婴幼儿鼻内型神经胶质细胞瘤1例
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1.郑州大学附属儿童医院 河南省儿童医院郑州儿童医院;2.河南省儿童医院郑州儿童医院

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河南省医学科技攻关 LHGJ20220717


1 case of infants and young children intranasal glioma cell
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[Department of Otorhinolaryngology Head and Neck Surgery,Children’s Hospital Affiliated of Zhengzhou University Henan Provincial Children’s Hospital Zhengzhou Children’s Hospital,Zhengzhou

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    摘要:

    目的:提高对鼻内型神经胶质细胞瘤的认识,减少误诊。方法:收集我院1例婴幼儿鼻内型神经胶质细胞瘤病例资料,查询并复习国内外神经胶质细胞瘤相关文献。结果:鼻内型神经胶质细胞瘤主要症状是鼻塞,鼻腔内可见灰白色半透明样新生物。其多见于婴幼儿,可伴随喂养困难,不具有家族遗传性。该病需与鼻息肉和脑膜膨出相鉴别,主要治疗方法为手术切除,经病理学诊断可确诊。结论:新生儿或婴幼儿持续性鼻塞伴有新生物时在排除脑膜脑膨出后应考虑到鼻内型神经胶质细胞瘤的可能,结合病史,完善影像学及内镜等相关检查,尽早手术可避免骨和颅面部畸形,减少术后并发症的发生。

    Abstract:

    Objective: To improve the understanding of intranasal glioma cell and reduce misdiagnosis. Methods: collected from 1 case of infants and young children intranasal glioma cell cases data, query and review the intranasal glioma cell related literature at home and abroad.Results: intranasal glioma cell main symptom is stuffy nose,gray-white translucent neoplasms were seen in the nasal cavity. Its more than seen in infants and young children, can accompany feeding difficulties, do not have familial transmissibility. With nasal polyps and bulging meningocele identify the disease, the main treatment is surgical resection, pathological diagnosis can be confirmed.Conclusions: In neonates or infants with persistent nasal obstruction and neoplasms , when meningoencephalocele is excluded, the possibility of intranasal glioma cell should be considered. Combined with medical history, perfect imaging and endoscopy and other related examinations, early surgery can avoid bone and craniofacial deformities and reduce the occurrence of postoperative complications.

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  • 收稿日期:2024-06-17
  • 最后修改日期:2024-07-07
  • 录用日期:2024-07-08
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