited number of angiographic examinations. Duplex carotid sonography (DCS) is very useful to diagnose internal carotid artery occlusion 6 and can be easily repeated. We have performed serial DCS examinations on three patients with intracranial carotid artery occlusion and have found that DCS can indicate the exact time of recanaiization. Case Reports DCS examinations were carried out with a Diasonics DRF 400V (Milpitas, California). The duplex probe consisted of a 10-MHz imaging transducer and a 4.5-MHz pulsed Doppler transducer. From the Department of Neurology, Tokyo Saiseikai Central Hospital (H.H., M.T., I.T., T.A., Y.T.) and the Department of Neurology, Tokyo Saiseikai Mukoujima Hospital (S.E.), Tokyo, Japan. Address for correspondence: Haruhiko Hoshino, MD, Department of Neurology, Tokyo Saiseikai Central Hospital, 1-4-17 Mita, Minato, Tokyo 108, Japan. Received August 1, 1988; accepted October 25, 1988. From April 1984 to December 1987, we performed 1,586 DCS examinations. Among them, 66 patients had internal carotid artery occlusion, 48 at the origin and 18 at the siphon. We performed serial DCS examinations during the acute period of cerebral infarction in 17 of these 66 patients; nine had occlusion at the origin and eight at the siphon. Angiography was performed in six of the nine patients and confirmed that all six had occlusion at the origin of the internal carotid artery, but serial angiography was not performed. We performed angiography in all eight patients with occlusion at the siphon, and the results indicated that five indeed had occlusion at the siphon and three had recanaiization by the time of angiography. Recanaiization was noted on serial angiograms in three of the five patients who had occlusion at the siphon. In these three patients, internal carotid artery blood flow patterns on DCS have been studied and can be classified into three patterns: 1) distal occiusive flow pattern: blood flow signals are detected only during the systolic phase but cannot be detected during the diastolic phase; 2) median flow pattern: between 1 and 3; and 3) normal flow pattern: blood flow is the same as in normal persons. Case 1. A 60-year-old man was admitted to our hospital because of an inability to speak. He had been living alone and did well until a day before admission, when a friend noted his inability to speak. On admission he was somnolent, his temperature was 36.1 C, his pulse was 60/min and regular,

Hoshino et al RecanaUzation Detected by Duplex 681 FIGURE 1. Case 1. Left: internal carotid artery on admission. Right: Frontal view of left carotid angiogram on admission. ISEIKfll CHUO ANCLE 43* AVG VEL VEt PNGf Sfil SEIKRI «MCL E «42- M 3«^S C CHUO ^^^^ Us AVG V? VEL BNC 22 CS1 _, -I t ***** FIGURE 2. Case 1. Left: internal carotid artery on seventh hospital day. Right: Frontal view of left carotid angiogram on eighth hospital day. FIGURE 3. Case 1. Left: internal carotid artery on 15th hospital day. Right: Frontal view of left carotid angiogram on 28th hospital day. t I CO

