Lymphatic malformations: a 9-year experience at the vascular anomaly clinic

IF 0.5 Q4 PEDIATRICS Egyptian Pediatric Association Gazette Pub Date : 2023-11-24 DOI:10.1186/s43054-023-00236-0
Amr Abdelhamid AbouZeid, Shaimaa Abdelsattar Mohammad, Nihal Hussein Aly, Wael Ahmed Ghanem, Mohammad Seada, Iman A. Ragab, Osama El-Naggar, Mohamed Aly AbdelBaky
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Abstract

To share our experience in the management of a specific type of vascular malformations (lymphatic) at a specialized multidisciplinary clinic for vascular anomalies. Data of patients attending the vascular anomaly clinic during the period 2015 through 2023 were retrospectively analyzed. The study included cases diagnosed primarily as lymphatic malformations (LMs). We excluded cases associated with complex/syndromic vascular malformations. Available data included regional distribution of the LMs, age at presentation, sex, imaging studies, and different modes of treatment. The study included 131 cases of LMs whose data were available for retrospective analysis. Generally, LMs had a benign course with good prognosis apart from two recorded mortalities (1.5%) during the 9-year period of the study. In this series, 93 cases were managed by injection sclerotherapy (Bleomycin). About 57 cases showed satisfactory response to injection sclerotherapy alone without the need to add other treatment modalities. Forty cases underwent surgical excision/debulking. Postoperative wound complications were recorded in 5 cases (12.5%). Sirolimus was offered for patients with LMs after the failure of conventional treatment (injection/surgery) to control associated significant complications. Lymphatic malformations represent a common presentation at the vascular anomaly clinic, which usually have a benign course. Complications are mainly cosmetic especially when involving the face, and sometimes superadded infections may occur. Airway compromise is a potential serious complication with submandibular lymphatic malformations in the neck.
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淋巴管畸形:在血管异常门诊9年的经验
分享我们在一个专门的多学科血管异常诊所处理一种特殊类型的血管畸形(淋巴管)的经验。回顾性分析2015 - 2023年在血管异常门诊就诊的患者资料。该研究包括主要诊断为淋巴畸形(LMs)的病例。我们排除了与复杂/综合征性血管畸形相关的病例。现有资料包括LMs的区域分布、发病年龄、性别、影像学研究和不同的治疗模式。本研究纳入了131例LMs病例,其资料可用于回顾性分析。总体而言,在9年的研究期间,除了2例死亡(1.5%)外,LMs的病程为良性,预后良好。93例患者采用注射硬化治疗(博莱霉素)。约57例患者对单纯注射硬化治疗反应满意,无需其他治疗方式。40例行手术切除/减体积。术后创面并发症5例(12.5%)。西罗莫司用于常规治疗(注射/手术)失败后的LMs患者,以控制相关的显著并发症。淋巴管畸形是血管异常临床的常见表现,通常有良性病程。并发症主要是美容方面的,特别是当涉及到面部时,有时可能会发生额外的感染。呼吸道损害是颈部下颌淋巴畸形的潜在严重并发症。
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来源期刊
自引率
0.00%
发文量
32
审稿时长
9 weeks
期刊介绍: The Gazette is the official journal of the Egyptian Pediatric Association. The main purpose of the Gazette is to provide a place for the publication of high-quality papers documenting recent advances and new developments in both pediatrics and pediatric surgery in clinical and experimental settings. An equally important purpose of the Gazette is to publish local and regional issues related to children and child care. The Gazette welcomes original papers, review articles, case reports and short communications as well as short technical reports. Papers submitted to the Gazette are peer-reviewed by a large review board. The Gazette also offers CME quizzes, credits for which can be claimed from either the EPA website or the EPA headquarters. Fields of interest: all aspects of pediatrics, pediatric surgery, child health and child care. The Gazette complies with the Uniform Requirements for Manuscripts submitted to biomedical journals as recommended by the International Committee of Medical Journal Editors (ICMJE).
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