Background: Intraosseous vascular anomalies (IOVA) are rare in the craniofacial skeleton and present a diagnostic and therapeutic challenge. This study aims to describe the clinical management based on a large case series. Methods: A retrospective chart review was performed and 9 IOVA were identified over a 15-year period. Data on demographics, diagnostic features, clinical management, and outcomes were reviewed. Results: Five frontal bone IOVA and 4 orbital IOVA were identified. The postoperative follow-up ranged from 4 months to 4 years. All 9 lesions were diagnosed with computed tomography (CT) imaging. Magnetic resonance imaging (MRI) was used to delineate soft tissue involvement in 2 patients presenting with oculo-orbital dystopia and ophthalmoplegia. En bloc excision was performed in all patients. Preoperative interventional embolization was critical in the successful resection of an orbital IOVA following 2 previously failed attempts that were aborted secondary to hemorrhage. Intraoperative 3-dimensional stereotactic navigation was used for the accurate en bloc excision of a frontal IOVA to prevent injury to the frontal sinus. Reconstruction of esthetic and functional deformities was successfully accomplished. Conclusion: The diagnosis of IOVA relies primarily on clinical assessment and CT imaging. Further interpretation of the involvement of periorbital, facial, and intracranial soft tissue is best defined by MRI. Multidisciplinary care with interventional radiology and neurosurgery must be considered for ensuring the safe and adequate en bloc excision of craniofacial IOVA. (C) 2017 by Mutaz B. Habal, MD.
http://ift.tt/2zQXCTA
Σφακιανάκης Αλέξανδρος
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5 Άγιος Νικόλαος
Κρήτη 72100
00302841026182
00306932607174
alsfakia@gmail.com
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- Do Bacteria and Biofilm Play a Role in Double-Caps...
- Subfascial Primary Breast Augmentation with Fat Gr...
- Five Steps to Internal Mammary Vessel Preparation ...
- Establishment of an Acquired Lymphedema Model in t...
- Evidence-Based Clinical Practice Guideline: Autolo...
- Discussion: Mixed Reality with HoloLens: Where Vir...
- Fat Grafting in Hollow Upper Eyelids and Volumetri...
- Reply: Late Surgical-Site Infection in Immediate I...
- Breast Cleavage Remodeling with Fat Grafting: A Sa...
- Evidence-Based Medicine: Face Lift
- Impact of Patient Subtype and Surgical Variables o...
- Optimizing Outcomes in Pharyngoesophageal Reconstr...
- Injection of Compressed Diced Cartilage in the Cor...
- ASPS/PSF Sponsored Symposia and Workshops
- Managing Alar Flare in Rhinoplasty
- Gender Affirmation: Medical & Surgical Perspectives
- The Evolution of Chemical Peeling and Modern-Day A...
- Reply: The Anterior Intercostal Artery Flap: Anato...
- Denosumab-induced cutaneous hypersensitivity react...
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- Acquired Bleeding Disorders
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- Large-Scale Network Topology Reveals Heterogeneity...
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- From the archive: Sydney turns 100
- An estimated carbon footprint of NHS primary denta...
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- Eavesdroppers and nosey neighbours required
- Alternative sugars: Syrup
- Is it time to digitally enable dentistry with the ...
- How Was Your Otology Training? A Survey of Recent ...
- Spreading the word about a devastating disease
- Bone-conducted Vestibular-evoked Myogenic Potentia...
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- Abscess with osteomyelitis of the clivus after ade...
- OR004 Safe and effective implementation of chemoth...
- P275 Refractory hypereosinophilia manifesting as n...
- P283 Pneumococcal osteomyelitis: a rare diagnosis ...
- P282 Recurrent candidal esophagitis in an otherwis...
- P337 Remission of cow’s milk allergy during rituxi...
- P222 Effects of immunoglobulin e concentration, eo...
- OR001 Drug rash eosinophilia and systemic symptoms...
- P280 Severe combined immunodeficiency in cartilage...
- OR002 Testing strategies for immediate and delayed...
- P206 Effect of inhaled corticosteroid use on weigh...
- OR003 Common misconceptions in the recognition and...
- P296 Hypogammaglobulinemia in a patient with Turne...
- P275 Refractory hypereosinophilia manifesting as n...
- P283 Pneumococcal osteomyelitis: a rare diagnosis ...
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