Wilson D A, Nelson M D, Fenstermacher M J, Bohan T P, Hopper K D, Tilton A, Mitchell W G, Contant C F, Maeder M A, Donfield S M
Magnetic Resonance Center of Oklahoma, Oklahoma Medical Center, Oklahoma City 73104.
Radiology. 1992 Nov;185(2):553-8. doi: 10.1148/radiology.185.2.1410372.
Cranial magnetic resonance (MR) imaging was performed in 124 male patients (aged 7-19 years), from 14 institutions, in whom a diagnosis of moderate to severe hemophilia was made. Blood tests in all subjects were negative for human immunodeficiency virus. Findings in MR studies were abnormal in 25 (20.2%) subjects. Six lesions in five subjects were classified as congenital. The most commonly identified congenital lesion was a posterior fossa collection of cerebrospinal fluid (five cases). Twenty-two subjects had acquired lesions that were probably related to the hemophilia or its treatment. The most commonly acquired lesions were single- or multifocal areas of high signal intensity within the white matter on T2-weighted images noted in 14 (11.3%) subjects. Two subjects had large focal areas of brain atrophy, and six had some degree of diffuse cerebral cortical atrophy. Three subjects (2.4%) had hemorrhagic lesions. To the authors' knowledge, the unexpected finding of small, focal, nonhemorrhagic white matter lesions has not previously been reported.
对来自14家机构的124名男性患者(年龄7至19岁)进行了头颅磁共振成像(MR)检查,这些患者均被诊断为中度至重度血友病。所有受试者的血液检测结果显示人类免疫缺陷病毒呈阴性。MR研究结果显示,25名(20.2%)受试者存在异常。5名受试者的6处病变被归类为先天性病变。最常见的先天性病变是后颅窝脑脊液聚集(5例)。22名受试者有后天性病变,可能与血友病或其治疗有关。最常见的后天性病变是14名(11.3%)受试者在T2加权图像上白质内出现的单灶或多灶高信号区。2名受试者有大面积局灶性脑萎缩,6名受试者有一定程度的弥漫性大脑皮质萎缩。3名受试者(2.4%)有出血性病变。据作者所知,此前尚未有关于小的、局灶性、非出血性白质病变这一意外发现的报道。