Chen Runzhe, Yu Zhengping, Zhang Hongming, Ding Jiahua, Chen Baoan
Department of Hematology and Oncology (Key Department of Jiangsu Medicine), Zhongda Hospital, Medical School, Southeast University, Nanjing, Jiangsu Province, People's Republic of China.
Onco Targets Ther. 2015 Jan 29;8:265-8. doi: 10.2147/OTT.S78171. eCollection 2015.
Primary malignant lymphoma of the uterus and broad ligament is rare. Here, we present a rare case of primary diffuse large B-cell lymphoma (DLBCL) of uterus and broad ligament in a 63-year-old female. The patient presenting with lower abdominal distention was referred to our hospital. Subsequent abdominal and pelvic ultrasound revealed the presence of a large mass, which was highly suspected as subserosal uterine leiomyoma. A large tumor was found with unclear boundary with right posterior wall, broad ligament and bilateral adnexa during surgery. Her uterus and the tumor of a broad ligament and bilateral adnexa were all excised as a result. Postoperative pathological examination showed DLBCL in uterus and broad ligament. Further examinations excluded metastatic diseases, which supported the diagnosis of primary DLBCL of the uterus and broad ligament. The patient received six cycles of R-CHOP (21 days) regimen. During the 8 months follow-up, no evidence of disease recurrence was identified. As the prevalence of primary extranodal lymphoma is increasing, the details of this rare case may highlight the importance and facilitate treatment of similar diseases. A summary focusing on the presentation and prognosis as well as a review of current management is also discussed.
原发性子宫和阔韧带恶性淋巴瘤较为罕见。在此,我们报告一例63岁女性原发性子宫和阔韧带弥漫性大B细胞淋巴瘤(DLBCL)的罕见病例。该患者因下腹胀就诊于我院。随后的腹部和盆腔超声检查发现一个大肿块,高度怀疑为浆膜下子宫肌瘤。手术中发现一个大肿瘤,与右后壁、阔韧带和双侧附件边界不清。因此,切除了她的子宫、阔韧带肿瘤及双侧附件。术后病理检查显示子宫和阔韧带存在DLBCL。进一步检查排除了转移性疾病,支持原发性子宫和阔韧带DLBCL的诊断。患者接受了六个周期的R-CHOP(21天)方案治疗。在8个月的随访中,未发现疾病复发迹象。由于原发性结外淋巴瘤的患病率在增加,该罕见病例的细节可能会凸显类似疾病的重要性并有助于其治疗。本文还讨论了该病例的临床表现、预后总结以及当前治疗方法的综述。