Yu Y Y, Ogino T, Okada S
First Department of Pathology, Okayama University Medical School, Japan.
Acta Pathol Jpn. 1992 Sep;42(9):684-7.
A rare alpha-fetoprotein (AFP)-producing carcinoma that originated in the rectum of a 54-year-old man is reported. High levels of AFP are found in the serum (5,126 ng/ml) and homogenate of the tumor tissue (2,600 ng/g). Two morphologic patterns were noted in the tumor. One was that of well differentiated tubular adenocarcinoma and the other was more polymorphous, in which the tumor cells grow in a solid-sheet with occasional glandular and papillary structures. Hyaline bodies and Schiller-Duval body-like structures were also found in the polymorphous area. There was a gradual transition between the well differentiated and the polymorphous area. AFP was positive in the polymorphous area and negative in the well differentiated area on immunohistochemical examination. These morphologic and immunohistochemical characteristics may suggest a differentiation toward embryonal carcinoma of the polymorphous component. Moreover, the polymorphous component showed marked vascular invasion and metastasis of liver as well as regional lymph nodes. AFP-producing carcinoma cells may be more aggressive than ordinary adenocarcinoma.
报道了一例起源于一名54岁男性直肠的罕见的产生甲胎蛋白(AFP)的癌。在血清(5126 ng/ml)和肿瘤组织匀浆(2600 ng/g)中发现了高水平的AFP。肿瘤呈现出两种形态学模式。一种是高分化管状腺癌模式,另一种则更为多形性,其中肿瘤细胞呈实性片状生长,偶尔有腺管和乳头结构。在多形性区域还发现了透明小体和席勒-杜瓦尔体样结构。高分化区域和多形性区域之间存在逐渐过渡。免疫组化检查显示,AFP在多形性区域呈阳性,在高分化区域呈阴性。这些形态学和免疫组化特征可能提示多形性成分向胚胎癌分化。此外,多形性成分显示出明显的血管侵犯以及肝和区域淋巴结转移。产生AFP的癌细胞可能比普通腺癌更具侵袭性。