Literature DB >> 26807370

Vascular anomalies of the head and neck in children.

Kate Mahady1, Stefanie Thust1, Rupert Berkeley1, Sam Stuart1, Alex Barnacle1, Fergus Robertson1, Kshitij Mankad1.   

Abstract

Sixty percent of vascular anomalies in children are found in the head and neck. These lesions can present throughout antenatal, perinatal and childhood development. They broadly fall into two categories: vascular tumours and vascular malformations. Their clinical and, often, psychological impact is determined by both pathological type and location: many lesions follow an uncomplicated natural course and other more complex, extensive or progressive lesions can present a threat to life from mass effect, haemorrhage or large volume arteriovenous shunting. Vascular tumours include infantile haemangioma (IH), congenital haemangioma (CH) and kaposiform hemangioendothelioma (KH); of which IH is the most common. Management options for vascular tumours include conservative approaches, oral medications and surgical intervention as determined by tumour type, location and associated complications. Vascular malformations can be categorised into low flow and high flow lesions. Low flow lesions include capillary, venous and lymphatic malformations (LMs). High flow lesions describe the arteriovenous malformations (AVMs), a highly heterogeneous group of lesions which can present in a variety of ways-the mainstay of treatment for these dynamic lesions is endovascular or surgical obliteration. We provide a practical framework for clinical classification of vascular anomalies of the head and neck in children. We also explore principles of their clinical and radiological assessment along with management, highlighting the importance of a multi-disciplinary approach.

Entities:  

Keywords:  Vascular; arteriovenous; birthmark; haemangioma; infantile; kaposiform; malformation

Year:  2015        PMID: 26807370      PMCID: PMC4700245          DOI: 10.3978/j.issn.2223-4292.2015.04.06

Source DB:  PubMed          Journal:  Quant Imaging Med Surg        ISSN: 2223-4306


  35 in total

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4.  Thrombocytopenic coagulopathy (Kasabach-Merritt phenomenon) is associated with Kaposiform hemangioendothelioma and not with common infantile hemangioma.

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7.  Lymphatic malformations of the head and neck. A proposal for staging.

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8.  Rapidly involuting congenital hemangioma: clinical and histopathologic features.

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3.  Neonatal venolymphatic malformation with spontaneous parotid duct rupture: first case report.

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4.  A pediatric posterior neck venous malformation with an endocranial extension.

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5.  The Relationship Between the Effectiveness of HMME-PDT and the Dermoscopic Features of Port-wine Stains in Chinese Pediatric Patients: A Retrospective Study.

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Review 6.  Interdisciplinary Management of Head and Neck Vascular Anomalies: Clinical Presentation, Diagnostic Findings and Minimalinvasive Therapies.

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7.  Massive Nasal Arterio-Venous Malformation (AVM) Excision and Reconstruction with Expanded Forehead Flap: A Case Report.

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9.  Aqueous intralesional bleomycin sclerotherapy in lymphatic malformation: Our experience with children and adult.

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10.  Retropharyngeal vascular malformation removed using transoral robotic surgery-A case report.

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