医学科普
发表者:邱占东 人已读
在专科门诊或好大夫平台,总会碰到来自MOG抗体相关疾病(MOGAD)患儿的爸爸/妈妈的咨询,笔者非儿科医生,因病房也曾收治过MOGAD患儿,加之认真研读过不少相关文章,有一些浅薄的经验及体会,故就患儿父母最关心的几个问题试着进行汇总、解答,以期提供帮助。
一、儿童MOGAD流行病学特征是什么?常见临床表现有哪些?
MOGAD在儿童较成人常见,男女比例为1:1-2。MOGAD似乎没有明显的种族差异性。10岁以下男女发病率相似,在青少年和成人,女性发病率略高[1]。荷兰最近的一项研究报告称,每年平均每10万名儿童中有0.31人患病,相比之下,每10万名成年人中有0.13人患病[2]。儿童MOGAD主要临床表现包括急性播散性脑脊髓炎(ADEM)、视神经炎(ON)、横贯性脊髓炎(TM)、视神经炎合并横贯性脊髓炎(ON+TM)及其他类型[3]。
图1. 儿童MOGAD临床表型比例
ADEM是儿童(<18岁)MOGAD最常见的症状,成人仅5%出现。在儿童中,40-50%的MOGAD病例中可见典型的ADEM MRI表现[4]。MOGAD视神经发炎表现为单侧或双侧视力障碍,包括视力丧失、中央暗点或视野缩小和色觉受损,并常伴有眼运动疼痛[5],儿科MOGAD-ON主要是13至18岁的青少年[6, 7]。一项回顾性研究包括54例MOG-TM患者,其中16例儿科患者(30%),其中孤立性TM占54%、ADEM的脊髓受累占17%,ON占6%;几乎所有患者发病时都有显著功能缺损,包括运动和感觉缺陷;无论发病时疾病的严重程度如何,大多数MOG-TM患者表现出良好的运动恢复[8]。具有视神经脊髓炎谱系疾病样表型(NMOSD-like)的儿童患者中,MOG抗体阳性者约占56%,较AQP4抗体阳性的NMOSD更为普遍[9]。
此外,新发现表型或非典型临床表型也陆续见诸报道,包括脑炎、重叠综合征和癫痫、脑白质营养不良样表型、中枢及外周联合脱髓鞘[10, 11]及尚不能分类的临床表型[12]。不到10%的儿童MOGAD患者(典型者<7岁)可表现为白质脑病样表型,核磁表现为大的融合显著强化的白质病变,随着时间推移出现显著的脑萎缩[13]。
二、儿童MOGAD急性期及缓解期治疗如何抉择?
目前国内尚无儿童MOGAD诊断与治疗相关共识或指南,笔者根据欧洲儿童MOGAD联合共识试做简要概述[14]。
急性期治疗:首选甲强龙冲击,剂量为20-30mg/kg/d(max. 1g/d),依据疾病负担及治疗反应,持续3-5天。3天后无改善或5天后改善不充分,可加用丙种球蛋白或行血浆置换。也可先使用丙球,1-2g/kg(max. 1g/kg/d),持续1-5天,如无充分改善,可再行血浆置换。之后口服醋酸泼尼松,起始剂量为1-2mg/kg/d(max. 60mg/d),以起始量维持4周,再逐渐减量至0.5mg/kg/d或更少。强的松剂量<0.5 mg/kg/d及停药后应密切监测,因为在这一时期经常出现复发。
图2. 儿童MOGAD急性期治疗专家联合推荐
维持期治疗:对于首次发病且急性期治疗反应良好的患者,密切观察(首次发病且及急性期治疗1-3个月后恢复较差者不在此列,应积极开始维持治疗)。对于复发者,开始维持期治疗:吗替麦考酚酯/硫唑嘌呤,加用低剂量激素3-6个月;或利妥昔单抗;或丙种球蛋白。如再次复发,除急性期治疗药物外,可选择利妥昔单抗或丙种球蛋白。如再复发,可联用利妥昔单抗及丙种球蛋白。如再复发,可联合应用利妥昔单抗、丙种球蛋白及低剂量激素。如疾病稳定两年以上且无复发,考虑降级治疗,直至停药。
图3. 儿童MOGAD维持期治疗专家联合推荐
三、儿童MOGAD容易复发吗?预后如何?
5年内成人MOGAD复发率为40%左右,儿童复发风险较低,约为30%,多数为单相型[15]。部分复发患者表现为ADEM继发1次或多次ON (ADEM-ON)、多相弥散性脑脊髓炎(MDEM)、复发性ON (RON)或复发性视神经脊髓炎(NMOSD)样综合征[3, 7, 15-17]。
复发的严重性及预后与年龄相关,儿童患者症状更重,但恢复更快更完全[18]。9岁以下的儿童患者更容易出现严重的脑部症状,在传统影像上表现出更多的病灶负荷,但是他们比年长儿童和成人恢复更快,这种情况并非特异性,在儿童和成人MS患者中也有类似发现[19]。相比青少年和成人,幼儿更容易有脑部受累,50%的复发且脑部受累的儿童认知功能受影响[16]。上文提到的白质脑病样表型患儿预后欠佳,伴有持续的认知和运动残障[13]。总之,儿童MOGAD的预后似与临床表型相关,单相病程及非白质脑病样患者预后良好[20]。
四、随访过程中MOG抗体阳性的意义大吗?
早期研究表明高MOG抗体滴度可预测临床复发事件[7],但是近来的数据显示患者可能多年血清学阳性但并未复发,也可能有患者MOG-IgG转阴但是仍然复发[15]。即使纵向长期测定抗体滴度,也不能明确显示其与功能障碍结局相关[21]。
总结
①儿童MOGAD发病率高于成年人,以ADEM和ON为主要表现;②急性期及缓解期治疗有迹可循;③复发率低于成人,常见表型预后良好;④随访过程中MOG抗体阳性意义并不显著。
声明:上文根据笔者有限的临床经验及总结相关文献所写,可能具备一定的临床参考意义,不具指导意义,不合理或错漏之处敬请指正。
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发表于:2022-01-10