多学科方法治疗极罕见的阴道子宫纵隔肉瘤--病例报告

Evelina-Elena Stoica, L. Bohiltea, Adrian Dumitru, Cătălin Aliuș, M. Cirstoiu
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引用次数: 0

摘要

原发性阴道肉瘤是妇科疾病中极为罕见的恶性肿瘤。我们介绍了一例 53 岁患者的病例,该患者无妇科疾病史或相关合并症,因绝经期反复阴道出血而就诊。我们要强调的是诊断管理的重要性,从局部妇科检查到阴道活检的所有必要步骤都要进行,并通过先进的成像技术优化结果。组织病理学诊断确定为阴道良性肌瘤后,由妇科医生、外科医生和肿瘤学家组成的多学科委员会讨论了治疗方法。结果,患者在就诊后较快地接受了量身定制的手术治疗,随后转诊至肿瘤科,目前正在接受第三个疗程的辅助化疗。我们目前的目标是对患者进行长期随访,获取有关其生存和生活质量的数据。这些事实可能有助于今后针对这种罕见疾病实施标准化治疗指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Multidisciplinary Approach to Vaginal Leiomyosarcoma, an Extremely Rare Diagnosis - Case Report
Primary vaginal sarcoma is an extremely rare malignant condition within the field of gynecological pathologies. We present the case of a 53-year old patient with no history of gynecological issues or associated comorbidities who presented to our clinic with recurrent vaginal bleeding during menopause. We want to emphasize the importance of diagnostic management, going through all the necessary steps from local gynecological examination to vaginal biopsy, optimizing results with advanced imaging techniques. Once the histopathological diagnosis of vaginal leiomyosarcoma was established, the therapeutic approach was discussed within a multidisciplinary committee consisting of a gynecologist, surgeon, and oncologist. As a result, the patient underwent tailored surgical intervention relatively quickly after presentation, followed by referral to the oncology department, where she is currently undergoing her third course of adjuvant chemotherapy. Our current objective is the long-term follow-up of the patient and the acquisition of data regarding her survival and quality of life. These facts may contribute in the future to the implementation of standardized therapeutic guidelines for such a rare condition
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