Spread C, Berkel H, Jewell L, Jenkins H, Yakimets W
Department of Surgery, University Hospital, University of Alberta, Edmonton, Canada.
Dis Colon Rectum. 1994 May;37(5):482-91. doi: 10.1007/BF02076196.
The aim of our investigation was to evaluate the clinical presentation of patients with carcinoid tumors of the colon and to estimate the survival and potential prognostic factors of this tumor type.
A population-based study was performed using data from the Alberta Cancer Registry between 1964 and 1988 (inclusive). The clinical records and the pathologic material of eligible patients were reviewed. Survival was estimated both as crude survival and with the Kaplan-Meier method.
During the 25-year study period (1964-1988), 36 true carcinoid tumors of the colon were diagnosed in Alberta. Carcinoids of the ileocecal region and of the rectum were excluded from the study. The average age at time of diagnosis was 68.4 years; there were 20 males and 16 females. Symptoms (abdominal pain, diarrhea, weakness, anorexia) occurred late in the course of the disease: 64 percent of the lesions were in Dukes D stage and 22 percent were Dukes C at diagnosis. Only one patient presented with a malignant carcinoid syndrome. Lesions occurred most frequently in the cecum (39 percent), followed by transverse and sigmoid colon. Most of the patients were managed surgically. The perioperative mortality rate was with 22 percent, which is quite high. The average size of the lesions was 5.8 (range, 2-10) cm, and most tumors (31/36) had invaded the pericolic fat. The most common immunohistochemical pattern was argentaffin/argyrophil negative and neuron-specific enolase positive. Two-year and five-year actuarial (Kaplan-Meier) survival was 34 percent and 26 percent, respectively. Survival for carcinoids of the colon was significantly lower compared with carcinoids of the rectum or appendix, and with colon adenocarcinomas. Size of the tumor and tumor invasion into the muscularis propria--the two major histopathologic prognostic factors for carcinoids of the gastrointestinal tract--were not found to influence survival significantly. Rather, tumor stage, histologic pattern, tumor differentiation, nuclear grade, and mitotic rate were found to significantly influence the survival rate.
Carcinoid tumors of the colon are extremely rare tumors, diagnosed late in the course of the disease, and they carry a bad prognosis. Prognostic factors are tumor stage, histologic pattern, differentiation, nuclear grade, and mitotic rate of the tumor.
我们研究的目的是评估结肠类癌患者的临床表现,并估计该肿瘤类型的生存率及潜在预后因素。
利用艾伯塔癌症登记处1964年至1988年(含)的数据进行一项基于人群的研究。对符合条件患者的临床记录和病理材料进行了回顾。生存率的估计采用粗生存率和Kaplan-Meier法。
在25年的研究期间(1964 - 1988年),艾伯塔省共诊断出36例真正的结肠类癌。回盲部和直肠类癌被排除在研究之外。诊断时的平均年龄为68.4岁;男性20例,女性16例。症状(腹痛、腹泻、虚弱、厌食)在疾病过程中出现较晚:64%的病变在诊断时处于Dukes D期,22%为Dukes C期。仅有1例患者出现恶性类癌综合征。病变最常发生于盲肠(39%),其次为横结肠和乙状结肠。大多数患者接受了手术治疗。围手术期死亡率为22%,相当高。病变的平均大小为5.8(范围2 - 10)cm,大多数肿瘤(31/36)侵犯了结肠周围脂肪。最常见的免疫组化模式为嗜银/亲银阴性和神经元特异性烯醇化酶阳性。两年和五年精算(Kaplan-Meier)生存率分别为34%和26%。与直肠或阑尾类癌以及结肠腺癌相比,结肠类癌的生存率显著更低。未发现肿瘤大小和肿瘤侵犯固有肌层(胃肠道类癌的两个主要组织病理学预后因素)对生存率有显著影响。相反,发现肿瘤分期、组织学模式、肿瘤分化、核分级和有丝分裂率对生存率有显著影响。
结肠类癌是极其罕见的肿瘤,在疾病过程中诊断较晚,预后不良。预后因素为肿瘤分期、组织学模式、分化、核分级和肿瘤的有丝分裂率。