Yang Chenyu, Wang Xinjia, Lin Huaitai, Zhu Jinhao, Xu Zijian, Wang Weidong
Bone and Soft Tissue Tumor Department, Shantou University Medical College Affiliated Cancer Hospital, Shantou, China.
Front Oncol. 2024 May 10;14:1395233. doi: 10.3389/fonc.2024.1395233. eCollection 2024.
Alveolar Rhabdomyosarcoma is a profoundly malignant soft-tissue sarcoma that predominantly affects children and adolescents. However, the medical field lacks consensus regarding the optimal surgical approach to be undertaken in cases where this tumor causes local bone destruction in the upper limb.
A 17-year-old male presented a mass in his left forearm and CT and MRI indicated that the mass had penetrated the ulnar cortex and infiltrating the medulla, resulting in the formation of an eccentric trans-ventricular tumor focus. The sizable tumor affected the volar muscles of the forearm as well as the ulnar bone marrow, exerting pressure on the ulnar artery and vein. It was confirmed by needle biopsy that the mass is alveolar rhabdomyosarcoma. Following two courses of neoadjuvant chemotherapy, the tumor was widely excised en bloc. Autologous fibula with a vascular pedicle was utilized for reconstruction during the procedure. In the postoperative follow-up, no local recurrence of the tumor was observed. Furthermore, the patient retained satisfactory wrist flexion and pronation function in the left forearm.
Alveolar rhabdomyosarcoma is an uncommon and highly aggressive form of soft tissue sarcoma. Scientific management necessitates a multidisciplinary approach, combining chemotherapy with surgery. In cases where the tumor invaded into compartment of the bone, careful consideration should be given to the boundaries of tumor resection, the extent of osteotomy, and the approach to musculoskeletal reconstruction when designing the surgical plan. Through reporting our own case and thoroughly reviewing previous clinical experiences, we aim to provide valuable insights for the treatment of this particular disease.
肺泡状横纹肌肉瘤是一种高度恶性的软组织肉瘤,主要影响儿童和青少年。然而,对于该肿瘤导致上肢局部骨质破坏的病例,医学领域在最佳手术方式上缺乏共识。
一名17岁男性患者左前臂出现肿块,CT和MRI显示该肿块穿透尺骨皮质并浸润髓质,形成一个偏心的经心室肿瘤灶。这个较大的肿瘤影响了前臂掌侧肌肉以及尺骨髓腔,对尺动脉和静脉产生压迫。经穿刺活检确诊为肺泡状横纹肌肉瘤。经过两个疗程的新辅助化疗后,肿瘤被整块广泛切除。术中采用带血管蒂的自体腓骨进行重建。术后随访未观察到肿瘤局部复发。此外,患者左前臂腕关节屈曲和旋前功能保留良好。
肺泡状横纹肌肉瘤是一种罕见且侵袭性很强的软组织肉瘤形式。科学的治疗需要多学科方法,将化疗与手术相结合。在肿瘤侵犯骨腔的病例中,制定手术方案时应仔细考虑肿瘤切除边界、截骨范围以及肌肉骨骼重建方法。通过报告我们自己的病例并全面回顾以往临床经验,我们旨在为这种特殊疾病的治疗提供有价值的见解。