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首页> 外文期刊>Annals of diagnostic pathology >Florid reactive lymphoid hyperplasia (lymphoma-like lesion) of the uterine cervix
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Florid reactive lymphoid hyperplasia (lymphoma-like lesion) of the uterine cervix

机译:子宫颈的花样反应性淋巴样增生(淋巴瘤样病变)

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摘要

Lymphoma-like lesion (LLL) of the female genital tract is an older term in the literature that describes a florid reactive lymphoid proliferation that can be misinterpreted as lymphoma. Multiple causes of LLL have been suggested but most cases remain unexplained. We describe the clinicopathologic features of 6 patients with LLL involving the uterine cervix. Five patients presented with abnormal Papanicolaou test (Pap smear), and 3 patients had a biopsy procedure performed prior to detection of LLL in a loop electrosurgical excision procedure (LEEP). In each specimen, surface epithelial erosion was associated with a superficial, polymorphous lymphoid infiltrate with numerous scattered large cells, without cellular necrosis or sclerosis. Squamous dysplasia was present in 4 patients. Immunohistochemical studies revealed a mixed population of B- and T-lymphoid cells. T-cells were more numerous but B-cells and formed aggregates or sheets in areas. The large cells were predominantly B-cells positive for CD20 and negative for CD3 in all cases. CD30 was positive 3 cases, and Epstein-Barr virus-encoded RNA was positive in 3 cases. Assessment for clonality in 1 patient using polymerase chain reaction (PCR) methods revealed monoclonal immunoglobulin heavy chain (IgH) gene rearrangements. At last clinical follow-up there was no evidence of progressive or systemic disease. We conclude that LLL of the cervix has a number of etiologies and that a prior surgical procedure, present in 3 patients in this study, is another possible etiology. As has been reported by others, monoclonal IgH gene rearrangements can be detected in this entity which has a benign clinical course.
机译:女性生殖道的淋巴瘤样病变(LLL)是文献中的一个较旧的术语,描述了可能被误解为淋巴瘤的轻度反应性淋巴样增生。已经提出了引起LLL的多种原因,但是大多数情况仍无法解释。我们描述了6例LLL累及子宫颈的临床病理特征。五名患者出现Papanicolaou试验异常(巴氏涂片检查),三名患者在回路电外科切除术(LEEP)中检测到LLL之前进行了活检。在每个标本中,表面上皮侵蚀与浅表性多形淋巴样浸润伴有大量散布的大细胞,而没有细胞坏死或硬化。鳞状不典型增生存在4例。免疫组织化学研究显示B和T淋巴样细胞混合。 T细胞数量众多,但B细胞却在区域内形成聚集体或薄片。在所有情况下,大细胞主要是对CD20呈阳性的B细胞,对CD3呈阴性。 CD30阳性3例,爱泼斯坦-巴尔病毒编码的RNA阳性3例。使用聚合酶链反应(PCR)方法对1位患者的克隆性评估显示单克隆免疫球蛋白重链(IgH)基因重排。在最后的临床随访中,没有任何进行性或全身性疾病的证据。我们得出结论,子宫颈LLL具有多种病因,并且本研究中有3位患者进行的先前手术是另一种可能的病因。正如其他人所报道的,可以在具有良好临床过程的该实体中检测到单克隆IgH基因重排。

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