682 Stroke Vol 20, No 5, May 1989 FIGURE 4. Case 1. Unenhanced computed tomograms on Geft) second, (center) 14th, and (right) 49th hospital day. Hemorrhagic infarction was noted on 14th hospital day. and his respiration rate was 20/min. His supine blood pressure was 128/80 mm Hg. Neurologic examination revealed that he had nonfluent aphasia, left conjugate deviation of his eyes, right hemiparesis, and right homonymous hemianopsia. Laboratory examinations showed increased serum creatine kinase concentration, up to 1,053 (normal range 3364) IU/ml, but electrocardiography (ECG) showed no evidence of myocardial infarction. On admission, a distal occlusive flow pattern was noted in the left internal carotid artery by DCS (Figure 1, left). Diagnosis by DCS was an occlusion of the left internal carotid artery at the siphon; this diagnosis was confirmed by angiography (Figure 1, right). On his seventh hospital day, DCSfindingschanged to a median flow pattern (Figure 2, left). On his eighth hospital day, angiography demonstrated that the embolus had moved distally and the left anterior cerebral artery was visualized from the ipsilateral internal carotid artery, but still no filling of the middle cerebral artery was noted (Figure 2, right). On his 15th hospital day, the DCS Doppler flow pattern of the left internal carotid artery improved to a normal flow pattern (Figure 3, left). On his 28th hospital day, recanalization was confirmed angiographically (Figure 3, right). During these episodes his clinical conditions were not aggravated, and transient atrial fibrillation was found on ECG. Hemorrhagic infarction was noted on a cranial computed tomogram (CT scan) on his 14th hospital day even though no anticoagulation therapy was given to this patient (Figure 4). Case 2. A 75-year-old woman had been treated for hypertension, cardiomegaly, and arrhythmia for the past 10 years. She was well until the evening of admission, when her family found her with disturbed consciousness. On admission she was somnolent, her temperature was 36.0 C, her pulse was 58/min and irregular, and her respiration rate was 24/min. Her blood pressure was 124/70 mm Hg. Neurologic examination revealed that she was totally aphasic and had left conjugate deviation of her eyes, right hemiplegia, and right homonymous hemianopsia. Results of laboratory examinations were unremarkable. Atrial fibrillation was noted on ECG. On admission, DCS demonstrated a distal occlusive flow pattern of the left internal carotid artery (Figure 5, left); the diagnosis was confirmed by angiography on her third hospital day (Figure 5, right). On her eighth hospital day, DCS findings changed to a median flow pattern. On her 10th hospital day, the DCS Doppler flow pattern of the left internal carotid artery improved to a normal flow pattern (Figure 6, left). On her 12th hospital day, recanalization was confirmed angiographically (Figure 6, right). During these episodes her clinical conditions were unchanged. Hemorrhagic infarction was noted by cranial CT on her 10th hospital day even though no anticoagulation therapy was administered (Figure 7). Case 3. A 76-year-old woman had been treated for angina pectoris and atrial fibrillation for 3 years prior to admission. She was well until the morning of admission, when her family found her with disturbed consciousness. On admission she was somnolent but fully oriented. Her temperature was 36.0 C, her pulse was 76/min and irregular. Her supine blood pressure was 170/80 mm Hg. Neurologic examination revealed left-sided neglect, right conjugate deviation of her eyes, left hemiplegia, and left homonymous hemianopsia. Results of laboratory examinations of her urine and blood were unremarkable. Atrial fibrillation was noted on ECG. On admission, a distal occlusive flow pattern of the right internal carotid artery was noted by DCS (Figure 8, left); the diagnosis was confirmed by angiography (Figure 8, right). On her second hospital day she complained of headache, and DCS findings changed to a median flow pattern. On her third hospital day she became semicomatose, but on her fifth day her level of consciousness improved to somnolence. On her sixth hospital day, the DCS Doppler flow pattern of the right internal carotid artery improved to a normal

Hoshino et al Recanalization Detected by Duplex 683 FIGURE 5. Case 2. Left: internal carotid artery on admission. Right: Lateral view of left carotid angiogram on third hospital day. FIGURE 6. Case 2. Left: internal carotid artery on 10th hospital day. Right: Lateral view of left carotid angiogram on 12th hospital day. FIGURE 7. Case 2. Unenhanced computed tomograms on (left) third, (center) 14th, and (right) 21st hospital day. Hemorrhagic infarction was noted on 10th hospital day.

684 Stroke Vol 20, No 5, May 1989 FIGURE 8. Case 3. Left: Doppler flow pattern of right internal carotid artery on admission. Right: Lateral view of right carotid angiogram on admission. SfllSEIKfll CHUO 31 SEC INVERTED W!^^Tl ^^^n I FIGURE 9. Case 3. Left: Doppler flow pattern of right internal carotid artery on sixth hospital day. Right: Lateral view of right carotid angiogram on sixth hospital day. FIGURE 10. Case 3. Unenhanced computed tomograms on (left) second and (right) 10th hospital day. Hemorrhagic infarction was noted on eighth hospital day.

