Liang J, Liu Q, Zhao D, Yu G, Shi X, Zhang H, Zhang L
Department of Rehabilitation Medicine, Shandong Provincial Third Hospital, China.
School of Clinical Medicine, Shandong Second Medical University, China.
S Afr J Surg. 2024 Dec;62(4):52-54.
Retroperitoneal lymphangioma is exceptionally rare. We present a case of a 41-year-old asymptomatic patient with a large abdominal cystic mass detected on contrast-enhanced computed tomography (CT) scan, initially suspected to be pseudomyxoma peritonei. Laparoscopic exploration revealed a 30 x 30 cm multilocular cystic tumour originating from the retroperitoneum. The tumour was successfully resected laparoscopically, and pathological analysis confirmed a lymphangioma. The patient recovered well with no recurrence over five years. For uncertain tumour types, transabdominal laparoscopic exploration should be prioritised. For treating retroperitoneal lymphangiomas with the origin in the retroperitoneum and a main body in the abdominal cavity, the transabdominal laparoscopic approach is a less invasive and effective treatment option.
腹膜后淋巴管瘤极为罕见。我们报告一例41岁无症状患者,在增强计算机断层扫描(CT)中发现腹部有一个巨大的囊性肿块,最初怀疑为腹膜假黏液瘤。腹腔镜探查发现一个起源于腹膜后的30×30厘米多房囊性肿瘤。该肿瘤通过腹腔镜成功切除,病理分析证实为淋巴管瘤。患者恢复良好,五年内无复发。对于肿瘤类型不确定的情况,应优先考虑经腹腹腔镜探查。对于起源于腹膜后且主体位于腹腔的腹膜后淋巴管瘤,经腹腹腔镜手术是一种侵入性较小且有效的治疗选择。