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累及生殖道的自然杀伤细胞淋巴瘤。

Natural killer-cell lymphoma involving the gynecologic tract.

作者信息

Mhawech P, Medeiros L J, Bueso-Ramos C, Coffey D M, Gei A F, Shahab I

机构信息

Departments of Pathology, University of Texas, M.D Anderson Medical Center, Houston, TX 77030, USA.

出版信息

Arch Pathol Lab Med. 2000 Oct;124(10):1510-3. doi: 10.5858/2000-124-1510-NKCLIT.

DOI:10.5858/2000-124-1510-NKCLIT
PMID:11035585
Abstract

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.

摘要

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。

相似文献

1
Natural killer-cell lymphoma involving the gynecologic tract.累及生殖道的自然杀伤细胞淋巴瘤。
Arch Pathol Lab Med. 2000 Oct;124(10):1510-3. doi: 10.5858/2000-124-1510-NKCLIT.
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CD3- CD56+ non-Hodgkin's lymphomas with an aggressive behavior related to multidrug resistance.具有与多药耐药相关的侵袭性行为的CD3-CD56+非霍奇金淋巴瘤。
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Nonnasal lymphoma expressing the natural killer cell marker CD56: a clinicopathologic study of 49 cases of an uncommon aggressive neoplasm.表达自然杀伤细胞标志物CD56的鼻外型淋巴瘤:49例罕见侵袭性肿瘤的临床病理研究
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Blastic natural killer cell leukemia/lymphoma presenting as overt leukemia.以明显白血病形式出现的母细胞性自然杀伤细胞白血病/淋巴瘤。
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Bone marrow involvement by nasal NK cell lymphoma at diagnosis is uncommon.鼻型NK细胞淋巴瘤诊断时骨髓受累并不常见。
Am J Clin Pathol. 2001 Feb;115(2):266-70. doi: 10.1309/E5PR-6A9R-Q02N-8QVW.
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Nasal T/natural killer (NK)-cell lymphomas are derived from Epstein-Barr virus-infected cytotoxic lymphocytes of both NK- and T-cell lineage.鼻T/自然杀伤(NK)细胞淋巴瘤源自爱泼斯坦-巴尔病毒感染的NK细胞和T细胞谱系的细胞毒性淋巴细胞。
Int J Cancer. 1997 Nov 4;73(3):332-8. doi: 10.1002/(sici)1097-0215(19971104)73:3<332::aid-ijc5>3.0.co;2-0.
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T-cell and T/natural killer-cell lymphomas involving ocular and ocular adnexal tissues: a clinicopathologic, immunohistochemical, and molecular study of seven cases.累及眼及眼附属器组织的T细胞和T/自然杀伤细胞淋巴瘤:7例临床病理、免疫组化及分子研究
Ophthalmology. 1999 Nov;106(11):2109-20. doi: 10.1016/S0161-6420(99)90492-X.

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2
What is CD4+CD56+ malignancy and how should it be treated?什么是CD4+CD56+恶性肿瘤,应如何治疗?
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