论文部分内容阅读
近来有报道指出,Gardner综合征和家族性腺瘤样息肉病(FAP)患者中,先天性视网膜色素上皮肥大(CHRPE)有很高的发病率(87.5%～100%).报道同时指出在有FAP的家族成员中进行眼科检查的重要性,因为CHRPE对FAP的高度诊断特异性.作者据此研究FAP和CHRPE并存的患者.在来自24个FAP家族的49个家庭成员中进行眼科检查.其中有43人患有FAP,另外6名直系亲属,尚未发现有结肠息肉.43个病人中有36人接受了胃十二
It has recently been reported that there is a high incidence of congenital retinal pigment epithelium hypertrophy (CHRPE) in patients with Gardner’s syndrome and familial adenomatous polyposis (FAP) (87.5% -100%). The report also pointed out that in patients with FAP Of the family members because of the high diagnostic specificity of CHRPE for FAP The authors studied patients with FAP and CHRPE coexisting and conducted an ophthalmic examination among 49 family members from the 24 FAP families, Forty-three had FAP and another six had immediate family history, with no colon polyps yet, and 36 of the 43 patients underwent gastric twelve