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表现为贝尔麻痹的播散性神经母细胞瘤:一例报告

Presentation of disseminated neuroblastoma mimicking Bell's palsy: a case report.

作者信息

Gunawardana Shamaali, Jogaprajahpan Geerthana, Dayasiri Kavinda

机构信息

Postgraduate Institute of Medicine, University of Colombo, Colombo, Sri Lanka.

Faculty of Medicine, University of Kelaniya, Kelaniya, Sri Lanka.

出版信息

J Med Case Rep. 2025 Jan 31;19(1):40. doi: 10.1186/s13256-025-05064-x.

Abstract

BACKGROUND

Neuroblastoma is an embryological malignancy of neural crest cells that may have diverse presentations owing to direct effects, metastases, or paraneoplastic syndromes. Facial nerve palsy is an extremely rare presentation of neuroblastoma.

CASE PRESENTATION

A previously healthy 1-year-and-10-month-old Sinhalese girl presented with difficulty in closing her left eye for 2 weeks, preceded by deviation of her mouth to opposite side. Initial physical examination was normal, apart from left lower-motor-type facial nerve palsy. Initial laboratory investigations were also normal. A tentative diagnosis of Bell's palsy was made. However, magnetic resonance imaging of the brain was performed owing to the incidental detection of a painless bulge in the left zygomatic region with overlying skin bruising, in the absence of any preceding trauma. Magnetic resonance imaging of the brain revealed a soft-tissue mass in the left lateral orbital wall, extending to the body of the sphenoid and bulging into the left anterior fossa. Contrast-enhanced computed tomography of the abdomen, performed subsequently, showed an intra-abdominal large paravertebral soft-tissue mass. Histology of the abdominal mass confirmed poorly differentiated neuroblastoma.

CONCLUSION

Facial nerve palsy is well recognized to have a myriad of underlying etiologies, including hematological malignancies, solid tumors, and paraneoplastic syndromes. However, its timely diagnosis is often challenging in the absence of other supportive clinical features. These children need careful and thorough evaluation for malignancies before commencing steroids, especially when underlying malignancy is likely.

摘要

背景

神经母细胞瘤是一种神经嵴细胞的胚胎性恶性肿瘤,由于直接影响、转移或副肿瘤综合征,可能有多种表现形式。面神经麻痹是神经母细胞瘤极为罕见的一种表现。

病例介绍

一名此前健康的1岁10个月大的僧伽罗族女孩,先是嘴向对侧歪斜,2周后出现左眼闭合困难。除左下面神经运动型麻痹外,初次体格检查正常。初次实验室检查也正常。初步诊断为贝尔氏麻痹。然而,由于在无任何先前外伤的情况下,偶然发现左侧颧区有一无痛性肿块且皮肤有瘀伤,遂进行了脑部磁共振成像检查。脑部磁共振成像显示左侧眶外侧壁有一软组织肿块,延伸至蝶骨体并突入左前颅窝。随后进行的腹部增强计算机断层扫描显示腹内有一巨大的椎旁软组织肿块。腹部肿块的组织学检查证实为低分化神经母细胞瘤。

结论

面神经麻痹有多种潜在病因,包括血液系统恶性肿瘤、实体瘤和副肿瘤综合征,这是广为人知的。然而,在没有其他支持性临床特征的情况下,其及时诊断往往具有挑战性。在开始使用类固醇之前,尤其是在可能存在潜在恶性肿瘤的情况下,这些儿童需要针对恶性肿瘤进行仔细而全面的评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/829e/11783695/c95f3cab9714/13256_2025_5064_Fig1_HTML.jpg

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