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上鼓室胆脂瘤的发病机制:对内陷理论与增殖理论相结合的临床及免疫组化支持

Pathogenesis of attic cholesteatoma: clinical and immunohistochemical support for combination of retraction theory and proliferation theory.

作者信息

Sudhoff H, Tos M

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, St. Elisabeth Hospital, University of Bochum, Germany.

出版信息

Am J Otol. 2000 Nov;21(6):786-92.

Abstract

OBJECTIVE

The aim of the current study was to provide support for a combination of the retraction and proliferation theories of acquired cholesteatoma.

BACKGROUND

There is clinical evidence for formation of a retraction, but there is a lack of explanation for the transition from a retraction pocket to an active and expanding attic cholesteatoma.

METHODS

Epidemiologic studies on the incidence of attic retractions and follow-up studies on patients with attic retractions were performed. Additionally, expression of proliferation marker and analysis of basement membrane were studied in samples of attic cholesteatoma.

RESULTS

The prevalence of attic retractions was between 14% and 25% of investigated ears. In children with manifest secretory otitis, there were some attic cholesteatomas and 5% to 6% severe retractions. Some of them became precholesteatomas, requiring treatment and controls. Immunohistochemistry of attic cholesteatomas showed that proliferating keratinocytes were very often seen within epithelial cones growing toward the underlying stroma. These growth cones exhibited focal discontinuities of the basement membrane, especially in areas of intense subepithelial inflammation.

CONCLUSIONS

As a possible explanation based on clinical and immunohistochemical findings, the authors propose a four-step concept for the pathogenesis of cholesteatoma that combines the retraction and proliferation theories: (a) the retraction pocket stage; (b) the proliferation stage of the retraction pocket, subdivided into cone formation and cone fusion; (c) the expansion stage of attic cholesteatoma; and (d) bone resorption.

摘要

目的

本研究的目的是为后天性胆脂瘤的回缩和增殖理论的结合提供支持。

背景

有临床证据表明存在回缩形成,但对于从回缩袋向活跃且不断扩大的上鼓室胆脂瘤的转变缺乏解释。

方法

对上鼓室回缩的发病率进行了流行病学研究,并对有上鼓室回缩的患者进行了随访研究。此外,对上鼓室胆脂瘤样本进行了增殖标志物表达和基底膜分析。

结果

上鼓室回缩的患病率在被调查耳的14%至25%之间。在患有明显分泌性中耳炎的儿童中,存在一些上鼓室胆脂瘤和5%至6%的严重回缩。其中一些发展为胆脂瘤前期,需要治疗和监测。上鼓室胆脂瘤的免疫组织化学显示,在朝着下方基质生长的上皮锥体内经常可见增殖的角质形成细胞。这些生长锥在基底膜处表现出局灶性中断,尤其是在强烈的上皮下炎症区域。

结论

基于临床和免疫组织化学结果,作者提出了一个结合回缩和增殖理论的胆脂瘤发病机制的四步概念:(a)回缩袋阶段;(b)回缩袋的增殖阶段,细分为锥体形成和锥体融合;(c)上鼓室胆脂瘤的扩展阶段;以及(d)骨吸收。

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