Solitary Metastasis in the Tibia as a Feature of Primary Squamous Vaginal Carcinoma

Q4 Medicine
Jelena Pavić Mamula, L. Tkalčić, D. Miletic, D. Veljković Vujaklija
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引用次数: 0

Abstract

Aim: Primary vaginal cancer is rare, comprising about 3% of all gynaecological malignancies. Solitary bone metastases to appendicular skeleton are extremely rare and there are only few published reports. We report the case of isolated metastasis in the tibia as a feature of primary squamous vaginal carcinoma. We present this case because of its rarity and for documentation and discussion purposes. Case report: We present a case of a 44-year old woman diagnosed with squamos vaginal cancer in June 2015. Computed tomography of the thorax, abdomen and pelvis revealed no distant metastases. She was treated with interstitial intracavitary brachytherapy and concomitant chemoradiotherapy. In March 2016 she was admitted to our hospital because of the swelling and the pain in the lower right leg. There was no history of trauma and plain radiographs were normal. Two months later, after further progression of pain, plain radiographs showed intramedullary permeative bone lesion with cortical disruption of tibial dyaphisis and local soft tissue swelling. MRI and core needle biopsy confirmed vaginal cancer metastasis containing tumor cells identical to the primary tumor. The patient was treated with radiotherapy and chemotherapy. Despite the treatment there was further progression of the disease with multiple bone metastases and eventually lung and brain metastases. Conclusion: This case report is another reminder that although extremely rare, solitary metastatic bone lesions of vaginal cancer are possible. Since symptoms mimic various benign conditions, it is important to consider bone metastasis as possible diagnosis in patients with progressive bone pain not responding to analgesic treatment.
胫骨单发转移是原发性阴道鳞状癌的一个特征
目的:原发阴道癌是罕见的,约占所有妇科恶性肿瘤的3%。孤立的骨转移到附肢骨骼是非常罕见的,只有少数发表的报道。我们报告的情况下,孤立转移在胫骨作为原发鳞状阴道癌的一个特点。我们提出这种情况,因为它的罕见性和文档和讨论的目的。病例报告:我们报告一位44岁女性,于2015年6月被诊断为阴道鳞状细胞癌。胸部、腹部和骨盆的计算机断层扫描未发现远处转移。她接受了间质腔内近距离放疗和同步放化疗。2016年3月因右下肢肿胀疼痛入住我院。无外伤史,x线平片正常。2个月后,疼痛进一步恶化,x线平片显示髓内穿透性骨病变伴胫骨失稳皮质破坏和局部软组织肿胀。MRI和穿刺活检证实阴道癌转移,肿瘤细胞与原发肿瘤相同。病人接受了放疗和化疗。尽管接受了治疗,但病情仍进一步发展为多发性骨转移,最终出现肺和脑转移。结论:本病例报告再次提醒我们,尽管极其罕见,但阴道癌的单独转移性骨病变是可能的。由于症状类似于各种良性疾病,因此在对止痛治疗无反应的进行性骨痛患者中,考虑骨转移作为可能的诊断是很重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicina Fluminensis
Medicina Fluminensis Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
34
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