Kim J C, Roh S A, Yu C S, Lee H I, Gong G
Department of Surgery, University of Ulsan College of Medicine, Seoul, Korea.
Am J Gastroenterol. 1997 Oct;92(10):1913-5.
Familial juvenile polyposis has been known to have malignant potential, but their genetic relation to familial adenomatous polyposis has not been proven yet. Two young brothers with intermittent rectal bleeding revealed multiple juvenile polyposis. Their father had a history of rectal cancer with multiple colonic polyps. Four frequent exons of APC gene mutation were tested from these patients' white blood cells by polyacrylamide gel electrophoresis and sequencing. The 21-yr-old brother had a missense mutation (GAA-->GGA) at codon 1309, whereas the 18-yr-old brother showed a missense mutation (ATA-->GTA) at codon 1304 in exon 15 of APC gene. Three of four first-degree relatives were affected with familial juvenile polyposis, familial juvenile polyposis with adenomatous change, and rectal cancer with multiple polyps. The APC gene mutation of familial juvenile polyposis in this case suggests a genetic relationship with familial adenomatous polyposis.
家族性幼年性息肉病已知具有恶变潜能,但其与家族性腺瘤性息肉病的遗传关系尚未得到证实。两名有间歇性直肠出血的年轻兄弟被发现患有多发性幼年性息肉病。他们的父亲有直肠癌病史且伴有多个结肠息肉。通过聚丙烯酰胺凝胶电泳和测序对这些患者白细胞中的APC基因突变的四个常见外显子进行了检测。21岁的哥哥在APC基因第15外显子的第1309密码子处有一个错义突变(GAA→GGA),而18岁的弟弟在第1304密码子处有一个错义突变(ATA→GTA)。四个一级亲属中有三人患有家族性幼年性息肉病、伴有腺瘤样改变的家族性幼年性息肉病以及伴有多个息肉的直肠癌。本例家族性幼年性息肉病的APC基因突变提示其与家族性腺瘤性息肉病存在遗传关系。