Hosing C, Freedman R S, McLaughlin P, Malpica A, Fornage B D, Kudelka A P
Division of Cancer Medicine, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Am J Clin Oncol. 2001 Apr;24(2):204-8. doi: 10.1097/00000421-200104000-00021.
Vaginal involvement in non-Hodgkin's lymphoma is uncommon and is often secondary to disseminated disease. Primary disease at this site is quite rare. We present here an unusual case of a patient who developed a diffuse large B-cell lymphoma presenting as a vaginal mass after having been treated for primary intestinal mucosa-associated lymphoid tissue (MALT) lymphoma 4 years earlier. Combined chemotherapy and radiation therapy for the intestinal MALT lymphoma produced complete remission that lasted for 2 years. Chemotherapy given for the diffuse large B-cell lymphoma with secondary vaginal involvement produced a second complete remission. The second remission was consolidated with high-dose chemotherapy and autologous bone marrow transplantation. Although the patient died from complications related to the transplant procedure, the disease was in complete remission at the time of her death. Given the rarity of primary intestinal MALT lymphoma and primary vaginal lymphoma, no standard treatment has been established. Treatment options have included chemotherapy, radiation therapy, or surgery, given alone or in combination.
阴道受累于非霍奇金淋巴瘤并不常见,且常继发于播散性疾病。该部位的原发性疾病相当罕见。我们在此报告一例不寻常的病例,一名患者在4年前接受原发性肠道黏膜相关淋巴组织(MALT)淋巴瘤治疗后,出现了以阴道肿块为表现的弥漫性大B细胞淋巴瘤。针对肠道MALT淋巴瘤的联合化疗和放疗产生了持续2年的完全缓解。针对继发阴道受累的弥漫性大B细胞淋巴瘤进行的化疗产生了第二次完全缓解。第二次缓解通过大剂量化疗和自体骨髓移植得以巩固。尽管患者死于与移植手术相关的并发症,但在她去世时疾病处于完全缓解状态。鉴于原发性肠道MALT淋巴瘤和原发性阴道淋巴瘤的罕见性,尚未确立标准治疗方案。治疗选择包括单独或联合使用化疗、放疗或手术。