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鼻咽血管纤维瘤:简明分类系统与适宜治疗方案。

Nasopharyngeal angiofibroma: a concise classification system and appropriate treatment options.

机构信息

Department of Otolaryngology, First Affiliated Hospital of Fujian Medical University, Fuzhou, China.

出版信息

Am J Otolaryngol. 2013 Mar-Apr;34(2):133-41. doi: 10.1016/j.amjoto.2012.10.004. Epub 2013 Jan 16.

Abstract

OBJECTIVES

To describe a clear and simplified classification system for juvenile nasopharyngeal angiofibroma (JNA), and to describe suitable management options.

STUDY DESIGN

Retrospective medical record review.

METHODS

The clinical and imaging materials of 51 cases of JNA diagnosed at our hospital between 1981 and 2011 were collected and studied. Based on our experiences, we prefer to divide JNAs into three types. Type I includes JNAs fundamentally localized to the nasal cavity, paranasal sinus, nasopharynx, or pterygopalatine fossa. Type II is a JNA extending into the infratemporal fossa, cheek region, or orbital cavity, with anterior and/or minimal middle cranial fossa extension but intact dura mater. Type III is a calabash-like massive tumor lobe in the middle cranial fossa. The management and prognosis for the three types of JNA were compared and evaluated.

RESULTS

Among cases of type I JNA (n=16), the entire mass was removed by the initial operation in 15 cases and by a repeat operation in 1 case. Among cases of type II JNA (n=29), the entire mass was removed by the first operation in 24 cases and by repeat operation in 5 cases. In cases of type III JNA (n=6), the huge calabash-like lobe in the middle cranial fossa could not be completely excised; 4 cases underwent radiotherapy and 2 cases were lost to follow-up.

CONCLUSIONS

  1. The transnasal cavity approach with endoscopic guidance is suitable for type I JNA resection. 2) The transantral-infratemporal fossa-nasal cavity combined approach is reliable for resection of a type II JNA, which extends into the deep anterior cranial fossa and/or minimally into the middle cranial fossa, with intact dura mater. 3) The complete removal of a type III JNA is difficult, even through a combined extracranial and intracranial approach. Radiotherapy is useful for treating the residual intracranial tumor. The successful or failed experiences of 6 typical cases prove that this revised classification system is reasonable and reliable.
摘要

目的

描述一种用于青少年鼻咽血管纤维瘤(JNA)的清晰简化分类系统,并描述适用的治疗选择。

研究设计

回顾性病历回顾。

方法

收集并研究了我院 1981 年至 2011 年间诊断的 51 例 JNA 的临床和影像学资料。基于我们的经验,我们更倾向于将 JNA 分为三型。I 型包括基本局限于鼻腔、鼻窦、鼻咽或翼腭窝的 JNA。II 型是指延伸至颞下窝、面颊区或眼眶,伴前颅窝和/或中颅窝前份局限性扩展但硬脑膜完整的 JNA。III 型是指中颅窝的葫芦状巨大肿瘤叶。比较和评估了这三种类型 JNA 的治疗和预后。

结果

I 型 JNA(n=16)中,15 例患者在初次手术中整块切除肿瘤,1 例患者在重复手术后整块切除肿瘤。II 型 JNA(n=29)中,24 例患者在初次手术中整块切除肿瘤,5 例患者在重复手术后整块切除肿瘤。III 型 JNA(n=6)中,无法完全切除中颅窝巨大葫芦状肿瘤叶;4 例患者接受放疗,2 例患者失访。

结论

1)经鼻内镜引导的经鼻入路适用于 I 型 JNA 的切除。2)经蝶-颞下窝-鼻腔联合入路适用于 II 型 JNA 的切除,该型肿瘤延伸至前颅窝深部和/或中颅窝前份,硬脑膜完整。3)III 型 JNA 完全切除困难,即使采用颅内外联合入路也难以实现。放疗对于治疗残留的颅内肿瘤是有效的。6 个典型病例的成功或失败经验证明,该改良分类系统是合理可靠的。

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