Roach E S, Kerr J, Mendelsohn D, Laster D W, Raeside C
Division of Pediatric Neurology, University of Texas Southwestern Medical School, Dallas 75235.
Neurology. 1991 Feb;41(2 ( Pt 1)):262-5. doi: 10.1212/wnl.41.2_part_1.262.
We performed a detailed physical examination and MRI without gadolinium DTPA contrast in 60 couples with at least 1 child having tuberous sclerosis (TS). Eight parents had TS diagnosed by physical examination, family history, or various diagnostic procedures including MRI. Eight additional subjects and 6 control subjects had nonspecific high-signal white matter changes on MRI. MRI confirmed the diagnosis of TS in only 1 parent without physical findings of the disease, similar to the results of earlier studies using computed cranial tomography. CT may be less sensitive than MRI but is probably more specific for TS. Either CT or MRI may occasionally help substantiate the diagnosis of TS in a parent with few other findings. Both studies may need to be done in some parents to maximize the accuracy of genetic counseling.
我们对60对夫妇进行了详细的体格检查,并在未使用钆喷酸葡胺造影剂的情况下进行了MRI检查,这些夫妇中至少有一个孩子患有结节性硬化症(TS)。通过体格检查、家族史或包括MRI在内的各种诊断程序,有8名父母被诊断患有TS。另外8名受试者和6名对照受试者在MRI上有非特异性的高信号白质改变。MRI仅在1名无该病体格检查结果的父母中确诊了TS,这与早期使用计算机头颅断层扫描的研究结果相似。CT可能比MRI敏感性低,但对TS可能更具特异性。CT或MRI偶尔可能有助于在其他表现较少的父母中证实TS的诊断。在一些父母中可能需要同时进行这两项检查,以最大限度地提高遗传咨询的准确性。