Surgical treatment and outcome of posterior fossa arachnoid cysts in infants.
Arachnoid Cysts
/ diagnostic imaging
Cerebrospinal Fluid Shunts
Cranial Fossa, Posterior
/ diagnostic imaging
Female
Follow-Up Studies
Humans
Hydrocephalus
/ surgery
Infant
Infant, Newborn
Magnetic Resonance Imaging
Male
Neuroendoscopy
/ methods
Neuronavigation
Neurosurgical Procedures
/ methods
Prenatal Diagnosis
Reoperation
/ statistics & numerical data
Retrospective Studies
Treatment Outcome
arachnoid cysts
congenital
craniotomy
hydrocephalus
infancy
neuroendoscopy
pediatric neurosurgery
posterior fossa
prenatal MRI
shunt
Journal
Journal of neurosurgery. Pediatrics
ISSN: 1933-0715
Titre abrégé: J Neurosurg Pediatr
Pays: United States
ID NLM: 101463759
Informations de publication
Date de publication:
20 Aug 2021
20 Aug 2021
Historique:
received:
28
02
2021
accepted:
07
05
2021
entrez:
1
11
2021
pubmed:
2
11
2021
medline:
12
11
2021
Statut:
epublish
Résumé
The aim of this cohort study was to describe and analyze the surgical treatment and outcome of posterior fossa arachnoid cysts (PFACs) in infants. Patients presenting with a PFAC at infancy or prenatally, between the years 2000 and 2019, and who were surgically treated before the age of 2 years, were included in this study. Patient data were retrospectively collected including baseline characteristics and surgical variables. Factors related to revision surgery were analyzed through uni- and multivariate analysis. Thirty-five patients, of whom 54.3% were male, were included. The cyst was diagnosed prenatally in 23 patients (65.7%). Surgery was typically recommended after a mean cyst follow-up of 3.4 ± 3.9 months, with a mean age at surgery of 6.1 ± 5.1 months. In 54.3% of patients (n = 19), surgery was performed before the age of 6 months. The PFAC was treated purely neuroendoscopically in 57.1% of patients (n = 20), while 28.6% of patients underwent open cyst procedures (n = 10), 5.7% (n = 2) were treated with a shunt, and 8.6% (n = 3) underwent a combined procedure. Additional surgery was required in 31.4% of patients (n = 11; mean 2.36 ± 2.11 surgeries per patient). At the last follow-up (61.40 ± 55.33 months), no mortality or permanent morbidity was seen; radiological improvement was apparent in 83.9% of the patients. Those patients treated before the age of 6 months (p = 0.09) and who presented before surgery with a stable cyst size that was maintained throughout preoperative monitoring (p = 0.08) showed a trend toward higher revision rates after surgical treatment. PFACs in infancy may require surgical treatment before the age of 6 months. Navigated endoscopy was a valid surgical option. Overall mortality or permanent morbidity was rare. Additional surgery was required in up to 30% of the patients; younger age and a preoperatively stable cyst might be risk factors for revision surgery.
Identifiants
pubmed: 34724647
doi: 10.3171/2021.5.PEDS21119
doi:
Types de publication
Journal Article
Video-Audio Media
Langues
eng
Sous-ensembles de citation
IM