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首页> 外文期刊>Surgical Neurology International >An autopsy case of widespread brain dissemination of glioblastoma unnoticed by magnetic resonance imaging after treatment with bevacizumab
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An autopsy case of widespread brain dissemination of glioblastoma unnoticed by magnetic resonance imaging after treatment with bevacizumab

机译:贝伐单抗治疗后,磁共振成像未发现胶质母细胞瘤广泛分布于大脑的尸检病例

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Background: Although glioblastoma has been shown to be able to disseminate widely in the intracranially after treatment with bevacizumab without any significant radiological findings, reports on such cases with subsequent autopsy findings are lacking. Case Description: A 36-year-old man presented with a general seizure and a mass of the right frontal lobe, which was diagnosed as diffuse astrocytoma (WHO Grade II). The patient underwent a total of four surgeries from 2005 to 2017. He showed tumor recurrence, progression, and malignant transformation to glioblastoma (GBM) (WHO Grade IV) despite repeated tumor resections, radiotherapy, and chemotherapies with temozolomide and carmustine wafers. Bevacizumab (10 mg/kg body weight) was started following the fourth surgery. After bevacizumab administration, the patient’s clinical condition improved to a Karnofsky performance status (KPS) score of 50–60, and he was stable for several months before finally deteriorating and passing away. Although sequential magnetic resonance imaging (MRI) showed shrinkage of the lesion and a reduction of edema, an autopsy showed widespread tumor invasion that was not revealed on MRI. Neoplastic foci were identified extensively in the cerebral cortex, basal ganglia, pituitary gland, cerebellum, and brainstem, imposing as gliomatosis cerebri. Conclusion: Imaging follow-up of malignant gliomas needs to be interpreted with caution as marked improvement in radiological response after bevacizumab treatment may not be indicating tumor regression. Despite the notable lack of evidence to increase overall survival in GBM patients with bevacizumab, the increase in progression-free survival and the observed relief of symptoms due to a decrease in edema should be considered relevant for patient management.
机译:背景:尽管已显示出胶质母细胞瘤在用贝伐单抗治疗后能够在颅内广泛散布,而没有任何明显的放射学发现,但尚无有关此类病例随后尸检的报道。病例描述:一名36岁的男性,表现为全身性癫痫发作和右额叶肿块,被诊断为弥漫性星形细胞瘤(WHO II级)。自2005年至2017年,该患者共进行了四次手术。尽管反复进行了肿瘤切除,放疗以及替莫唑胺和卡莫斯汀片的化学疗法,他仍显示出肿瘤的复发,进展以及恶性转化为胶质母细胞瘤(GBM)(WHO IV级)。在第四次手术后开始使用贝伐单抗(10 mg / kg体重)。贝伐单抗给药后,患者的临床状况改善到卡诺夫斯基病情状态(KPS)评分为50-60,并且他稳定了几个月,直到病情恶化并死亡。尽管顺序磁共振成像(MRI)显示病变缩小和水肿减轻,但尸检显示广泛的肿瘤浸润,而MRI没有显示。在大脑皮层,基底神经节,垂体,小脑和脑干中广泛发现了肿瘤灶,表现为脑胶质瘤病。结论:恶性神经胶质瘤的影像学随访需要谨慎解释,因为贝伐单抗治疗后放射学反应明显改善可能并不表明肿瘤消退。尽管明显缺乏增加贝伐单抗的GBM患者总体生存率的证据,但应将无进展生存率的提高和因水肿减少引起的症状缓解视为与患者管理有关。

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