Suppr超能文献

[内淋巴囊肿瘤(ELST)的肿瘤分期手术]

[Tumour staged surgery of endolymphatic sac tumors (ELST)].

作者信息

Schipper J, Maier W, Rosahl S, Berlis A, Laszig R

机构信息

Universitätsklinik für Hals-, Nasen- und Ohrenheilkunde und Poliklinik, Universitätsklinikum Freiburg.

出版信息

Laryngorhinootologie. 2004 Aug;83(8):493-500. doi: 10.1055/s-2004-814395.

Abstract

BACKGROUND

Endolymphatic sac tumours (ELST) have only been known as own tumour entities since 1984. ELST might occur solitarily and sporadically as well as hereditary connected to von Hippel-Lindau disease (VHL). This connection has been observed in 1992 for the first time and confirmed by molecular genetic analyses of the VHL gen. There is no agreement yet concerning diagnostics and therapy.

METHODS

Our attempt of classifying this type of tumour is the first one. According to our own experience and to literature, we suggest the following classification: ELST type A is locally confined without erosions of the temporal bone nor infiltration of the subarachnoidal area; ELST type B with bony infiltration of the labyrinth block and clinical hearing loss, and ELST type C with additional infiltration of the sigmoid sinus and the vein of jugular bulb. Preoperative diagnostics are performed according to defined radiological criteria in CT and MRI scans including MR-angiography.

RESULTS

In 6 patients, including two with a VHL syndrome, ELST was completely sanitized by stage-compatible surgery, using translabyrintine to infratemporal approaches, according to the tumour classification that we developed. The VII (th) nerve could be saved in all tumour stages, and in stage ELST type A the VIII (th) nerve as well. All patients remained without local recurrence in MRI check during the observation period of 4 to 38 months.

CONCLUSION

Our stage-compatible surgery of ELST allows total tumor removal with minor morbidity. In contrast to the antero-, retrosigmoidal and suboccipital approaches, the tumour matrix can be safely removed via transmastoidal approach to exclude local recurrences.

摘要

背景

自1984年以来,内淋巴囊肿瘤(ELST)才被认为是独立的肿瘤实体。ELST可能单独、散发性出现,也可能与冯·希佩尔-林道病(VHL)相关的遗传性疾病有关。这种关联于1992年首次被观察到,并通过VHL基因的分子遗传学分析得到证实。关于诊断和治疗尚未达成共识。

方法

我们对这类肿瘤进行分类的尝试尚属首次。根据我们自己的经验和文献,我们建议如下分类:A型ELST局限于局部,无颞骨侵蚀及蛛网膜下腔浸润;B型ELST伴有迷路骨块浸润及临床听力丧失;C型ELST伴有乙状窦及颈静脉球静脉的额外浸润。术前诊断根据CT和MRI扫描(包括磁共振血管造影)中确定的放射学标准进行。

结果

在6例患者中,包括2例患有VHL综合征的患者,根据我们制定的肿瘤分类,采用经迷路至颞下的手术入路,通过与分期相适应的手术,ELST被完全清除。在所有肿瘤分期中,面神经均可保留;在A型ELST分期中,听神经也可保留。在4至38个月的观察期内,所有患者在MRI检查中均未出现局部复发。

结论

我们对ELST进行的与分期相适应的手术能够在低发病率的情况下实现肿瘤全切。与前、乙状窦后和枕下手术入路不同,通过经乳突手术入路可以安全地切除肿瘤基质以排除局部复发。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验