Mhawech P, Medeiros L J, Bueso-Ramos C, Coffey D M, Gei A F, Shahab I
Departments of Pathology, University of Texas, M.D Anderson Medical Center, Houston, TX 77030, USA.
Arch Pathol Lab Med. 2000 Oct;124(10):1510-3. doi: 10.5858/2000-124-1510-NKCLIT.
Non-Hodgkin lymphomas (NHL) can involve the gynecologic tract, most often as a manifestation of systemic involvement, and most cases reported have been of B-cell lineage. We describe 2 women with natural killer (NK)-cell lymphoma involving the gynecologic tract that initially presented with vaginal bleeding. In case 1, the patient had a stage IE nasal-type NK-cell lymphoma involving the cervix. The tumor was composed of medium-sized, irregular lymphoid cells with angioinvasion and necrosis. In case 2, the patient had a stage IV blastoid NK-cell lymphoma/leukemia infiltrating all organs in a hysterectomy and bilateral salpingo-oophorectomy specimen. Subsequent biopsy specimens revealed that the bone marrow and lymph nodes were also involved. The neoplasm was composed of small to medium lymphoid cells with fine nuclear chromatin. Case 1 was assessed immunohistochemically and the neoplastic cells were positive for CD3, CD56, and TIA-1. Case 2 was analyzed using both immunohistochemical and flow cytometry methods. The neoplastic cells were positive for cytoplasmic CD3, CD4, CD7, CD43, CD45, and CD56 and were negative for surface CD3. Both cases were negative for Epstein-Barr virus (EBV) ribonucleic acid (RNA) and molecular studies showed no evidence of T-cell receptor gamma chain gene rearrangements. The immunophenotype and absence of T-cell receptor gene rearrangements support NK-cell origin. We report these cases to illustrate that NK-cell lymphomas can involve, and rarely arise in, the gynecologic tract.
非霍奇金淋巴瘤(NHL)可累及生殖道,多数情况下是全身受累的一种表现,且报道的大多数病例为B细胞谱系。我们描述了2例自然杀伤(NK)细胞淋巴瘤累及生殖道的女性患者,她们最初均表现为阴道出血。病例1中,患者为IE期鼻型NK细胞淋巴瘤累及宫颈。肿瘤由中等大小、形态不规则的淋巴细胞组成,伴有血管浸润和坏死。病例2中,患者为IV期母细胞样NK细胞淋巴瘤/白血病,在子宫切除及双侧输卵管卵巢切除标本中可见肿瘤浸润所有器官。随后的活检标本显示骨髓和淋巴结也受累。肿瘤由核染色质细腻的小至中等淋巴细胞组成。病例1进行了免疫组化评估,肿瘤细胞CD3、CD56和TIA-1呈阳性。病例2采用免疫组化和流式细胞术方法进行分析。肿瘤细胞胞质CD3、CD4、CD7、CD43、CD45和CD56呈阳性,表面CD3呈阴性。两例患者的爱泼斯坦-巴尔病毒(EBV)核糖核酸(RNA)均为阴性,分子研究未显示T细胞受体γ链基因重排的证据。免疫表型及T细胞受体基因重排的缺失支持NK细胞起源。我们报告这两例病例以说明NK细胞淋巴瘤可累及生殖道,且很少起源于生殖道。