Ma Minglei, Wu Mingxing, Li Yanbin, Wu Di, Zhang Bingke
Department of Neurosurgery, Capital Institute of Pediatrics, Chaoyang District, Beijing, 100020, People's Republic of China.
Childs Nerv Syst. 2018 Jul;34(7):1417-1421. doi: 10.1007/s00381-018-3753-6. Epub 2018 Feb 27.
Methylmalonic acidemia (MMA) with early-onset severe hydrocephalus is rare. In this paper, we described two cases of MMA with hydrocephalus and review the literature to elucidate the clinical features of the disease, treatment options, and follow-up results.
The PubMed and Embase databases were searched for clinical reports on MMA with severe hydrocephalus, and two unreported cases were presented to illustrate the clinical spectrum.
Six cases of MMA with severe hydrocephalus were observed in the previous literature. Our two patients with severe hydrocephalus but not bulging fontanelle received a ventriculo-peritoneal shunt, and intracranial hypertension was confirmed in both cases during the operation. These patients' clinical symptoms significantly improved after the operation.
Intracranial hypertension can exist in early-onset severe hydrocephalus in MMA, even if the bulging anterior fontanelle is not apparent. These patients could benefit from a ventriculo-peritoneal shunt.
甲基丙二酸血症(MMA)合并早发性严重脑积水较为罕见。在本文中,我们描述了两例MMA合并脑积水的病例,并回顾文献以阐明该疾病的临床特征、治疗选择和随访结果。
检索PubMed和Embase数据库中关于MMA合并严重脑积水的临床报告,并展示两例未报告的病例以说明临床谱。
既往文献中观察到6例MMA合并严重脑积水的病例。我们的两名严重脑积水但囟门未膨出的患者接受了脑室-腹腔分流术,术中均证实存在颅内高压。术后这些患者的临床症状明显改善。
MMA早发性严重脑积水患者即使前囟未明显膨出也可能存在颅内高压。这些患者可从脑室-腹腔分流术中获益。