Tamura Ryosuke, Yokoyama Yoshihito, Kobayashi Asami, Osawa Yuuki, Shigeto Tatsuhiko, Futagami Masayuki, Mizunuma Hideki
Department of Obstetrics and Gynecology, Hirosaki University Graduate School of Medicine Japan.
Rare Tumors. 2013 Dec 5;5(4):e58. doi: 10.4081/rt.2013.e58. eCollection 2013.
Primary small cell carcinoma of the vagina is quite rare, and a standard treatment has not been established yet. Herein, we report a case of an 81-year-old woman who was diagnosed with a vaginal tumor without continuity with the uterine cervix. Histopathological diagnosis indicated alveolar solid growth of nuclear chromatin-rich atypical cells with a high N/C ratio and a partially recognized rosette-like structure, suggesting a differentiated neuroendocrine system. Chromogranin A and synaptophysin were positive. Stage I vaginal small cell carcinoma localized to the vagina was diagnosed. The tumor disappeared by radiation monotherapy with external beam irradiation and endocavitary irradiation. The patient remains alive without any disease 1 year and 8 months after the treatment, suggesting the efficacy of radiotherapy in small cell carcinoma of the vagina.
原发性阴道小细胞癌非常罕见,目前尚未确立标准治疗方案。在此,我们报告一例81岁女性,被诊断为阴道肿瘤,与子宫颈无连续性。组织病理学诊断显示,核染色质丰富的非典型细胞呈肺泡实性生长,核质比高,部分可见玫瑰花结样结构,提示为分化型神经内分泌系统。嗜铬粒蛋白A和突触素呈阳性。诊断为局限于阴道的I期阴道小细胞癌。通过外照射和腔内照射的放射单一疗法,肿瘤消失。治疗后1年8个月,患者仍存活且无任何疾病,提示放射治疗对阴道小细胞癌有效。