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CSF Rhinorrhea: A Rare Clinical Presentation of Choroid Plexus Papilloma
Layth Mula-Hussain1, Julia Malone1, Marlise P Dos Santos2
1Radiation Oncology Division, The Ottawa Hospital-University of Ottawa, Ottawa, ON K1H 8L6, Canada.
Insights
Choroid plexus papilloma, a rare brain tumor, can occur in adults and present atypically. This case highlights successful treatment with subtotal resection and CyberKnife radiosurgery for a cerebellopontine angle tumor causing CSF rhinorrhea.
Area of Science:
- Neuro-oncology
- Neurosurgery
- Radiation Oncology
Background:
- Choroid plexus papilloma (CPP) is a rare intracranial tumor predominantly affecting pediatric populations.
- Intraventricular location and increased intracranial pressure (ICP) are typical presentations of CPP.
- Cerebellopontine angle (CPA) location and cerebrospinal fluid (CSF) rhinorrhea are atypical manifestations.
Observation:
- A middle-aged female presented with spontaneous CSF rhinorrhea.
- The causative lesion was identified as a CPA tumor.
- Initial management involved craniotomy and subtotal tumor resection.
Findings:
- The patient remained progression and rhinorrhea-free for several years post-surgery.
- Recurrence or progression led to treatment with CyberKnife stereotactic radiosurgery.
- The patient exhibited clinical improvement and favorable radiologic response to radiosurgery.
Implications:
- This case expands the understanding of CPP presentation in adults.
- It underscores the efficacy of a multimodal treatment approach including radiosurgery for recurrent or residual CPA tumors.
- Highlights the potential for long-term disease control with advanced treatment modalities.
Abstract:
Choroid plexus papilloma (CPP) is a rare brain tumour occurring mostly in infants and children. Most CPPs are intraventricular and present with symptoms and signs of increased intracranial pressure (ICP). This case report describes a middle-aged female who presented with spontaneous cerebrospinal fluid (CSF) rhinorrhea from a tumour located in the cerebellopontine angle (CPA). She underwent craniotomy with subtotal tumour resection and remained progression and rhinorrhea-free for several years. Upon clinical progression, the patient was treated with Cyberknife stereotactic radiosurgery. The patient clinically improved and demonstrated a favourable radiologic response to radiosurgery.
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