急性白质脑病伴弥散受限 - 病例系列

Badiginchala Naga Jyothi, C. P. R. Kumar, Ravindra B. Kamble, Shanthi Manivannan
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摘要

急性白质脑病伴弥散受限(ALERD)是一种临床病理诊断,其特征是严重的脑病和癫痫发作,脑实质内有广泛的弥散受限区。病例 1:表面健康的 13 个月大男婴出现急性发热性脑病,并伴有颅内压升高的阵发性癫痫发作。检查结果符合多器官功能障碍,同时伴有严重的代谢性酸中毒、酮病和高氨血症。最初的脑磁共振成像(MRI)正常。但随后的脑部磁共振成像显示出弥漫性 ALERD 的特征。经过免疫治疗和支持性治疗,他的病情有所好转,出院时没有留下后遗症。病例 2:一名 9 个月大的男婴,病前精神正常,但出现发热、癫痫状态和脑病。核磁共振脑成像提示为中枢疏松性 ALERD。在康复治疗的建议下,他带着后遗症出院了。不幸的是,他因误吸而死亡。病例 3:一名出生 10 天的新生儿出现拒食、多次抽搐和脑病。核磁共振脑成像显示他患有中枢性疏松性 ALERD。经免疫治疗后病情好转,五个月大时发育正常。ALERD 是一种临床放射综合征,其特征是急性脑病,核磁共振成像显示皮层下白质弥散受限。报告的 ALERD 分为弥漫型和中枢疏松型两类。弥漫型 ALERD 表现严重。然而,病例 1 的预后良好,这表明预后是可变的。中枢疏松型 ALERD 的症状较轻,但当基底节受累时,其预后可能会恶化,如病例 2 所示。病例 3 患有中枢疏松型 ALERD,如文献所述,预后良好。本研究强调了 ALERD 的各种症状和体征,包括新生儿发病年龄。诊断的依据是弥散加权成像显示的白质弥散受限和脑部核磁共振成像显示的表观弥散系数。核磁共振成像在最初的病程中可能是正常的;因此,如果有强烈的怀疑,必须进行复查。应强调及时的免疫治疗和支持性护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute leukoencephalopathy with restricted diffusion – Case Series
Acute leukoencephalopathy with restricted diffusion (ALERD) is a clinicopathological diagnosis that is characterized by severe encephalopathy and seizures with extensive areas of restricted diffusion in cerebral parenchyma. Case 1: Apparently healthy 13-month-old male child presented with acute febrile encephalopathy with a flurry of seizures with raised intracranial pressure. Investigations were consistent with multiorgan dysfunction along with severe metabolic acidosis, ketosis, and hyperammonemia. Initial magnetic resonance imaging (MRI) Brain was normal. However subsequent MRI brain suggested features of diffuse ALERD. With immunotherapy and supportive management, he improved and was discharged without sequelae. Case 2: A 9-month-old male child who was premorbidly normal presented with fever, status epilepticus, and encephalopathy. MRI Brain was suggestive of central sparing ALERD. He was discharged with sequelae with the advice of rehabilitation. Unfortunately, he got succumbed due to aspiration. Case 3: A 10-day-old neonate presented with the refusal of feeds, multiple seizures, and encephalopathy. MRI Brain revealed central sparing ALERD. Improved with immunotherapy and was developmentally normal at five months of age. ALERD is a clinic-radiological syndrome characterized by acute encephalopathy with restricted areas of diffusion in subcortical white matter on MRI. Reported two categories are Diffuse and Central sparing ALERD. Diffuse ALERD has severe manifestations. However, Case 1 had a good outcome, suggesting a variable prognosis. Central sparing ALERD is a milder form, but when basal ganglia are involved, it may have a worsened outcome, as seen in Case 2. Case 3 had central sparing ALERD, and had a good prognosis as described in literature. This study highlights the varied signs and symptoms of ALERD, including neonatal age of onset. Diagnosis is based on the restricted diffusion in white matter on diffusion-weighted imaging and the apparent diffusion coefficient in MRI of the brain. MRI may be normal in the initial course; hence, it’s important to repeat if strongly suspected. Prompt immunotherapy and supportive care are emphasised.
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