Department of Orthopedic Surgery, Hokkaido University Graduate School of Medicine, Sapporo, Hokkaido, Japan; Department of Orthopedic Surgery, Teine Keijinkai Hospital, Teine-Ku, Sapporo, Hokkaido, Japan.
Department of Orthopedic Surgery, Hokkaido University Graduate School of Medicine, Sapporo, Hokkaido, Japan.
Knee. 2021 Jan;28:151-158. doi: 10.1016/j.knee.2020.11.019. Epub 2020 Dec 23.
Hemarthrosis after total knee arthroplasty (TKA) is a relatively rare complication. Although most cases are effectively treated with conservative therapy, some cases require angiographic embolization or surgical intervention. Angiosarcoma is a rare malignant tumor derived from the vascular endothelium with neovascular hyperplasia and mainly arises in the skin and superficial soft tissue, and less frequently in deep soft tissue and bone. Although malignant neoplasms such as angiosarcoma in the vicinity of orthopedic implants were reported, the causal relationship between development of the malignant tumor and the orthopedic implant is widely debated in the literature.
We report the case of a 68-year-old female with angiosarcoma that developed in the knee joint 2 years after revision TKA. The patient exhibited severe persistent bleeding, which reached 1000-1400 ml per day for 4 months. Histological analysis of the synovial tissue in the knee joint showed large cells with nuclear atypia. Immunohistochemical staining showed cells that were positive for CD31, CD34, and D2-40, and she was diagnosed with angiosarcoma. The patient underwent an amputation at the level of the thigh, and her general condition immediately improved after the operation. The patient did not exhibit bleeding from the site of amputation, and no local recurrence or distant metastases were detected 1 year after the amputation.
To the best of our knowledge, this represents the first report of angiosarcoma 2 years after revision TKA. Further careful follow up is needed, given the high-grade malignancy.
全膝关节置换术后关节内血肿(hemarthrosis after total knee arthroplasty,TKA)是一种相对罕见的并发症。虽然大多数病例通过保守治疗即可有效治疗,但有些病例需要血管造影栓塞或手术干预。血管肉瘤是一种罕见的来源于血管内皮细胞的恶性肿瘤,具有新生血管增生,主要发生于皮肤和浅表软组织,较少发生于深部软组织和骨骼。虽然有报道称在骨科植入物附近发生了血管肉瘤等恶性肿瘤,但该恶性肿瘤的发生与骨科植入物之间的因果关系在文献中仍存在广泛争议。
我们报告了一例 68 岁女性患者,在接受翻修全膝关节置换术后 2 年时发生膝关节血管肉瘤。患者表现为严重持续出血,每天出血量达 1000-1400ml,持续了 4 个月。膝关节滑膜组织的组织学分析显示,细胞核异型性较大的细胞。免疫组织化学染色显示,细胞对 CD31、CD34 和 D2-40 呈阳性,诊断为血管肉瘤。患者接受了大腿水平的截肢手术,术后一般情况立即改善。截肢部位无出血,截肢 1 年后未发现局部复发或远处转移。
据我们所知,这是首例翻修全膝关节置换术后 2 年发生血管肉瘤的报告。鉴于其高度恶性,需要进一步密切随访。