Cerebral ischaemia after repair of coarctation of the aorta

2014 ◽  
Vol 25 (4) ◽  
pp. 780-782
Author(s):  
Maria Gogou ◽  
Anastasia Keivanidou ◽  
Andreas Giannopoulos

AbstractA 9-year-old boy, with a history of repair of severe coarctation of the aorta through balloon angioplasty 2 weeks ago, presented in the emergency paediatric department with symptoms consistent with transient cerebral ischaemia. MRI revealed an area of cerebral infarction in the right frontal lobe. Causes of cerebral ischaemia after aortic coarctation repair are briefly discussed.

1992 ◽  
Vol 76 (1) ◽  
pp. 137-142 ◽  
Author(s):  
Francis H. Tomlinson ◽  
David G. Piepgras ◽  
Douglas A. Nichols ◽  
Daniel A. Rüfenacht ◽  
Sue C. Kaste

✓ A neonate presented with anatomically discrete cerebral arteriovenous fistulae located in the right sylvian fissure and the cerebellar vermis that were initially detected by prenatal ultrasonography. Following delivery of the baby by Caesarean section, both malformations were treated by surgical obliteration. These intracranial vascular lesions were associated with cardiac anomalies and a periductal coarctation of the aorta, which was treated with a left subclavian rotational arterial pedicle repair. Follow-up examination of the infant at age 13 months demonstrated an excellent clinical result with normalization of the circulation. The pathophysiology of this syndrome is discussed and the literature reviewed.


Author(s):  
Vityala Yethindra ◽  
Elmira Mamytova ◽  
Tugolbai Tagaev ◽  
Sagynali Mamatov

A 36-year-old male with non-lesional refractory frontal-lobe epilepsy, diagnosed at 16 years of age, and with a history of four hospitalizations for refractory status epilepticus and admitted to the intensive care unit with focal seizures in the right upper limb, impaired consciousness, and recurrent progression to bilateral tonic-clonic seizures.


2021 ◽  
Vol 9 ◽  
Author(s):  
Julia Moosmann ◽  
Ariawan Purbojo ◽  
Susanne Eder ◽  
Sven Dittrich

Primary surgical repair remains the traditional treatment for patients with critical duct-dependent coarctation of the aorta (CoA). Initial surgical repair might not be possible or associated with higher risks if additional comorbidities arise in small infants and neonates. Balloon angioplasty (BA) has been described as a rescue strategy for these children. We describe the feasibility of a palliative BA and rescue stent implantation via an alternative antegrade right-axillary artery approach in an initially inoperable infant with pneumonia and respiratory failure and severe CoA, where the stenosis was not passable by traditional retrograde femoral access. This case adds new aspects to the therapy of critical CoA: Stent implantation provides a bridge to surgery in critically ill infants and does not preclude successful surgical repair. Further, if the classic retrograde approach is not possible, the right axillary artery access should be considered as an alternative to pass the stenosis.


2011 ◽  
Vol 22 (4) ◽  
pp. 475-477 ◽  
Author(s):  
Pawel Dryzek ◽  
Sebastian Goreczny ◽  
Marek Kopala

AbstractThe authors describe successful balloon angioplasty of aortic coarctation in a preterm neonate weighing 670 grams. The intervention was performed in an open incubator to ensure stable temperature comfort and to minimise the risk of hypothermia during the procedure of obtaining surgical vessel access, performing balloon angioplasty, and closure of the wound.


2021 ◽  
Author(s):  
Huajun Jiang ◽  
Qu Wei ◽  
Liang Zhanhua ◽  
Yang Jingjing

