Chamberlain M C
Department of Neurosciences, University of California, San Diego, 92103.
J Child Neurol. 1993 Apr;8(2):175-81. doi: 10.1177/088307389300800212.
Fourteen consecutive children with acquired immune deficiency syndrome (AIDS) (age range, 4 months to 11 years; median 4 years) were studied prospectively comparing nonenhanced cranial magnetic resonance imaging (MRI) and computed tomographic (CT) scans. MRI and CT were performed twice: at time of entry into protocol and again at 1 year. In addition, sequential neurologic (every 2 months) and neuropsychological examinations (every 6 months) were performed. At entry, 12 children had abnormal neurologic examinations; of these, 10 had developmental delay; two children were normal by developmental history and neurologic examination. Five children performed in the normal range on a standardized neuropsychological test, whereas nine children showed significant delays in verbal or motor/perceptual development. Following 1 year of study, four children had normal and six had abnormal neurologic examinations (six stable and four improved). Neuropsychological examinations were normal in five children and abnormal in five (seven stable, one improved, and two deteriorated). At entry, the following neuroradiographic abnormalities were seen: brain parenchymal volume loss (eight, MR = CT), cervical lymphatic enlargement (four, MR = CT), striatal-thalamic calcification (one, CT > MR), delayed myelination (one, MR > CT), and focal white-matter lesions (one, MR > CT). At 1 year the following neuroradiographic changes were seen: brain parenchymal volume loss (10, MR = CT; two improved, eight stable); cervical lymphatic enlargement (one, MR = CT; three improved, one stable), striatal-thalamic calcification (one, CT > MR; one new), and focal white-matter lesions (one, MR > CT; one stable).(ABSTRACT TRUNCATED AT 250 WORDS)
对14名连续的获得性免疫缺陷综合征(AIDS)儿童(年龄范围4个月至11岁;中位年龄4岁)进行了前瞻性研究,比较非增强头颅磁共振成像(MRI)和计算机断层扫描(CT)。MRI和CT均进行了两次:进入研究方案时一次,1年后再次进行。此外,还进行了连续的神经学检查(每2个月一次)和神经心理学检查(每6个月一次)。入组时,12名儿童神经学检查异常;其中10名有发育迟缓;2名儿童根据发育史和神经学检查结果正常。5名儿童在标准化神经心理学测试中表现正常,而9名儿童在语言或运动/感知发育方面有明显延迟。经过1年的研究,4名儿童神经学检查正常,6名异常(6名稳定,4名改善)。5名儿童神经心理学检查正常,5名异常(7名稳定,1名改善,2名恶化)。入组时,发现以下神经影像学异常:脑实质体积减少(8例,MRI = CT)、颈部淋巴结肿大(4例,MRI = CT)、纹状体-丘脑钙化(1例,CT > MRI)、髓鞘延迟形成(1例,MRI > CT)和局灶性白质病变(1例,MRI > CT)。1年后,发现以下神经影像学变化:脑实质体积减少(10例,MRI = CT;2例改善,8例稳定);颈部淋巴结肿大(1例,MRI = CT;3例改善,1例稳定)、纹状体-丘脑钙化(1例,CT > MRI;1例新增)和局灶性白质病变(1例,MRI > CT;1例稳定)。(摘要截断于250字)