Hamed Sherifa A, Mekkawy Mohamad A, Abozaid Hosam
Sherifa A Hamed, Department of Neurology and Psychiatry, Assiut University Hospital, Assiut 71516, Egypt.
World J Clin Cases. 2015 Nov 16;3(11):956-64. doi: 10.12998/wjcc.v3.i11.956.
We describe clinical, diagnostic features and follow up of a patient with a vanishing brain lesion. A 14-year-old child admitted to the department of Neurology at September 2009 with a history of subacute onset of fever, anorexia, vomiting, blurring of vision and right hemiparesis since one month. Magnetic resonance imaging (MRI) of the brain revealed presence of intra-axial large mass (25 mm × 19 mm) in the left temporal lobe and the brainstem which showed hypointense signal in T1W and hyperintense signals in T2W and fluid attenuated inversion recovery (FLAIR) images and homogenously enhanced with gadolinium (Gd). It was surrounded by vasogenic edema with mass effect. Intravenous antibiotics, mannitol (2 g/12 h per 2 d) and dexamethasone (8 mg/12 h) were given to relief manifestations of increased intracranial pressure. Whole craniospinal radiotherapy (brain = 4000 CGy/20 settings per 4 wk; Spinal = 2600/13 settings per 3 wk) was given based on the high suspicion of neoplastic lesion (lymphoma or glioma). Marked clinical improvement (up to complete recovery) occurred within 15 d. Tapering of the steroid dose was done over the next 4 mo. Follow up with MRI after 3 mo showed small lesion in the left antero-medial temporal region with hypointense signal in T1W and hyperintense signals in T2W and FLAIR images but did not enhance with Gd. At August 2012, the patient developed recurrent generalized epilepsy. His electroencephalography showed the presence of left temporal focus of epileptic activity. MRI showed the same lesion as described in the follow up. The diffusion weighted images were normal. The seizures frequency was decreased with carbamazepine therapy (300 mg/12 h). At October 2014, single voxel proton (1H) MR spectroscopy (MRS) showed reduced N-acetyl-aspartate (NAA)/creatine (Cr), choline (Cho)/Cr, NAA/Cho ratios consistent with absence of a neoplasm and highly suggested presence of gliosis. A solitary brain mass in a child poses a considerable diagnostic difficulty. MRS provided valuable diagnostic differentiation between tumor and pseudotumor lesions.
我们描述了一名患有脑病变消失的患者的临床、诊断特征及随访情况。一名14岁儿童于2009年9月入住神经内科,有一个月来亚急性发热、厌食、呕吐、视力模糊及右侧偏瘫病史。脑部磁共振成像(MRI)显示左颞叶和脑干存在轴内大肿块(25mm×19mm),在T1加权像上呈低信号,在T2加权像和液体衰减反转恢复(FLAIR)像上呈高信号,注射钆(Gd)后均匀强化。它被血管源性水肿包围并伴有占位效应。给予静脉抗生素、甘露醇(每2天2g/12小时)和地塞米松(8mg/12小时)以缓解颅内压升高的表现。基于高度怀疑肿瘤性病变(淋巴瘤或胶质瘤),给予全颅脊髓放疗(脑部=4000cGy/20次,每4周;脊髓=2600/13次,每3周)。15天内出现明显临床改善(直至完全恢复)。在接下来的4个月内逐渐减少类固醇剂量。3个月后MRI随访显示左前内侧颞区有小病变,在T1加权像上呈低信号,在T2加权像和FLAIR像上呈高信号,但注射Gd后不强化。2012年8月,患者出现复发性全身性癫痫。他的脑电图显示存在左侧颞叶癫痫活动灶。MRI显示与随访中描述的相同病变。扩散加权像正常。卡马西平治疗(300mg/12小时)后癫痫发作频率降低。2014年10月,单体素质子(1H)磁共振波谱(MRS)显示N-乙酰天门冬氨酸(NAA)/肌酸(Cr)、胆碱(Cho)/Cr、NAA/Cho比值降低,符合无肿瘤表现,强烈提示存在胶质增生。儿童中的孤立性脑肿块带来了相当大的诊断困难。MRS为肿瘤和假瘤性病变之间提供了有价值的诊断鉴别。