Malik Muhammad Akbar, Zia-ur-Rehman Muhammad, Nadeem Malik Muhammad, Chaudhry Farooq Rasool, Qureshi Abid Ali, Nawaz Muhammad, Malik Hamza
Department of Paediatrics Neurology, The Children's Hospital, Lahore.
J Coll Physicians Surg Pak. 2012 Sep;22(9):570-4.
To analyze the clinical course and magnetic resonance angiographic (MRA) abnormalities in children with primary angiitis of the central nervous system (cPACNS).
Cohort study.
Neurosciences and Neuroradiology Department of the Children's Hospital, Lahore, from January 2009 to December 2010.
The cohort comprised consecutive patients diagnosed as having cPACNS based on clinical findings and identification of arterial stenosis on magnetic resonance angiography (MRA) in the absence of an underlying condition that could cause these findings. The treatment protocol for ischaemic infarcts consisted of induction therapy with intravenous steroids pulses and intravenous immunoglobulin followed by maintenance therapy with azathioprine and low dose aspirin. When indicated, they were treated with anticoagulants at least for 4 weeks along with induction therapy. Patients were followed at a single centre and systemically assessed for clinical presentation, classification of disease as progressive or non-progressive, adverse effects of anticoagulants, aspirin, azathioprine and their hospital course.
Sixty-eight children with medium-large vessel cPACNS (62% boys, 38% girls) with mean age of 8.5 ± 3.5 years were enrolled in this study. Motor deficit (70%); headache (64%) and fever (20%) were the commonest symptoms; whereas hemiparesis (60%); seizures 55% (focal 35%, generalized 20%) and decreased conscious level (30%), were the commonest neurological findings. Neuroradiological findings were ischaemic strokes in 50 (73.5%), haemorrhagic strokes in 10 (14.7%) and ischaemic haemorrhagic lesions in 8 cases (11.8%). Angiographically 51 (51/68, 75%) of the cohort had non-progressive (obliterative) and 17 (17/68, 25%) had evidence of progressive arteriopathy at the time of admission. No secondary haemorrhagic lesions were documented among infarcts strokes, which were treated with heparin and oral anticoagulants. Outcome was survival in 56 cases (81.5%) and death in 12 cases (18.5%). All survivors were discharged on long-term oral aspirin; 15 of them were also commenced on azathioprine. Neurological findings among the 56 survivors were; normal 20%, minor disabilities in 25%, moderate disabilities in 20% and severe disabilities in 35%.
The spectrum of cPACNS includes both progressive and non-progressive forms with significant morbidity and mortality. This treatment protocol of immunosuppressive therapy may improve long-term neurological outcome in children with medium-large vessel childhood primary angiitis of the CNS.
分析中枢神经系统原发性血管炎(cPACNS)患儿的临床病程及磁共振血管造影(MRA)异常情况。
队列研究。
2009年1月至2010年12月,拉合尔儿童医院神经科学与神经放射科。
该队列包括根据临床表现及磁共振血管造影(MRA)发现动脉狭窄而确诊为cPACNS的连续患者,且不存在可导致这些表现的基础疾病。缺血性梗死的治疗方案包括静脉注射类固醇脉冲和静脉注射免疫球蛋白进行诱导治疗,随后用硫唑嘌呤和低剂量阿司匹林进行维持治疗。如有指征,在诱导治疗期间至少4周给予抗凝剂治疗。患者在单一中心接受随访,并对临床表现、疾病分类为进行性或非进行性、抗凝剂、阿司匹林、硫唑嘌呤的不良反应及其住院病程进行系统评估。
本研究纳入了68例中大型血管cPACNS患儿(男孩62%,女孩38%),平均年龄8.5±3.5岁。运动功能障碍(70%)、头痛(64%)和发热(20%)是最常见的症状;而偏瘫(60%)、癫痫发作55%(局灶性35%,全身性20%)和意识水平下降(30%)是最常见的神经学表现。神经放射学表现为缺血性卒中50例(73.5%)、出血性卒中10例(14.7%)和缺血性出血性病变8例(11.8%)。血管造影显示,该队列中51例(51/68,75%)为非进行性(闭塞性),17例(17/68,25%)在入院时有进行性动脉病变的证据。在接受肝素和口服抗凝剂治疗的梗死性卒中中,未记录到继发性出血性病变。结果为56例(81.5%)存活,12例(18.5%)死亡。所有幸存者出院时均服用长期口服阿司匹林;其中15例还开始服用硫唑嘌呤。56例幸存者的神经学表现为:正常20%,轻度残疾25%,中度残疾20%,重度残疾35%。
cPACNS的范围包括进行性和非进行性形式,具有显著的发病率和死亡率。这种免疫抑制治疗方案可能改善中大型血管儿童中枢神经系统原发性血管炎患儿的长期神经学预后。