Spontaneous middle-ear encephalocele: report of two cases and brief review

H Alkhalidi1, L N de Tilly, R Fenton

  • 1Department of Laboratory Medicine and Pathobiology, St. Michael's Hospital and Li Ka Shing Knowledge Institute, University of Toronto, Ontario, Canada.

Clinical Neuropathology
|September 24, 2008
PubMed

Insights

Spontaneous middle-ear encephalocele, a rare condition, was observed in two elderly patients. This finding highlights the importance of considering encephalocele in diagnosing ear masses and otorrhea.

Area of Science:

  • Neurology
  • Otolaryngology

Background:

  • Spontaneous (idiopathic) encephalocele is a rare condition involving brain tissue protrusion through a defect in the skull.
  • Middle-ear encephalocele specifically affects the temporal bone, presenting diagnostic challenges.

Observation:

  • Two cases of middle-ear encephalocele are presented in patients aged 69 and 82 years.
  • The 82-year-old patient represents the oldest reported individual with this condition.
  • Microscopic analysis revealed disorganized neuropil with inflammation and cystic changes.

Findings:

  • The study documents rare instances of spontaneous middle-ear encephalocele in elderly individuals.
  • Histopathological examination identified characteristic neurological and inflammatory changes.
  • The presence of ciliated epithelium in one case suggests a potential developmental or acquired component.

Implications:

  • Middle-ear encephalocele should be considered in the differential diagnosis of unexplained otorrhea.
  • This condition warrants inclusion in the differential diagnosis for middle ear masses, especially in older populations.
  • Accurate diagnosis is crucial for appropriate management and to prevent complications.