Anatomy-based treatment strategy for abdominal and retroperitoneal cystic lymphatic malformations in children

D. Diehtiarova
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Abstract

Lymphatic malformations (LMs) are rare congenital benign malformations of the lymphatic system, consisting of fluid‑filled cysts or channels with unusual growth. The low incidence of LMs leads to a challenging differential diagnosis and a complicated choice of further treatment strategies. In this study, we analyzed our experience in the treatment of abdominal and retroperitoneal cystic LMs and proposed an anatomy‑based treatment strategy that could improve the treatment outcomes. Objective —  to prove that the anatomical localization of LM influences treatment effectiveness and should be taken into account when making treatment decisions. Materials and methods. Out of 240 pediatric patients who underwent treatment for cystic LMs at a single center from December 2012 to December 2020, 43 (19.1 %) were diagnosed with abdominal and retroperitoneal LMs. The follow‑up period was 3.50 ± 2.16 years. Results. Surgical resection of abdominal LMs without evident connection with cisterna chyli does not lead to a recurrence. Sclerotherapy is the best treatment option for retroperitoneal LMs. Diffuse mesentery affection can be successfully treated by sirolimus systemic therapy. According to a logistic regression model, initial choice of LM treatment without considering anatomical localization influences the risks of LM treatment failure (p = 0.000503). All patients in our study group received the following treatments: laparoscopic resections (n = 10, 23.2 %), videoassisted resections (n = 11, 25.5 %), laparotomy resections (n = 9, 20.9 %), sclerotherapy (n = 4, 9.3 %), sclerotherapy and surgery combination (n = 1, 2.3 %), sirolimus systemic therapy (n = 2, 4.6 %), and splenectomy (n = 1, 2.3 %). Six (13.4 %) patients are under dynamic observation. The recommended technique for treating abdominal LMs produced excellent outcomes in 35 (81.4 %) patients, good outcomes in 5 (11.6 %) patients, satisfactory outcomes in 2 (4.7 %) patients, and unsatisfactory outcomes in 1 (2.3 %) patient. Conclusions. Treatment strategies for abdominal and retroperitoneal LMs should be based on their anatomical localization. Retroperitoneal localization indicates a high risk of surgical treatment failure (p = 0.0006).  
儿童腹腔及腹膜后囊性淋巴畸形的解剖学治疗策略
淋巴畸形(LMs)是一种罕见的先天性淋巴系统良性畸形,由异常生长的充满液体的囊肿或通道组成。LMs的低发病率导致了鉴别诊断的挑战和进一步治疗策略的复杂选择。在本研究中,我们分析了我们治疗腹部和腹膜后囊性LMs的经验,并提出了一种基于解剖学的治疗策略,可以改善治疗效果。目的:证明LM的解剖定位影响治疗效果,在制定治疗决策时应予以考虑。材料和方法。2012年12月至2020年12月,在同一中心接受囊性LMs治疗的240名儿童患者中,43名(19.1%)被诊断为腹部和腹膜后LMs。随访时间为3.50±2.16年。结果。手术切除与乳糜池无明显联系的腹部LMs不会导致复发。硬化疗法是腹膜后LMs的最佳治疗选择。弥漫性肠系膜病变可通过西罗莫司全身治疗成功。根据logistic回归模型,不考虑解剖定位的LM治疗初始选择影响LM治疗失败的风险(p = 0.000503)。本研究组所有患者均接受了以下治疗:腹腔镜切除(n = 10, 23.2%)、视频辅助切除(n = 11, 25.5%)、剖腹切除(n = 9, 20.9%)、硬化治疗(n = 4, 9.3%)、硬化治疗和手术联合(n = 1, 2.3%)、西罗莫司全身治疗(n = 2, 4.6%)和脾切除术(n = 1, 2.3%)。动态观察6例(13.4%)。推荐的治疗腹部LMs的技术在35例(81.4%)患者中获得了良好的结果,5例(11.6%)患者获得了良好的结果,2例(4.7%)患者获得了满意的结果,1例(2.3%)患者获得了不满意的结果。结论。腹部和腹膜后LMs的治疗策略应基于其解剖定位。腹膜后定位提示手术治疗失败的高风险(p = 0.0006)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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