Università Cattolica del Sacro Cuore, Largo Francesco Vito n. 1, 00168, Rome, Italy.
Dipartimento Scienze Mediche e Chirurgiche, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Largo Agostino Gemelli 8, 00168, Rome, Italy.
BMC Surg. 2020 Nov 20;20(1):291. doi: 10.1186/s12893-020-00966-7.
Angiosarcoma is a rare malignant tumor, originating from vascular endothelial cells, accounting for approximatively 1-2% of soft tissue sarcomas. It is characterized by a rapid proliferation and high metastatic potential. Some cases of angiosarcoma are described in association with vascular prosthesis, orthopedic devices and foreign bodies. Hereby, we report a case of a patient treated with the endovascular placement of a PTFE aorto bis-iliac prosthesis for aortic aneurysm, who developed a graft-related angiosarcoma with bone and peritoneal localizations. The peritoneal "sarcomatosis" led to an acute presentation with hemoperitoneum and anemia. We perform a thorough review of the literature summarizing the description of similar cases, their epidemiology and the possibilities for treatment.
An 84-year-old male with a history of abdominal aortic aneurysm endovascular repair presented to our emergency department complaining with low back pain radiating to the left limb. He underwent a type II endoleak embolization of the aneurysmal sac nine days before. During hospitalization he underwent a spine MRI which documented a vertebral alteration of non-univocal interpretation. Vertebral biopsy was performed revealing groups of cells of uncertain nature. He lately underwent percutaneous L2-L4 arthrodesis. Forty-two days after admission, he developed acute anemia. Emergency laparotomy revealed a massive hemoperitoneum and actively bleeding peritoneal nodules. Abdominal packing was performed, and several nodules were sent for definitive histological examination. After surgery, he developed progressive and severe hypovolemic shock and expired on postoperative day 5.
Angiosarcoma associated with foreign bodies, especially vascular prosthesis, is a very rare entity. In patients who have a history of prosthetic vascular graft placement that present with lumbar pain, osteolytic changes at radiologic imaging or the development of ascites, angiosarcoma should be considered in the differential diagnosis. Despite the poor prognosis, a prompt diagnosis might give access to an adequate treatment planning, with the aim for disease control and increased survival.
血管肉瘤是一种罕见的恶性肿瘤,起源于血管内皮细胞,约占软组织肉瘤的 1-2%。它的特点是快速增殖和高转移潜能。有些血管肉瘤病例与血管假体、骨科器械和异物有关。在此,我们报告一例患者,因主动脉瘤行血管内放置 PTFE 主动脉双髂假体治疗,后发生与移植物相关的血管肉瘤,并伴有骨和腹膜局灶性病变。腹膜“肉瘤样转移”导致急性表现为血腹和贫血。我们对文献进行了全面回顾,总结了类似病例的描述、流行病学和治疗可能性。
一名 84 岁男性,有腹部主动脉瘤血管内修复史,因腰痛放射至左下肢就诊于我院急诊科。他在 9 天前接受了 II 型腹主动脉瘤腔内修复术的内漏栓塞治疗。住院期间,他接受了脊柱 MRI 检查,发现脊柱改变无法明确诊断。脊柱活检显示为一组性质不明的细胞。他最近接受了经皮 L2-L4 融合术。入院后第 42 天,他出现急性贫血。紧急剖腹手术发现大量血腹和活跃性出血性腹膜结节。进行了腹部填塞,送几个结节进行明确的组织学检查。手术后,他出现进行性和严重的低血容量性休克,并于术后第 5 天死亡。
与异物相关的血管肉瘤,特别是血管假体,是一种非常罕见的实体瘤。对于有血管假体植入史、影像学检查有溶骨性改变或出现腹水的患者,出现腰痛时应考虑血管肉瘤的鉴别诊断。尽管预后不良,但及时诊断可能有助于制定适当的治疗计划,以控制疾病并提高生存率。