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腘窝软组织肉瘤的治疗结果:15年经验总结

Outcome of Soft Tissue Popliteal Sarcomas: 15 Years of Experience.

作者信息

Tepedelenlioğlu Hüseyin Emre, Tolunay Tolga, Orhan Özlem, Arikan Şefik Murat, Akgün Erkan, Toğral Güray

机构信息

Department of Orthopedics and Traumatology, Ankara Etlik City Hospital, Ankara, Turkey.

Department of Orthopedics and Traumatology, Faculty of Medicine, Gazi University, Ankara, Turkey.

出版信息

Indian J Orthop. 2024 Sep 25;59(1):34-39. doi: 10.1007/s43465-024-01263-8. eCollection 2025 Jan.

Abstract

BACKGROUND

Soft-tissue sarcoma involving the popliteal fossa remains challenging because it is difficult to achieve wide margins with limb salvage in this location. Adjuvant therapy is frequently necessary, and limb function can be adversely affected. We reviewed our experience with these tumors. A variety of lesions can be identified within the posterior knee, ranging from simple Baker's cysts to malignant lesions. We present a review of frequently encountered and less common entities using an anatomic sieve, with the aim of providing a diagnostic approach to popliteal fossa masses Soft-tissue sarcomas (STSs) arising from the popliteal fossa present a challenge with regard to local control of primary tumors.

METHOD

In the study, patients who were operated for a mass in the popliteal region between 2007 and 2018 in our clinic were retrospectively analyzed. Patients were categorized by parameters such as age, gender, extremity direction, type of surgery, AJCC scores, surgical margin, tumor size, presence of distant metastases, mass pathology, follow-up time and MSTS score.

RESULTS

Our study included 13 patients (eight women and five men). The mean age was 48 (range 12-84) years. The mass was located in the left knee in nine patients and the right knee in four patients. Frequent histologic diagnoses were for maliğn soft-tissue tumor liposarcoma (= 5), synovial sarcoma (= 3) and pleomorphic sarcoma (= 2), rabdomyorsarcoma, clear cell sarcoma, peripheral nerve sheath tumor (=1). Tumor size varied from 3 to 14 cm (median 7 cm). American Joint Committee on Cancer staging was as follows: three patients had stage IIA disease, five patients had stage IIB disease, two patients had stage III and stage IB and 1 patient had stage IV disease. The mean duration of follow-up was 39 (range 12-96) months. All patients underwent wide resection. Recurrence developed in four of these patients during the 5-year follow-up period. Recurrence resection was performed in three of the patients who developed recurrence, while recurrence resection + femur distal tumor resection arthroplasty was performed in one patient. In addition, 3 of these 13 patients received neoadjuvant chemotherapy, while 5 received adjuvant chemotherapy treatment. Neoadjuvant RT was applied to 4 patients with a mass greater than 9 cm. Margins were negative in seven of 13 patients and microscopically positive in five patients. Complications included wound infections in four patients and thrombophlebitis in two patients and one patients peroneal nerve nöropraxy. Of the patients undergoing limb-salvaging procedures, two experienced local recurrences after limb salvage and four experienced lung metastases. Local recurrence was always associated with positive margins. The mean MusculoskeletalTumor Society 1987 score was 50 ( range 35-68). At latest follow-up, six patients had died of disease, one was alive with disease, and five patients remained free of disease.

CONCLUSION

The popliteal region is a rare area in terms of mass localizations. Inpatients presenting with knee pain, regardless of external findings such as swelling ornot, tumors located in the popliteal region should be considered in patients withoutpathology on direct radiography.

摘要

背景

累及腘窝的软组织肉瘤治疗仍具有挑战性,因为在此部位进行保肢手术时难以获得广泛的手术切缘。辅助治疗常常是必要的,且肢体功能可能受到不利影响。我们回顾了我们治疗这些肿瘤的经验。膝关节后方可发现多种病变,从单纯的贝克囊肿到恶性病变。我们使用解剖筛选法对常见和少见的实体进行综述,旨在为腘窝肿块提供一种诊断方法。起源于腘窝的软组织肉瘤在原发性肿瘤的局部控制方面存在挑战。

方法

在本研究中,对2007年至2018年期间在我们诊所因腘窝区肿块接受手术的患者进行回顾性分析。根据年龄、性别、肢体方向、手术类型、美国癌症联合委员会(AJCC)评分、手术切缘、肿瘤大小、远处转移情况、肿块病理、随访时间和肌肉骨骼肿瘤学会(MSTS)评分等参数对患者进行分类。

结果

我们的研究包括13例患者(8例女性和5例男性)。平均年龄为48岁(范围12 - 84岁)。肿块位于左膝9例,右膝4例。常见的组织学诊断为恶性软组织肿瘤脂肪肉瘤(= 5例)、滑膜肉瘤(= 3例)和多形性肉瘤(= 2例)、横纹肌肉瘤、透明细胞肉瘤、周围神经鞘瘤(= 1例)。肿瘤大小从3厘米至14厘米不等(中位数7厘米)。美国癌症联合委员会分期如下:3例患者为IIA期疾病,5例患者为IIB期疾病,2例患者为III期和IB期,1例患者为IV期疾病。平均随访时间为39个月(范围12 - 96个月)。所有患者均接受了广泛切除。在5年随访期内,其中4例患者出现复发。3例复发患者接受了复发切除,1例患者接受了复发切除 + 股骨远端肿瘤切除关节成形术。此外,这13例患者中有3例接受了新辅助化疗,5例接受了辅助化疗。4例肿块大于9厘米的患者接受了新辅助放疗。13例患者中有7例切缘阴性,5例显微镜下阳性。并发症包括4例患者伤口感染、2例患者血栓性静脉炎和1例患者腓总神经神经失用。在接受保肢手术的患者中,2例在保肢后出现局部复发,4例出现肺转移。局部复发总是与切缘阳性相关。1987年肌肉骨骼肿瘤学会平均评分为50分(范围35 - 68分)。在最近一次随访时,6例患者死于疾病,1例带瘤生存,5例患者无病生存。

结论

就肿块定位而言,腘窝区是一个少见部位。对于出现膝关节疼痛的患者,无论有无肿胀等外部表现,在X线平片无病变的患者中应考虑腘窝区肿瘤。

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