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原发性胃滤泡性淋巴瘤伴滤泡旁单核样B细胞和淋巴上皮病变,酷似黏膜相关淋巴组织结外边缘区淋巴瘤。

Primary gastric follicular lymphoma with parafollicular monocytoid B-cells and lymphoepithelial lesions, mimicking extranodal marginal zone lymphoma of MALT.

作者信息

Tzankov Alexandar, Hittmair Anton, Müller-Hermelink Hans-Konrad, Rüdiger Thomas, Dirnhofer Stephan

机构信息

Institute of Pathology, University of Innsbruck, Müllerstr. 44, Austria.

出版信息

Virchows Arch. 2002 Dec;441(6):614-7. doi: 10.1007/s00428-002-0670-5. Epub 2002 Oct 26.

Abstract

The incidence of B-cell non-Hodgkin lymphomas (B-NHL) at nodal and extranodal sites is fairly different. Follicular lymphomas (FL) occur predominantly at nodal sites and rarely in the gastrointestinal tract, while marginal zone lymphomas (MZL) of the mucosa-associated lymphatic tissue (MALT) type predominate in the digestive organs and especially in the stomach. We report a 72-year-old female patient admitted for gastroscopy because of epigastric pain. The antral biopsies showed dense lymphocytic infiltrates, partially forming follicles with widened marginal zones and monocytoid cells. Multiple lymphoepithelial lesions (LEL) were also observed. A MZL of the MALT type was suspected morphologically. Immunohistochemical analysis revealed the lymphatic infiltrates to be CD20, bcl-2, bcl-6 and CD10 positive, and negative for CD43, CD5 and cyclin D1. PCR-based analysis showed a JH/bcl-2 rearrangement, corresponding to the translocation t(14;18). An extranodal FL mimicking MZL was diagnosed. The present case is remarkable, as it demonstrates that the detection of LEL and monocytoid B-cells, although suggestive for MZL, is not entirely specific and can also be observed in FL. Pathologists should be aware of this diagnostic pitfall in classifying gastric B-NHL. In equivocal cases, a careful morphological examination, supported by specific immunohistochemical and molecular findings, should lead to the correct diagnosis.

摘要

B细胞非霍奇金淋巴瘤(B-NHL)在淋巴结和结外部位的发病率有很大差异。滤泡性淋巴瘤(FL)主要发生在淋巴结部位,很少发生在胃肠道,而黏膜相关淋巴组织(MALT)型边缘区淋巴瘤(MZL)则在消化器官尤其是胃中占主导。我们报告一名72岁女性患者,因上腹部疼痛入院接受胃镜检查。胃窦活检显示密集的淋巴细胞浸润,部分形成边缘区增宽和单核细胞样细胞的滤泡。还观察到多个淋巴上皮病变(LEL)。形态学上怀疑为MALT型MZL。免疫组化分析显示淋巴细胞浸润CD20、bcl-2、bcl-6和CD10阳性,CD43、CD5和细胞周期蛋白D1阴性。基于PCR的分析显示有JH/bcl-2重排,对应于t(14;18)易位。诊断为模仿MZL的结外FL。本病例值得注意,因为它表明LEL和单核细胞样B细胞的检测虽然提示MZL,但并不完全特异,也可见于FL。病理学家在对胃B-NHL进行分类时应意识到这一诊断陷阱。在疑难病例中,仔细的形态学检查,辅以特定的免疫组化和分子结果,应能得出正确诊断。

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