Philippe P G, Rao B N, Rogers D A, Fontanesi J, Bowman L, Parham D, Shapiro D, Lobe T E, Fleming I
Department of Surgery, St Jude Children's Research Hospital, University of Tennessee, Memphis 38103.
J Pediatr Surg. 1992 Aug;27(8):964-7. doi: 10.1016/0022-3468(92)90541-e.
Successful management of sarcomas of the extremities in children implies not only achievement of local control but also satisfactory function and maintenance of the growth potential. The popliteal and antecubital fossae, because of their complex neurovascular anatomy, all of which is essential, make resection with satisfactory margins difficult. We reviewed our experience with 14 patients (3 to 20 years old; median, 13 years) with soft tissue sarcomas arising in the popliteal (11 patients) or antecubital (3 patients) fossae. There were four rhabdomyosarcomas (3 alveolar, 1 embryonal) and 10 other sarcomas, the most frequent being synovial sarcoma (5 patients). Chemotherapy was given to all patients with rhabdomyosarcomas. The one patient presenting with metastatic disease was treated, after biopsy of the primary, by chemotherapy and radiation and survived 21 months. In three patients, the primary management was an above-the-knee amputation and two of three survived (3 and 43 months). In 10 patients a wide local excision of the primary tumor was performed. Radiation therapy was administered to five, either as external beam (3 patients) or as brachytherapy (2 patients). In this group, there were no local recurrences. Four patients remain free of disease (4 months to 18 years) and one developed pulmonary metastasis. Among the five non-irradiated patients, three developed local recurrences, requiring above-the-knee amputation for disease. The fourth patient relapsed in the lung and only one of the five is free of disease at 36 months. Of the 8 patients not treated with amputation, one acquired a leg length discrepancy, which required correction, and one has a minimal extension deficit of the knee.(ABSTRACT TRUNCATED AT 250 WORDS)
成功治疗儿童肢体肉瘤不仅意味着实现局部控制,还意味着获得满意的功能以及维持生长潜力。腘窝和肘前窝因其复杂的神经血管解剖结构(所有这些都至关重要),使得在保证切缘满意的情况下进行切除手术变得困难。我们回顾了14例患者(年龄3至20岁,中位年龄13岁)的治疗经验,这些患者的软组织肉瘤发生于腘窝(11例)或肘前窝(3例)。其中有4例横纹肌肉瘤(3例肺泡型,1例胚胎型)和10例其他肉瘤,最常见的是滑膜肉瘤(5例)。所有横纹肌肉瘤患者均接受了化疗。1例出现转移性疾病的患者在对原发灶进行活检后,接受了化疗和放疗,存活了21个月。3例患者最初采取了膝上截肢术,其中2例存活(分别为3个月和43个月)。10例患者对原发肿瘤进行了广泛局部切除。5例患者接受了放射治疗,其中3例采用外照射,2例采用近距离放疗。在这组患者中,没有出现局部复发。4例患者无疾病复发(时间为4个月至18年),1例出现肺转移。在5例未接受放疗的患者中,3例出现局部复发,因疾病进展需要进行膝上截肢。第4例患者肺部复发,5例患者中只有1例在36个月时无疾病复发。在8例未接受截肢治疗的患者中,1例出现了腿长差异,需要进行矫正,1例膝关节伸展功能有轻微缺损。