City University of New York (CUNY) School of Medicine, New York, USA.
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Department of Otolaryngology-Head and Neck Surgery, Hempstead, NY, USA; Cohen Children's Medical Center, Division of Pediatric Otolaryngology, New Hyde Park, NY, USA.
Int J Pediatr Otorhinolaryngol. 2021 Nov;150:110942. doi: 10.1016/j.ijporl.2021.110942. Epub 2021 Oct 14.
The management of arteriovenous malformations (AVMs) can be challenging in the pediatric population. It is of utmost importance to keep in mind various management options as these lesions can have disastrous outcomes. This is a systematic review of the treatment AVMs describing the current practices so that practitioners can be aware of what is currently reported in the literature. The challenges of AVM management can be mitigated when approaching these patients through a multidisciplinary team-based approach.
A systematic review of the literature was performed using the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines to gain insight into pediatric mandibular AVMs. Demographics, arterial involvement, clinical symptoms, imaging, treatment, complications, follow-up, and outcomes were reviewed.
63 articles were included in the systematic review with 106 distinct cases. The age range was from 3 to 17 years with a mean of 12 years. 51% of the patients were female. The most common clinical presentation was emergency hemorrhage (37.4%), swelling or edema (33.0%), and persistent bleeding (31.9%). The most common CT findings were osteolytic changes and radiolucencies (60.8%). With regards to treatment, 56.6% of patients had embolization alone and 34.9% were treated with embolization in combination with other surgical treatments. Of the patients who had surgical resection of the lesion, 50% had resection followed by reconstruction, 23.7% had curettage of the lesion, and 13.2% had resection/curettage then immediate reimplantation of the mandible segment. The most common complications after intervention included bleeding in 17.9% of patients and infection in 8.3% of patients. 89.5% of patients were clinically cured without recurrence at follow-up.
Diagnosing AVMs can be difficult as they have variable clinical and radiographical presentations. Although rare, because of risk of massive hemorrhage, it is important for healthcare professionals to be aware of this pathology. Many surgical techniques, routes of embolization, embolic material, and other experimental therapies have been described and this review shows that the most cases had embolization as a part of the treatment. The role of therapies targeted at the molecular level still needs to be further explored.
儿童动静脉畸形(AVM)的治疗极具挑战性。了解各种治疗选择至关重要,因为这些病变可能会导致灾难性的后果。本系统综述旨在描述 AVM 的治疗方法,以了解当前文献中的报道,使临床医生能够了解这方面的知识。通过多学科团队合作的方式来治疗 AVM,可以减轻治疗的挑战。
采用 PRISMA(系统评价和荟萃分析的首选报告项目)指南对文献进行系统综述,以深入了解儿童下颌 AVM。评估了人口统计学、动脉受累、临床症状、影像学、治疗、并发症、随访和结果。
本系统综述共纳入 63 篇文章,涉及 106 个不同的病例。年龄范围为 3 至 17 岁,平均 12 岁。51%的患者为女性。最常见的临床表现是急诊出血(37.4%)、肿胀或水肿(33.0%)和持续性出血(31.9%)。最常见的 CT 表现为溶骨性改变和透光区(60.8%)。在治疗方面,56.6%的患者仅接受栓塞治疗,34.9%的患者接受栓塞联合其他手术治疗。在接受病变切除术的患者中,50%的患者行病变切除后重建,23.7%的患者行病变刮除术,13.2%的患者行切除/刮除后立即进行下颌骨段再植术。干预后最常见的并发症包括出血(17.9%)和感染(8.3%)。89.5%的患者在随访时无复发,临床治愈。
由于 AVM 的临床表现和影像学表现多样,因此诊断可能具有挑战性。尽管罕见,但由于大出血的风险,医护人员了解这种病理非常重要。已经描述了许多手术技术、栓塞途径、栓塞材料和其他实验性治疗方法,本综述表明,大多数病例的治疗都包括栓塞。靶向分子水平的治疗方法的作用仍需要进一步探索。