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Systematic review of pineal cysts surgery in pediatric patients
被引:12
作者:
Choque-Velasquez, Joham
[1
,2
,3
]
Colasanti, Roberto
[4
,5
]
Baluszek, Szymon
[6
,7
]
Resendiz-Nieves, Julio
[1
,2
]
Muhammad, Sajjad
[1
,2
,8
]
Ludtka, Christopher
[9
]
Hernesniemi, Juha
[1
,2
,3
]
机构:
[1] Univ Helsinki, Dept Neurosurg, Helsinki, Finland
[2] Helsinki Univ Hosp Helsinki, Helsinki, Finland
[3] Henan Prov Peoples Hosp, Juha Hernesniemi Int Ctr Neurosurg, Zhengzhou, Peoples R China
[4] Univ Politecn Marche, Umberto I Gen Hosp, Dept Neurosurg, Ancona, Italy
[5] Osped Riuniti Marche Nord, Dept Neurosurg, Pesaro, Italy
[6] Nencki Inst Expt Biol, Lab Mol Neurobiol, Warsaw, Poland
[7] Minist Interior, Cent Clin Hosp, Clin Dept Neurosurg, Warsaw, Poland
[8] Univ Hosp Dusseldorf, Dept Neurosurg, Dusseldorf, Germany
[9] Univ Florida, Dept Biomed Engn, Gainesville, FL USA
关键词:
Microneurosurgery;
Pineal cysts;
Sitting position;
Supracerebellar infratentorial approach;
SYMPTOMATIC GLIAL CYSTS;
STEREOTAXIC MANAGEMENT;
CASE SERIES;
FOLLOW-UP;
GLAND;
LESIONS;
REGION;
TUMORS;
PREVALENCE;
DIAGNOSIS;
D O I:
10.1007/s00381-020-04792-3
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Introduction We present a consecutive case series and a systematic review of surgically treated pediatric PCs. We hypothesized that the symptomatic PC is a progressive disease with hydrocephalus at its last stage. We also propose that PC microsurgery is associated with better postoperative outcomes compared to other treatments. Methods The systematic review was conducted in PubMed and Scopus. No clinical study on pediatric PC patients was available. We performed a comprehensive evaluation of the available individual patient data of 43 (22 case reports and 21 observational series) articles. Results The review included 109 patients (72% females). Ten-year-old or younger patients harbored smaller PC sizes compared to older patients (p< 0.01). The pediatric PCs operated on appeared to represent a progressive disease, which started with unspecific symptoms with a mean cyst diameter of 14.5 mm, and progressed to visual impairment with a mean cyst diameter of 17.8 mm, and hydrocephalus with a mean cyst diameter of 23.5 mm in the final stages of disease (p< 0.001). Additionally, 96% of patients saw an improvement in their symptoms or became asymptomatic after surgery. PC microsurgery linked with superior gross total resection compared to endoscopic and stereotactic procedures (p< 0.001). Conclusions Surgically treated pediatric PCs appear to behave as a progressive disease, which starts with cyst diameters of approximately 15 mm and develops with acute or progressive hydrocephalus at the final stage. PC microneurosurgery appears to be associated with a more complete surgical resection compared to other procedures.
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页码:2927 / 2938
页数:12
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