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Odyssey of an Elbow Synovial Chondromatosis

机译:肘部滑膜软骨瘤病的奥德赛

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Synovial chondromatosis of the elbow is an uncommon condition. However, a chondrosarcoma arising from the former is remarkably rare. The authors report a case of an elbow chondrosarcoma secondary to synovial chondromatosis in a 38-year-old woman. Before the development of chondrosarcoma, the patient underwent 3 operations and 3 sessions of radiosynovectomy because of continuous recurrence of synovial chondromatosis on the left elbow. After the last radiosynovectomy, magnetic resonance imaging and biopsy showed a grade II chondrosarcoma secondary to synovial chondromatosis. The patient underwent further surgery and custom-made arthroplasty because of aseptic loosening of the prosthesis. Four months after the last intervention, 3 subcutaneous nodes appeared on the patient's elbow and were histologically found to be a recurrence of chondrosarcoma (grade III). Amputation by disarticulation of the shoulder was performed in addition to biopsy of another subcutaneous node on the abdomen. The biopsy showed metastasis of chondrosarcoma. At final follow-up, the patient had lung metastasis 7 years after the initial diagnosis. A reason for the manifestation of primary synovial chondromatosis and its progression to chondrosarcoma has not been found. Synovial chondromatosis progressing to chondrosarcoma in the elbow was reported in only 1 case, with no clear initial diagnosis. The role of radiosynovectomy in the development of chondrosarcoma is unknown, and no reports have described the treatment of elbow synovial chondromatosis. Although synovial chondromatosis is benign, its metaplastic nature is a marker of possible malignancy, especially with signs of recurrence and aggression. The role of radiosynovectomy in malignant changes should be examined in future studies.
机译:肘部的滑膜软骨瘤是一种罕见的条件。然而,前者产生的软骨肉瘤非常罕见。作者报告了一个38岁的女性中继发于滑膜软骨病的肘部软骨菌病的案例。在开发乳房肉瘤之前,由于在左肘上连续复发,患者接受了3次操作和3次收集性术后的疗效。在最后的可收音术后,磁共振成像和活组织检查显示出次级肺泡软骨病的II级Chondrosarcoma。由于假体的无菌松动,患者接受了进一步的手术和定制关节成形术。在最后一次干预后四个月,患者肘部出现了3个皮下节,并在组织学上发现是软骨肉瘤的复发(III级)。除了腹部上另一个皮下节点的活检之外,还进行肩部截肢。活组织检查显示了软骨肉瘤的转移。在最终随访时,患者在初步诊断后7年肺转移。尚未发现初级滑膜软骨瘤化表现的原因及其对软骨糖瘤的进展。在肘部中进展到肘部的软骨菌病的滑膜瘤病进展,只有1例,没有明确的初步诊断。无雷诺术后术在软骨肉瘤发育中的作用是未知的,并且没有报道已经描述了肘部滑纹软骨病的治疗。虽然滑膜软骨瘤是良性的,但其常规性质是可能恶性肿瘤的标志,特别是具有复发和侵略的迹象。在未来的研究中,应检查收差距切除在恶性变化中的作用。

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