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A subcutaneous mass due to a glioblastoma which invaded and destroyed the bone: A case report

机译:由于侵入和摧毁骨骼的胶质母细胞瘤引起的皮下肿块:案例报告

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BackgroundGlioblastoma multiforme (GBM) is the most common and aggressive primary malignant brain tumor. However, it rarely invades and destroys bone. We report the first case of GBM of a very old patient, which eroded the dura and bone and finally resulted in a large facio-cranial subcutaneous lesion in the absence of prior surgery or radiation.Case descriptionA 93-year-old woman was presumed with a low-grade glioma (LGG), and the lesion was followed up with magnetic resonance imaging (MRI). Serial monitoring revealed no tumor growth until 2?years later, when the patient was admitted to our institution for anorexia and lack of spontaneity and flow of conversation. On admission, she oftentimes complained of severe right forehead skin pain. Computed tomography (CT) revealed enhancing mass lesions in the right frontal lobe and bone destruction. Upon inspection and palpation, a soft and swelling subcutaneous mass was evident at the forehead, the site of bone destruction. Contrast-enhanced MRI revealed ring-enhancing lesions with irregular borders, and the malignant transformation of LGG into GBM was suspected. The patient had severe skin pain at the region of the subcutaneous mass, so tumor resection of the subcutaneous mass was performed for removing the pain and a definitive diagnosis. The pathological diagnosis was isocitrate dehydrogenase (IDH)-mutated glioblastoma. Immunostaining revealed that the tumor was positive for IDH-1 and p53mutations but negative for ATRX. The patient died due to aspiration pneumonitis.ConclusionsWe report a first case of GBM in a very old patient untreated with surgery or radiation that invaded and destroyed the calvaria during the natural progression of the disease. Calvarial destruction without prior surgery or radiation in very old patients association with extra- and intra-axial neoplasm should include GBM in the differential diagnosis, although this is very rare.
机译:Backgroundglioblastoma multiforme(GBM)是最常见和最具侵略性的原发性恶性脑肿瘤。然而,它很少侵入并摧毁骨骼。我们报告了一个非常老患者的GBM的第一种情况,它侵蚀了硬脑膜和骨骼,最终导致在没有先前的手术或辐射的情况下发生了大的面部颅皮下病变.Case Descriptiona 93岁的女子被推出低级胶质瘤(LGG)和病变随访磁共振成像(MRI)。连续监测显示肿瘤生长直到2年后,当患者被厌食的机构录取和缺乏自发性和谈话流动时。入学时,她曾抱怨严重的额外肤色疼痛。计算机断层扫描(CT)显示出右前叶和骨破坏中的增强质量病变。在检查和触诊时,在额头上柔软和肿胀的皮下肿块,骨质破坏部位是明显的。对比增强的MRI显示出具有不规则边界的环增强病变,怀疑LGG变为GBM的恶性转化。患者在皮下肿块的区域处具有严重的皮肤疼痛,因此进行皮下肿块的肿瘤切除,用于去除疼痛和明确的诊断。病理诊断是异柠檬酸脱氢酶(IDH) - 融化的胶质母细胞瘤。免疫染色显示肿瘤对于IDH-1和P53浆质为阳性,但为ATRX为阴性。患者因吸汗肺炎而死亡.Conclusionswe在一个非常古老的患者中报告了一个在疾病自然进展过程中侵入和摧毁了Calvaria的手术或辐射的非常古老的患者中的第一个GBM。颅骨破坏没有先前的手术或辐射,患者与高度和轴上肿瘤的关联应包括差异诊断中的GBM,虽然这是非常罕见的。

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