scholarly journals Spontaneous regression of a mandibular arteriovenous malformation in a 9-year-old boy: Case report with twelve month follow up

2017 ◽  
Vol 1 (0) ◽  
pp. 10
Author(s):  
Carolina Carneiro Soareas Macedo ◽  
Vinícius Rabelo Torregrossa ◽  
Márcio Ajudarte Lopes ◽  
Alan Roger dos Santos Silva
2020 ◽  
Vol 8 (2) ◽  
Author(s):  
Sobri M ◽  
Mezlina WZ ◽  
Subramaniam JH

Dural arteriovenous malformation (DAVM) is relatively rare and defined as abnormal connections or shunts between the arterial and the venous side of vascular tree located within the dura mater. Spontaneous closures of DAVM are rare and have been scarcely reported. This case report will describe the neuroimaging findings and classification of DAVM. A 50 year old lady presented with headache. Neuroimaging showed prominent serpinginous flow-void structures, cerebral angiogram confirmed the presence of DAVM at the occipital region. She had defaulted treatment and follow up for 3 years. On second admission, she had a cerebral angiogram which showed normal findings with no evidence of fistulas or malformation. She was discharged well. Causes of spontaneous closure of DAVM are discussed.


2017 ◽  
Vol 70 (7-8) ◽  
pp. 241-244
Author(s):  
Bojan Jelaca ◽  
Tomislav Cigic ◽  
Vladimir Papic ◽  
Mladen Karan ◽  
Jagos Golubovic ◽  
...  

Introduction. Treatment of cerebral arteriovenous malformations is very challenging and controversial in spite of current recommendations. Surgery is recommended in patients with hemorrhagic stroke, but in patients with good neurological status, when symptoms improve rapidly, the risk of surgical morbidity may be much higher than the risk of rebleeding. Case report. We report a case of a patient with an intracranial hemorrhage due to a ruptured arteriovenous malformation located in the right temporal region of the brain. Because of angiographic and anatomical features of the arteriovenous malformation (deep location and deep venous drainage, but also small arteriovenous malformation nidus size), radiosurgery was the preferred treatment modality. The patient was treated conservatively in the acute stage, and the arteriovenous malformation was subsequently completely eradicated with gamma knife radiosurgery. During the 3-year imaging follow-up, no sings of rebleeding were found. Also, angiography demonstrated that the arteriovenous malformation was completely excluded from the cerebral circulation. The patient was in a good condition and presented without neurological deficits or seizures during the follow-up period. Conclusion. All treatment modalities carry a risk of neurological compromise, but gamma knife radiosurgery may be a good option, even in cases with hemorrhagic presentation. It needs to be mentioned that complete obliteration takes approximately 1 to 3 years after the treatment, and in some cases it cannot be obtained.


2018 ◽  
Vol 52 ◽  
pp. 146-151
Author(s):  
Michael E. Kritikos ◽  
Nikhil Sharma ◽  
Neda Sedora-Roman ◽  
Bryan A. Pukenas ◽  
Robert W. Hurst ◽  
...  

Cephalalgia ◽  
2009 ◽  
Vol 29 (9) ◽  
pp. 980-985 ◽  
Author(s):  
WS Lesley

Intracranial arteriovenous malformation (AVM) is a rare cause of trigeminal neuralgia (TN). Successful resolution of AVM-related TN following embolization surgery using Onyx has not been reported. In this case report, a posterior fossa AVM was embolized in two separate, staged endovascular surgeries using Onyx. The AVM was reduced in size, and the TN resolved. The patient subsequently underwent radiosurgery for the small, residual AVM, and he has maintained an uneventful follow-up. A thorough literature review was also performed for AVM-associated TN. Fifty-nine reports of AVM-related TN have been described to date, of which only three were treated with embosurgery. None of the prior two embosurgical reports utilized Onyx, and no AVM was obliterated with embosurgery alone. TN secondary to AVM can be resolved with embosurgery utilizing Onyx; however, complete elimination of the underlying AVM requires adjuvant surgery.


2021 ◽  
Vol 14 (1) ◽  
pp. e239482
Author(s):  
Kelvin Yong Jie Lim ◽  
Alvin Yong Quan Soon ◽  
Jian Li Tan

Extracranial manifestation of arteriovenous malformations (AVMs) is uncommon. Nasoseptal AVMs are an even rarer entity. In this case report, we present an interesting and first-of-its-kind case of the development of a left nasoseptal AVM in a 60-year-old man after a fall. This was likely post-traumatic, unlike the usual congenital AVMs described in the literature. The patient was managed conservatively with regular follow-up for the AVM as he was asymptomatic.


2014 ◽  
Vol 72 (4) ◽  
pp. 730-736 ◽  
Author(s):  
Rúbia da Rocha Vieira ◽  
Éder Ricardo Biasoli ◽  
Marcelo Macedo Crivelini ◽  
Glauco Issamu Miyahara

2017 ◽  
Vol 55 (10) ◽  
pp. e106
Author(s):  
Juergen Schlabe ◽  
Ketan Shah ◽  
Fintan Sheerin ◽  
Miranda Payne ◽  
Adekunmi Fasanmade

2009 ◽  
Vol 82 (980) ◽  
pp. e148-e150 ◽  
Author(s):  
U ZÄTTERSTRÖM ◽  
J P AANESEN ◽  
A KOLBENSTVEDT

Neurosurgery ◽  
1991 ◽  
Vol 29 (6) ◽  
pp. 920-923 ◽  
Author(s):  
Shin-ichi Wakabayashi ◽  
Kikuo Ohno ◽  
Tsuneo Shishido ◽  
Masashi Tamaki ◽  
Yoshiharu Matsushima ◽  
...  

Abstract A case demonstrating the marked growth of an angiographically occult arteriovenous malformation is presented. A review of 58 cases in which an increase in the size of an arteriovenous malformation occurred suggested that the patient's initial age may have had an important role in such growth and that both the age and the duration of follow-up were related to the extent of growth. Follow-up neuroradiological examinations are thought to be necessary for patients who have had an episode of intracranial hemorrhage of unknown cause during childhood, even if the initial angiograms revealed no vascular lesion.


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