Hyvönen Hanna, Aronniemi Johanna, Salminen Päivi, Kyrklund Kristiina
New Children's Hospital, Department of Pediatric Surgery, Helsinki University Hospital and University of Helsinki, P.O. Box 347 (Stenbäckinkatu 9), 00029 HUS, Helsinki, Finland.
HUS Diagnostic Center, Department of Radiology, New Children's Hospital, Helsinki University Hospital and University of Helsinki, P.O. Box 347 (Stenbäckinkatu 9), 00029 HUS, Helsinki, Finland.
J Pediatr Surg. 2024 Sep;59(9):1875-1878. doi: 10.1016/j.jpedsurg.2024.05.011. Epub 2024 May 23.
Intra-abdominal lymphatic malformations (LMs) are relatively rare congenital anomalies and can be divided into intra- and retroperitoneal subgroups. This study aims to evaluate the outcomes after surgical resection of intraperitoneal LMs in children.
The records of all patients ≤16 years of age with intraperitoneal LMs managed at our tertiary center between 2007-2022 were reviewed. Patients with retroperitoneal LMs were excluded. Our preferred approach is surgical exploration for large (>5 cm), symptomatic lesions if they are potentially resectable on imaging.
A total of 12 patients (10 males) were diagnosed with intraperitoneal LMs located in the small bowel mesentery or omentum at a median age of 6.6 (range, 0.6-14.4) years. Ten (83%) patients presented with acute symptoms, including abdominal pain (n = 8; 67%) and vomiting (n = 3; 25%). Two (17%) intraperitoneal LMs were found on imaging performed for other reasons. Surgical exploration was performed in 11/12 (92%) cases. Intestinal volvulus around a mesenteric macrocyst had occurred in 4 (36%) patients. Complete macroscopic resection was achieved in 10/11 (91%) patients. Most lesions were localized to a short intestinal segment. One mixed type LM with an extensive mesenteric involvement was biopsied as the lesion was deemed to be unresectable in preoperative imaging and the diagnosis was initially unclear. There was one recurrence (8%) during postoperative follow-up on imaging (median 3.6 (range, 1.5-6.9) years) but the patient has remained asymptomatic and not undergone interventions. 6/8 (75%) of screened intraperitoneal LMs were positive for a somatic PIK3CA mutation.
Most large, pedunculated macrocystic LMs in the small bowel mesentery or omental location were amenable to macroscopic resection. Intraperitoneal LMs tend to present with acute symptoms including a risk for intestinal volvulus based on anatomical location. Our results suggest low recurrence rates or need for further interventions over follow-up.
III.
腹腔内淋巴管畸形(LMs)是相对罕见的先天性异常,可分为腹腔内和腹膜后亚组。本研究旨在评估儿童腹腔内LMs手术切除后的结果。
回顾了2007年至2022年期间在我们三级中心接受治疗的所有年龄≤16岁的腹腔内LMs患者的记录。排除腹膜后LMs患者。如果影像学检查显示大的(>5 cm)、有症状的病变可能可切除,我们首选的方法是手术探查。
共有12例患者(10例男性)被诊断为腹腔内LMs,位于小肠系膜或网膜,中位年龄为6.6岁(范围0.6 - 14.4岁)。10例(83%)患者出现急性症状,包括腹痛(8例;67%)和呕吐(3例;25%)。2例(17%)腹腔内LMs是在因其他原因进行的影像学检查中发现的。11/12(92%)例患者进行了手术探查。4例(36%)患者发生了围绕肠系膜大囊肿的肠扭转。10/11(91%)例患者实现了肉眼下完全切除。大多数病变局限于一小段肠管。1例广泛累及肠系膜的混合型LMs因术前影像学检查认为不可切除且最初诊断不明确而进行了活检。术后影像学随访(中位时间3.6年(范围1.5 - 6.9年))中有1例复发(8%),但该患者仍无症状且未接受干预。筛查的腹腔内LMs中有6/8(75%)存在体细胞PIK3CA突变。
大多数位于小肠系膜或网膜部位的带蒂大囊型LMs适合进行肉眼下切除。腹腔内LMs倾向于出现急性症状,基于解剖位置有肠扭转风险。我们的结果表明随访期间复发率低或无需进一步干预。
III级