首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Pathology >Intravascular large B-cell lymphoma manifesting as cholecystitis: report of an Asian variant showing gain of chromosome 18 with concurrent deletion of chromosome 6q
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Intravascular large B-cell lymphoma manifesting as cholecystitis: report of an Asian variant showing gain of chromosome 18 with concurrent deletion of chromosome 6q

机译:表现为胆囊炎的血管内大B细胞淋巴瘤:亚洲变种的报告显示18号染色体的获得与6q号染色体的同时缺失

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摘要

Intravascular large B-cell lymphoma (IVLBCL), which involves the lumen of small vessels, is a rare variant of extranodal diffuse large B-cell lymphomas. Herein, we present a case of IVLBCL manifesting as cholecystitis in a 77-year-old Japanese man. He presented with fever, fatigue, and weight loss. Physical examination revealed tenderness of the right upper quadrant. The white blood cell count and C-reactive protein levels were elevated. Computed tomography revealed gallbladder thickening and pericholecystic fluid collection; these observations were consistent with the diagnosis of cholecystitis. Serum soluble interleukin-2 receptor levels were highly elevated, and gallium scintigraphy revealed an abnormal accumulation in the spleen, implying lymphoma. Consequently, G-banding analysis of the patient’s bone marrow aspirates revealed the presence of different abnormal clones, including those with gain of chromosome 18 and deletion of chromosome 6q. As cholecystectomy was necessary, a concurrent splenectomy was performed to diagnose the disease definitively. Histopathologically, atypical large lymphoid cells were observed to be localized in the vasculature in both the spleen and gallbladder; the atypical cells expressed high levels of CD20, CD5, and CD10, immunohistochemically. These findings were consistent with IVLBCL. The patient underwent post-operative treatment with rituximab, cyclophosphamide, adriamycin, vincristine, and prednisolone. However, a pancreatic fistula developed during chemotherapy, causing left pleural effusion and peritoneal effusion; the patient developed sepsis from multidrug-resistant microorganisms, and subsequently died of multi-organ failure 6 months after the diagnosis. No obvious recurrence of the tumor was found during autopsy. We discuss the characteristic karyotype and immunohistochemical status observed in this case.
机译:涉及小血管腔的血管内大B细胞淋巴瘤(IVLBCL)是结外弥漫性大B细胞淋巴瘤的罕见变体。在本文中,我们介绍了一名在77岁的日本男子中表现为胆囊炎的IVLBCL病例。他表现出发烧,疲劳和体重减轻。体格检查显示右上腹压痛。白细胞计数和C反应蛋白水平升高。计算机断层扫描显示胆囊增厚和胆囊积液。这些观察结果与胆囊炎的诊断是一致的。血清可溶性白细胞介素2受体水平高度升高,镓闪烁显像显示脾脏中异常堆积,这意味着淋巴瘤。因此,对患者骨髓抽吸物的G谱带分析显示存在不同的异常克隆,包括具有18号染色体扩增和6q染色体缺失的克隆。由于必须进行胆囊切除术,因此需要同时进行脾切除术以明确诊断该病。从组织病理学上看,非典型大淋巴样细胞位于脾和胆囊的脉管系统中。非典型细胞通过免疫组织化学表达高水平的CD20,CD5和CD10。这些发现与IVLBCL一致。病人接受了利妥昔单抗,环磷酰胺,阿霉素,长春新碱和泼尼松龙的术后治疗。然而,在化疗过程中出现了胰瘘,导致左胸腔积液和腹膜积液。该患者因多药耐药微生物而导致败血症,并在诊断后6个月死于多器官衰竭。尸检期间未发现明显的肿瘤复发。我们讨论在这种情况下观察到的特征性核型和免疫组化状态。

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