基础医学与临床 ›› 2026, Vol. 46 ›› Issue (9): 1272-1276.doi: 10.16352/j.issn.1001-6325.2026.09.1272

• 疑难病例 • 上一篇    下一篇

一例45 cm腹膜后去分化脂肪肉瘤报告

王君, 华祎炜, 赵奕, 刘广华, 东洁*   

  1. 中国医学科学院北京协和医学院 北京协和医院 泌尿外科,北京 100730
  • 收稿日期:2026-06-02 修回日期:2026-07-12 出版日期:2026-09-05 发布日期:2026-08-18
  • 通讯作者: *pumchdongjie@163.com
  • 基金资助:
    北京协和医学院课程思政教改专项基金(2025kcsz001)

One case report of a 45 cm retroperitoneal dedifferentiated liposarcoma

WANG Jun, HUA Yiwei, ZHAO Yi, LIU Guanghua, DONG Jie*   

  1. Department of Urology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China
  • Received:2026-06-02 Revised:2026-07-12 Online:2026-09-05 Published:2026-08-18
  • Contact: *pumchdongjie@163.com

摘要: 目的 探讨腹膜后去分化脂肪肉瘤(DDLPS)的临床特点、诊断过程、手术治疗及围手术期管理,以提高对该巨大罕见肿瘤的认识,为临床诊治提供参考。方法 本文报道北京协和医院泌尿外科2025年9月收治的一例57岁男性患者。回顾性分析此例患者电子病历资料,包括就诊记录、住院病历及辅助检查结果,患者住院期间的治疗。结果 患者门诊就诊时查体扪及左侧腹部巨大包块,影像学显示肿瘤推挤脾脏、胰腺体尾部、左肾及左肾上腺移位,同时压迫左侧输尿管导致上尿路积水。肿瘤完整切除后测量最大径达45 cm,重约12.5 kg。病理荧光原位杂交(FISH)检测示鼠双微体2(MDM2)信号扩增,提示DDLPS诊断。患者术后恢复良好,术后11 d出院,术后1个月随访一般情况可。结论 该病例影像学表现复杂,伴多形性钙化者较为罕见;对于此类巨大腹膜后肿物,应结合影像学、病理学及MDM2扩增检测明确诊断,并通过充分术前评估和完整手术切除以改善患者压迫症状及预后。

关键词: 去分化脂肪肉瘤, 腹膜后肿瘤, 罕见病, 鼠双微体2(MDM2)扩增

Abstract: Objective To investigate the clinical characteristics, diagnostic process, surgical treatment and peri-operative management of retroperitoneal dedifferentiated liposarcoma (DDLPS) and to improve awareness of this type of rare giant tumor while providing a reference for future clinical diagnosis and treatment. Methods A case of a 57-year-old male patient admitted to the Department of Urology, Peking Union Medical College Hospital in September 2025. The patient′s electronic medical records were retrospectively reviewed, including outpatient and inpatient records, laboratory and radiology results, and treatments during hospitalization. Results Physical examination revealed a giant palpable mass in the left abdomen. Radiology imaging showed significant displacements of the spleen, pancreas, left kidney, and left adrenal gland by the tumor and a compressed left ureter, resulting in upper urinary tract hydronephrosis. After en bloc resection, the tumor measured up to 45 cm in maximum diameter and weighed approximately 12.5 kg. Pathological fluorescence in situ hybridization (FISH) demonstrated amplification of murine double minute 2 (MDM2), supporting the diagnosis of DDLPS. The patient recovered uneventfully after surgery, was discharged on postoperative day 11, and remained in generally good condition at the 1-month follow-up. Conclusions The case demonstrated complex imaging features, since DDLPS with polymorphic calcification is relatively rare. For retroperitoneal masses of this size, diagnosis should be established based on a combination of imaging findings, pathological examination, and MDM2 amplification testing. Adequate preoperative assessment and complete surgical resection are also essential for relieving compression-related symptoms and improving prognosis.

Key words: dedifferentiated liposarcoma, retroperitoneal tumor, rare disease, murine double minute 2(MDM2) amplification

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