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Vaginal Primary Malignant Melanoma: A Rare and Aggressive Tumor

机译:阴道原发性恶性黑色素瘤:罕见且侵袭性肿瘤

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摘要

Vaginal primary malignant melanoma is a rare and very aggressive tumor. It most commonly occurs in postmenopausal women, with a mean age of 57 years. Our patient is an 80-year-old, postmenopausal Greek woman presented with a complaint of abnormal vaginal bleeding. On gynecologic examination there was a pigmented, raised, ulcerated, and irregular lesion 5 × 4.5 cm in the upper third of anterior vaginal wall. She underwent a wide local excision of the lesion. The histopathology revealed vaginal primary malignant melanoma with ulceration and no clear surgical margins. She denied any additional surgical interventions and underwent to postoperative adjuvant radiotherapy. Follow up 5 months after initial diagnosis revealed no evidence of local recurrence or distant metastasis. The prognosis of vaginal primary malignant melanoma is very poor despite treatment modality, because most of the cases are diagnosed at advanced stage. Particularly patients with no clear surgical margins and tumor size >3 cm needed postoperative adjuvant radiotherapy.
机译:阴道原发性恶性黑色素瘤是一种罕见且非常具有侵略性的肿瘤。它最常见于绝经后妇女,平均年龄为57岁。我们的患者是一名80岁的绝经后希腊女性,主诉阴道异常出血。在妇科检查中,阴道前壁的上三分之一处有一个色素沉着,凸起,溃疡和不规则的病变,面积5×4.5 cm。她对病变进行了广泛的局部切除。组织病理学显示阴道原发性恶性黑色素瘤有溃疡,没有明确的手术切缘。她否认有任何其他手术干预措施,并接受了术后辅助放疗。初步诊断后5个月进行随访,未发现局部复发或远处转移的迹象。尽管有治疗方式,但阴道原发性恶性黑色素瘤的预后很差,因为大多数病例都是在晚期诊断出来的。特别是没有明确的手术切缘且肿瘤大小> 3 cm的患者需要术后辅助放疗。

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