Schneiderian papilloma of the temporal bone

Lisa van der Putten1, Elisabeth Bloemena, Paul Merkus

  • 1Department of Otorhinolaryngology, Head and Neck Surgery, VU University Medical Center, Amsterdam, The Netherlands.

BMJ Case Reports
|December 7, 2013
PubMed

Insights

Primary temporal bone Schneiderian papilloma is rare and can recur frequently. Early detection and consistent follow-up are crucial for managing this middle ear tumor.

Area of Science:

  • Otolaryngology
  • Pathology
  • Oncology

Background:

  • Schneiderian papillomas (SPs) are rare tumors that can arise primarily in the temporal bone or extend from sinonasal disease.
  • Primary temporal bone SPs are exceptionally rare, with only 18 cases documented, often originating in the middle ear and mastoid.

Observation:

  • This case highlights a primary temporal bone SP, presenting a unique clinical scenario.
  • The patient remained disease-free post-excision, but the high recurrence rate of temporal bone SPs mirrors that of sinonasal SPs with extrasinus extension.

Findings:

  • Malignant progression is less common in primary temporal bone SPs compared to those extending from the sinonasal tract.
  • Human papillomavirus (HPV) positivity, a known prognostic factor in sinonasal SPs, was observed in this case, though infrequent in temporal bone disease.

Implications:

  • The high recurrence rate and potential for malignant transformation necessitate vigilant monitoring.
  • Stringent follow-up protocols, including otoscopy, nasendoscopy, and imaging, are essential due to the lack of reliable prognostic markers.