Stabile B E, Passaro E
Am J Surg. 1985 Jan;149(1):144-50. doi: 10.1016/s0002-9610(85)80024-6.
The advent of the histamine H2-receptor antagonists and the renewed interest in curative surgery in patients with gastrinoma have made the differentiation between benign and malignant tumors of critical importance. An analysis of 65 patients with gastrinoma followed for an average of 93 months revealed two distinct clinical groups: those with and those without hepatic tumors at initial examination or operation. Among the 14 patients with hepatic tumors, 12 had multiple liver metastases from pancreatic or duodenal primary tumors, and 2 had primary hepatic gastrinomas. Ten of the 14 patients (71 percent) died from tumor progression, and the total tumor-related mortality for this group was 79 percent. In contrast, only 1 of 15 patients (7 percent) with tumor in the lymph nodes died from a tumor-related cause (recurrent ulcer hemorrhage), and none died from tumor progression. Only a single patient with lymph node metastases at initial exploration went on to the development of liver metastases, which was found incidentally at autopsy 313 months later. Among 23 patients with either primary tumors only or no tumors found at laparotomy, there was only one tumor-related death and no deaths from tumor spread. Life-table analysis demonstrated a significantly decreased length of survival for patients with liver tumor compared with those without liver involvement. Multiple endocrine adenopathy syndrome was not a significant factor in survival. Serum gastrin levels were likewise nondiscriminatory. Six of 52 patients (12 percent), including three with tumor in the lymph nodes, were apparently cured by excision of all gastrinoma recognized at laparotomy. The cure rate was 23 percent for patients without multiple endocrine adenopathy syndrome or liver metastases. Hepatic metastases is a definitive marker for clinically malignant disease and portends a poor prognosis. Patients with gastrinoma confined to the lymph nodes uncommonly follow a malignant clinical course. Such patients have at least a 20 percent probability of surgical cure if they do not have multiple endocrine adenopathy syndrome.
组胺H2受体拮抗剂的出现以及对胃泌素瘤患者根治性手术重新燃起的兴趣,使得区分胃泌素瘤的良性与恶性肿瘤变得至关重要。对65例平均随访93个月的胃泌素瘤患者进行分析,发现了两个不同的临床组:初诊或手术时伴有肝肿瘤的患者和不伴有肝肿瘤的患者。在14例有肝肿瘤的患者中,12例有来自胰腺或十二指肠原发性肿瘤的多发肝转移,2例有原发性肝胃泌素瘤。14例患者中有10例(71%)死于肿瘤进展,该组总的肿瘤相关死亡率为79%。相比之下,15例有淋巴结肿瘤的患者中只有1例(7%)死于肿瘤相关原因(复发性溃疡出血),无1例死于肿瘤进展。初次探查时有淋巴结转移的患者中只有1例后来发生了肝转移,这是在313个月后的尸检中偶然发现的。在23例仅患有原发性肿瘤或剖腹探查未发现肿瘤的患者中,只有1例死于肿瘤相关原因,无1例死于肿瘤扩散。寿命表分析显示,与无肝受累的患者相比,有肝肿瘤的患者生存时间显著缩短。多发性内分泌腺病综合征不是影响生存的重要因素。血清胃泌素水平同样无鉴别意义。52例患者中有6例(12%),包括3例有淋巴结肿瘤的患者,经剖腹手术切除所有发现的胃泌素瘤后明显治愈。无多发性内分泌腺病综合征或肝转移的患者治愈率为23%。肝转移是临床恶性疾病的决定性标志,预示预后不良。局限于淋巴结的胃泌素瘤患者很少出现恶性临床病程。如果这些患者没有多发性内分泌腺病综合征,手术治愈的概率至少为20%。