Department of Radiology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Department of Internal Medicine, Division of Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
J Neuroradiol. 2019 May;46(3):193-198. doi: 10.1016/j.neurad.2018.05.002. Epub 2018 Jun 18.
To increase the knowledge of central nervous system (CNS) imaging features in deficiency of adenosine deaminase 2 (DADA2) by examining magnetic resonance imaging (MRI) studies of a relatively large number of patients.
We retrospectively examined neuroimages of 12 patients (7 male, 5 female) diagnosed with DADA2. The mean age of the patients at the time of initial brain MRI was 16.7±10.2 years. Seven patients (58.3%) fulfilled the classification criteria of polyarteritis nodosa. Brain MRI studies were assessed with respect to findings of ischemia, intracranial hemorrhages, focal parenchymal signal abnormalities, cerebral/cerebellar volume loss, and abnormal contrast enhancement. Angiographic studies of 7 patients were evaluated for the signs of vasculitis.
The most frequent finding was acute and/or chronic lacunar ischemic lesions in the brainstem and/or deep gray matter (n=9, 75%). Six patients (50%) revealed MRI findings compatible with recurrent ischemic attacks. Small nodular contrast enhancement (n=2, 16.6%), acute putaminal hemorrhage (n=1, 8.3%) and findings compatible with posterior reversible encephalopathy syndrome (n=1, 8.3%) were also detected. Slight-to-moderate diffuse cerebral and/or cerebellar volume loss (n=7, 58.3%), decreased T1 signal of the bone marrow (n=6, 50%) and optic atrophy (n=1, 8.3%) were the other findings on brain MRI. The only abnormal angiographic finding was reduced caliber of the right distal posterior cerebral artery in MRA of a patient (14.6%).
DADA2 should be included in the differential diagnosis of young patients presenting with ischemic and/or hemorrhagic lesions located in the brainstem and deep gray matter, especially if they have a family history or additional systemic abnormalities.
通过检查相当数量患者的磁共振成像(MRI)研究,增加对腺苷脱氨酶 2(DADA2)缺乏症中枢神经系统(CNS)成像特征的认识。
我们回顾性检查了 12 名(7 名男性,5 名女性)被诊断为 DADA2 的患者的神经影像。患者首次脑部 MRI 时的平均年龄为 16.7±10.2 岁。7 名患者(58.3%)符合结节性多动脉炎的分类标准。评估了脑 MRI 研究中缺血、颅内出血、局灶性实质信号异常、脑/小脑体积损失和异常对比增强的发现。对 7 名患者的血管造影研究评估了血管炎的迹象。
最常见的发现是脑桥和/或深部灰质的急性和/或慢性腔隙性缺血性病变(n=9,75%)。6 名患者(50%)显示与复发性缺血性发作相符的 MRI 发现。还检测到小的结节性对比增强(n=2,16.6%)、急性壳核出血(n=1,8.3%)和符合后部可逆性脑病综合征的发现(n=1,8.3%)。轻度至中度弥漫性脑和/或小脑体积损失(n=7,58.3%)、骨髓 T1 信号降低(n=6,50%)和视神经萎缩(n=1,8.3%)是脑部 MRI 的其他发现。唯一异常的血管造影发现是 MRA 中一名患者(14.6%)右侧大脑后动脉远端口径减小。
如果年轻患者出现位于脑桥和深部灰质的缺血和/或出血性病变,尤其是有家族史或其他系统异常的患者,应将 DADA2 纳入鉴别诊断。