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原发性结直肠淋巴瘤

Primary colorectal lymphoma.

作者信息

Aragón Sánchez F J, García Molina F J, Rodríguez Fernández A, de Dios Franco Osorio J, Ortegón Castellano B, Márquez Platero R, López Hurtado M, Medina Díez J

机构信息

Service of General Surgery, Jerez de la Frontera Hospital of the S.A.S, Cádiz, Spain.

出版信息

Rev Esp Enferm Dig. 1997 Dec;89(12):903-18.

PMID:9494378
Abstract

OBJECT

To analyze our experience in the treatment of primary colorectal lymphomas.

PATIENTS

During the recent period from 1989 to 1995, a total number of 406 cases of malignant neoplasms of large intestine were treated at Department of Surgery, Hospital del S.A.S de Jerez de la Frontera. There were 5 cases of primary colorectal Non-Hodgkin's lymphomas, constituting 1.2% of all colorectal malignancies.

METHODS

Medical records of all five patients were carefully reviewed. Surgical pathology specimens were retrospectively reexamined to confirm the diagnosis, and immunohistochemistry staining methods were performed. Dawson, Cornes and Morson criteria were used to distinguish primary colonic lymphoma. For tumor staging, a modification of the Ann-Arbor system for gastrointestinal lymphoma proposed by Musshoff and Schmidt-Vollmer was used.

RESULTS

All cases were Non-Hodgkin's lymphomas. There were no cases of lymphoma of the rectum. There were 2 males and 3 females. Their ages ranged from 12 to 73 years, with an average age of 31 years. The cecum was the site of the lesions in 4 patients and the other was located in the sigmoid colon. Acute abdomen in three cases, undiagnosed abdominal mass in one and intussusception in the other one were the clinical presentation. Inmunohistochemical studies showed B-cell phenotype in 4 and non-B non-T Ki-1-positive phenotype in 1 patient. Chemotherapy was administered following resection in 100% of patients.

CONCLUSIONS

Intraoperative diagnosis of lymphoma was not suspected in all cases but the malignancy was always present. The cecum is the commonest site of involvement. Both of our two patients presented with perforated lymphoma were associated with a poor short term prognosis. It is necessary to unify the staging system and the histologic classifications enabling a comparison of several studies.

摘要

目的

分析我们治疗原发性结直肠淋巴瘤的经验。

患者

在1989年至1995年最近这段时间里,赫雷斯德拉弗龙特拉市圣安东尼奥医院外科共治疗了406例大肠恶性肿瘤患者。其中有5例原发性结直肠非霍奇金淋巴瘤,占所有结直肠恶性肿瘤的1.2%。

方法

仔细查阅了所有5例患者的病历。对手术病理标本进行回顾性复查以确诊,并进行了免疫组织化学染色。采用道森、科恩斯和莫森标准来区分原发性结肠淋巴瘤。对于肿瘤分期,采用了穆肖夫和施密特 - 福尔默提出的对安阿伯胃肠淋巴瘤分期系统的改良方法。

结果

所有病例均为非霍奇金淋巴瘤。无直肠淋巴瘤病例。男性2例,女性3例。年龄范围为12至73岁,平均年龄31岁。4例患者病变位于盲肠,另1例位于乙状结肠。临床表现为3例急性腹痛、1例未确诊的腹部肿块和1例肠套叠。免疫组织化学研究显示4例为B细胞表型,1例为非B非T Ki - 1阳性表型。100%的患者在切除术后接受了化疗。

结论

并非所有病例术中均怀疑为淋巴瘤,但恶性肿瘤始终存在。盲肠是最常受累的部位。我们的2例穿孔性淋巴瘤患者短期预后均较差。有必要统一分期系统和组织学分类,以便能够对多项研究进行比较。

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