Kilçiksiz S, Gökçe T, Somali I, Duransoy A, Aydin A, Yiğit S
Department of Radiation Oncology, Atatürk Training and Research Hospital, Izmir, Turkey.
J BUON. 2006 Jul-Sep;11(3):355-8.
A 37-year-old man was admitted with an extrathoracic desmoid tumor invading the brachial plexus. Magnetic resonance imaging (MRI) of the thorax demonstrated a 20 x 9 x 14 cm mass in the supraclavicular fossa, axillary fossa and the right side of the chest. It invaded the brachial plexus and circumscribed the subclavian and axillary arteries concentrically. Biopsy revealed desmoid tumor which was resected subtotally with the brachial plexus. The gross residual mass was treated postoperatively with radiotherapy (60 Gy) which resulted in major regression of the mass. Following radiotherapy, ethodolac with ascorbic acid were administered. The tumor was clinically indiscernible 35 months post-radiotherapy. This case shows the high effectiveness of radiotherapy along with less toxic medical treatment modalities in instances where local control is hard to achieve with surgery and highlights the importance of using multidisciplinary treatments to maintain good functional results.
一名37岁男性因胸外硬纤维瘤侵犯臂丛神经入院。胸部磁共振成像(MRI)显示,在锁骨上窝、腋窝及右侧胸部有一个20×9×14 cm的肿块。该肿块侵犯臂丛神经,并同心包绕锁骨下动脉和腋动脉。活检显示为硬纤维瘤,遂将其与臂丛神经一并大部分切除。术后对肉眼可见的残留肿块进行了放射治疗(60 Gy),肿块明显缩小。放疗后,给予依托度酸和维生素C。放疗35个月后,临床上已无法辨认该肿瘤。该病例表明,在手术难以实现局部控制的情况下,放射治疗联合低毒的药物治疗方式具有很高的有效性,并突出了采用多学科治疗以保持良好功能结果的重要性。