Foramen of Monro choroid plexus papilloma: An extremely rare location managed by endoscopic resection
Mahmoud Abdallat, Mohammed Aloqaily, Wafi Aloqaily, Mohammad Al-Qob, Saleh Al-Jbour, Abdallah Al-Muhtaseb, Nosaiba Al Ryalat, Fatima Obeidat

TL;DR
A rare brain tumor in an unusual location was successfully treated with endoscopic surgery in a 30-year-old woman.
Contribution
Reports a first-in-adults case of choroid plexus papilloma in the Foramen of Monro managed via endoscopic resection.
Findings
The tumor was located in the Foramen of Monro, an extremely rare site in adults.
Endoscopic resection was successfully performed without complications.
The case highlights the potential of endoscopic approaches for similar rare tumors.
Abstract
Choroid plexus papillomas are rare brain neoplasms, primarily observed in children, and typically manifest with symptoms indicative of heightened intracranial pressure and cerebral irritation. In addition, the tumor's localization varies with the patient's age, and diagnostic and therapeutic approaches predominantly rely on imaging findings and surgical interventions, with histopathological examination being essential for confirmation. This study outlines a unique instance of choroid plexus papilloma in a 30-year-old female, who presented with severe headache and vomiting, subsequently revealing hydrocephalus on Brain CT. Remarkably, the tumor was identified in the Foramen of Monro, an exceedingly rare and unreported location in adults. Notably, the patient underwent successful endoscopic resection without complications, a technique sparsely documented in similar cases. Choroid plexus…
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Taxonomy
TopicsCerebrospinal fluid and hydrocephalus · Head and Neck Surgical Oncology · Fetal and Pediatric Neurological Disorders
