Hayama M, Niitsu N, Tamaru J, Higashihara M
Department of Hematology and Internal Medicine, Kitasato University School of Medicine.
Rinsho Ketsueki. 2001 Jul;42(7):565-70.
Primary vaginal non-Hodgkin's lymphomas (NHL) are rare, and are clinically difficult to differentiate from inflammatory diseases or vaginal cancer. Here, we present such a case in a 74-year-old woman complaining of fever and difficulty with urination. Pelvic examination revealed a tumor involving most of the vaginal wall, and pelvic MRI demonstrated vaginal wall thickening. A biopsy of this lesion confirmed NHL (diffuse large B-cell lymphoma), and the patient was admitted. Abdominal CT and MRI detected a vaginal tumor, and Ga scintigraphy confirmed accumulation in the pelvis, but no abnormalities were seen in other areas. Therefore, the patient was diagnosed as having NHL at clinical stage IB with low-intermediate risk (international prognosis index) (LDH 1,309 IU/L). The patient underwent three courses of CHOP therapy followed by radiotherapy, and complete remission was achieved. Primary vaginal NHL often affects women younger than 50 years of age, and abnormal hemorrhage is the initial symptom in many cases. There have been a number of reports of long-term survival following appropriate early chemotherapy and radiation therapy, suggesting that early diagnosis and treatment based on vaginal biopsy findings greatly influence the prognosis.
原发性阴道非霍奇金淋巴瘤(NHL)较为罕见,临床上很难与炎症性疾病或阴道癌相鉴别。在此,我们报告一例74岁女性患者,主诉发热和排尿困难。盆腔检查发现肿瘤累及大部分阴道壁,盆腔磁共振成像(MRI)显示阴道壁增厚。该病变活检确诊为NHL(弥漫大B细胞淋巴瘤),患者入院。腹部CT和MRI检测到阴道肿瘤,镓闪烁扫描证实盆腔有放射性聚集,但其他部位未见异常。因此,该患者被诊断为临床ⅠB期低中危NHL(国际预后指数)(乳酸脱氢酶[LDH] 1309 IU/L)。患者接受了3个疗程的CHOP化疗,随后进行放疗,实现了完全缓解。原发性阴道NHL常发生于50岁以下女性,许多病例的初始症状为异常出血。有多项关于早期进行适当化疗和放疗后长期生存的报道,提示基于阴道活检结果的早期诊断和治疗对预后有很大影响。