Intraventricular Craniopharyngiomas—Overcoming Their Relative Inaccessibility: Institutional Experience With a Review of Literature

2021 
Introduction: Craniopharyngiomas constitute 2 to 4 % of intracranial neoplasms. Intraventricular craniopharyngiomas (IVCrs) are the rarely encountered varieties of these lesions. Objective: To study the special features in clinical presentation, imaging, management, and surgical outcome of IVCrs. Materials and Methods: This retrospective analysis included the combined experience of the two senior authors (from two tertiary care institutions). Medical records of histopathologically proven cases of IVCrs from January 1994 to June 2021, were assessed and images analysed, based on the criteria by Migliore et al. for inclusion of solely intraventricular lesion with the third ventricular ependyma demarcating it from the suprasellar cistern. Results: Among the 25 patients included (mean age: 34.5 years), the most common presentation included headache (n=21; 84%), vomiting and other features of raised ICP (n=18,72%), visual complaints (n=12, 48%) and endocrinopathies (n=11, 44%). Fifteen had predominantly cystic tumours, 2 were purely solid and 8 were of mixed consistency. Primary open microsurgical procedures were performed in 18(72%) patients, of which 4(16%) were endoscope-assisted. Seven (28%) underwent a purely endoscopic procedure. One underwent a staged surgery with endoscopic cyst fenestration and intracystic interferon [IFN]-alpha therapy, followed by microsurgical excision. Complete excision was achieved in 10 patients, near-total in 9, and partial excision in 6. Four patients underwent a ventriculoperitoneal shunt (one before the definitive procedure). At a median follow-up of 36 months (range:11-147 months), 5 patients developed a recurrence, and one had a stable small residue. This patient and two others with small cystic recurrences, were observed. One patient was managed with radiotherapy alone. Another underwent re-surgery after a trial of radiotherapy, and the last patient developed a local recurrence which was managed with radiotherapy; he then later developed an intraparenchymal recurrence, which was operated. Conclusion: Purely IVCrs present with raised intracranial pressure and visual disturbances are less common. Their deep-seated location and limited surgical field-of-view makes minimally invasive endoscopic-assisted surgery most suitable for their excision. The thin-walled cystic lesions may be occasionally adherent to the ependymal wall in close vicinity to the thalamus-hypothalamus complex, making complete excision difficult. Their responsiveness to radiotherapy, often leads to a gratifying long-term outcome.
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