Giant glioependymal cyst in an infant
Ryoma Morigaki1, Kiyohito Shinno, Kyong-Hon Pooh
1Department of Neurosurgery, National Hospital Organization, Kagawa Children's Hospital, Kagawa, Japan. morigakiryoma@hotmail.com
Insights
A giant glioependymal cyst in an infant was successfully treated with endoscopic fenestration. This case suggests the tela choroidea as the origin of these rare brain cysts.
Area of Science:
- Neuroscience
- Pediatric Neurosurgery
- Pathology
Background:
- Glioependymal cysts are rare intracranial lesions.
- Their precise origin, particularly in infants, remains debated.
- Potential origins include the tela choroidea or ependymal/glial elements.
Observation:
- A 35-month-old girl presented with truncal ataxia and hydrocephalus.
- MRI revealed a giant cystic mass spanning the anterior and posterior cranial fossae, obstructing the sylvian aqueduct.
- Endoscopic fenestration of the cyst was performed.
Findings:
- Histochemical and immunohistochemical analysis confirmed the lesion as a glioependymal cyst.
- Post-operative MRI suggested the cyst originated from the tela choroidea.
- A 5-year follow-up showed no recurrence and complete recovery.
Implications:
- This case supports the tela choroidea as a potential origin for glioependymal cysts.
- Endoscopic fenestration is a viable treatment for giant glioependymal cysts causing hydrocephalus.
- Further research into the embryological development of glioependymal cysts is warranted.
Abstract:
The authors report the case of an infant with a giant glioependymal cyst. Although it has been suggested that these cysts originate from the tela choroidea, their origin remains controversial. This 35-month-old girl with truncal ataxia was referred to the authors' hospital. Magnetic resonance imaging revealed a giant cystic mass extending from the anterior to the posterior cranial fossa. Hydrocephalus was caused by obstruction of the sylvian aqueduct. Endoscopic fenestration of the cyst wall was performed. Histochemical and immunohistochemical staining identified the lesion as a glioependymal cyst. Magnetic resonance imaging performed 8 months later suggested that the cyst originated from the tela choroidea. At 5-year follow-up, there was no tumor recurrence and she had fully recovered. The origin of glioependymal cysts is discussed, and the authors suggest that their origin is the tela choroidea.
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