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[原发性结直肠非霍奇金淋巴瘤的诊断与治疗:52例分析]

[Diagnosis and treatment of primary colorectal non-Hodgkin's lymphoma: analysis of 52 cases].

作者信息

Huang Shuai, Zheng Zhao-xu, Xu Quan, Yuan Xing-hua

机构信息

Department of Abdominal Surgery, Cancer Institute & Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2013 Apr;35(4):305-8. doi: 10.3760/cma.j.issn.0253-3766.2013.04.014.

Abstract

OBJECTIVE

To summarize and analyze the diagnosis, clinical features and therapy of primary colorectal non-Hodgkin's lymphoma (NHL).

METHODS

The clinicopathological data of 52 patients with primary colorectal NHL diagnosed and treated in our department from January 2000 to January 2010 were reviewed and analyzed retrospectively in this study.

RESULTS

This group of patients was composed of 45 cases of B cell and 7 T cell lymphomas, including 33 males and 19 females, with a male to female ratio of 1.7:1, and the age at diagnosis was 16 - 74 years old, with a median age of 50 years. The ileocecal region was most frequently involved site, acounted for 48.1%. The common symptoms encountered were abdominal pain (66.7%), diarrhea (15.6%), blood stool (24.4%), and body weight loss (8.9%). All patients were eventually diagnosed by histopathology, and the DLBCL subtype took up 64.4%. Among the 45 cases of B cell subtype, 33 cases (73.3%) were of early stage (IE and IIE confirmed), and the 5-year survival rate was 78.1%, while those of stage IIIE and IVE comprised 26.7%, with a 5-year survival rate of 45.5% (P < 0.05). The 5-year survival rate of all patients was 71.1%. Surgery was employed in 36 cases, and 9 patients received chemotherapy alone. Radical surgery could significantly increase the patients' overall survival rate, as compared with the chemotherapy alone group and palliative surgery group (P < 0.05).

CONCLUSIONS

Colorectal non-Hodgkin's lymphoma is a rare malignancy of the gastrointestinal tract. B cell type, male predominance and DLBCL subtype are most encountered manifestations in clinics. Multi-modality management with radical surgical resection of the primary lesion followed by standard chemotherapy, affords better local disease control, and a better survival outcome. Early detection and tailored immunotherapy can obviously prolong the long-term survival time.

摘要

目的

总结并分析原发性结直肠非霍奇金淋巴瘤(NHL)的诊断、临床特征及治疗方法。

方法

回顾性分析2000年1月至2010年1月在我科诊治的52例原发性结直肠NHL患者的临床病理资料。

结果

该组患者包括45例B细胞淋巴瘤和7例T细胞淋巴瘤,其中男性33例,女性19例,男女比例为1.7∶1,确诊年龄为16~74岁,中位年龄50岁。回盲部是最常累及的部位,占48.1%。常见症状有腹痛(66.7%)、腹泻(15.6%)、便血(24.4%)和体重减轻(8.9%)。所有患者最终均经组织病理学确诊,弥漫大B细胞淋巴瘤(DLBCL)亚型占64.4%。45例B细胞亚型中,33例(73.3%)为早期(确诊为IE期和IIE期),5年生存率为78.1%,而IIIE期和IVE期患者占26.7%,5年生存率为45.5%(P<0.05)。所有患者的5年生存率为71.1%。36例行手术治疗,9例单纯接受化疗。与单纯化疗组和姑息手术组相比,根治性手术可显著提高患者的总生存率(P<0.05)。

结论

结直肠非霍奇金淋巴瘤是一种罕见的胃肠道恶性肿瘤。B细胞型、男性居多和DLBCL亚型是临床上最常见的表现。采用对原发性病变进行根治性手术切除并辅以标准化化疗的多模式治疗,可更好地控制局部疾病,并获得更好的生存结果。早期发现并进行针对性免疫治疗可明显延长长期生存时间。

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