[Intraosseous arteriovenous malformations].

Rev Stomatol Chir Maxillofac

Service de chirurgie maxillofaciale, centre hospitalier Lyon-Sud, 69310 Pierre-Bénite, France.

Published: February 2010

Intraosseous arteriovenous maxillomandibular malformations are rare. The diagnosis is primarily clinical (children with pulsatile osseous tumefaction, bleeding at cingulum), completed with imaging techniques (TDM and/or MRI). Arteriography is indicated only at the time of therapeutic management. The evolution may vary greatly (four levels: quiescence, expansion, destruction, decompensation) and usually evolves because of hormonal changes or trauma. Radiotherapy and vascular ligatures are no longer recommended. The best treatment is direct or transarterial embolization. Surgical resection, when feasible, must be thorough. It is indicated in case of failure or recurrence after embolization.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.stomax.2009.12.001DOI Listing

Publication Analysis

Top Keywords

[intraosseous arteriovenous
4
arteriovenous malformations]
4
malformations] intraosseous
4
intraosseous arteriovenous
4
arteriovenous maxillomandibular
4
maxillomandibular malformations
4
malformations rare
4
rare diagnosis
4
diagnosis clinical
4
clinical children
4

Similar Publications

Article Synopsis
  • - Arteriovenous malformations (AVMs) in facial bones, while rare, can lead to serious issues like aesthetic concerns, pain, and significant complications such as life-threatening bleeding.
  • - A case study showcased a surgical approach involving preoperative embolization and sclerotherapy followed by the use of specialized devices (Sonopet® and Aquamantys™) to successfully resect AVMs from the maxilla while preserving important structures.
  • - The report emphasizes the importance of careful planning and surgical techniques to manage bleeding and ensure effective removal of deformed bone, presenting a promising method for maintaining facial integrity during treatment.
View Article and Find Full Text PDF

Objective: An intraosseous arteriovenous fistula (AVF) is a rare fistula with an intracranial shunted pouch. A case of an intraosseous AVF at the squamous part of the occipital bone with spontaneous occlusion of diploic venous drainage is described.

Case Presentation: The patient, a Japanese woman in her 80s, presented with headaches at the back of the head and a history of multiple unruptured cerebral aneurysms but no recent head trauma.

View Article and Find Full Text PDF

: Intraosseous vascular anomalies in the facial skeleton present significant diagnostic and therapeutic challenges due to complex anatomy. These anomalies represent about 0.5-1% of bony neoplastic and tumor-like lesions, usually presenting as a firm, painless mass.

View Article and Find Full Text PDF
Article Synopsis
  • A rare case of spinal epidural arteriovenous fistulas (SEAVFs) with intraosseous shunts was observed in a woman in her 70s who experienced severe weakness and urinary retention due to spinal issues.
  • Imaging revealed spinal cord edema and venous dilation caused by compressed vertebrae, with angiography showing shunts connected to lumbar arteries.
  • Successful treatment involved transarterial embolization, leading to complete closure of the shunt and significant improvement in the patient’s symptoms post-surgery.
View Article and Find Full Text PDF

Intraosseous occurrence of a spinal AVM is anecdotal, with only four such cases reported previously. This is the first report of a spinal intraosseous AVM in the cervical vertebrae. A 44-year-old male patient presented with a 2-month history of progressive quadriparesis and bladder dysfunction.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!