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Spontaneous Regression of Congenital Cholesteatoma: A Report of Two Cases with Differing Ossicle Involvement

Author(s): Yoshimasa Tsuchiya, Taichi Kan*, Mayuko Kishimoto, Yasue Uchida, Tetsuya Ogawa, Hiromi Ueda

The mechanism of congenital cholesteatoma has not been clarified yet. Usually, middle ear cholesteatoma (congenital and acquired) is a progressive and destructive disease that requires surgery for complete cure. In recent years, early detection of congenital cholesteatomas has become more frequent due to advances in endoscopy and microscopy. Along with these developments, there have been reports of congenital cholesteatoma regressing spontaneously, as seen by tympanic and computed tomography findings over time. Herein, we report two cases of spontaneous regression of cholesteatoma, both with ossicular chain malformation. One cholesteatoma was close to the ossicles. In the other case, the cholesteatoma and ossicle were separated; however, the ossicular morphology was inconsistent with that of congenital ossicular malformation. Further similarities and differences between these two cases are discussed herein.

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    Editor In Chief

    Yasuo Iwasaki

  • Division of Neurology, Department of Internal Medicine
    Toho University School of Medicine
    Ota-ku, Tokyo, Japan

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