Congenital or acquired? A case report of extensive congenital cholesteatoma
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 mon...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
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Penerbit UKM
2010
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| Online Access: | http://journalarticle.ukm.my/2087/ http://journalarticle.ukm.my/2087/1/08MS090_4144.pdf |
| _version_ | 1848809754338525184 |
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| author | Roslenda AR, Asma A, Iqbal FRW, Iqbal FRW, |
| author_facet | Roslenda AR, Asma A, Iqbal FRW, Iqbal FRW, |
| author_sort | Roslenda AR, |
| building | UKM Institutional Repository |
| collection | Online Access |
| description | 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. |
| first_indexed | 2025-11-14T23:19:38Z |
| format | Article |
| id | oai:generic.eprints.org:2087 |
| institution | Universiti Kebangasaan Malaysia |
| institution_category | Local University |
| language | English |
| last_indexed | 2025-11-14T23:19:38Z |
| publishDate | 2010 |
| publisher | Penerbit UKM |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | oai:generic.eprints.org:20872016-12-14T06:30:51Z http://journalarticle.ukm.my/2087/ Congenital or acquired? A case report of extensive congenital cholesteatoma Roslenda AR, Asma A, Iqbal FRW, Iqbal FRW, 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. Penerbit UKM 2010 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/2087/1/08MS090_4144.pdf Roslenda AR, and Asma A, and Iqbal FRW, and Iqbal FRW, (2010) Congenital or acquired? A case report of extensive congenital cholesteatoma. Medicine & Health, 5 (2). pp. 103-107. ISSN 1823-2140 http://www.ppukm.ukm.my/ukmmcjournal/index.php |
| spellingShingle | Roslenda AR, Asma A, Iqbal FRW, Iqbal FRW, Congenital or acquired? A case report of extensive congenital cholesteatoma |
| title | Congenital or acquired? A case report of extensive
congenital cholesteatoma |
| title_full | Congenital or acquired? A case report of extensive
congenital cholesteatoma |
| title_fullStr | Congenital or acquired? A case report of extensive
congenital cholesteatoma |
| title_full_unstemmed | Congenital or acquired? A case report of extensive
congenital cholesteatoma |
| title_short | Congenital or acquired? A case report of extensive
congenital cholesteatoma |
| title_sort | congenital or acquired? a case report of extensive
congenital cholesteatoma |
| url | http://journalarticle.ukm.my/2087/ http://journalarticle.ukm.my/2087/ http://journalarticle.ukm.my/2087/1/08MS090_4144.pdf |