Ji Yuan, Zhu Xiong-zeng, Lou Wen-hui, Wang Dong-qing, Jin Da-yong, Zeng Meng-su, Zeng Hai-ying
Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Zhonghua Bing Li Xue Za Zhi. 2007 Mar;36(3):160-5.
To study the clinicopathologic and immunohistochemical features of cystic neoplasms of the pancreas.
Ninety-two cases of cystic neoplasm of pancreas were retrieved from the Department archival file during the period from 1999 to 2005. Histologic features were studied and the tumors were typed according to WHO classification. Immunohistochemistry was also carried out using paraffin-embedded tissues.
The age of patients ranged from 16 to 80 years. The patients included 33 males and 59 females. The tumors varied from 2 cm to 21 cm in diameter. They consisted of intraductal papillary mucinous neoplasm (36/92), serous cystic neoplasm (18/92), solid pseudopapillary tumor (18/92), mucinous cystic neoplasm (14/92), cystic pancreatic ductal adenocarcinoma (4/92) and cystic pancreatic endocrine neoplasm (2/92). Immunohistochemical study revealed variable staining patterns, with frequent overlaps between different tumor types. In general, serous cystic neoplasm expressed MUC1, while mucinous cystic neoplasm was positive for MUC-5AC, intraductal papillary mucinous neoplasm for MUC-2 and cystic pancreatic ductal adenocarcinoma for MUC-1. On the other hand, solid pseudopapillary tumor expressed alpha-antitrypsin, alpha-antichymotrypsin, vimentin and progesterone receptor.
Accurate diagnosis of pancreatic cystic neoplasms requires correlation of clinical findings, radiologic examination, histologic features and immunostaining results. Pathologic distinction is important because of different prognostic significance. Two-thirds of pancreatic cystic neoplasms are premalignant or malignant and warrant surgical resection, whereas the remaining one-third (including pseudocyst and serous cystadenoma) are benign and can be treated conservatively.
研究胰腺囊性肿瘤的临床病理及免疫组化特征。
从1999年至2005年期间的科室存档文件中检索出92例胰腺囊性肿瘤病例。研究其组织学特征,并根据世界卫生组织分类对肿瘤进行分型。同时对石蜡包埋组织进行免疫组化检测。
患者年龄在16岁至80岁之间。其中男性33例,女性59例。肿瘤直径从2厘米至21厘米不等。包括导管内乳头状黏液性肿瘤(36/92)、浆液性囊性肿瘤(18/92)、实性假乳头状肿瘤(18/92)、黏液性囊性肿瘤(14/92)、囊性胰腺导管腺癌(4/92)和囊性胰腺内分泌肿瘤(2/92)。免疫组化研究显示出不同的染色模式,不同肿瘤类型之间常有重叠。一般来说,浆液性囊性肿瘤表达MUC1,黏液性囊性肿瘤MUC - 5AC呈阳性,导管内乳头状黏液性肿瘤表达MUC - 2,囊性胰腺导管腺癌表达MUC - 1。另一方面,实性假乳头状肿瘤表达α - 抗胰蛋白酶、α - 抗糜蛋白酶、波形蛋白和孕激素受体。
胰腺囊性肿瘤的准确诊断需要结合临床发现、影像学检查、组织学特征和免疫染色结果。由于预后意义不同,病理鉴别很重要。三分之二的胰腺囊性肿瘤为癌前病变或恶性,需要手术切除,而其余三分之一(包括假性囊肿和浆液性囊腺瘤)为良性,可保守治疗。