肝母细胞瘤
家族性腺瘤性息肉病
医学
结直肠癌
胃肠病学
内科学
大肠腺瘤性息肉病
腺癌
肿瘤科
癌症
作者
Ilaria Lazzareschi,Giuseppe Barone,Stefano Mastrangelo,Ilaria Furfaro,Giacomo Rando,Riccardo Riccardi
标识
DOI:10.1177/030089160909500629
摘要
Familial adenomatous polyposis is an inherited disorder characterized by the development of hundreds of colorectal adenomas during adolescence, which in many cases will transform into colorectal cancer by the fourth decade of life, along with the development of various malignant tumors including hepatoblastoma. We report on a female patient with a de novo interstitial deletion of 5q21.3-q23.3, encompassing the APC gene, associated with adenomatous polyposis and early colorectal cancer, hepatoblastoma, epidermoid cysts, mental retardation, several mild dysmorphic signs and lower limb venous thrombosis.
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