Abstract Background: Familial hypercholesterolemia has various presentations mostly including early-onset cardiovascular diseases, remarkable skin and tendon xanthomas. By comparison, Cerebral Infarction due to familial hypercholesterolemia is extremely rare. Case presentation: We present a 41-year-old man who was admitted to our hospital with dizziness, vertigo, slurred speech, weakness in his left limbs. He had family history of Hyperlipidemia in older sister . Head CT scan demonstrated multiple acute cerebral infarction in the right frontal and parietal lobes, and arterial plaques was found in the bifurcation of common carotid artery. The severe carotid stenosis was located in the initial segment of the right internal carotid artery. Histopathologic findings were consistent with xanthoma. Especially, molecular analysis of the LDLR gene was made, which identified heterozygous missense mutation in exon 12 of the LDLR gene. The final diagnosis of cerebral infarction associated with familial hypercholesterolemia was made. The patient was referred to a nutritionist for dietary advice, and was treated with Tab. Finally, the patient recovered well. The symptoms of brain infarct vanished and no recurrence occurred during follow-up.Conclusions: In the present case, the acute cerebral infarction is most likely due to hypercholesterolemia, as his family history of hypercholesterolemia, and arterial plaques and severe carotid stenosis was found by CTA. This case highlights the importance of the early diagnosis and treatment of hypercholesterolemia, which may help in preventing the development of cardiovascular and cerebrovascular diseases.


1994 ◽  
Vol 4 (1) ◽  
pp. 75-78 ◽  
Author(s):  
Masaaki Yoshigi ◽  
Kazuo Momma ◽  
Yasuharu Imai

SummaryWe report a two-year-old boy with a rare combination of tetralogy of Fallot and aortic coarctation. The obstruction in this patient had an hourglass-like configuration, with a pressure difference of 15 mm Hg. There was a right aortic arch, bilateral brachiocephalic arteries, and persistent left superior caval vein. Percutaneous transluminal balloon angioplasty was performed to lower the resistance to the left ventricular ejection, considered a risk factor for subsequent corrective surgery of tetralogy. Six months later, he underwent combined repair of tetralogy of Fallot and coarctectomy with end-to-end anastomosis, thus avoiding the future potential for restenosis. During surgery, a ligament was found extending from the right subclavian artery to the distal side of the coarctation. The perioperative course was uneventful, indicating the success of the preoperative balloon angioplasty. We speculate that the embryogenesis of the coarctation could be related to an abnormal involution of the aortic arches.


Neurosurgery ◽  
2011 ◽  
Vol 68 (1) ◽  
pp. E258-E262 ◽  
Author(s):  
Kyung-Jae. Park ◽  
Shin-Hyuk. Kang ◽  
Yang-Seok. Chae ◽  
Yong-Gu. Chung

abstract BACKGROUND AND IMPORTANCE: Arachnoid cysts have not been reported to be located within the brain parenchyma. We present a case of an arachnoid cyst that was contained entirely within the right frontal lobe devoid of communication with the subarachnoid space and ventricle. CLINICAL PRESENTATION: A 65-year-old woman presented with a 1-year history of progressive headache and nausea. Computed tomographic and magnetic resonance imagining scans showed a well-defined, nonenhancing mass measuring 5 × 5 × 3.5 cm in the right frontal lobe. The mass appeared to be contained entirely within the brain parenchyma. The patient underwent a right frontal craniotomy, at which time the cystic mass was identified in the brain parenchyma without any communication with the arachnoid space. The cyst contained a clear fluid, and its wall was excised. The fluid contents demonstrated a composition similar to that of normal cerebrospinal fluid. Histological and immunohistochemical examinations of the cyst wall were compatible with the diagnosis of an arachnoid cyst. Postoperatively, the symptoms of the patient resolved, and no recurrence was observed up to 6 months after removal. CONCLUSION: The present case showed an intraparenchymal arachnoid cyst arising in the frontal lobe. Although the etiology is not known, an arachnoid cyst should be included in the differential diagnosis of primary intracerebral cysts.


2012 ◽  
Vol 23 (1) ◽  
pp. 138-140 ◽  
Author(s):  
Ahmet Çağrı Aykan ◽  
Mustafa Yıldız ◽  
Mehmet Özkan

AbstractCoarctation of the aorta is a rare congenital anomaly usually accompanying bicuspid aortic valve. Adult patients with aortic coarctation can be managed either with surgery or percutaneously. Here we present a case of percutaneously treated aortic coarctation complicated with infective endocarditis of the aortic valve, thoracic aortitis, and thoracic mycotic aneurysm.


