Yuan Chun-hui, Xiu Dian-rong, Shi Xue-ying, Ma Zhao-lai, Li Zhi-fei, Tao Ming, Jia Yi-mu, Xiong Jing-wei, Zhang Tong-lin
Department of General Surgery, Peking University Third Hospital, Beijing 100191, China.
Zhonghua Wai Ke Za Zhi. 2012 Jan 1;50(1):11-4.
To study the clinicopathologic and immunohistochemical features, biological behavior, diagnosis and treatment of solid pseudopapillary tumor of the pancreas (SPTP).
A retrospective clinical and clinicopathologic analysis was made on 33 cases of SPTP admitted from May 2001 to 2010 July. There were 7 male and 26 female patients, aging from 13 to 66 years with a mean of 34.3 years.
The tumor was located in pancreatic head of 10 patients, in pancreatic neck of 5 patients, in pancreatic body and tail of 18 patients. Of the 33 patients treated with surgery, 8 underwent simple resection of pancreatic tumor, 6 underwent pancreaticoduodenectomy, 3 underwent tumor resection plus pancreaticojejunostomy, 1 underwent tumor resection plus pancreaticogastrostomy, 11 underwent distal pancreatectomy, 4 underwent distal pancreatectomy plus spleen resection (1 underwent mesohepatectomy for hepatic metastasis). Sixteen of the 33 operations were completed by laparoscopy. Histologically, tumors were composed of papillary and microcystic solid structures, with uniformed population of cells. The pancreas and blood vessels invasion were identified in 3 cases, one of them was combined with liver metastasis, and they are male. Immunohistologically, the tumors were positive for α1-antitrypsin, α1-antichymotrypsin, β-catenin, CD10, CD56 and vimentin (all cases), neuron-specific enolase (3 cases), synaptophysin (6 cases), chromogranin A (4 cases), progesterone receptor (28 cases), estrogen receptor (3 cases), S-100 (6 cases). Totally 33 cases were followed up with a median period of 49 months without tumor recurrence.
SPTP is of low graded malignancy. It primarily affects young women. It may be located in any part of pancreas. Immunohistochemistry is very important for the diagnosis and differential diagnosis of SPTP. Surgical resection is recommended as the treatment of choice. Laparoscopic distal pancreatectomy or tumor resection is feasible and safe for some selected patients, and the prognosis is good.
探讨胰腺实性假乳头状瘤(SPTP)的临床病理及免疫组化特征、生物学行为、诊断及治疗方法。
对2001年5月至2010年7月收治的33例SPTP患者进行回顾性临床及临床病理分析。其中男性7例,女性26例,年龄13~66岁,平均34.3岁。
肿瘤位于胰头10例,胰颈5例,胰体尾18例。33例行手术治疗的患者中,8例行单纯胰腺肿瘤切除术,6例行胰十二指肠切除术,3例行肿瘤切除加胰空肠吻合术,1例行肿瘤切除加胰胃吻合术,11例行远端胰腺切除术,4例行远端胰腺切除术加脾切除术(1例因肝转移行肝中叶切除术)。33例手术中16例通过腹腔镜完成。组织学上,肿瘤由乳头状和微囊性实性结构组成,细胞群体均匀。3例见胰腺及血管侵犯,其中1例合并肝转移,均为男性。免疫组化结果显示,肿瘤α1 -抗胰蛋白酶、α1 -抗糜蛋白酶、β -连环蛋白、CD10、CD56及波形蛋白均呈阳性(所有病例),神经元特异性烯醇化酶3例阳性,突触素6例阳性,嗜铬粒蛋白A 4例阳性,孕激素受体28例阳性,雌激素受体3例阳性,S - 100 6例阳性。33例均获随访,中位随访时间49个月,无肿瘤复发。
SPTP恶性程度低。主要累及年轻女性。可发生于胰腺任何部位。免疫组化对SPTP诊断及鉴别诊断非常重要。推荐手术切除作为首选治疗方法。对于部分合适的患者,腹腔镜远端胰腺切除术或肿瘤切除术可行且安全,预后良好。