| Literature DB >> 30604654 |
Jun Sugata1,2, Tessei Ueda1, Natsuko Tanoue1, Kazuho Hirahara3, Kiyohisa Kamimura4, Kazunori Arita1,2, Koji Yoshimoto1.
Abstract
An otherwise healthy 22-month-old boy suffered high fever, irritability, nausea, dysphagia, dysarthria and right hemiparesis. Magnetic resonance imaging showed a cystic mass, 15 mm in diameter, with surrounding oedema in the base of the lower pons. The symptoms subsided in about 10 days after onset, followed by a rapid decrease of the cyst size to 5 mm. Thereafter, the patient's psychomotor growth has been normal. Annual follow-up magnetic resonance imaging scans showed very gradual enlargement of the cyst located on the ventral surface of the pontomedullary junction, reaching 16 mm in diameter in 21 years after onset. It was hyperintense on T1-weighted and isointense on T2-weighted magnetic resonance imaging. No haemosiderin deposition or gadolinium enhancement was seen. This is a rare report of a two decade longitudinal follow-up of a midline prepontine cyst showing asymptomatic and very slow growth. The possible nature of the cyst includes neurenteric, dermoid and epidermoid cyst.Entities:
Keywords: Neurenteric cyst; endodermal cyst; prepontine cyst; rupture
Mesh:
Year: 2019 PMID: 30604654 PMCID: PMC6410450 DOI: 10.1177/1971400918821085
Source DB: PubMed Journal: Neuroradiol J ISSN: 1971-4009