Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology · 2007
Porencephalic cyst: a review of the literature and management of a rare cause of cerebrospinal fluid otorrhea.
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Ryzenman John M, Rothholtz Vanessa S, Wiet Richard J
Аннотация
OBJECTIVE: To discuss the first reported case of spontaneous cerebrospinal fluid (CSF) otorrhea caused by a massive CSF-containing porencephalic cyst.
STUDY DESIGN: A case report and review of the literature (MEDLINE 1962-2005).
SETTING: A tertiary neurotologic referral center.
PATIENT: A 65-year-old woman with congenital hemiplegia presented with left-sided spontaneous CSF otorrhea of 4-month duration. An audiogram revealed a mixed hearing loss. High-resolution computed tomography revealed a thinning of the tegmen and epitympanum without an obvious defect. Magnetic resonance imaging revealed a massive porencephalic cyst essentially replacing the entire left cerebral hemisphere.
INTERVENTION: A transmastoid approach with three-layered closure was used to successfully repair the sieve-like defects that were discovered in her tegmen.
RESULTS: The patient remains free of drainage, and the conductive hearing loss has resolved.
CONCLUSION: Spontaneous CSF otorrhea caused by a porencephalic cyst is an uncommon cause of conductive hearing loss that has never been reported before. Only a few cases of traumatic CSF otorrhea/rhinorrhea associated with a porencephalic cyst have been reported. A high level of suspicion, a beta2-transferrin assay, and appropriate radiographic imaging are required for diagnosis in adults without a history of trauma, meningitis, chronic ear disease, or previous ear surgery.
STUDY DESIGN: A case report and review of the literature (MEDLINE 1962-2005).
SETTING: A tertiary neurotologic referral center.
PATIENT: A 65-year-old woman with congenital hemiplegia presented with left-sided spontaneous CSF otorrhea of 4-month duration. An audiogram revealed a mixed hearing loss. High-resolution computed tomography revealed a thinning of the tegmen and epitympanum without an obvious defect. Magnetic resonance imaging revealed a massive porencephalic cyst essentially replacing the entire left cerebral hemisphere.
INTERVENTION: A transmastoid approach with three-layered closure was used to successfully repair the sieve-like defects that were discovered in her tegmen.
RESULTS: The patient remains free of drainage, and the conductive hearing loss has resolved.
CONCLUSION: Spontaneous CSF otorrhea caused by a porencephalic cyst is an uncommon cause of conductive hearing loss that has never been reported before. Only a few cases of traumatic CSF otorrhea/rhinorrhea associated with a porencephalic cyst have been reported. A high level of suspicion, a beta2-transferrin assay, and appropriate radiographic imaging are required for diagnosis in adults without a history of trauma, meningitis, chronic ear disease, or previous ear surgery.