首页> 外文期刊>Pathology International >Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) arising in the small intestine with monoclonal cryoglobulinemia.
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Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) arising in the small intestine with monoclonal cryoglobulinemia.

机译:黏膜相关淋巴样组织的结外边缘区B细胞淋巴瘤(MALT淋巴瘤)在单克隆小球蛋白血症的小肠中发生。

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A case of small intestinal extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) with monoclonal cryoglobulinemia is described. The patient was a woman in her mid-sixties with purpura of the bilateral lower legs and abdominal pain. An immunoserological investigation showed expression of IgM-kappa type monoclonal cryoglobulin. A renal biopsy specimen revealed proliferative glomerulonephritis with cryoglobulin deposition. Physical examination disclosed a stenosis, edematous changes and ascariasis in the small intestine. In aspiration cytology of the ascites, proliferation of the atypical lymphoid cells with plasmacytoid differentiation was observed. These cells were positive for B-lineage antigens in immunocytochemistry, and showed an immunoglobulin heavy-chain gene rearrangement in Southern blotting and chromosomal alteration in G-banded karyotype analysis. Although medicinal treatment was used, the patient died of general prostration. The diagnosis of intestinal MALT lymphoma was made at autopsy. Expression of API2-MALT1 fusion transcripts was detected by reverse transcription-polymerase chain reaction analysis using formalin-fixed, paraffin-embedded tissue. Intestinal MALT lymphomas with API2-MALT1 expression have distinctive forms of infiltration compared with those without translocation. Therefore, detection of API2-MALT1 fusion transcripts is useful for evaluating the prognosis and clinical behavior of the disease.
机译:描述了一例黏膜相关淋巴组织小肠结外边缘区B细胞淋巴瘤(MALT淋巴瘤)伴单克隆冷球蛋白血症。该患者是一名六十多岁的女性,患有双侧小腿紫癜和腹痛。免疫血清学研究显示IgM-κ型单克隆冷球蛋白的表达。肾脏活检标本显示增生性肾小球肾炎伴冷球蛋白沉积。体格检查发现小肠狭窄,水肿,changes虫病。在腹水的抽吸细胞学中,观察到具有浆细胞样分化的非典型淋巴样细胞的增殖。这些细胞在免疫细胞化学中对B谱系抗原呈阳性,在Southern印迹法中显示免疫球蛋白重链基因重排,在G型核型分析中显示染色体改变。尽管使用了药物治疗,但患者因全身虚脱而死亡。尸检时诊断为肠道MALT淋巴瘤。使用福尔马林固定,石蜡包埋的组织通过逆转录-聚合酶链反应分析检测API2-MALT1融合转录本的表达。与没有转运的人相比,具有API2-MALT1表达的肠道MALT淋巴瘤具有独特的浸润形式。因此,API2-MALT1融合转录本的检测对于评估疾病的预后和临床行为非常有用。

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