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首页> 外文期刊>Surgical neurology >Choroid plexus papilloma of the cerebellopontine angle: a twelve patient series.
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Choroid plexus papilloma of the cerebellopontine angle: a twelve patient series.

机译:小脑桥脑角的脉络丛乳头状瘤:十二个病人系列。

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BACKGROUND: Choroid plexus papillomas (CPPs), of the cerebellopontine angle (CPA), are a rare entity and no surgical series have been reported so far. We reviewed all the pertinent literature of 12 patients operated on in the last 20 years at our institution. METHODS: All the patients were adults, ranging from 19 to 61 years. The group included 6 males and 6 females. Preoperatively, on computerized tomography (CT) (n = 10) or magnetic resonance imaging (MRI) (n = 4), differential diagnosis was difficult to achieve, especially with meningiomas. Hydrocephalus was disclosed in 8 cases. Angiography (n = 11) showed tumor blush with typical vascular supply in almost half the cases. RESULTS: In 6 patients a midline approach via the cerebellomedullary fissure was used; in the remaining 6 patients the retromastoid route was adopted. We found 2 "unconnected" tumors; no hilum was identified at surgery. Total tumor removal was achieved in 6 patients, predominantly in the last cases. Two patients died in the postoperative period, 3 patients had mild additional deficits, whereas 7 patients were stable or improved. All the patients were followed up for a mean period of 8.2 years. Conventional radiotherapy was carried out in 5 patients; 1 of them after tumor recurrence. Stereotactic radiotherapy was performed in 3 patients; 2 of them after recurrences. Two patients showed tumor progression and died during the follow-up. One of them presented a suprasellar metastasis and died much earlier (2 versus 7 years). CONCLUSION: Careful assessment and surgical planning is accomplished with the combined information from CT, MRI, and angiography. Typical characteristics are the following: vascular supply from the choroidal arteries, ventral extension, adhesion to the brainstem, and lower cranial nerves. Nowadays, total removal of CPPs of the CPA can be achieved with acceptable morbidity and mortality. In our experience, conventional radiotherapy did not prove effective.
机译:背景:桥小脑角(CPA)的脉络丛乳头状瘤(CPP)是一种罕见的实体,迄今为止尚无外科手术报道。我们回顾了过去20年在我们机构接受手术的12例患者的所有相关文献。方法:所有患者均为成年人,年龄在19至61岁之间。该组包括6名男性和6名女性。术前,在计算机断层扫描(CT)(n = 10)或磁共振成像(MRI)(n = 4)上,很难实现鉴别诊断,尤其是脑膜瘤。脑积水8例。血管造影(n = 11)在几乎一半的病例中显示出具有典型血管供应的脸红。结果:6例患者采用中线经脑小脑裂孔入路。其余6例患者采用了后乳突途径。我们发现了2个“未连接”的肿瘤。手术时未发现肺门。 6例患者实现了总的肿瘤切除,主要是最后一批病例。术后有2例患者死亡,3例有轻度的其他缺陷,7例稳定或好转。所有患者均获随访,平均随访8。2年。常规放疗治疗5例;其中1例在肿瘤复发后。 3例患者进行了立体定向放疗。复发后其中2例。两名患者表现出肿瘤进展并在随访期间死亡。其中一名出现了鞍上转移,并较早死亡(2岁对7岁)。结论:结合来自CT,MRI和血管造影的信息,可以进行仔​​细的评估和手术计划。典型特征如下:来自脉络膜动脉的血管供应,腹侧延伸,对脑干的粘附以及下颅神经。如今,可以以可接受的发病率和死亡率完全清除CPA中的CPP。根据我们的经验,常规放疗并未证明有效。

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