Heniford B T, Iannitti D A, Evans P, Gagner M, Henderson J M
Department of General Surgery, Cleveland Clinic Foundation, Ohio, USA.
Am Surg. 1998 Dec;64(12):1165-9.
Primary duodenal adenocarcinoma not involving the ampullary region is rare. Our aim was to review the outcome of these patients and determine the factors that affect survival. We performed a retrospective review of all patients with primary, nonampullary duodenal adenocarcinoma at the Cleveland Clinic Foundation from January 1986 through December 1996. Twenty-six patients with primary, nonampullary duodenal malignancies were identified. There were 16 adenocarcinomas, 3 gastrinomas, 3 stromal tumors, 3 leiomyosarcomas, and 1 carcinoid tumor. Patients with adenocarcinoma had symptoms present an average of 6.1 months. Tumors were identified by upper gastrointestinal contrast study and esophagogastroduodenoscopy in 90 per cent and 87 per cent of patients, respectively. Twelve of 13 (93%) cancers found in the third or fourth portion of the duodenum were adenocarcinomas. Seven of the 16 adenocarcinomas were resectable on exploration. Those that were contained within the serosa have not recurred (mean, 6 years); one of the two patients with locally invasive adenocarcinoma remains disease free. The average survival for patients with unresectable disease was 6.7 months. The 5-year survival rates were: all adenocarcinoma, 38 per cent; resectable, 86 per cent; and unresectable, 0 per cent. All patients presenting with weight loss or obstructive symptoms died of disease; those with melena survived long term. Patients with tumors other than adenocarcinoma had a 90 per cent 5-year survival. We conclude that patients typically present with a long history of symptoms. Distal duodenal malignancies are most frequently adenocarcinomas. Upper gastrointestinal contrast study or endoscopy is often diagnostic. Patients with weight loss and/or obstructive symptoms had invasive disease and a morbid prognosis. Aggressive surgery is warranted, and most with resectable disease (86%) had long-term survival.
原发性十二指肠腺癌不累及壶腹区域者较为罕见。我们的目的是回顾这些患者的治疗结果并确定影响生存的因素。我们对1986年1月至1996年12月在克利夫兰诊所基金会就诊的所有原发性非壶腹十二指肠腺癌患者进行了回顾性研究。确定了26例原发性非壶腹十二指肠恶性肿瘤患者。其中有16例腺癌、3例胃泌素瘤、3例间质瘤、3例平滑肌肉瘤和1例类癌。腺癌患者出现症状的平均时间为6.1个月。分别有90%和87%的患者通过上消化道造影和食管胃十二指肠镜检查发现肿瘤。在十二指肠第三或第四部分发现的13例癌症中有12例(93%)为腺癌。16例腺癌中有7例在探查时可切除。那些局限于浆膜层内的肿瘤未复发(平均6年);2例局部浸润性腺癌患者中有1例仍无疾病复发。不可切除疾病患者的平均生存期为6.7个月。5年生存率分别为:所有腺癌患者为38%;可切除患者为86%;不可切除患者为0%。所有出现体重减轻或梗阻症状的患者均死于疾病;有黑便的患者长期存活。非腺癌患者的5年生存率为90%。我们得出结论,患者通常有较长的症状史。十二指肠远端恶性肿瘤最常见的是腺癌。上消化道造影或内镜检查通常具有诊断价值。出现体重减轻和/或梗阻症状的患者患有浸润性疾病且预后不良。应积极进行手术,大多数可切除疾病患者(86%)可长期存活。