鼻窦内翻性乳头状瘤的临床表现、手术处理及预后

Tariq Tatwani
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摘要

鼻窦内翻性乳头状瘤(IP)又称施耐德乳头状瘤,是鼻腔和副鼻窦最有趣的病理之一。它是一种良性上皮性肿瘤,起源于鼻窦和副鼻窦周围的施耐德上皮。这种肿瘤的其他名称包括上皮乳头状瘤、林格兹瘤、移行细胞乳头状瘤、绒毛状癌和尤因乳头状瘤b[3]。它占所有鼻窦乳头状瘤的70%,其余30%为外生性乳头状瘤或柱状细胞乳头状瘤,尽管它不是很常见的疾病(占所有鼻和鼻窦肿瘤的0.5-4%)。然而,IP引起了相当大的兴趣,因为它是局部侵袭性的,具有很高的复发倾向,并且与恶性转化显著相关-最常见的是鳞状细胞癌,约10-15%的病例[4,5]。
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Clinical Presentations, Surgical Management and Outcome of Sinonasal Inverted Papilloma
Sinonasal inverted papilloma (IP) also known as Schneiderian papilloma is one of the most intriguing pathology of nasal cavity and paranasal sinuses [1]. It is a benign epithelial neoplasm arising from the Schneiderian epithelium that lines the nose and paranasal sinuses [2]. Other names for this tumor include epithelial papilloma, Ringertz’s tumour, transitional cell papilloma, villiform cancer and Ewing’s papilloma [3]. It accounts for 70% of all sinonasal papillomas, remaining 30% are either exophyticpapillomas or columnar cell papillomas despite that it is not very common diseases (0.5-4% of all nasal and sinus tumours). However, IP attracts considerable interest because it is locally aggressive, has a high propensity to recur, and is significantly associated with malignant transformation-most frequently to squamous cell carcinoma in about 10-15% cases [4,5].
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