原发性子宫恶性淋巴瘤2例。免疫组织化学研究。

T. Nishikawa, T. Kasajima, Y. Takeo, A. Andoh, A. Masuda, M. Kawakami
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摘要

恶性淋巴瘤起源于子宫是极为罕见的报道。自从Epperson在1950年描述了第一例病例以来,全世界报道的病例不超过50例。在此,我们报告两例根据Fox和More标准诊断的原发性子宫恶性淋巴瘤。其中一名患者是一名39岁的家庭主妇,她患有非典型生殖器出血。行子宫切除术,组织学检查发现恶性淋巴瘤,弥漫性,中等大小。经免疫组化检查,肿瘤细胞对多种B淋巴细胞抗体和CD74 (LN2)阳性。手术后,病人目前还活着,状况良好。另一名患者为80岁的家庭主妇,腹部不适。临床检查发现子宫异常增大,尿路梗阻。入院后8天,患者死于一般性肺病,并进行尸检。子宫明显增大,肿瘤延伸到肠浆膜和腹膜,并累及一个淋巴结。然而,在其他器官中未发现其他肿瘤。组织学上,肿瘤细胞弥漫性分布于整个子宫壁,为中等大小的淋巴样细胞。免疫组化分析显示为b淋巴细胞,L26、CD20、CD22、CD74 (LN2)和sIgD(表面IgD)阳性,但T淋巴细胞和组织细胞标志物均为阴性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two cases of primary malignant lymphoma of uterus. An immunohistochemical study.
Malignant lymphoma originating from the uterus is reported extremely rarely. Since Epperson described the first case in 1950, no more than about fifty cases have been reported world wide. Here we report two cases of primary uterine malignant lymphoma diagnosed according to Fox and More's criteria. One of the patients was a 39-year-old housewife who suffered from atypical genital bleeding. Hysterectomy was performed and histological examination revealed malignant lymphoma, diffuse, medium sized. Upon immunohistochemical examination, the tumor cells were positive for several antibodies against B lymphocytes and also for CD74 (LN2). The patient is currently alive and well after surgery. The other patient was an 80-year-old housewife who suffered from abdominal discomfort. Clinical examination revealed abnormal enlargement of the uterus and obstruction of the urinary tract. Eight days after admission, she died of general consumption, and autopsy was performed. The uterus was markedly enlarged with a tumor, which extended to the serosa of the intestine and the peritoneum, involving one lymph node. However, there were no other tumors in other organs examined. Histologically, the tumor cells were distributed diffusely throughout the entire uterine wall and were medium-sized lymphoid cells. Immunohistochemical analysis revealed a B-lymphocyte nature, with positivity for L26, CD20, CD22, CD74 (LN2) and sIgD (surface IgD), but both T lymphocytic and histiocytic markers were negative.
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