Roth J A, Berman E, Befeler D, Johnson F B
Am J Surg Pathol. 1982 Jun;6(4):375-82. doi: 10.1097/00000478-198206000-00010.
A hepatocellular carcinoma which was predominately black was surgically excised from a noncirrhotic, asymptomatic 62-year-old white man. Brown-black, pigment granules, found only in the tumor cells, were histochemically and ultrastructurally identical to the hepatocellular pigment found in Dubin-Johnson syndrome. The latter pigment is thought to accumulate as a consequence of a genetically determined abnormality in the excretion of catecholamines and related substances. It is postulated that the pigment formation in this tumor developed via a similar, though epigenetic, mechanism. This occurrence has not been previously described. Unusual PAS-negative, globular cytoplasmic inclusions were also found in the tumor cells and these proved to be Mallory bodies by electron microscopy.
从一名62岁无症状的非肝硬化白人男性身上手术切除了一个以黑色为主的肝细胞癌。仅在肿瘤细胞中发现的棕黑色色素颗粒,在组织化学和超微结构上与杜宾-约翰逊综合征中发现的肝细胞色素相同。后者的色素被认为是由于儿茶酚胺及相关物质排泄的基因决定异常而积累的。据推测,该肿瘤中的色素形成是通过类似的、尽管是表观遗传的机制发展而来的。这种情况以前没有被描述过。在肿瘤细胞中还发现了不寻常的PAS阴性、球状细胞质包涵体,通过电子显微镜证实这些是马洛里小体。