School of Clinical Medicine, Shandong Second Medical University, Weifang, China.
Affiliated Yantai Yuhuangding Hospital of Qingdao University, No. 20 East Yuhuangding Road, Yantai, 264000, Shandong, China.
BMC Nephrol. 2024 Aug 29;25(1):281. doi: 10.1186/s12882-024-03701-z.
Retroperitoneal liposarcoma (RPLPS) is a relatively rare disease. Liposarcomas vary in size, but sizeable RPLPS larger than 30 cm in diameter are very rare, and their diagnosis and treatment present significant challenges.
We report a 58-year-old male patient who was admitted to the hospital with an increased abdominal circumference and was later diagnosed with a giant RPLPS. The liposarcoma was found to adhere to the right kidney and the entire ureter, invading the ascending colon. The patient underwent complete combined surgical resection. The tumor was removed intact, measured 55.0 cm × 30.0 cm × 18.0 cm, and weighed 19.8 kg. Histopathologic analysis revealed well-differentiated liposarcoma (WDLPS). The patient was successfully discharged from the hospital and followed up for 6 months with no signs of recurrence.
RPLPS is a rare tumor with atypical clinical presentation. Surgery remains the most effective method of treatment for retroperitoneal sarcomas, with complete removal if there is local invasion. Preoperative examination, including three-dimensional (3D) reconstruction, is essential for surgical success. The role of adjuvant radiotherapy or chemotherapy remains controversial. However, clinicians should not rule them out as viable options.
腹膜后脂肪肉瘤(RPLPS)是一种相对罕见的疾病。脂肪肉瘤大小不一,但直径大于 30cm 的巨大 RPLPS 非常罕见,其诊断和治疗极具挑战性。
我们报告了一位 58 岁男性患者,因腰围增大就诊,后被诊断为巨大 RPLPS。脂肪肉瘤与右肾和整个输尿管粘连,侵犯升结肠。患者接受了完整的联合手术切除。肿瘤完整切除,大小为 55.0cm×30.0cm×18.0cm,重量为 19.8kg。组织病理学分析显示为高分化脂肪肉瘤(WDLPS)。患者成功出院,随访 6 个月无复发迹象。
RPLPS 是一种罕见的肿瘤,临床表现不典型。手术仍然是治疗腹膜后肉瘤最有效的方法,如果存在局部侵犯则需要完全切除。术前检查,包括三维(3D)重建,对手术成功至关重要。辅助放疗或化疗的作用仍存在争议。但临床医生不应排除这些治疗方法。