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Systematic review of pineal cysts surgery in pediatric patients.
Choque-Velasquez, Joham; Colasanti, Roberto; Baluszek, Szymon; Resendiz-Nieves, Julio; Muhammad, Sajjad; Ludtka, Christopher; Hernesniemi, Juha.
Affiliation
  • Choque-Velasquez J; Department of Neurosurgery, University of Helsinki and Helsinki University Hospital Helsinki, Helsinki, Finland. johchove@hotmail.com.
  • Colasanti R; Juha Hernesniemi International Center for Neurosurgery, Henan Provincial People's Hospital, Zhengzhou, China. johchove@hotmail.com.
  • Baluszek S; Department of Neurosurgery, Umberto I General Hospital, Università Politecnica delle Marche, Ancona, Italy.
  • Resendiz-Nieves J; Department of Neurosurgery, Ospedali Riuniti Marche Nord, Pesaro, Italy.
  • Muhammad S; Laboratory of Molecular Neurobiology, Nencki Institute of Experimental Biology, Warsaw, Poland.
  • Ludtka C; Clinical Department of Neurosurgery, Central Clinical Hospital Ministry of Interior, Warsaw, Poland.
  • Hernesniemi J; Department of Neurosurgery, University of Helsinki and Helsinki University Hospital Helsinki, Helsinki, Finland.
Childs Nerv Syst ; 36(12): 2927-2938, 2020 12.
Article in En | MEDLINE | ID: mdl-32691194
ABSTRACT

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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pineal Gland / Brain Neoplasms / Central Nervous System Cysts / Cysts Type of study: Systematic_reviews Limits: Child / Female / Humans / Male Language: En Journal: Childs Nerv Syst Journal subject: NEUROLOGIA / PEDIATRIA Year: 2020 Document type: Article Affiliation country: Finland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pineal Gland / Brain Neoplasms / Central Nervous System Cysts / Cysts Type of study: Systematic_reviews Limits: Child / Female / Humans / Male Language: En Journal: Childs Nerv Syst Journal subject: NEUROLOGIA / PEDIATRIA Year: 2020 Document type: Article Affiliation country: Finland