From the Departments of Radiology (E.S., D.R.P., J.M.P.), and.
Department of Radiology (C.L., M.Z.), Wake Forest University, Winston-Salem, North Carolina.
AJNR Am J Neuroradiol. 2020 Apr;41(4):725-728. doi: 10.3174/ajnr.A6475. Epub 2020 Mar 19.
In the medicolegal literature, notching of the corpus callosum has been reported to be associated with fetal alcohol spectrum disorders. Our purpose was to analyze the prevalence of notching of the corpus callosum in a fetal alcohol spectrum disorders group and a healthy population to determine whether notching occurs with increased frequency in the fetal alcohol spectrum disorders population.
We performed a multicenter search for cases of fetal alcohol spectrum disorders and included all patients who had a sagittal T1-weighted brain MR imaging. Patients with concomitant intracranial pathology were excluded. The corpus callosum was examined for notches using previously published methods. A χ test was used to compare the fetal alcohol spectrum disorders and healthy groups.
Thirty-three of 59 patients with fetal alcohol spectrum disorders (0-44 years of age) identified across all centers had corpus callosum notching. Of these, 8 had an anterior corpus callosum notch (prevalence, 13.6%), 23 had a posterior corpus callosum notch (prevalence, 39%), and 2 patients demonstrated undulated morphology (prevalence, 3.4%). In the healthy population, the anterior notch prevalence was 139/875 (15.8%), posterior notch prevalence was 378/875 (43.2%), and undulating prevalence was 37/875 (4.2%). There was no significant difference among the anterior (= .635), posterior (= .526), and undulating (= .755) notch prevalence in the fetal alcohol spectrum disorders and healthy groups.
There was no significant difference in notching of the corpus callosum between patients with fetal alcohol spectrum disorders and the healthy population. Although reported to be a marker of fetal alcohol spectrum disorders, notching of the corpus callosum should not be viewed as a specific finding associated with fetal alcohol spectrum disorders.
在法医学文献中,胼胝体切迹已被报道与胎儿酒精谱系障碍有关。我们的目的是分析胎儿酒精谱系障碍组和健康人群中胼胝体切迹的患病率,以确定在胎儿酒精谱系障碍人群中胼胝体切迹是否更频繁发生。
我们进行了一项多中心搜索,以寻找胎儿酒精谱系障碍的病例,并纳入了所有具有矢状 T1 加权脑 MRI 的患者。排除伴有颅内病变的患者。使用先前发表的方法检查胼胝体是否有切迹。使用 χ2 检验比较胎儿酒精谱系障碍组和健康组。
在所有中心鉴定的 59 例胎儿酒精谱系障碍患者(0-44 岁)中,有 33 例存在胼胝体切迹。其中,8 例存在胼胝体前切迹(患病率为 13.6%),23 例存在胼胝体后切迹(患病率为 39%),2 例患者表现为波状形态(患病率为 3.4%)。在健康人群中,前切迹的患病率为 139/875(15.8%),后切迹的患病率为 378/875(43.2%),波状的患病率为 37/875(4.2%)。胎儿酒精谱系障碍组和健康组的前切迹(=0.635)、后切迹(=0.526)和波状切迹(=0.755)的患病率无显著差异。
胎儿酒精谱系障碍患者与健康人群的胼胝体切迹无显著差异。虽然胼胝体切迹已被报道为胎儿酒精谱系障碍的标志物,但不应将其视为与胎儿酒精谱系障碍相关的特定发现。