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2型神经纤维瘤病自然病史研究联盟受试者的前庭神经鞘瘤生长速率

Vestibular schwannoma growth rates in neurofibromatosis type 2 natural history consortium subjects.

作者信息

Slattery William H, Fisher Laurel M, Iqbal Zarina, Oppenhiemer Mark

机构信息

House Ear Institute, Los Angeles, California 90057, USA.

出版信息

Otol Neurotol. 2004 Sep;25(5):811-7. doi: 10.1097/00129492-200409000-00027.

Abstract

OBJECTIVE

To determine the amount of growth in vestibular schwannomas in Neurofibromatosis type 2 (NF2) patients from diagnosis through short-term (up to 2 yr) and long-term (up to 4 yr) follow-up.

STUDY DESIGN

Retrospective magnetic resonance imaging (MRI) films were obtained on subjects enrolled in the NF2 Natural History study and examined for changes in vestibular schwannoma size over time.

SETTING

Data were collected from nine foreign and domestic NF2 centers, including hospital-based, academic, and tertiary care centers.

SUBJECTS

NF2 patients with MRI data and at least one follow-up examination within 9 months to 2 years of diagnosis were included; n=56 patients with 84 lesions for evaluation of growth.

INTERVENTION

Routine, clinically obtained, magnetic resonance images were digitized and measured using image management software. Short-term follow-up was defined as up to 2 years (n=84 lesions), and long-term follow-up was defined as 3 to 4 years (n=29 lesions).

OUTCOME MEASURES

Vestibular schwannoma size was assessed using anterior-posterior, medial-lateral, and greatest diameter linear measurements.

RESULTS

Vestibular schwannomas increased in size (at least 5 mm) in 8% of the vestibular schwannomas across short-term follow-up. At long-term follow-up, 13% of the tumors had increased in size. On average, schwannomas increased in greatest diameter 1.3 mm per year across short-term follow-up.

CONCLUSION

Slightly greater than 1 in 10 diagnosed NF2-related vestibular schwannomas increased in size by at least 5 mm by 4 years of follow-up, if still untreated at that time.

摘要

目的

确定2型神经纤维瘤病(NF2)患者从诊断到短期(最长2年)和长期(最长4年)随访期间前庭神经鞘瘤的生长量。

研究设计

对纳入NF2自然病史研究的受试者进行回顾性磁共振成像(MRI)检查,并观察前庭神经鞘瘤大小随时间的变化。

研究地点

数据收集自9个国内外NF2中心,包括医院、学术和三级护理中心。

研究对象

纳入有MRI数据且在诊断后9个月至2年内至少进行过一次随访检查的NF2患者;56例患者共84个病灶用于生长评估。

干预措施

将常规临床获得的磁共振图像数字化,并使用图像管理软件进行测量。短期随访定义为最长2年(84个病灶),长期随访定义为3至4年(29个病灶)。

观察指标

使用前后径、内外径和最大直径线性测量来评估前庭神经鞘瘤大小。

结果

在短期随访中,8%的前庭神经鞘瘤大小增加(至少5mm)。在长期随访中,13%的肿瘤大小增加。短期随访期间,神经鞘瘤平均最大直径每年增加1.3mm。

结论

如果在诊断后4年仍未治疗,每10例确诊的NF2相关前庭神经鞘瘤中,略多于1例会增大至少至少5mm。

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