Boor P J, Swanson M R
Am J Surg Pathol. 1979 Feb;3(1):69-75. doi: 10.1097/00000478-197902000-00008.
A case of an unusual pancreatic tumor with a characteristic papillary-cystic microscopic morphology is presented. Review of four previously reported similar cases suggests a distinct clinical picture of a large abdominal mass occurring in a young person which apparently, after resection, does not rapidly recur. The histopathology of this tumor consists of papillary and cystic patterns, regular homogeneous cells with a few mitoses, glassy eosinophilic cytoplasm, and mucin and PAS positivity. Ultrastructural detail, including eccentric nucleoli, numerous mitochondria, sparse endoplasmic reticulum, and little evidence of secretory activity, suggests a duct cell origin for this rare tumor.
本文报告了一例具有特征性乳头-囊性微观形态的罕见胰腺肿瘤。回顾之前报道的4例类似病例发现,其临床表现具有明显特征,即发生于年轻人的巨大腹部肿块,切除后显然不会迅速复发。该肿瘤的组织病理学表现为乳头和囊性结构,细胞形态规则、均匀,有少量有丝分裂象,胞质呈玻璃样嗜酸性,黏液和PAS染色呈阳性。超微结构细节包括偏心核仁、大量线粒体、稀疏的内质网以及几乎没有分泌活动的迹象,提示这种罕见肿瘤起源于导管细胞。