resection of GCT

  • 文章类型: Case Reports
    巨细胞瘤(GCT)是一种常见的良性侵袭性肿瘤,主要发生在胫骨近端,桡骨远端,和股骨远端,但很少在肱骨远端看到。它最初在30至50岁之间出现突然发生的疼痛。治疗通常是必要时刮宫辅助治疗,必要时重建。在我们的案例报告中,我们提出了临床和放射学发现,诊断,并对一名33岁的女性患者进行了治疗,该患者患有巨细胞瘤(GCT)并伴有左肱骨远端继发性动脉瘤性骨囊肿(ABC),患者经历了多年的疼痛而没有明显的创伤史。经临床检查,患者肘部内侧出现压痛,但未发现肿胀,发红,或热。她有一个无痛的全方位运动,完整的远端神经血管检查。影像学结论为GCT继发ABC。活检证实了诊断,排除转移病灶.患者接受了手术干预,用钢板固定,产生了极好的结果。
    Giant cell tumor (GCT) is a common benign aggressive tumor that mostly occurs in the proximal tibia, distal radius, and distal femur but is rarely seen in the distal region of the humerus. It originally presents between the ages of 30 and 50 with suddenly occurring pain. Treatment is generally curettage adjuvant treatment if necessary and reconstruction if required. In our case report, we present the clinical and radiological findings, diagnosis, and management of a 33-year-old female patient with a giant cell tumor (GCT) accompanied by a secondary aneurysmal bone cyst (ABC) in the left distal humerus, where the patient experienced pain for many years without significant history of trauma. Upon clinical examination, the patient displayed tenderness over the medial side of the elbow but no noted swelling, redness, or hotness. She had a painless full range of motion, with an intact distal neurovascular examination. Imaging concluded GCT with secondary ABC. A biopsy confirmed the diagnosis, ruling out metastatic lesions. The patient underwent surgical intervention, with plate fixation, which yielded excellent outcomes.
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  • 文章类型: Case Reports
    背景:骨巨细胞瘤(GCT)是一种常见的良性原发性骨肿瘤,常见于股骨远端,胫骨近端和桡骨远端。据报道,肱骨远端很少有GCT病例。我们报告了一名25岁男性在左肱骨内侧髁和上髁复发性巨细胞瘤的不寻常表现。
    方法:患者3年前出现左肘溶解性病变。因为它是一个不常见的肿瘤部位,误诊为结核性骨髓炎,刮除不充分。患者在初次手术后一年出现肿瘤复发。我们对肿瘤进行了整块切除,明智地移除部分滑车。尽管计划重建,由于每次手术肘部稳定,因此发现没有必要。患者恢复了接近正常的肘部运动,没有不稳定。他的MayoElbow性能得分从30提高到85。随访2年无复发或转移。
    结论:虽然在肱骨远端很少见骨肿瘤,需要进行活检以确认该区域任何溶解性病变的诊断,以便进行适当的治疗。
    BACKGROUND: Giant cell tumour of bone (GCT) is a common benign primary bone tumour, seen commonly in the distal Femur, proximal Tibia and distal Radius. Very few cases of GCT are reported in distal humerus. We report an unusual presentation of recurrent Giant cell tumour in a 25 year old male in the medial condyle and epicondyle of left Humerus.
    METHODS: Patient presented elsewhere with lytic lesion of left elbow three years ago. As it is an uncommon site for tumors, it was misdiagnosed as tuberculous osteomyelitis and was inadequately curetted. Patient presented to us with recurrence of tumor one year after the primary surgery. We did en-bloc resection of the tumour, with judicious removal of partial trochlea. Though reconstruction was planned, it was found to be not necessary as the elbow was stable per-operatively. Patient regained near normal movements of the elbow with no instability. His Mayo Elbow Performance score improved from 30 to 85. There is no recurrence or metastasis of the tumor in the two-year follow-up.
    CONCLUSIONS: Though bone tumors are rare in distal Humerus, biopsy is needed to confirm the diagnosis of any lytic lesion in this region for proper management.
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