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首页> 外文期刊>Case Reports in Oncology >Vaginal Lymphoma with Immune Thrombocytopenic Purpura: An Unusual Case Report
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Vaginal Lymphoma with Immune Thrombocytopenic Purpura: An Unusual Case Report

机译:伴免疫性血小板减少性紫癜的阴道淋巴瘤:不寻常的病例报告

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摘要

The female genital tract is rarely the initial site of presentation in lymphoma or leukemia. We report a case of non-Hodgkin’s lymphoma (NHL) presenting initially in the vagina. The patient, a 75-year-old woman, had a history of immune thrombocytopenic purpura (ITP). She presented with a chief complaint of genital bleeding and introital pain. On transvaginal ultrasonography, a vaginal tumor with an irregular wall was detected, and the internal echo showed a hypoechoic and echogenic pattern. Ultrasonography and magnetic resonance imaging (MRI) suggested that the vaginal tumor was likely to be a hematoma or a hemorrhagic tumor arising from ITP. Incision and resection for a hematoma or a hemorrhagic tumor were carried out in response to genital bleeding, introital pain, and pathological diagnosis. Postoperative microscopic examination confirmed that the tumor was a vaginal NHL. The final diagnosis using the Ann Arbor staging system was high-stage (stage IV) NHL. The patient received chemotherapy, and she remains in remission for 42 months after treatment.
机译:女性生殖道很少是淋巴瘤或白血病中出现的最初部位。我们报告了最初出现在阴道中的非霍奇金淋巴瘤(NHL)病例。该患者为75岁的女性,有免疫性血小板减少性紫癜(ITP)病史。她主诉生殖器出血和肛门疼痛。经阴道超声检查,发现阴道壁壁不规则,内部回声呈低回声和回声模式。超声和磁共振成像(MRI)提示阴道肿瘤很可能是ITP引起的血肿或出血性肿瘤。血肿或出血性肿瘤的切开和切除是针对生殖器出血,腹痛和病理诊断而做出的。术后显微镜检查证实该肿瘤是阴道NHL。使用Ann Arbor分期系统进行的最终诊断是高阶段(IV期)NHL。该患者接受了化疗,治疗后仍保持缓解42个月。

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