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유양동에 발생한 거대 선천성 진주종 1예

A Case of Giant Congenital Cholesteatoma on Mastoid Process

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초록

Congenital cholesteatoma is a rare lesion of the temporal bone. It accounts for only 2 to 5% of all cholesteatoma, though that number is throught to be on the rise due to improved imaging techniques. The diagnosis of a congenital cholesteatoma includes a pearly white mass behind an intact tympanic membrane without history of otitis media, otorrhea, or otological surgical procedure. Congenital cholesteatoma may develop in various temporal bone sites including the middle ear cavity, petrous apex, cerebellopontine angle, external auditory canal and mastoid process. The most frequent site of origin is the middle ear cavity, whereas the rarest is the mastoid. The clinical presentation is usually an symptomatic white mass behind an intact tympanic membrane. The congenital cholesteatoma that originates in the mastoid is more difficult to diagnose due to variable clinical presentation. We recently experienced a case of congenital cholesteatoma with facial palsy in 33 year old male patient who showed normal tympanic membrane without prior history of ear disease and otologic surgical procedure. We report this case with brief review of the literatures

Abstract

Congenital cholesteatoma is a rare lesion of the temporal bone. It accounts for only 2 to 5% of all cholesteatoma, though that number is throught to be on the rise due to improved imaging techniques. The diagnosis of a congenital cholesteatoma includes a pearly white mass behind an intact tympanic membrane without history of otitis media, otorrhea, or otological surgical procedure. Congenital cholesteatoma may develop in various temporal bone sites including the middle ear cavity, petrous apex, cerebellopontine angle, external auditory canal and mastoid process. The most frequent site of origin is the middle ear cavity, whereas the rarest is the mastoid. The clinical presentation is usually an symptomatic white mass behind an intact tympanic membrane. The congenital cholesteatoma that originates in the mastoid is more difficult to diagnose due to variable clinical presentation. We recently experienced a case of congenital cholesteatoma with facial palsy in 33 year old male patient who showed normal tympanic membrane without prior history of ear disease and otologic surgical procedure. We report this case with brief review of the literatures

참고문헌 (11)

  1. Paparella MM, "Congenital cholesteatoma", Otolaryngol Clin North Am, 11(1), pp.113~120 (1978)
  2. Kang MK, "A case of congenital cholesteatoma with labyrithine fistula", J Clinical Otolaryngol, 9(1), pp.132~136 (1998)
  3. Hidaka H, "Congenital cholesteatoma of mastoid region manifesting as acute mastoiditis: case report and literature review", J Laryngol Otol, 124(7), pp.810~815 (2010)
  4. Derlacki EL, "Congenital cholesteatoma of the middle ear and mastoid", Trans Am Otol Soc, 53, pp.208~231 (1965)
  5. Warren FM, "Congenital cholesteatoma of the mastoid temporal bone", Laryngoscope, 117(8), pp.1389~1394 (2007)
  6. Lee JH, "Congenital cholesteatoma of mastoid origin", J Laryngol Otol, 121(11), pp.e20~ (2007)
  7. Cvorovic L, "Giant destructive congenital mastoid cholesteatoma with minimal clinical presentation", Otolaryngol Head Neck Surg, 144(5), pp.821~822 (2011)
  8. Mafee MF, "MRI and CT in the evaluation of acquired and congenital cholesteatoma of the temporal bone", J Otolaryngol, 22(4), pp.239~248 (1993)
  9. Luntz M, "Congenital cholesteatoma isolated to the mastoid", Ann Otol Rhinol Laryngol, 106, pp.608~610 (1997)
  10. Park OH, "Congenital cholesteatoma of the mastoid", Korean J Otolaryngol, 25(2), pp.370~375 (1982)
  11. Geven LI, "Giant Cholesteatoma: recommendations for follow up", Skull Base, 18(5), pp.353~359 (2008)

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