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宫颈原发性恶性黑色素瘤:一种罕见疾病。

Primary malignant melanoma of the cervix: a rare disease.

作者信息

Julião Ivo, Carvalho Sonia Dias, Patricio Vanda, Raimundo Ana

机构信息

Medical Oncology, Instituto Português de Oncologia do Porto Francisco Gentil, Porto, Portugal.

Department of Pathology, Instituto Português de Oncologia do Porto Francisco Gentil, Porto, Portugal.

出版信息

BMJ Case Rep. 2017 Apr 21;2017:bcr-2017-219361. doi: 10.1136/bcr-2017-219361.

Abstract

Malignant melanoma (MM) arising primarily in the cervix is exceedingly rare and has a poor prognosis. We report the case of a primary MM of the cervix in a 64-year-old woman with vaginal bleeding. She presented with a cervical amelanotic lesion which on biopsy rendered the diagnosis of MM. The patient was staged as International Federation of Gynecology and Obstetrics IIB and underwent Wertheim-Meigshysterectomy followed by brachytherapy. One year later, she was diagnosed with a large pelvic relapse for which surgery was performed. She then presented with a vaginal relapse and an isolated hepatic lesion, both of which were proposed for surgery. The diagnosis of MM of the cervix is a clinical and pathological challenge due to its rarity and overlapping features. Cytology cannot accurately diagnose it. Moreover, amelanotic MMs must be distinguished from other poorly differentiated carcinomas by diagnosis that ultimately relies on immunohistochemical staining. Radical surgery is the only treatment showing predictive benefit.

摘要

原发性宫颈癌恶性黑色素瘤(MM)极为罕见,预后较差。我们报告了一例64岁阴道出血女性的原发性宫颈MM病例。她表现为宫颈无黑色素病变,活检后诊断为MM。患者分期为国际妇产科联盟IIB期,接受了Wertheim-Meigs子宫切除术,随后进行近距离放疗。一年后,她被诊断为盆腔大面积复发并接受了手术。之后她又出现阴道复发和孤立性肝转移灶,二者均建议手术治疗。宫颈MM的诊断因其罕见性和特征重叠而成为临床和病理上的挑战。细胞学检查无法准确诊断。此外,无黑色素MM必须通过最终依赖免疫组化染色的诊断与其他低分化癌相鉴别。根治性手术是唯一显示出有预测益处的治疗方法。

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Primary Melanoma of the Cervix Uteri: A Systematic Review and Meta-Analysis of the Reported Cases.
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本文引用的文献

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Primary malignant melanoma of the cervix: report of a case.
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