Lieberman J, Silton R M, Agliozzo C M, McMahon J
Am J Clin Pathol. 1975 Sep;64(3):304-10. doi: 10.1093/ajcp/64.3.304.
A case history of a 16-year-old boy with hepatocellular carcinoma and an intermediate deficiency of alpha1-antitrypsin (MZ phenotype) is presented. Previous reports have suggested that hepatocellular carcinoma may be associated with the Z variant of antitrypsin and either a severe or intermediate antitrypsin deficiency. The present case is unusual because of the rather high level of the serum trypsin inhibitory capacity for an MZ heterozygote (1.633 units), which may be due to involvement of the liver by the tumor or to a recent partial hepatectomy. PAS-positive antitrypsin globules were seen in the primary tumor and in nodules metastatic to the mesentery, as well as in nonneoplastic portions of the liver. Hepatocellular carcinoma is another disease state that may occur preferentially in individuals with either severe or intermediate deficiencies of alpha1-antitrypsin.
本文报告了一名16岁患有肝细胞癌且α1 -抗胰蛋白酶中度缺乏(MZ表型)男孩的病例史。既往报道提示肝细胞癌可能与抗胰蛋白酶的Z变体以及严重或中度抗胰蛋白酶缺乏有关。本病例不同寻常之处在于,作为MZ杂合子,其血清胰蛋白酶抑制能力相当高(1.633单位),这可能是由于肿瘤累及肝脏或近期进行了部分肝切除术所致。在原发性肿瘤、转移至肠系膜的结节以及肝脏的非肿瘤部分均可见PAS阳性的抗胰蛋白酶小球。肝细胞癌是另一种可能优先发生于α1 -抗胰蛋白酶严重或中度缺乏个体的疾病状态。