Abdul-Hafez Hamza A, Aljouda Sulaiman, Aldarwish Asad, Soubh Bashar N, Najar Alaa, Mansour Mamoun
Department of Medicine, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine.
Department of Neurosurgery, Al-Makassed Hospital, Jerusalem, Palestine.
Int J Surg Case Rep. 2025 Jun;131:111410. doi: 10.1016/j.ijscr.2025.111410. Epub 2025 May 6.
Brain metastases are the most common intracranial tumors in adults, yet they remain rare in sarcoma patients, occurring in <6 % of cases. Metastatic spread of sarcomas typically involves the lungs, bones, and liver, with brain involvement being an unusual and poorly understood occurrence. Given the limited data, management strategies remain challenging, and prognosis is generally poor.
A previously healthy 16-year-old female presented with left shoulder pain and restricted movement. Imaging revealed a pathological fracture of the proximal humerus with a destructive mass lesion, and biopsy confirmed a diagnosis of high-grade sarcoma. She underwent chemotherapy, tumor resection, and later a pneumonectomy for lung metastases. Thirty months post-diagnosis, she developed progressive left-sided weakness, and brain MRI demonstrated a right insular metastatic lesion. She underwent gross total resection via microscopic right pterional craniotomy, followed by whole-brain radiotherapy and rehabilitation. At 42 months post-diagnosis, she remained recurrence-free with stable neurological function.
Brain metastases from sarcomas are rare and associated with poor prognosis. Pulmonary metastases are the strongest risk factor, and survival remains limited despite treatment. Surgical resection improves neurological function and extends survival in select patients with a high Karnofsky Performance Scale score and controlled systemic disease. Stereotactic radiosurgery is an option for multiple lesions, while WBRT and chemotherapy are reserved for widespread disease.
This case highlights the potential for favorable outcomes in sarcoma brain metastases with a multidisciplinary approach. Early detection and tailored intervention may improve survival and quality of life in such patients.
脑转移瘤是成人中最常见的颅内肿瘤,但在肉瘤患者中仍然罕见,发生率<6%。肉瘤的转移扩散通常累及肺、骨和肝,脑受累情况不常见且了解甚少。鉴于数据有限,管理策略仍然具有挑战性,且预后通常较差。
一名既往健康的16岁女性因左肩疼痛和活动受限就诊。影像学检查显示肱骨近端病理性骨折伴破坏性肿块病变,活检确诊为高级别肉瘤。她接受了化疗、肿瘤切除,后来因肺转移接受了肺切除术。诊断后30个月,她出现进行性左侧肢体无力,脑部MRI显示右侧岛叶转移瘤。她通过显微镜下右翼点开颅术进行了全切术,随后接受了全脑放疗和康复治疗。诊断后42个月,她无复发,神经功能稳定。
肉瘤脑转移罕见且预后不良。肺转移是最强的危险因素,尽管接受了治疗,生存期仍然有限。手术切除可改善神经功能,并延长部分卡氏功能状态评分高且全身疾病得到控制的患者的生存期。立体定向放射外科是治疗多发病变的一种选择,而全脑放疗和化疗则用于广泛病变。
本病例强调了多学科方法治疗肉瘤脑转移可能取得良好结果。早期检测和针对性干预可能改善此类患者的生存期和生活质量。