Hoshino et al Recanalization Detected by Duplex 685 Case 1 2 3 Duplex CT Autography Duplex CT Angwgraphy Duplex CT Angwgraphy Onset 1 3 5 7 9 11 13 15 17 19 21 28 days 9 O A A A A B D O 0 A A A A A A A 0 D A A A A A A a FIGURE 11. Summary of results of duplex carotid sonography, computed tomography (CT), and angiography. For duplex, flow pattern of internal carotid artery is designated, distal occlusive flow pattern;, median flow pattern; and O, normal flow pattern. For CT, area of cerebral infarction is designated A, low-density area; and A, high-density area. For angiography,findingsof internal carotid artery at siphon are designated, complete occlusion; D, partial recanalization; anda, recanalization. flow pattern (Figure 9, left) and recanalization was confirmed angiographically (Figure 9, right). During these episodes we did not use any anticoagulation therapy. Hemorrhagic infarction was noted by cranial CT on her eighth hospital day (Figure 10). Discussion We describe three patients with internal carotid artery occlusion at the siphon with subsequent recanalization and associated hemorrhagic infarction. Since these patients had atrial fibrillation without substantial atherosclerosis, cerebral embolism was the most likely diagnosis. In these patients, DCS showed three flow patterns of the internal carotid artery. The first pattern was the distal occlusiveflow pattern, in which angiography showed complete occlusion of the internal carotid artery at the siphon. The third flow pattern was the normal flow pattern that is usually found in persons who do not have any occlusion; when DCS showed this pattern, angiography showed no occlusion in the internal carotid artery nor in the Ml portion of the middle cerebral artery. The second flow pattern was the median flow pattern, a pattern in between the first and third patterns. This second pattern indicates that the embolus has moved or incompletely lysed and partial recanalization has occurred; blood flow of the internal carotid artery was slightly increased, and this second pattern was observed only transiently. We found that the embolus moved distally and that only the anterior cerebral artery was visualized by angiography during this period in Case 1. In these three patients recanalization was noted by DCS and confirmed by angiography. We consider that DCS alone is sufficient to recognize recanalization of an internal carotid artery occlusion. Compared with CT findings, previous cerebral infarction changed to hemorrhagic infarction concurrent with recanalization, which was promptly detected by DCS (Figure 11). In 1958, Lehrer 1 initially demonstrated recanalization by serial angiography. Since then, angiography has been performed serially in cerebral infarction to detect recanalization. Recanalization usually occurs within 48-72 hours after the onset of occlusion, but it has been difficult to tell the exact time of recanalization angiographically. 5 We have previously demonstrated the distal occlusive flow pattern in the internal carotid artery in five of five patients with carotid artery occlusion at the siphon and in three of four patients with middle cerebral artery occlusion at the Ml portion. 6 Analysis of these three current patients suggest that the internal carotid artery flow pattern on DCS is a simple and easy way to detect recanalization. Fisher and Adams 7 postulated that downstream migration of the embolus after its initial impact leads to extravasation of blood via reflow into the damaged vessels. In our three patients, the appearance of hemorrhagic infarction on CT scans correlated with recanalization detected by DCS. Hemorrhagic infarction occurs by several hypothetical mechanisms. 8 Our study supports the importance of recanalization in hemorrhagic transformation. Acknowledgment Professor Teruyuki Kurihara, MD, Toho University, School of Medicine, Tokyo kindly reviewed the manuscript. References 1. Lehrer GM: Arteriographic demonstration of collateral circulation in cerebrovascular disease. Neurology 1958;8:27-32 2. Dalai PM, Shah PM, Sheth SC, Deshpande CK: Cerebral embolism. Angiographic observations on spontaneous clot lysis. Lancet 1965; 1:61-64 3. Liebeskind A, Chinichian A, Schechter MM: The moving embolus seen during serial cerebral angiography. Stroke 1971^:440-443

686 Stroke Vol 20, No 5, May 1989 4. Irino T, Tancda M, Minami T: Angiographic manifestations 7. Fisher CM, Adams RD: Observations on brain embolism in postrecanalized cerebral infarction. Neurology 1977; with special reference to the mechanism of hemorrhagic 27:471-475 infarction. J Neuropathol Exp Neurol 1951 ;10:92-93 5. Irino T: Review of the clinical reports about recanalization 8. Hart RG, Easton JD: Hemorrhagic infarcts. Stroke 1986; of occluded cerebral artery. No To Shinkei 1978^0:135-151 17:586-589 6. Hoshino H, Takagi M, Komagamine M, Takagi Y, Ebihara S: Diagnosis of internal carotid artery occlusion by duplex ultrasonography. Jpn J Stroke 1988;10:169-174 KEYWORDS carotid artery diseases ultrasonics