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起源于脊髓的黏液乳头型室管膜瘤的子宫颈转移

Uterine Cervix Metastasis of Myxopapillary Ependymoma Originated from the Spinal Cord.

作者信息

Güzin Kadir, Bozdağ Halenur, Aydın Abdullah, Şahin Sadık, Özkanlı Şeyma

机构信息

Department of Obstetrics and Gynecology, İstanbul Medeniyet University Göztepe Training and Research Hospital, İstanbul, Turkey.

Department of Pathology, İstanbul Medeniyet University Faculty of Medicine, İstanbul, Turkey.

出版信息

Balkan Med J. 2016 Mar;33(2):235-8. doi: 10.5152/balkanmedj.2015.151101. Epub 2016 Mar 1.

Abstract

BACKGROUND

Myxopapillary ependymomas are well differentiated low-grade tumors which have been documented to local or distant metastasis. In the literature, this is a unique case of myxopapillary ependymoma with metastasis to the uterine cervix. Here, we present a rare case of extra neural metastasis of spinal ependymoma that developed over a long period.

CASE REPORT

A 34-year-old woman was referred to our hospital for pelvic mass. A mass (110×100 mm) localized between the sacrococcygeal region and the uterus was detected by magnetic resonance imaging. In 2004, she had been operated upon for myxopapillary ependymoma seated in the sacrococcygeal region for the first time. She underwent tumor resection eight times due to the recurrence of spinal tumor in the same region in nine years. Under the diagnosis of uterine neoplasm, we carried out radical hysterectomy, omentectomy and pelvic lymphadenectomy as the surgical procedure. The pathological findings were reported as myxopapillary ependymoma. Immunohistochemically, the myxopapillary ependymal cells showed strong positivity for glial fibrillary acidic protein, whereas they were negative for low molecular weight cytokeratin. The Ki-67 labeling index was about 2-3%. The patient had an uneventful postoperative period. She has remained free of symptoms in the year since surgery.

CONCLUSION

Extra-spinal myxopapillary ependymoma is very rare, but it must be considered in the differential diagnosis of pelvic mass lesions.

摘要

背景

黏液乳头型室管膜瘤是分化良好的低级别肿瘤,已有文献记载其可发生局部或远处转移。在文献中,这是一例黏液乳头型室管膜瘤转移至子宫颈的独特病例。在此,我们报告一例长期发生的脊髓室管膜瘤神经外转移的罕见病例。

病例报告

一名34岁女性因盆腔肿物被转诊至我院。磁共振成像检测到一个位于骶尾区域与子宫之间的肿物(110×100毫米)。2004年,她首次因骶尾区域的黏液乳头型室管膜瘤接受手术。由于同一区域脊髓肿瘤在9年内复发,她接受了8次肿瘤切除术。在诊断为子宫肿瘤后,我们实施了根治性子宫切除术、大网膜切除术和盆腔淋巴结清扫术作为手术操作。病理检查结果报告为黏液乳头型室管膜瘤。免疫组织化学检查显示,黏液乳头型室管膜细胞胶质纤维酸性蛋白呈强阳性,而低分子量细胞角蛋白呈阴性。Ki-67标记指数约为2%-3%。患者术后恢复顺利。自手术以来,她在这一年中一直没有症状。

结论

脊髓外黏液乳头型室管膜瘤非常罕见,但在盆腔肿物病变的鉴别诊断中必须予以考虑。

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