Bhatia Ritika, Singh Himanshi, Sadeque Jafor, Mathur Kushagra
General Medicine, Dartford and Gravesham NHS Trust, Dartford, GBR.
General Medicine, Chelsea and Westminster NHS Foundation Trust, London, GBR.
Cureus. 2024 Dec 20;16(12):e76081. doi: 10.7759/cureus.76081. eCollection 2024 Dec.
Glioblastoma multiforme (GBM) is a World Health Organisation (WHO) grade IV glioma originating from astrocytes. It is the most common malignant primary tumour of the brain and central nervous system (CNS) and is associated with fast progression and violent local spread, with a median overall survival of approximately 15 months after diagnosis. Due to its late and varied presentation, it is often diagnosed only after it has grown considerably. The symptomatology can vary from the individual being completely asymptomatic to mild sensory or sensorimotor symptoms. The symptoms usually arise due to compression of the fibres rather than pressure on vital structures. We discuss a case of a 72-year-old male who presented with complaints of tingling in the left upper limb for one day, improving spontaneously. A noncontrast CT head was nondiagnostic, and an MRI reported a likely metastatic lesion, and further imaging was advised. A detailed history was taken from an oncology point of view but the patient denied any weight loss, fever, recent travel, and family history of cancers. The scans were discussed at a neuroradiology multidisciplinary team (MDT) discussion an MRI with contrast was planned. After a thorough discussion and further review by neuroradiology consultants, the patient was diagnosed with a grade IV glioblastoma - a primary tumour of the brain - which was confirmed by a biopsy and immunohistochemistry. He was treated with two cycles of radiotherapy initially, followed by chemotherapy. Unfortunately, he died eight months after the start of the treatment due to a massive pulmonary embolism, complicated by nosocomial infection. This report highlights the importance of early diagnosis and treatment for patients with glioma. It also sheds light on the symptomatology and difficulties faced in the diagnosis of gliomas. Treating physicians should adopt an MDT approach in such cases and discuss the various possibilities and differentials.
多形性胶质母细胞瘤(GBM)是世界卫生组织(WHO)IV级胶质瘤,起源于星形胶质细胞。它是脑和中枢神经系统(CNS)最常见的恶性原发性肿瘤,与快速进展和局部侵袭性生长相关,诊断后的中位总生存期约为15个月。由于其发病较晚且表现多样,通常在肿瘤生长到相当程度后才被诊断出来。症状可能从个体完全无症状到轻度感觉或感觉运动症状不等。症状通常是由于纤维受压而非重要结构受压引起的。我们讨论一例72岁男性患者,他因左上肢刺痛一天前来就诊,症状自行缓解。头颅非增强CT检查未明确诊断,MRI报告可能为转移瘤,并建议进一步检查。从肿瘤学角度详细询问了病史,但患者否认有任何体重减轻、发热、近期旅行史及癌症家族史。在神经放射学多学科团队(MDT)讨论中对扫描结果进行了讨论,并计划进行增强MRI检查。经过神经放射学顾问的深入讨论和进一步复查,患者被诊断为IV级胶质母细胞瘤——一种原发性脑肿瘤——活检及免疫组化确诊。患者最初接受了两个周期的放疗,随后进行化疗。不幸的是,治疗开始八个月后,他因大面积肺栓塞并伴有医院感染而死亡。本报告强调了胶质瘤患者早期诊断和治疗的重要性。它还揭示了胶质瘤的症状学及诊断中面临的困难。在这种情况下,治疗医生应采用MDT方法,讨论各种可能性及鉴别诊断。