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腺苷脱氨酶 2 缺乏症;特别关注中枢神经系统成像。

Deficiency of adenosine deaminase 2; special focus on central nervous system imaging.

机构信息

Department of Radiology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

Department of Internal Medicine, Division of Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

出版信息

J Neuroradiol. 2019 May;46(3):193-198. doi: 10.1016/j.neurad.2018.05.002. Epub 2018 Jun 18.

Abstract

PURPOSE

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.

METHODS

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.

RESULTS

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%).

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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