Fujiwara Arisa, Nagayama Shiho, Amada Satoshi, Shimamoto Tomihiro, Shimao Yoshiya, Hayashi Tohru
Department of Obstetrics and Gynecology, Miyazaki Prefectural Miyazaki Hospital, 5-30 Kitatakamatu-machi, Miyazaki City, Miyazaki 880-8510, Japan.
Acta Cytol. 2010 Sep-Oct;54(5 Suppl):787-92.
Intravascular lymphoma is a rare subtype of extranodal lymphoma. Most instances of the disease are of B-cell lineage. Diagnosis is difficult because of its nonspecific clinical signs, and many cases are diagnosed at autopsy. Uterine involvement is rare, and it is commonly manifested as genital bleeding. In this case, the chief complaint was fever, which is also very rare.
A 62-year-old woman presented with fever of unknown origin. Computed tomography revealed no localized lesion except for swelling of the right internal iliac nodes. A cytologic smear of the endometrium by liquid-based cytology demonstrated malignant cells. Based on the curettage material, the lesion was diagnosed as an undifferentiated malignant tumor. Total abdominal hysterectomy with bilateral salpingo-oophorectomy and pelvic/paraaortic lymphadenectomy revealed widely scattered lymphoma cells of B-cell lineage mainly in the vascular lumina of the uterus, right ovary and lymph nodes.
The final histologic type was established on the basis of the surgical material of hysterectomy. Diagnosis was difficult because of prominent cellular atypia and rare location of the tumor. Immunocytochemical examination of liquid-based samples can lead to a correct diagnosis of malignant lymphoma, even at the stage of endometrial cytologic examination.
血管内淋巴瘤是结外淋巴瘤的一种罕见亚型。该疾病的大多数病例为B细胞谱系。由于其临床症状不具特异性,诊断较为困难,许多病例在尸检时才得以确诊。子宫受累罕见,通常表现为生殖器出血。在本病例中,主要症状为发热,这也非常罕见。
一名62岁女性因不明原因发热就诊。计算机断层扫描显示除右侧髂内淋巴结肿大外无局部病变。子宫内膜液基细胞学涂片显示有恶性细胞。根据刮宫材料,该病变被诊断为未分化恶性肿瘤。全腹子宫切除术加双侧输卵管卵巢切除术及盆腔/腹主动脉旁淋巴结清扫术显示,主要在子宫、右侧卵巢和淋巴结的血管腔内广泛散在B细胞谱系的淋巴瘤细胞。
最终的组织学类型是根据子宫切除的手术材料确定的。由于肿瘤细胞异型性明显且位置罕见,诊断困难。即使在子宫内膜细胞学检查阶段,液基样本的免疫细胞化学检查也可导致恶性淋巴瘤的正确诊断。