Vazhayil Vikas, Sadashiva Nishanth, Nayak Nithish, Prabhuraj A R, Shukla Dhaval, Somanna Sampath
Department of Neurosurgery, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India.
Childs Nerv Syst. 2018 Jun;34(6):1215-1220. doi: 10.1007/s00381-018-3760-7. Epub 2018 Feb 27.
Colloid cysts are uncommon lesions in the pediatric age group, which most commonly occur in the fourth through fifth decades. The authors hereby report a series of 36 patients with colloid cysts in the pediatric age group.
A retrospective chart review was conducted on all patients with colloid cyst who underwent surgery in our institute between November 2003 and December 2016 (13 years). Patients above the age of 18 were excluded from the study. They were analyzed based on clinical presentation, radiological findings, surgical approaches, and outcome.
There were 36 pediatric patients selected for the study. Age ranged from 8 to 18 years. The male-to-female ratio was 3.5:1. Headache and vomiting were the most common symptoms, and papilledema is the most common clinical sign. The mean duration of symptoms was 9 months (range 1 day to 5 years), but 27 (75%) of the children had precipitous symptoms just before presentation. Preoperative CT showed a hyperdense non-enhancing lesion in the majority of cases. Endoscopic excision was done in 13; 5 patients underwent transcortical transventricular excision, while transcallosal approach was opted for in 17 patients. In one patient, the colloid cyst could not be removed endoscopically and had to be converted to transcortical transventricular approach. Postoperatively, five patients developed CSF leak. They were successfully managed conservatively. One patient had operative site extra dural hematoma and underwent re-exploration, and two patients had transient hemiparesis which improved spontaneously. The median follow-up period was 9 months in the 30 available patients. Though no formal neuropsychological testing was done at follow-up, all children appeared to be doing well without memory disturbances.
Pediatric colloid cysts are less common and may show rapid deterioration. Timely surgery results in a permanent cure with minimum morbidity. The results of either micro neurosurgical or endoscopic operative excision of colloid cysts in children are excellent. All children who are symptomatic with raised intracranial pressure due to a third ventricular colloid cyst should undergo definitive surgery. There were no major permanent deficits in memory or disconnection syndromes observed with the limited anterior colostomy.
胶样囊肿在儿童年龄组中是罕见病变,最常见于40至50岁。作者在此报告一系列36例儿童年龄组的胶样囊肿患者。
对2003年11月至2016年12月(13年)间在我院接受手术的所有胶样囊肿患者进行回顾性病历审查。18岁以上患者被排除在研究之外。根据临床表现、影像学检查结果、手术方式和预后进行分析。
36例儿童患者入选本研究。年龄范围为8至18岁。男女比例为3.5:1。头痛和呕吐是最常见症状,视乳头水肿是最常见临床体征。症状平均持续时间为9个月(范围1天至5年),但27例(75%)儿童在就诊前症状急剧加重。术前CT在大多数病例中显示高密度无强化病变。13例行内镜下切除;5例患者接受经皮质经脑室切除,17例患者选择经胼胝体入路。1例患者内镜下无法切除胶样囊肿,不得不改为经皮质经脑室入路。术后,5例患者发生脑脊液漏。经保守治疗成功处理。1例患者手术部位硬膜外血肿并接受再次探查,2例患者出现短暂性偏瘫,随后自行好转。30例可随访患者的中位随访期为9个月。尽管随访时未进行正式神经心理学测试,但所有儿童似乎情况良好,无记忆障碍。
儿童胶样囊肿较少见,可能表现为病情迅速恶化。及时手术可实现永久治愈且并发症最少。儿童胶样囊肿的显微神经外科手术或内镜手术切除效果均良好。所有因第三脑室胶样囊肿导致颅内压升高出现症状的儿童均应接受确定性手术。有限的前入路手术未观察到明显的永久性记忆缺陷或分离综合征。