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头颈部大囊型淋巴管畸形的手术切除:短期和长期结果

Surgical resection of macrocystic lymphatic malformations of the head and neck: Short and long-term outcomes.

作者信息

Bonilla-Velez Juliana, Moore Brendan P, Cleves Mario A, Buckmiller Lisa, Richter Gresham T

机构信息

Division of Pediatric Otolaryngology and Center for the Investigation of Congenital Aberrancies of Vascular Development, Arkansas Children's Hospital, 1 Children's Way, Little Rock, AR, USA; Department of Otolaryngology-Head and Neck Surgery, University of Arkansas for Medical Sciences, 4301 W Markham St #543, Little Rock, AR, USA.

College of Medicine, University of Arkansas for Medical Sciences, 4301 W Markham St #550, Little Rock, AR, USA.

出版信息

Int J Pediatr Otorhinolaryngol. 2020 Jul;134:110013. doi: 10.1016/j.ijporl.2020.110013. Epub 2020 Mar 20.

Abstract

BACKGROUND

Controversy exists on management of lymphatic malformations, with schools of thought advocating for observation, surgery or sclerotherapy. This study sought to examine outcomes after surgical resection of pediatric cervicofacial macrocystic lymphatic malformations (MLM).

METHODS

Case series with planned data collection on pediatric patients with cervicofacial MLM who underwent surgical resection at a tertiary referral center for vascular anomalies from January 1995 to June 2016. For consistency in patient population analysis, patients who had pre-surgical sclerotherapy or had mixed or microcystic disease were excluded. The main outcome was complete response rate (CR) and long-term recurrence-free survival (RFS).

RESULTS

Sixty-three patients who underwent excision of MLM were included, 52.4% were female, 77.8% Caucasian. The majority had de Serres stage I-III (96.8%) affecting the neck (71.4%). Patients were discharged the same day (28.6%), or had a 1 day median length-of-stay (interquartile range (IQR) = 2). Surgical complications included seroma/hematoma (9.5%), transient nerve weakness (facial nerve, sympathetic chain, or phrenic nerve, 6.3%), and infection (1.6%). On long-term follow-up (median: 12 months, IQR 1-43 months), a single surgery achieved CR in 90.5% of patients. RFS was achieved in 86% of patients in our observation period of up to 15 years. Most patients requiring a second intervention failed within 6-months of initial procedure (4/5 patients, 90%); associated factors included bilaterality, advanced staging, and partial response at first-follow-up (p = 0.0051, 0.0051, and <0.0001, respectively).

CONCLUSIONS

Surgery is safe and effective as first line treatment for selected MLM. For stage I-III MLM CR and long-term RFS can be achieved with a single surgery. A direct and randomized comparison of treatment modalities is needed.

摘要

背景

关于淋巴管畸形的治疗存在争议,不同的观点主张观察、手术或硬化治疗。本研究旨在探讨小儿颈面部大囊型淋巴管畸形(MLM)手术切除后的疗效。

方法

对1995年1月至2016年6月在一家三级血管异常转诊中心接受手术切除的小儿颈面部MLM患者进行病例系列研究,并计划收集相关数据。为了使患者群体分析具有一致性,排除了术前接受过硬化治疗或患有混合型或微囊型疾病的患者。主要结局指标为完全缓解率(CR)和长期无复发生存率(RFS)。

结果

纳入63例行MLM切除术的患者,其中52.4%为女性,77.8%为白种人。大多数患者为de Serres I - III期(96.8%),病变累及颈部(71.4%)。患者于术后当天出院(28.6%),或中位住院时间为1天(四分位间距(IQR) = 2)。手术并发症包括血清肿/血肿(9.5%)、短暂性神经麻痹(面神经、交感神经链或膈神经,6.3%)和感染(1.6%)。在长期随访中(中位时间:12个月,IQR 1 - 43个月),单次手术使90.5%的患者达到CR。在长达15年的观察期内,86%的患者实现了RFS。大多数需要二次干预的患者在初次手术后6个月内复发(4/5例患者,90%);相关因素包括双侧病变、分期较晚以及首次随访时部分缓解(分别为p = 0.0051、0.0051和<0.0001)。

结论

手术作为特定MLM的一线治疗方法是安全有效的。对于I - III期MLM,单次手术可实现CR和长期RFS。需要对治疗方式进行直接的随机对照比较。

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