scholarly journals A rare case of pulmonary arterio-venous malformation with recurrent anemia: Hereditary hemorrhagic telangiectasia

Lung India ◽  
2015 ◽  
Vol 32 (4) ◽  
pp. 384 ◽  
Author(s):  
KamaleshTagadur Nataraju ◽  
Tirthankar Mukherjee ◽  
Ramachandra PrabhuHosahalli Doddaiah ◽  
NageshGabbadi Nanjappa ◽  
Lakshmikanth Narasegowda
Keyword(s):  
Hereditary Hemorrhagic Telangiectasia ◽  
Rare Case ◽  
Venous Malformation ◽  
Arterio Venous Malformation

scholarly journals Kombinasi Dexmedetomidine – Sevoflurane 0,5 MAC pada Bedah Mikro Reseksi Malformasi Arteri-Vena

2021 ◽  
Vol 10 (2) ◽  
pp. 113-118
Author(s):  
Adhy Tjahyanto ◽  
◽  
Ibnu Siena Samdani ◽  
M. Sofyan Harahap
Keyword(s):  
Rare Case ◽  
Venous Malformation ◽  
Young Patients ◽  
Anaesthetic Induction ◽  
Haemodynamic Stability ◽  
Brain Avm ◽  
Arterio Venous Malformation ◽  
Micro Surgery ◽  
Acting Agent ◽  
Fast Acting

Arterio-venous malformation (AVM) is a rare case, particularly among young patients (<40 years old). Maintaining haemodynamic stability and anticipating massive haemorrhage during micro surgery resection of AVM are fundamental for an anaesthetist. Total Intra Venous Anesthesia using propofol is still popular to control intracranial pressure as it is easily titrated and fast acting agent (both in onset and duration). Moreover, general neuruologic evaluation soon after anesthesia terminated is an integral important component of microsurgery of brain MAV. In this case report: a 20-year-old woman suddenly lost her consciousness and left-sided motors strength. Brain angiographic revealed an AVM in right frontal lobe. Microsurgery of brain AVM resection was performed. After 5-minute-preoxygenation, anaesthetic induction was performed by using propofol, fentanyl, rocuronium, and sevoflurane. The surgery went successfully using a combination of dexmedetomidine-sevoflurane 0.5MAC. Post-anaesthesia hemodynamic of this patient was in stable and without new neurologic deficit afterward.

A rare case of extradural arterio-venous malformation presenting as cervical radiculopathy

2019 ◽  
Vol 405 ◽  
pp. 313
Author(s):  
N. Kadam ◽  
S. Khadilkar ◽  
P. Ojha ◽  
G. Soni ◽  
B. Patel
Keyword(s):  
Rare Case ◽  
Venous Malformation ◽  
Cervical Radiculopathy ◽  
Arterio Venous Malformation

scholarly journals A Rare Case of Adrenal Arterio-Venous Malformation (AVM): A Case Report

2020 ◽  
Vol 01 (04) ◽  
Author(s):  
Rosanna Mamone ◽  
Rocco Minelli ◽  
Maria G. Giagnorio ◽  
Sonia Tamasi ◽  
Eugenio Rossi ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Venous Malformation ◽  
Arterio Venous Malformation

scholarly journals Extracranial Arterio-Venous Malformation in the Gluteal Region - A Rare Case Report

2017 ◽  
Vol 3 (3) ◽  
Author(s):  
Harpal Singh Seemar ◽  
Anika Mittal ◽  
Ramandeep Kaur ◽  
Jasneet Kaur ◽  
Ramesh Kumar Kundal
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Venous Malformation ◽  
Gluteal Region ◽  
Rare Case Report ◽  
Arterio Venous Malformation

scholarly journals A Rare Case of Subtentorial Arterio-Venous Malformation Case Report

2013 ◽  
Vol 6 (2) ◽  
pp. 135-138
Author(s):  
Nachko I. Totsev ◽  
Tihomir V. Andreev ◽  
Maya P. Danovska ◽  
Mladen E. Ovcharov
Keyword(s):  
Arteriovenous Malformations ◽  
Rare Case ◽  
Venous Malformation ◽  
Posterior Cranial Fossa ◽  
Unenhanced Ct ◽  
Rare Location ◽  
Cranial Fossa ◽  
Arterio Venous Malformation ◽  
Treatment Prognosis

Summary The majority - over 80%, of arteriovenous malformations (AVMs) are supratentorial. The infratentorial AVM are uncommon and different from other intracranial AVMs in terms of history, diagnosis, treatment, prognosis, and follow up. The authors present a case of an intracranial hemorrhage, caused by rupture of an AVM in the posterior cranial fossa. Native (unenhanced) CT and computed tomography angiography (CTA) images of this rare location of AVM are presented.

Arterio-venous malformation in the chest wall: a case report

1991 ◽  
Vol 27 (6) ◽  
pp. 796
Author(s):  
Yun Young Choi ◽  
Kyo Nam Kim ◽  
Heung Suk Seo
Keyword(s):  
Case Report ◽  
Chest Wall ◽  
Venous Malformation ◽  
Arterio Venous Malformation

Intraosseous venous malformation in the anterior mandible: Report of a rare case

2016 ◽  
Vol 3 ◽  
pp. 1-4
Author(s):  
Asha R. Iyengar ◽  
B. V. Subash ◽  
Shalini Dina Simon ◽  
M. H. Vani
Keyword(s):  
Rare Case ◽  
Venous Malformation ◽  
Anterior Mandible

A Rare Case: Primary Venous Malformation in Parietal Bone

2021 ◽  
pp. 1-4
Author(s):  
Serhat Yarar ◽  
Ilker Uyar ◽  
Mehmet Emin Cem Yildirim ◽  
Mehmet Dadacı ◽  
Bilsev Ince
Keyword(s):  
Vascular Malformation ◽  
Rare Case ◽  
Histopathological Examination ◽  
Vascular Malformations ◽  
Venous Malformation ◽  
Parietal Bone ◽  
Hair Density ◽  
Trichilemmal Cyst ◽  
Advancement Flaps ◽  
Rotation Advancement

Primary intraosseous vascular malformations (PIVMs) are rare intraosseous lesions, accounting for approximately 0.5–1% of all intraosseous tumours. In this case report, we aimed to present a rare case of intraosseous vascular malformation causing a large lytic area in the parietal bone. A 25-year-old male patient was admitted to the clinic with a mass on the parietal bone. On physical examination, it was observed that the hair density on the mass was decreased, the mass had a soft consistency, and there was no pain on palpation. The patient was operated under local anaesthesia with a provisional diagnosis of a trichilemmal cyst. However, intraoperative diagnosis was a vascular malformation. There was a 3-cm full-thickness defect on the parietal bone caused by the lesion. The mass was excised completely while preserving the integrity of the dura. The resulting defect was reconstructed with bilateral rotation advancement flaps. The calvarial defect was not reconstructed due to equipment inadequacy. No complications were encountered in the postoperative period. Ninety-three PIVM cases have been reported in the skull since 1845. In very few of these cases, the mass is located in the parietal bone. The pathogenesis of PIVMs is not completely understood. The definitive diagnosis is made by histopathological examination. The therapeutic gold standard is surgery. Surgeons should keep in mind that radiological examination before the operation could prevent undesirable complications.

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