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眶神经鞘黏液瘤伴眼外肌受累:1例罕见病例

Orbital nerve seath myxoma with extraocular muscle involvement: a rare case.

作者信息

Rodríguez-Uña Ignacio, Troyano-Rivas Juan A, González-García Cristina, Chícharo-de-Freitas Reinaldo, Ortiz-Zapata Juan J, Ortega-Medina Luis, Toledano-Fernández Nicolás, García-Feijoo Julián

机构信息

Department of Ophthalmology, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC) , Madrid , Spain .

出版信息

Semin Ophthalmol. 2015 Jul;30(4):316-20. doi: 10.3109/08820538.2013.874471. Epub 2014 Jan 29.

Abstract

A 66-year-old woman with breast cancer presented with a painless mass in the left orbit. MRI revealed a well-defined intraconal mass in the temporal quadrant of the orbit. Fifteen months later, a further MRI indicated the mass had grown, displacing the left optic nerve and making contact with the lateral rectus muscle, suggesting its possible intramuscular origin. Despite the clinical and radiological characteristics of the lesion and its slow growth, a PET/CT study was developed because of the history of malignant disease. No metabolic activity of the mass or malignant lesion in other locations was observed. After surgical excision, histopathological examination revealed an abundant myxoid matrix with few spindle-shaped cells and no signs of malignancy. The cells were immunopositive for CD34, positive for S-100 protein, and negative for EMA, actin, and CD57. A diagnosis was made of a nerve sheath myxoma. The orbital location of these tumors is extremely rare.

摘要

一名66岁的乳腺癌女性患者出现左侧眼眶无痛性肿块。磁共振成像(MRI)显示眼眶颞侧象限内有一个边界清晰的肌锥内肿块。15个月后,进一步的MRI检查显示肿块增大,压迫左侧视神经并与外直肌接触,提示其可能起源于肌肉内。尽管该病变具有临床和放射学特征且生长缓慢,但鉴于患者有恶性疾病史,仍进行了正电子发射断层扫描/计算机断层扫描(PET/CT)检查。未观察到肿块或其他部位有恶性病变的代谢活性。手术切除后,组织病理学检查显示有丰富的黏液样基质,梭形细胞较少,无恶性迹象。细胞CD34免疫阳性,S-100蛋白阳性,上皮膜抗原(EMA)、肌动蛋白和CD57阴性。诊断为神经鞘黏液瘤。这些肿瘤在眼眶部位极为罕见。

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