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[基于7例治疗病例的嗅神经母细胞瘤的分类与预后]

[Classification and prognosis of esthesioneuroblastoma based on 7 treated cases].

作者信息

Zumegen C, Michel O

机构信息

Klinik und Poliklinik für Hals-Nasen-Ohrenheilkunde der Universität zu Köln.

出版信息

Laryngorhinootologie. 2000 Dec;79(12):736-42. doi: 10.1055/s-2000-9142.

Abstract

BACKGROUND

The esthesioneuroblastoma is a rare tumour of neuroectodermal origin, which arises usually in the area of the olfactory epithelium and invades the paranasal sinuses, the orbit and the brain. The low incidence of this disease makes a development of standardised clinical and histological classification difficult. Up to now this tumour is considered to be slow progressive but strained by a high rate of local recurrences. Metastasis are usually seen late at an advanced stage.

PATIENTS

In the last 18 years 7 patients with an esthesioneuroblastoma were treated in our department. This relatively large number of patients allows a retrospective evaluation of the different already existing classifications concerning treatment and prognosis.

RESULTS AND CONCLUSIONS

In all cases of a disease limited on the paranasal sinuses the patients were successfully treated either by a combination of resection and radiation (4 cases) or resection alone (1 case). No patient underwent a chemotherapy. Two cases with lethal outcome showed an extremely aggressive tumour progression. In such cases of extensive disease an additional chemotherapy has always to be taken into account. Our experiences and the analysis of the literature gives some indications that middle-aged patients have a worse prognosis than young or old patients.

摘要

背景

嗅神经母细胞瘤是一种罕见的神经外胚层起源肿瘤,通常发生于嗅上皮区域,可侵犯鼻窦、眼眶及脑部。该疾病发病率低,难以制定标准化的临床及组织学分类。目前认为该肿瘤进展缓慢,但局部复发率高。转移通常在晚期出现。

患者

在过去18年中,我科共治疗了7例嗅神经母细胞瘤患者。相对较多的患者数量使得我们能够对现有的不同治疗及预后分类进行回顾性评估。

结果与结论

所有局限于鼻窦的病例,患者均通过手术切除联合放疗(4例)或单纯手术切除(1例)成功治疗。无一例患者接受化疗。2例死亡病例显示肿瘤进展极为迅速。对于此类广泛病变的病例,总是需要考虑额外进行化疗。我们的经验及文献分析表明,中年患者的预后比年轻或老年患者更差。

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