González Quarante Lain Hermes, Mena-Bernal José Hinojosa, Martín Beatriz Pascual, Ramírez Carrasco Marta, Muñoz Casado María Jesús, Martínez de Aragón Ana, de las Heras Rogelio Simón
Department of Pediatric Neurosurgery, Hospital General 12 de Octubre, Madrid, Spain.
Department of Neurosurgery, HGU Gregorio Marañón, Calle Doctor Esquerdo número 46, C.P, 28007, Madrid, Spain.
Childs Nerv Syst. 2016 May;32(5):857-63. doi: 10.1007/s00381-015-2954-5. Epub 2015 Nov 19.
In 1996, Hinchey and colleagues coined the term "Posterior reversible encephalopathy syndrome" (PRES) to describe a condition seen in patients with acute neurological symptoms and reversible subcortical vasogenic edema predominantly involving parieto-occipital areas demonstrated in brain MRI. The occurrence of this phenomenon after surgical resection of CNS tumors is typically linked to pediatric cases.
Two new cases of PRES after posterior fossa surgery are reported. A thorough review of the literature is carried out with the purpose of updating and summarizing the main features regarding PRES in similar cases. Seven cases of PRES after resection of a posterior fossa tumor have been hitherto reported (4 patients were <20 years old). There is another pediatric case described after a ventriculoperitoneal shunting procedure in a patient with fourth ventricle ependymoma. Two resected tumors were ependymomas, 2 hemangiopericytomas in one patient, 1 pilocyticastrocytoma, 1 vestibular schwannoma, and 1 of the reported cases did not describe the final pathology diagnosis.
We present 2 new cases of PRES after surgical resection of a posterior fossa tumor (medulloblastoma in case 1 and ependymoma in case 2) in pediatric patients. Case 1 developed delayed seizures and altered mental status(10 days after surgical resection) after receiving treatment with bromocriptine for cerebellar mutism. Case 2 presented with generalized seizures and altered mental status within the first 48 postoperative hours followed by right hemiparesis. Both patients fully recovered and returned to neurological baseline status. A thorough review of the literature was carried out with the purpose of updating and summarizing the main features regarding PRES in similar cases.
We report 2 new pediatric cases of posterior reversible encephalopathy syndrome (PRES) that developed after surgical resection of a posterior fossa tumor. Appropriate management includes supportive measures, antihypertensive agents, and antiepileptic drugs, if needed. Full recovery is the most likely outcome in line with previous articles.
1996年,欣奇等人创造了“后部可逆性脑病综合征”(PRES)一词,用于描述急性神经症状患者中出现的一种情况,即脑MRI显示主要累及顶枕区的可逆性皮质下血管源性水肿。这种现象在中枢神经系统肿瘤手术切除后出现的情况通常与儿科病例有关。
报告了两例后颅窝手术后发生PRES的新病例。对文献进行了全面回顾,目的是更新和总结类似病例中PRES的主要特征。迄今已报告了7例后颅窝肿瘤切除术后发生PRES的病例(4例患者年龄<20岁)。还有1例儿科病例,是在一名第四脑室室管膜瘤患者进行脑室腹腔分流术后出现的。切除的肿瘤中,2例为室管膜瘤,1例患者的2例为血管外皮细胞瘤,1例为毛细胞型星形细胞瘤,1例为前庭神经鞘瘤,1例报告病例未描述最终病理诊断。
我们介绍了2例儿科患者后颅窝肿瘤(病例1为髓母细胞瘤,病例2为室管膜瘤)手术切除后发生PRES的新病例。病例1在接受溴隐亭治疗小脑缄默症后(手术切除后10天)出现延迟性癫痫发作和精神状态改变。病例2在术后48小时内出现全身性癫痫发作和精神状态改变,随后出现右侧偏瘫。两名患者均完全康复并恢复到神经学基线状态。对文献进行了全面回顾,目的是更新和总结类似病例中PRES的主要特征。
我们报告了2例后颅窝肿瘤手术切除后发生的后部可逆性脑病综合征(PRES)儿科新病例。适当的处理措施包括支持性措施、降压药物,必要时使用抗癫痫药物。与之前的文章一致,最可能的结果是完全康复。