Author(s):  
Steven Wolf ◽  
Andrew Rhoads ◽  
William Gomes ◽  
Philip Overby ◽  
Patricia McGoldrick

AbstractTuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder affecting many organ systems. Patients commonly develop a variety of benign tumors as well as neurological disease, including seizures, autism, and cognitive delay. We report here the case of an adolescent patient with TSC and a history of mild COVID-19 who presented with a 1-day history of altered mental status. The patient was found to have ischemic cerebral infarction of the right MCA and ACA territories. Initial angiography showed an occlusion of the right internal carotid artery without a demonstrable etiology, with follow-up echocardiography and angiography revealing a large aortic thrombus. The patient was not a candidate for thrombus removal due to her cerebral infarct and received medical anticoagulation. Thrombosis progressed to involve the left ICA, with left cerebral infarction and subsequent death. Aortic thrombus embolization as a cause of cerebrovascular accident (CVA) is a novel finding in the setting of TSC and should be considered for pediatric patients with CVA of unknown etiology. It is unclear whether this was related to the prior COVID-19 infection.


2021 ◽  
Author(s):  
Zhe-Yuan Li ◽  
Li-Hong Si ◽  
Bo Shen ◽  
Xia Ling ◽  
Xu Yang

Abstract Background: Vestibular migraine (VM) is considered one of the most common cause of episodic central vestibular disorders, the mechanism of VM is currently still unclear. It is worth investigating whether VM belongs to the migraine subtype or is a separate disorder. The development of functional nuclear magnetic resonance (fMRI) in recent years offers the possibility to explore the pathogenesis of VM in depth. The study aimed to investigate resting-state functional brain activity alterations in patients with VM diagnosed based on the diagnostic criteria of the Bárány Society and the International Headache Society.Methods: Seventeen patients with VM who received treatment in our hospital from December 2018 to December 2020 were enrolled. Clinical data of all patients were collected. Eight patients with migraine and 17 health controls (HCs) were also included. All subjects underwent fMRI examination. The amplitude of low frequency fluctuation (ALFF), fractional amplitude of low frequency fluctuation (fALFF) and regional homogeneity (ReHo) were calculated to observe the changes in spontaneous brain activity in patients with VM. Then brain regions with altered spontaneous brain activity were selected for seeded-based functional connectivity (FC) analysis to explore the changes in FC in patients with VM.Results: Among 17 patients with VM, there were 7 males and 10 females with an average age of 39.47±9.78 years old. All patients with VM had a history of migraine. Twelve (70.6%) patients with VM had recurrent spontaneous vertigo, 2 (11.7%) patients had visually-induced vertigo, and 3 (17.6%) patients had head motion-induced vertigo. All 17 patients with VM reported worsening of dizziness vertigo during visual stimulation. The migraine-like symptoms were photophobia or phonophobia (n=15, 88.2%), migraine-like headache (n=8, 47.1%), visual aura during VM onset (n= 7, 41.2%). 5 (29.4%) patients with VM had hyperactive response during the caloric test, and 12 (70.6%) patients had caloric test intolerance. Eleven (64.7%) patients had a history of motion sickness. VM patients showed exhibited significantly increased ALFF and fALFF values in the right temporal lobe (STG and MTG), and significantly increased ReHo values in the right STG, MTG and ITG in comparison with HCs. Compared with patients with migraine, patients with VM showed significantly decreased ALFF values in the right median cingulate and paracingulate gyri, significantly increased fALFF values in the right parietal lobe (postcentral gyrus and superior parietal gyrus), and the right frontal lobe (supplementary motor areas and dorsolateral superior frontal gyrus), as well as significantly increased ReHo values in the right thalamus. Compared with HCs, patients with migraine showed significantly increased ALFF values in the right limbic lobe (right parahippocampal gyrus and right fusiform gyrus), left ITG and the right frontal lobe (supplementary motor areas, right median cingulate and paracingulate gyri, and right right inferior frontal gyrus), significantly decreased ALFF values in the pons and brainstem, significantly decreased ReHo values in the frontal cortex (including left and right supplementary motor areas, left dorsolateral superior frontal gyrus, left median cingulate and paracingulate gyri, right paracentral lobule, right dorsolateral superior frontal gyrus, left and right middle frontal gyrus). Conclusions: Ventral stream of visual processing and allocentric spatial cognition in patients with VM may be impaired. Vertigo attacks in patients with VM may be related to increased spontaneous activity in the right parietal lobe-frontal lobe-thalamus; patients with VM and migraine both had altered brain function, but the underlying mechanism seems to be different.


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