Published in:
Open Access
01-07-2016 | Paediatric Neuroradiology
MRI-based assessment of the pineal gland in a large population of children aged 0–5 years and comparison with pineoblastoma: part II, the cystic gland
Authors:
Selma Sirin, Marcus C. de Jong, Paolo Galluzzi, Philippe Maeder, Hervé J. Brisse, Jonas A. Castelijns, Pim de Graaf, Sophia L. Goericke, on behalf of the European Retinoblastoma Imaging Collaboration (ERIC)
Published in:
Neuroradiology
|
Issue 7/2016
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Abstract
Introduction
Pineal cysts are a common incidental finding on brain MRI with resulting difficulties in differentiation between normal glands and pineal pathologies. The aim of this study was to assess the size and morphology of the cystic pineal gland in children (0–5 years) and compare the findings with published pineoblastoma cases.
Methods
In this retrospective multicenter study, 257 MR examinations (232 children, 0–5 years) were evaluated regarding pineal gland size (width, height, planimetric area, maximal cyst(s) size) and morphology. We performed linear regression analysis with 99 % prediction intervals of gland size versus age for the size parameters. Results were compared with a recent meta-analysis of pineoblastoma by de Jong et al.
Results
Follow-up was available in 25 children showing stable cystic findings in 48 %, cyst size increase in 36 %, and decrease in 16 %. Linear regression analysis gave 99 % upper prediction bounds of 10.8 mm, 10.9 mm, 7.7 mm and 66.9 mm2, respectively, for cyst size, width, height, and area. The slopes (size increase per month) of each parameter were 0.030, 0.046, 0.021, and 0.25, respectively. Most of the pineoblastomas showed a size larger than the 99 % upper prediction margin, but with considerable overlap between the groups.
Conclusion
We presented age-adapted normal values for size and morphology of the cystic pineal gland in children aged 0 to 5 years. Analysis of size is helpful in discriminating normal glands from cystic pineal pathologies such as pineoblastoma. We also presented guidelines for the approach of a solid or cystic pineal gland in hereditary retinoblastoma patients.