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内翻性乳头状瘤的一种不寻常表现:病例报告及文献综述

An unusual presentation of inverted papilloma: case report and literature review.

作者信息

Visvanathan V, Wallace H, Chumas P, Makura Z G G

机构信息

Department of Otolaryngology - Head and Neck Surgery, Leeds General Infirmary, West Yorkshire, UK.

出版信息

J Laryngol Otol. 2010 Jan;124(1):101-4. doi: 10.1017/S0022215109990703. Epub 2009 Aug 3.

Abstract

OBJECTIVE

Inverted papilloma is a rare but locally aggressive tumour with the potential for malignant transformation. Intracranial extension or complications secondary to inverted papilloma are extremely rare. We report a case of inverted papilloma with a large frontal sinus mucocele eroding the frontal sinus, which presented with sudden neurological compromise. A literature review on intracranial extension of such tumours is also included.

METHODS

A Medline search of articles, using the terms 'inverted papilloma', 'Ringertz tumour', 'intracranial extension' and 'complication'. Suitable references from the collected articles were also reviewed. Articles published in English were selected and reviewed.

RESULTS

A total of 10 cases was identified. Intracranial spread was more commonly seen in recurrent cases, especially if the recurrence involved the cribriform plate, fovea ethmoidalis or orbits. Cases with extradural disease seemed to have a better prognosis than those with intradural spread.

CONCLUSIONS

Intracranial involvement of inverted papilloma is extremely rare, and is usually seen in recurrent cases. This case report highlights an unusual but serious case of inverted papilloma presenting with acute neurological deterioration secondary to a large frontal sinus mucocele eroding the frontal sinus. A literature review on intracranial extension of inverted papilloma indicated that common sites of intracranial spread include the cribriform plate, fovea ethmoidalis and orbits. The prognosis for patients with such tumours depends on the type of dural involvement, with intradural extension carrying a poorer prognosis.

摘要

目的

内翻性乳头状瘤是一种罕见但具有局部侵袭性且有恶变潜能的肿瘤。内翻性乳头状瘤继发颅内扩展或并发症极为罕见。我们报告一例内翻性乳头状瘤合并巨大额窦黏液囊肿侵蚀额窦,表现为突发神经功能障碍的病例。本文还包括对此类肿瘤颅内扩展的文献综述。

方法

利用“内翻性乳头状瘤”“林格茨瘤”“颅内扩展”和“并发症”等术语在医学文献数据库中检索文章。对所收集文章中的合适参考文献也进行了综述。选取并审阅了英文发表的文章。

结果

共确定了10例病例。颅内扩散在复发病例中更常见,尤其是复发累及筛板、筛凹或眼眶时。硬膜外病变的病例预后似乎比硬膜内扩散的病例要好。

结论

内翻性乳头状瘤颅内受累极为罕见,通常见于复发病例。本病例报告强调了一例不寻常但严重的内翻性乳头状瘤病例,其因巨大额窦黏液囊肿侵蚀额窦而出现急性神经功能恶化。关于内翻性乳头状瘤颅内扩展的文献综述表明,颅内扩散的常见部位包括筛板、筛凹和眼眶。此类肿瘤患者的预后取决于硬脑膜受累的类型,硬膜内扩展的预后较差。

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