Department of Gynecology, Affiliated Hospital of Jining Medical University, Jining Medical University.
School of Clinical Medicine Jining Medical University, Shandong, China.
Medicine (Baltimore). 2021 Jan 22;100(3):e24049. doi: 10.1097/MD.0000000000024049.
Primary female genital tract lymphomas are sporadic neoplasms, accounting for 0.2% to 1.1% of all cases of extranodal lymphoma. The most common genital localizations are the cervix, the uterine corpus and the ovary, while primary lymphomas of the fallopian tube are quite unusual. According to literature searching in PubMed, this is the first reported case of primary diffuse large B-cell lymphoma of the fallopian tube.
A 52-year-old woman presented with a more than 2 months history of intermittent lower abdominal pain. The gynecological examination showed that the uterus, as big as 3 months of pregnancy, had weak activity and no tenderness. The uterine rectum lacuna was like a hard nodule of about 3 × 2 cm, and an irregular solid mass was fixed and inactive in the right adnexa.
In accordance with Ann Arbor staging system, a stage IE primary diffuse large B-cell lymphoma of fallopian tube was diagnosed for this patient, based on the tumor pathology, the results of bone marrow biopsy and computed tomography (CT) scan.
After gynecological/urinary ultrasound, blood test, pelvic contrast enhanced CT scan and CT angiography of iliac artery, exploratory laparoscopy and following hysterectomy with bilateral salpingo-oophorectomy were performed. After the surgery, the patient was treated with combined Rituximab and chemotherapy and got complete response (CR).
After the operation and R-CHPOP, following up for more than 1 year so far, the patient has no tumor recurrence and is still in good condition.
It is very difficult to diagnose the primary diffuse large B-cell lymphoma of fallopian tube, not only because of its rarity, but also because of its non-specific clinical manifestations. It easily be treated as late ovarian cancer by gynecologist. So the pathology diagnosis and surgeons' decision is very important. Because lymphoma is pretty sensitive to chemotherapy and easy to get complete response, so we no need to do an operation like ovarian cancer and should put chemotherapy as a primary method for lymphomas of the female genital tract.
原发性女性生殖道淋巴瘤是散发性肿瘤,占结外淋巴瘤的 0.2%~1.1%。最常见的生殖部位定位是宫颈、子宫体和卵巢,而输卵管原发性淋巴瘤则相当罕见。根据 PubMed 文献检索,这是首例报道的原发性输卵管弥漫性大 B 细胞淋巴瘤。
一位 52 岁女性因间歇性下腹疼痛超过 2 个月就诊。妇科检查发现子宫如 3 个月妊娠大小,活动度差,无压痛。子宫直肠窝触及约 3×2cm 硬结节,右侧附件触及不规则实性肿块,固定无活动度。
根据肿瘤病理学、骨髓活检和计算机断层扫描(CT)结果,按照 Ann Arbor 分期系统,该患者诊断为原发性输卵管弥漫性大 B 细胞淋巴瘤,IE 期。
在进行妇科/泌尿科超声、血液检查、盆腔增强 CT 扫描和髂动脉 CT 血管造影、探查性腹腔镜检查和随后的子宫切除术及双侧输卵管卵巢切除术之后。手术后,患者接受了利妥昔单抗联合化疗,获得完全缓解(CR)。
手术后和 R-CHPOP 治疗后,随访至今已超过 1 年,患者无肿瘤复发,情况良好。
原发性输卵管弥漫性大 B 细胞淋巴瘤的诊断非常困难,不仅因为其罕见,还因为其临床表现不特异。它很容易被妇科医生误诊为晚期卵巢癌。因此,病理诊断和外科医生的决策非常重要。由于淋巴瘤对化疗非常敏感,容易获得完全缓解,因此我们不需要像卵巢癌那样进行手术,而应该将化疗作为女性生殖道淋巴瘤的主要治疗方法。