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孤立性蝶窦内翻性乳头状瘤:临床表现、影像学表现及治疗策略

Isolated inverting papilloma of the sphenoid sinus: clinical presentations, imaging manifestations, and therapeutic strategies.

作者信息

Cheng Kejia, Chen Haihong, Zhou Shuihong, Wang Shenqing, Zhong Baishu

机构信息

Department of Otolaryngology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, People's Republic of China.

出版信息

J Craniofac Surg. 2012 Jul;23(4):1109-14. doi: 10.1097/SCS.0b013e31825434fc.

Abstract

BACKGROUND

Isolated inverting papilloma (IP) of the sphenoid sinus is rare, with about 50 patients reported in the English-language literature. With its rarity, scientists have paid less attention to the clinical and radiographic characteristics of isolated IPs arising from the sphenoid sinus.

METHODS

We describe the clinical presentation, imaging manifestations, and surgical methods of isolated IPs from the sphenoid sinus in 3 patients and review the English-language literature from 1970 to 2011.

RESULTS

In total, 59 cases of isolated sphenoid sinus IPs (including our cases) have been reported, 40 patients with computed tomography or magnetic resonance imaging details. The most common presentation is headache. Lesions were found in the sphenoethmoidal recess in 26 cases. In 8 patients who underwent enhanced magnetic resonance imaging, the tumor was obviously intensified. We found 26 patients with bony destruction, and 8 lesions revealed the correct tumor origin.

CONCLUSIONS

A polyp-like mass in the sphenoethmoidal recess strongly implied the diagnosis of an IP in the sphenoid sinus. Bony destruction on computed tomography is a common characteristic of this disease and had a close relationship with the original tumor site in our study. Malignant transformation of IPs in the sphenoid sinus is much scarcer.

摘要

背景

蝶窦孤立性内翻性乳头状瘤(IP)较为罕见,英文文献报道约50例。因其罕见性,科学家们对蝶窦起源的孤立性IP的临床及影像学特征关注较少。

方法

我们描述了3例蝶窦孤立性IP的临床表现、影像学表现及手术方法,并回顾了1970年至2011年的英文文献。

结果

总共报道了59例蝶窦孤立性IP(包括我们的病例),40例患者有计算机断层扫描或磁共振成像细节。最常见的表现是头痛。26例病变位于蝶筛隐窝。8例行增强磁共振成像的患者中,肿瘤明显强化。我们发现26例有骨质破坏,8个病变显示了正确的肿瘤起源。

结论

蝶筛隐窝内的息肉样肿块强烈提示蝶窦IP的诊断。计算机断层扫描显示的骨质破坏是本病的常见特征,在我们的研究中与原发肿瘤部位密切相关。蝶窦IP的恶变更为少见。

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