Congenital or Acquired? A Case Report of Extensive Congenital Cholesteatoma

被引:0
|
作者
Roslenda, A. R. [1 ]
Asma, A. [1 ]
Iqbal, F. R. W. [1 ]
Jeevanan, J. [1 ]
机构
[1] Univ Kebangsaan Malaysia, Fac Med, Dept Otorhinolaryngol Head & Neck Surg, Kuala Lumpur, Malaysia
来源
MEDICINE AND HEALTH-KUALA LUMPUR | 2010年 / 5卷 / 02期
关键词
cholesteatoma; hearing loss; deafness; tympanoplasty; ossicles;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Congenital cholesteatoma (CC) is rare clinical condition and It is known as a pearly white mass medial to an intact tympanic membrane. In this case report, we describe a 6-year-old boy who presented with a one year history of left ear discomfort, reduced hearing, followed by ear discharge two months prior to admission. Otoscopic examination revealed a large attic perforation. Radiological investigation showed extensive cholesteatoma in the mastoid, mesotympanum and epitympanum with destruction of the ossicles including the stapes footplate. He underwent radical mastoidectomy in view of extensive cholesteatoma with tympanoplasty type V. In this case report, the classification, treatment and theories related to CC are discussed.
引用
收藏
页码:103 / 107
页数:5
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