Hashimoto L A, Walsh R M
Department of General Surgery, The Cleveland Clinic Foundation, OH 44195, USA.
J Am Coll Surg. 1999 Oct;189(4):368-73. doi: 10.1016/s1072-7515(99)00163-5.
Insulinomas are infrequent but are important to recognize and surgically remove. Several diagnostic tests have been used to increase the chances of operative success. The value of preoperative testing for insulinomas is the subject of this review.
All patients treated at the Cleveland Clinic for insulinoma between 1985 and 1995 were retrospectively reviewed. All patients had biochemical evidence of primary hyperinsulinemia.
There were 21 patients, 10 men and 11 women, with a median age of 58 years. Eighteen patients (85%) had a single insulinoma, two patients (10%) had multiple insulinomas, and one patient (5%) had nesidioblastosis. In addition, two patients (10%) had malignant insulinoma. A total of 13 patients (62%) had successful preoperative localization of their tumors, and all of these were found during exploration either by the surgeon (12 patients) or by intraoperative ultrasonography (1 patient). The remaining eight patients (38%) did not have their lesion localized by preoperative tests. In seven patients these tumors were found at operation, three by the surgeon and four by intraoperative ultrasonography. One patient failed preoperative and intraoperative localization and was later diagnosed with nesidioblastosis. Enucleation was performed in 13 patients and distal pancreatectomy in 7; the patient with nesidioblastosis had a negative laparotomy and a subsequent distal pancreatectomy. The mortality and morbidity rates were 0% and 14%, respectively. Only two patients, including the patient with nesidioblastosis, remained symptomatic after operation.
The diagnosis of an insulinoma does not require extensive localization studies before operation. The combination of surgical exploration and intraoperative ultrasonography identified more than 90% of insulinomas. When technically feasible, enudeation is curative and can be accomplished with low morbidity.
胰岛素瘤虽不常见,但识别并手术切除至关重要。已采用多种诊断测试以提高手术成功率。本综述探讨术前检测对胰岛素瘤的价值。
回顾性分析1985年至1995年间在克利夫兰诊所接受胰岛素瘤治疗的所有患者。所有患者均有原发性高胰岛素血症的生化证据。
共21例患者,10例男性,11例女性,中位年龄58岁。18例患者(85%)为单发胰岛素瘤,2例患者(10%)为多发胰岛素瘤,1例患者(5%)为胰岛细胞增殖症。此外,2例患者(10%)为恶性胰岛素瘤。共有13例患者(62%)术前成功定位肿瘤,其中12例由外科医生在探查时发现,1例由术中超声发现。其余8例患者(38%)术前检查未定位病变。其中7例患者的肿瘤在手术中发现,3例由外科医生发现,4例由术中超声发现。1例患者术前及术中均未定位,后来被诊断为胰岛细胞增殖症。13例患者行肿瘤剜除术,7例患者行远端胰腺切除术;患有胰岛细胞增殖症的患者剖腹探查阴性,随后行远端胰腺切除术。死亡率和发病率分别为0%和14%。术后仅2例患者(包括患有胰岛细胞增殖症的患者)仍有症状。
胰岛素瘤的诊断术前无需进行广泛的定位研究。手术探查与术中超声相结合可发现90%以上的胰岛素瘤。在技术可行时,剜除术可治愈疾病,且发病率低。