Results 21 to 30 of about 22,680 (203)

Arteriovenous Malformation of Face

Contemporary Clinical Dentistry, 2017
Arteriovenous malformations (AVMs) are rare congenital vascular malformations accounting only 1.5% of all vascular anomalies with 50% occurrence in the oral and maxillofacial region. It usually results from birth defects of the vasculature. A literature search revealed only few case reports of AVMs in the facial region.
Ashok Kumar, Meenu Mittal, Dhirendra Srivastava, Vipul Jaetli, Sunil Chaudhary   +4 more
openaire   +3 more sources

Radiocirurgia no tratamento de malformações arteriovenosas cerebrais.

Acta Médica Portuguesa, 2010
Stereotactic radiosurgery is one of the principle treatment options for small cerebral arteriovenous malformations, even in eloquent locations. Complete obliteration mainly depends on the applied single dose and treatment volume, although other potential
Fátima Amaral
doaj   +1 more source

Surgical lobectomy of pulmonary arteriovenous malformations in a patient with presentations regarded as sequela of tuberculosis: a case report

Journal of Cardiothoracic Surgery, 2020
Background Pulmonary arteriovenous malformations are uncommon conditions of abnormal communications between pulmonary arteries and veins, which are most commonly congenital in nature.
Peng Teng, Weidong Li, Yiming Ni
doaj   +1 more source

Catheter embolization for pulmonary arteriovenous malformations during chemotherapy for appendiceal adenocarcinoma: A case report of associated brain abscess

Radiology Case Reports
Pulmonary arteriovenous malformations are rare, abnormal, low-resistance vascular structures that connect a pulmonary artery to a vein. They are common in patients with hereditary hemorrhagic telangiectasia; however, acquired malformations can occur in ...
Toshinari Yagi, MD, Koji Takano, MD, PhD, Toru Umehara, MD, PhD, Hideyuki Arita, MD, PhD, Noboru Maeda, MD, PhD, Katsuyuki Nakanishi, MD, PhD   +5 more
doaj   +1 more source

Malformações arteriovenosas do lobo parietal: revisão clínico-cirúrgica de 17 casos

Arquivos de Neuro-Psiquiatria, 1968
The incidence, clinical occurences, diagnosis and surgical procedures registered in 17 cases of arteriovenous malformations of the parietal lobe are reported. The authors conclude: The arteriovenous anomalies located in the parietal lobe were mostly (65%)
Nelson Pires Ferreira, Sérgio Raupp, João A. M. Dahne   +2 more
doaj   +1 more source

Twenty-seven years follow-up of a patient with congenital retinocephalofacial vascular malformation syndrome and additional congenital malformations (Bonnet-dechaume-blanc syndrome or wyburn-mason syndrome)

European Journal of Medical Research, 2010
Purpose Follow-up of vascular changes in a patient with congenital retinocephalofacial vascular malformation syndrome. Methods MRI and cerebral angiography.
Schmidt D, Agostini H, Schumacher M
doaj   +1 more source

Diagnostic Pitfalls: Soft Tissue Lymphoma: Superficial Soft Tissue Lymphoma Mimicking a Venous Malformation

Journal of Vascular Anomalies
In this case report, 3 patients addressed to our vascular anomalies reference center to manage a slow-flow vascular anomaly were reported. Our objective is to highlight that a discrepancy between clinical and radiological data should suggest a ...
Victoire Roblot, Valérie Bousson, Annouk Bisdorff   +2 more
doaj   +1 more source

Complex Cerebrovascular Presentation in Central Nepal with Therapeutic Challenge

Nepal Journal of Neuroscience, 2016
Effective management of complex vascular malformation remains one of the more challenging problems faced in most of the developing countries where modern therapeutic resources are deficient.
Karuna T Karki , Pramod K Chaudhary , Binod Bhattarai , Sunil Munakomi   +3 more
doaj   +1 more source

Angiographic analysis on posterior fossa hemorrhages and vascular malformations beyond aneurysms by CT angiography and digital subtraction angiography

Egyptian Journal of Neurosurgery, 2022
Background Posterior fossa malformations are less common than supratentorial malformations, but hemorrhages in posterior fossa are more serious due to presence of vital structures within this region.
S. Vignesh, Surya Nandan Prasad, Vivek Singh, Zafar Neyaz, R. V. Phadke, Anant Mehrotra, Prabhakar Mishra   +6 more
doaj   +1 more source

Liver transplantation in a patient with hereditary haemorrhagic telangiectasia and pulmonary hypertension

Pulmonary Circulation, 2019
Hereditary haemorrhagic telangiectasia or Rendu-Osler-Weber syndrome is a systemic vascular disease with autosomal dominant inheritance, mucocutaneous telangiectasia, and repeated nasal bleeding due to vascular abnormalities.
Kentaro Ejiri, Satoshi Akagi, Kazufumi Nakamura, Naofumi Amioka, Keishi Ichikawa, Takahito Yagi, Hiroshi Ito   +6 more
doaj   +1 more source