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Metastatic patterns of extremity myxoid liposarcoma and their outcome.

机译:肢体黏液状脂肪肉瘤的转移模式及其预后。

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摘要

BACKGROUND AND OBJECTIVES: Extremity myxoid liposarcomas have a unique extrapulmonary metastatic potential. We studied the metastatic pattern of extremity liposarcomas to determine what types of posttreatment imaging may be of value in the follow-up these patients. METHODS: Twenty-two patients from a total of 128 patients with primary extremity liposarcoma were treated at a tertiary care institution for subsequent metastases from January 1981 to January 2000. Median follow-up was 45 months (range: 6-270 months). Data on these patients was prospectively collected and then retrospectively analyzed for effect of metastatic pattern and treatment on outcome. RESULTS: Of these 22 patients, extrapulmonary metastases developed in 10, combined pulmonary and extrapulmonary metastases developed in 6, and isolated pulmonary metastases developed in 6. Of the 16 patients with extrapulmonary metastases, 13 were of the myxoid subtype. Of the 49 patients with extremity myxoid liposarcomas, metastases developed in 14 (29%). The most common sites of metastases among these 14 patients include: the retroperitoneum, 10 patients (71)%; intra-abdominal extra-hepatic, 7 patients (50%); spinal/paraspinal, 6 patients (43%). Only 3 of the patients are alive and disease free and all 3 of these patients are from the subgroup of 10 patients with only extra-pulmonary metastases (2 intra-abdominal and 1 retroperitoneal). CONCLUSIONS: Extremity myxoid liposarcomas have an unusually high predilection for extra-pulmonary metastases, frequently without any pulmonary metastases. After treatment of the primary tumor, these patients should be followed with periodic chest X-ray and abdominal/pelvic computed tomography (CT) scans. Any back or neurologic complaints should prompt additional imaging of the appropriate spinal area. Consideration should be given to surgical and adjuvant treatment of metastatic disease when appropriate.
机译:背景与目的:四肢粘液性脂肪肉瘤具有独特的肺外转移潜能。我们研究了肢体脂肪肉瘤的转移模式,以确定哪些类型的治疗后影像学对这些患者的随访可能有价值。方法:从1981年1月至2000年1月,在三级医疗机构对总共128例原发性肢体脂肪肉瘤患者中的22例患者进行了后续转移治疗。中位随访时间为45个月(范围:6-270个月)。前瞻性收集这些患者的数据,然后回顾性分析转移模式和治疗对预后的影响。结果:在这22例患者中,有10例发生了肺外转移,在6例中发生了肺和肺外转移,在6例中出现了孤立性肺转移。在16例肺外转移患者中,有13例属于类胶质亚型。在49例四肢粘液样脂肪肉瘤患者中,有14例发生转移(29%)。在这14例患者中,最常见的转移部位包括:腹膜后,10例(71)%;腹内肝外治疗7例(50%);脊柱/脊柱旁的6例(43%)。只有3例患者活着并且没有疾病,并且所有3例患者均来自10例仅有肺外转移的患者(2例是腹腔内转移,1例是腹膜后转移)。结论:肢体黏液状脂肪肉瘤对肺外转移有很高的偏爱,通常无任何肺转移。在治疗原发性肿瘤后,应定期对这些患者进行胸部X射线和腹部/骨盆计算机断层扫描(CT)扫描。任何背部或神经系统不适都应提示对适当的脊柱区域进行额外的成像。适当时应考虑对转移性疾病进行手术和辅助治疗。

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