Congenital cholesteatoma: A case report

Yıl 2014, , 93 - 95, 01.06.2014

Süleyman Cesur Mahmut Sinan Yılmaz Mehmet Güven Muhammet Yeniay

https://doi.org/10.5505/sakaryamj.2014.97752

Cited By: 1

Öz

Congenital cholesteatomas are rare disorders, which may originate from the postpartum persistence of epidermoid formations.They have been defined as evidencing no tympanic perforation, that a pearly white mass medial to the tympanic membrane. Usually presentation as asymptomatic but rarely conductive hearing loss, otorrhea, vertigo may occur. Treatment of congenital cholesteatomas is surgical. In this article,we present a case with congenital cholesteatoma presenting hearing loss, otalgia ve otorrhea, also bone defect associated with carotis interna artery.

Anahtar Kelimeler

Congenital cholesteatoma, hearing loss, otalgia.

Konjenital kolesteatom: Bir olgu sunumu

Öz

Konjenital kolesteatom aberan epitelyal kalıntılardan kaynaklanan nadir bir durumdur. Genellikle sağlam timpanik membran arkasında beyaz yuvarlak kitle olarak kendini gösterir. Asemptomatik seyredebileceği gibi iletim tipi işitme kaybı, kulak akıntısı, baş dönmesine sebep olabilir. Cerrahi tedavi uygulanır. Bu yazıda, işitme kaybı, otalji ve otore ile kendini gösteren, internal karotid arter kemik duvarda defekt oluşturan konjenital kolesteatom olgusunu sunarak tartışmayı amaçladık.

Anahtar Kelimeler

Konjenital kolesteatom, işitme kaybı, kulak ağrısı

Kaynakça

• Potsic WP, Korman SB, Samadi DS, Wetmore RF. Congenital cholesteatoma: 20 years’ experience at The Children’s Hospital of Philadelphia. Otolaryngol Head Neck Surg 2002;126:409-14
• Mornet E, Martins Carvalho C, et al. Cholesteatome congenital lokalise chez I’adulte. Annales d’otolaryngologie et chirurgie cervico-faciale 2008;125:85-89
• Akyıldız N. Kulak Hastalıkları ve Mikrocerrahisi. Ankara: Bilimsel Tıp Yayınevi. 1998:354-418
• Derlacki EL, Clemis JD. Congenital cholesteatoma of middle ear and mastoid. Ann Otol Rhinol Laryngol 1965;74:706-27
• Levenson MJ, Michaels L, Parisier SC, et al. Congenital cholesteatomas of middle ear in children: origin and management. Otolaryngol Clin North Am 1989;22:941-54
• Michaels L. An epidermoid formation in the developing middle ear: possible source of cholesteatoma. J Otolaryngol 1986;15:169-74
• Sade J, Babiacki A, Pinkus G. The metaplastic and congenital orign of cholesteatoma. Acta Otolaryngol 1983;96:119-29
• Kashiwamura M, Fukuda S, Chida E, Matsumura M. Locations of congenital cholesteatoma in the middle ear in Japanese patients. Am J Otolaryngol 2005;26(6):372-6
• Peron DL, Schuknecht HF. Congenital cholesteatoma with other anomalies. Arch Otolaryngol 1975;101(8):498-505
• Aimi K. Role of the tympanic ring in the pathogenesis of congenital cholesteatoma. Laryngoscope 1983;93:1140-6
• Kojima H, Tanaka Y, Shiwa M, Sakurai Y, Moriyama H. Congenital cholesteatoma clinical features and surgical results. Am J Otolaryngol 2006;27(5):299-305
• Mevio E, Gorini E, Sbrocca M, Artesi L, Lenzi A, Lecce S, et al. Congenital cholesteatoma of the mastoid region. Otolaryngol Head Neck Surg 2002;127(4):346-8
• Potsic WP, Samadi DS, Marsh RR, Wetmore RF. A staging system for congenital cholesteatoma. Arch Otolaryngol Head Neck Surg 2002;128(9):1009-12
• El- Bitar MA, Choi SS. Bilateral occurrence of congenital middle ear cholesteatoma. Otolaryngol Head Neck Surg 2002;127(5):480-2
• Benhammou A, Nguyen D-Q, et al. Resultats a long terme des cholesteatomes congenitaux de I’oreille moyenne de I’enfant. Ann Otolaryngol Chir Cervicofac 2005;122:113-9