Kim Soo-Hong, Kim Hyun-Young, Lee Cheol, Min Hye Sook, Jung Sung-Eun
Department of Pediatric Surgery, Pusan National University Yangsan Hospital, Yangsan, Korea.
Department of Pediatric Surgery, Seoul National University Children's Hospital, Seoul, Korea.
J Pediatr Surg. 2016 Apr;51(4):582-7. doi: 10.1016/j.jpedsurg.2015.11.021. Epub 2015 Dec 9.
Mesenteric lymphatic malformations (MLs) are a heterogeneous group of benign diseases of the lymphatic system that present with cystic dilated lymphatics of the mesentery. MLs are rare and represent less than 5% of all lymphatic malformations. The aims of this study were to analyze the characteristics of MLs in children and to suggest a modified classification.
We investigated 25 patients who underwent ML surgery. The clinical data and pathological findings were reviewed retrospectively. We divided the patients into 4 groups according to the operative findings. Group 1 included patients with MLs involving the intestinal walls. Group 2 included patients with pedicle-type MLs with no relationship to the mesenteric vessels. Group 3 patients presented with MLs located in the mesenteric boundaries near the mesenteric vessels. Group 4 patients had multicentric and diffusely infiltrated MLs.
The male-to-female ratio was 11:14, and the median age at diagnosis was 5years of age. The most common symptom was abdominal pain. The jejunal mesentery was the most frequently involved site in this study. Five patients showed the macrocystic type and 20 patients showed the mixed cystic type. With the exception of one patient with a large mixed cystic-type ML who underwent incomplete mass excision, 24 patients underwent complete mass excision. The group 1 patients (n=14) underwent mass excision performed with segmental resection of the bowel. The group 2 patients (n=3) only underwent mass excision surgery. The patients in group 3 (n=7) underwent mass excision with segmental resection of the intestine because ML excision altered the blood supply of the adjacent intestines. The group 4 patients (n=1) presented with MLs involving the entire mesentery and underwent incomplete excision.
The relationships between MLs and the neighboring organs determine the surgical strategy, and the size and location of MLs affect the operative methods. The modified classification based on these findings can facilitate effective treatment planning.
肠系膜淋巴管瘤(MLs)是淋巴系统的一组异质性良性疾病,表现为肠系膜的囊性扩张淋巴管。MLs较为罕见,占所有淋巴管瘤的比例不到5%。本研究的目的是分析儿童MLs的特征并提出一种改良分类方法。
我们调查了25例行ML手术的患者。回顾性分析临床资料和病理结果。根据手术所见将患者分为4组。第1组包括累及肠壁的MLs患者。第2组包括与肠系膜血管无关的蒂型MLs患者。第3组患者的MLs位于靠近肠系膜血管的肠系膜边界处。第4组患者有多中心且弥漫浸润性的MLs。
男女比例为11:14,诊断时的中位年龄为5岁。最常见的症状是腹痛。空肠系膜是本研究中最常受累的部位。5例表现为大囊型,20例表现为混合囊型。除1例大的混合囊型ML患者行肿物不完全切除外,24例患者行肿物完全切除。第1组患者(n = 14)行肿物切除并肠段切除术。第2组患者(n = 3)仅行肿物切除术。第3组患者(n = 7)因ML切除改变了相邻肠管的血供而行肿物切除并肠段切除术。第4组患者(n = 1)的MLs累及整个肠系膜,行不完全切除。
MLs与邻近器官的关系决定手术策略,MLs的大小和位置影响手术方法。基于这些发现的改良分类有助于制定有效的治疗方案。