Su Tieshan, Li Chaoyuan, Song Bin, Song Defeng, Feng Ye
Departments of Gastrointestinal Colorectal Anus Surgery, China-Japan Union Hospital, Jilin University, Changchun, China.
Departments of Orthopedics Surgery, China-Japan Union Hospital, Jilin University, Changchun, China.
Front Surg. 2023 Jan 17;10:1074067. doi: 10.3389/fsurg.2023.1074067. eCollection 2023.
Cystic lymphangioma is a rare benign tumor of the lymphatic system, which is most commonly observed in the neck, head and armpit.Less than 5% of lymphangiomas occur in the abdominal cavity and even less in the retroperitoneum.
A 65-year-old male patient was diagnosed with an "abdominal mass that had persisted for 1 year, accompanied by abdominal pain, abdominal distension and dyspnea for 7 days". After abdominal computerd tomography, a giant multilobed abdominal lymphangioma was suspected, which squeezed the intestinal canal and was closely related to the inferior vena cava. The patient underwent an exploratory laparotomy, during which, it was found that the tumor formed extensive adhesions to the transverse colon, small intestine and pelvic wall, and enveloped the abdominal aorta, superior mesenteric artery, inferior mesenteric artery and inferior vena cava to varying degrees. It was diffcult to remove the cyst completely. Postoperative pathology confirmed the diagnosis of retroperitoneal cystic lymphangioma. The patient recovered well after the operation, was eating normally by 5 days postoperatively,and was discharged 10 days postoperatively.The patient was followed up 1 month after postoperatively and no evidence of recurrence was observed.
In this case, we report a patient with giant retroperitoneal cystic lymphangioma who underwent exploratory laparotomy combined with preoperative abdominal computerd tomography and acute abdominal pain, abdominal distension and dyspnea. Because of the large volume of the tumor and its close relationship with the superior mesenteric artery and other blood vessels, the surgeon used scissors to separate the tumor sharply and removed the whole tumor completely.
囊性淋巴管瘤是一种罕见的淋巴系统良性肿瘤,最常见于颈部、头部和腋窝。腹腔内发生的淋巴管瘤不到5%,腹膜后发生的更少。
一名65岁男性患者被诊断为“腹部肿块持续1年,伴有腹痛、腹胀和呼吸困难7天”。腹部计算机断层扫描后,怀疑是巨大的多叶腹腔淋巴管瘤,其压迫肠道并与下腔静脉关系密切。患者接受了剖腹探查术,术中发现肿瘤与横结肠、小肠和盆腔壁形成广泛粘连,并不同程度地包绕腹主动脉、肠系膜上动脉、肠系膜下动脉和下腔静脉。难以完全切除囊肿。术后病理证实为腹膜后囊性淋巴管瘤。患者术后恢复良好,术后5天正常进食,术后10天出院。术后1个月对患者进行随访,未观察到复发迹象。
在本病例中,我们报告了一名患有巨大腹膜后囊性淋巴管瘤的患者,其接受了剖腹探查术,术前进行了腹部计算机断层扫描,伴有急性腹痛、腹胀和呼吸困难。由于肿瘤体积大且与肠系膜上动脉及其他血管关系密切,外科医生用剪刀锐性分离肿瘤并完整切除了整个肿瘤。