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儿童胆脂瘤

Cholesteatoma in children.

作者信息

Sadé J, Shatz A

机构信息

Department of Otolaryngology, Meir Hospital, Kfar Saba, Israel.

出版信息

J Laryngol Otol. 1988 Nov;102(11):1003-6. doi: 10.1017/s0022215100107121.

Abstract

Of 325 previously untreated cholesteatomas, 109 were found to be in children 13 years old and younger--however, these 109 ears were not found to consist of one clinical entity. Sixty-three of the 109 ears presented a marginal perforation or a retraction pocket, at the level of Shrapnell's membrane or beyond the postero-superior quadrant. In this group the cholesteatoma was distributed mainly in the attic and mastoid and was associated with a non-cellular mastoid. A second group comprising 31 ears presented with cholesteatoma behind an intact drum and were considered to be primary cholesteatomas. These were distributed mostly in the tympanic cavity as cystic epidermoid formations--their mastoid was usually pneumatized. Eight cholesteatomas were related to a central perforation. These ears presented features very similar to the primary cholesteatomas i.e., a pneumatized mastoid and tympanic cavity distribution. The similar features of this group make us think that they may have also originated as primary cholesteatomas which eventually perforated and bring the percentage of primary cholesteatomas in children to 38.3%. Seven of the 109 ears with cholesteatoma were of an indeterminate character.

摘要

在325例未经治疗的胆脂瘤中,发现109例发生在13岁及以下儿童中——然而,这109只耳朵并非属于同一临床类型。109只耳朵中有63只在Shrapnell膜水平或后上象限以外出现边缘穿孔或内陷袋。在这一组中,胆脂瘤主要分布在鼓室上隐窝和乳突,并与无细胞乳突相关。第二组包括31只耳朵,胆脂瘤出现在完整鼓膜后方,被认为是原发性胆脂瘤。这些胆脂瘤大多以囊性表皮样结构分布在鼓室内——其乳突通常为气化型。8例胆脂瘤与中央穿孔有关。这些耳朵呈现出与原发性胆脂瘤非常相似的特征,即气化型乳突和鼓室分布。这一组的相似特征使我们认为它们可能也起源于原发性胆脂瘤,最终穿孔,使儿童原发性胆脂瘤的比例达到38.3%。109例胆脂瘤患儿中有7例性质不确定。

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