Lioe T F, Biggart J D
Department of Histopathology, Belfast City Hospital, Northern Ireland.
J Clin Pathol. 1990 Jul;43(7):533-6. doi: 10.1136/jcp.43.7.533.
Between 1954 and 1988 only a total of twenty five cases of primary adenocarcinoma of the small bowel (excluding periampillary tumours) were recorded at the Department of Histopathology, Belfast City Hospital. Of these, 14 tumours were located in the jejunum: the remainder arose in the ileum. The average age at presentation was 61.3 years and a slight female to male preponderance of 1:7:1 was noted. The adenocarcinoma arose from a preexisting villous adenoma in six cases. The overall prognosis was poor, with a five year survival of 15.7%. All the survivors had tumours located in the jejunum. The single most important prognostic indicator was the depth of tumour invasion or stage at the time of diagnosis. Tumour size and grade did not seem to correlate well with survival. It is concluded that the rarity of these tumours and their inaccessibility hinder detection and treatment and that surgical resection is more effective than chemotherapy.
1954年至1988年间,贝尔法斯特市医院组织病理学部门仅记录了25例原发性小肠腺癌(不包括壶腹周围肿瘤)。其中,14例肿瘤位于空肠,其余发生于回肠。就诊时的平均年龄为61.3岁,女性与男性比例略高,为1.7:1。6例腺癌由先前存在的绒毛状腺瘤发展而来。总体预后较差,五年生存率为15.7%。所有幸存者的肿瘤均位于空肠。最重要的单一预后指标是诊断时肿瘤浸润深度或分期。肿瘤大小和分级似乎与生存率没有很好的相关性。结论是,这些肿瘤罕见且难以触及,阻碍了检测和治疗,手术切除比化疗更有效。