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骨纤维结构不良样骨化性嗅神经母细胞瘤:罕见变异型,易与纤维结构不良混淆。

Hyperostotic esthesioneuroblastoma: rare variant and fibrous dysplasia mimicker.

机构信息

Neuroradiology Section, Imaging Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.

Director of Facial Plastic and Reconstructive Surgery, Associate Professor of Otolaryngology, UCSF School of Medicine, San Fransisco, CA 94143, USA.

出版信息

Korean J Radiol. 2014 Jan-Feb;15(1):156-60. doi: 10.3348/kjr.2014.15.1.156. Epub 2014 Jan 8.

Abstract

A 65-year-old male presented with a 3-year history of orbital symptoms. An imaging-based diagnosis of fibrous dysplasia involving the skull base was made at another institution. CT showed a diffuse sinonasal mass and ground-glass appearance of the bones of the anterior skull base with bony defects and mucocele formation. MRI demonstrated an accompanying intracranial and orbital rind of soft tissue mass along the hyperostotic bones. FDG-PET showed corresponding intense hypermetabolism. Small cysts were observed at the tumor-brain interface. Biopsy revealed esthesioneuroblastoma with bone infiltration that is compatible with the hyperostotic variant of esthesioneuroblastoma. There are a few cases of hyperostotic esthesioneuroblastoma reported in the literature.

摘要

一位 65 岁男性,以 3 年的眶症状就诊。另一医疗机构基于影像学诊断为累及颅底的纤维结构不良。CT 显示弥漫性鼻旁窦肿块和前颅底骨的磨玻璃样外观,伴有骨缺损和黏液囊肿形成。MRI 显示沿骨肥厚的颅腔和眶周软组织肿块。FDG-PET 显示相应的强烈高代谢。在肿瘤-脑界面观察到小囊肿。活检显示伴有骨浸润的嗅神经母细胞瘤,符合嗅神经母细胞瘤的骨肥厚型。文献中有少数几例骨肥厚型嗅神经母细胞瘤的报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f08c/3909850/8995e86e2ef9/kjr-15-156-g001.jpg

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