首页> 外文期刊>The journal of obstetrics and gynaecology research >Lymphoepithelioma-like carcinoma of the vagina: A rare case report and review of the literature
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Lymphoepithelioma-like carcinoma of the vagina: A rare case report and review of the literature

机译:阴道的淋巴素样癌:一个罕见的案例报告和对文献的审查

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摘要

A 78-year-old woman with the chief complaint of vaginal bleeding was referred to our institution. Pelvic magnetic resonance imaging showed a 2.1 cm x 2.0 cm soft tissue mass in the left vaginal area with left inguinal lymph node enlargement. A positron emission tomography/computer tomography scan showed a focal hypermetabolic lesion in the left vaginal area with involvement of vulvar area. Pelvic examination showed a vaginal wall mass and the patient underwent surgical excision of the mass. The results of pathology indicated lymphoepithelioma-like carcinoma (LELC) in the vagina. The patient was admitted subsequently in the oncological department for additional chemoradiation treatment. LELC is extremely rare in the vagina, and only three cases have been reported in the literature. Here we report an extremely rare case of this tumor and review of the previous literature.
机译:一位以阴道出血为主诉的78岁女性被转诊到我们的机构。盆腔磁共振成像显示左侧阴道区域有一个2.1厘米x 2.0厘米的软组织肿块,伴有左侧腹股沟淋巴结肿大。正电子发射断层扫描/计算机断层扫描显示左侧阴道区域有局灶性高代谢病变,累及外阴区域。盆腔检查显示阴道壁肿块,患者接受了手术切除。病理结果显示阴道内有淋巴上皮瘤样癌(LELC)。该患者随后在肿瘤科接受了额外的放化疗。LELC在阴道中极为罕见,文献中仅报告了三例。我们在此报告一例极为罕见的肿瘤病例,并回顾以往的文献。

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