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[小肠原发性非霍奇金淋巴瘤:34例临床分析]

[Primary non-Hodgkin lymphoma of small bowel: a clinical analysis of 34 cases].

作者信息

Chen Chun-qiu, Yin Lu, Peng Cheng-hong, Zhao Ren, Chen Gui-ming, Zhou Hui-jiang, Li Hong-wei

机构信息

Department of General Surgery, Ruijin Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200025, China.

出版信息

Zhonghua Wei Chang Wai Ke Za Zhi. 2007 May;10(3):249-52.

Abstract

OBJECTIVE

To study the clinical characteristics,treatment and prognosis of primary non-Hodgkin's lymphoma of small bowel.

METHODS

The records of 34 patients with a confirmed diagnosis of primary non-Hodgkin's lymphoma of small bowel, registered between Jan. 1996 and Dec. 2005 at our hospital, were retrieved and analysed retrospectively.

RESULTS

Twenty-seven patients had B-cell lymphoma and 7 had T-cell lymphoma of the small bowel. The major symptoms included abdominal pain and intestinal obstruction. According to Ann Arbor staging classification, 22 patients belonged to stage III, including 20 cases of B-cell lymphoma and 2 cases of T-cell lymphoma, and 12 patients belonged to stage IIIIV, including 7 cases of B-cell lymphoma and 5 cases of T-cell lymphoma. Compared with T-cell lymphoma patients, B-cell lymphoma patients had lower lymphoma stages (P<0.05). Twenty-seven patients were treated with surgical resection. Fourteen patients were treated with six cycles of cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP) chemotherapy, and 8 patients were treated with Rituximab at the same time. T-cell lymphoma patients were more often treated with emergent operation than B-cell lymphoma patients would (P<0.05). It happened more frequently that B-cell lymphoma patients reached complete remission and their accumulative survival rate was longer than T-cell lymphoma patients did (P<0.05).

CONCLUSION

Patients with stages I and II B-cell lymphoma of small bowel respond well to surgery and chemotherapy, and the treatment and prognosis of patients with T-cell lymphoma of small bowel are unsatisfactory.

摘要

目的

研究小肠原发性非霍奇金淋巴瘤的临床特征、治疗方法及预后。

方法

回顾性检索并分析1996年1月至2005年12月在我院确诊的34例小肠原发性非霍奇金淋巴瘤患者的病历资料。

结果

27例为小肠B细胞淋巴瘤,7例为小肠T细胞淋巴瘤。主要症状包括腹痛和肠梗阻。根据Ann Arbor分期标准,22例患者为ⅠⅡ期,其中B细胞淋巴瘤20例,T细胞淋巴瘤2例;12例患者为ⅢⅣ期,其中B细胞淋巴瘤7例,T细胞淋巴瘤5例。与T细胞淋巴瘤患者相比,B细胞淋巴瘤患者的淋巴瘤分期较低(P<0.05)。27例患者接受了手术切除治疗。14例患者接受了6个周期的环磷酰胺、阿霉素(多柔比星)、长春新碱和泼尼松(CHOP)化疗,8例患者同时接受了利妥昔单抗治疗。T细胞淋巴瘤患者比B细胞淋巴瘤患者更常接受急诊手术(P<0.05)。B细胞淋巴瘤患者达到完全缓解的情况更常见,其累积生存率也长于T细胞淋巴瘤患者(P<0.05)。

结论

小肠Ⅰ、Ⅱ期B细胞淋巴瘤患者对手术和化疗反应良好,而小肠T细胞淋巴瘤患者的治疗及预后并不理想。

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