Li Zu-Gui, Mu Hai-Yu
Department of Nuclear Medicine Department of Oncology, Pingjin Hospital, Logistics university of Chinese People's Armed Police Force, Tianjin, People's Republic of China.
Medicine (Baltimore). 2017 Jun;96(23):e7123. doi: 10.1097/MD.0000000000007123.
Extracranial bone metastases from astrocytoma are rare and frequently detected as part of multiorgan metastases. It is extremely rare for astrocytoma to have extracranial bone metastases alone. The importance of whole-body fluorodeoxyglucose positron emission tomography/computed tomography (FDG PET/CT) imaging in evaluating extracranial metastasis (ECMs) has not been described effectively due to the rarity of this event. The purpose of our case report is to emphasize the role of FDG PET/CT in the assessment of tumor recurrence and extracranial bone metastases from anaplastic astrocytoma.
A 25-year-old woman was firstly admitted with a 4-month history of progressive blurred vision, and 2-month history of intermittent headache. Presurgical MRI imaging revealed a large mass in the left trigone of lateral ventricle. Subsequently, she underwent tumor resection, radiotherapy and chemotherapy. A final pathological diagnosis of anaplastic astrocytoma (WHO III) was made. Nearly 12 months after the surgery, the follow-up brain MR imaging revealed a contrast-enhanced lesion in the site of operative region. Whole-body FDG PET/CT imaging was performed to evaluate the situation.
Postoperative brain FDG PET/CT showed an abnormal focal FDG uptake corresponding to the contrast-enhanced lesion in the operative area, suggesting a tumor recurrence. Whole-body FDG PET/CT also showed multiple FDG-avid osteosclerotic lesions in the body. It was highly suggestive of extracranial bone metastases. A subsequent open bone biopsy of FDG-avid lesion in right iliac crest was performed. Histopathological and immunohistochemical findings indicated characteristic of glioma. The patient died 1 month later, nearly 13 months after the initial diagnosis.
ECMs from anaplastic astrocytoma are extremely rare but they do occur. Whole-body FDG PET/CT imaging with inclusion of brain was valuable in differentiating tumor recurrence from radiation necrosis and in detecting uncommon extracranial bone metastases from anaplastic astrocytoma, which were closely related to prognosis of this disease.
星形细胞瘤的颅外骨转移罕见,常作为多器官转移的一部分被发现。星形细胞瘤单独发生颅外骨转移极为罕见。由于该情况罕见,全身氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG PET/CT)成像在评估颅外转移(ECM)中的重要性尚未得到有效描述。本病例报告的目的是强调FDG PET/CT在评估间变性星形细胞瘤的肿瘤复发和颅外骨转移中的作用。
一名25岁女性首次因进行性视力模糊4个月、间歇性头痛2个月入院。术前MRI成像显示侧脑室左三角区有一个大肿块。随后,她接受了肿瘤切除、放疗和化疗。最终病理诊断为间变性星形细胞瘤(WHO III级)。术后近12个月,随访脑部MR成像显示手术区域有一个强化病灶。进行全身FDG PET/CT成像以评估情况。
术后脑部FDG PET/CT显示与手术区域强化病灶相对应的异常局灶性FDG摄取,提示肿瘤复发。全身FDG PET/CT还显示体内有多个FDG摄取增高的骨硬化病灶。高度提示颅外骨转移。随后对右髂嵴FDG摄取增高的病灶进行了开放性骨活检。组织病理学和免疫组化结果显示为胶质瘤特征。患者在初始诊断后近13个月,1个月后死亡。
间变性星形细胞瘤的颅外骨转移极为罕见,但确实会发生。包括脑部的全身FDG PET/CT成像在区分肿瘤复发与放射性坏死以及检测间变性星形细胞瘤罕见的颅外骨转移方面具有价值,这些转移与该疾病的预后密切相关。