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[岩部和乳突先天性胆脂瘤:两例报告]

[Congenital cholesteatoma of the petrous process and mastoid: a report of two cases].

作者信息

Pérez Obón J, Fernández Liesa R, Marín García J, Valero J, Eiras Ajuria J, Ortiz García A

机构信息

Servicio de ORL, Hospital Miguel Servet, Zaragoza.

出版信息

Acta Otorrinolaringol Esp. 1995 Sep-Oct;46(5):349-52.

PMID:8554803
Abstract

Congenital cholesteatoma are unusual. They may arise in different sites of the temporal bone: petrous process, middle ear and mastoid. Primary cholesteatomas originate from embryonary ectodermal inclusions but the pathogenesis is not clear and many different hypotheses regarding its origin have been suggested. The clinical diagnosis is not easy if the tympanic membrane is normal, and computerized tomography and magnetic resonance imaging are useful. We report two cases of congenital cholesteatoma: One located in the petrous process and the other in the mastoid without affection of the tympanic cavity.

摘要

先天性胆脂瘤并不常见。它们可能出现在颞骨的不同部位:岩部、中耳和乳突。原发性胆脂瘤起源于胚胎外胚层包涵体,但其发病机制尚不清楚,关于其起源已提出许多不同的假说。如果鼓膜正常,临床诊断并不容易,计算机断层扫描和磁共振成像很有用。我们报告两例先天性胆脂瘤病例:一例位于岩部,另一例位于乳突,鼓室未受影响。

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