Goodin Geoffrey S, McCarville M Beth, Thibodeau Stephen N, Skapek Stephen X, Khoury Joseph D, Spunt Sheri L
Department of Radiological Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Pediatr Blood Cancer. 2008 Feb;50(2):409-12. doi: 10.1002/pbc.20985.
Familial adenomatous polyposis (FAP) is an inherited condition causing numerous adenomatous colorectal polyps and a markedly elevated risk of colon cancer. FAP may be associated with various extracolonic manifestations such as desmoid fibromatosis and osteomas (termed Gardner's syndrome) and brain tumors, usually medulloblastoma or glioma [termed Brain Tumor Polyposis (BTP) syndrome type 2]. We describe a pediatric patient who initially presented with prolactinoma and later was found to have Gardner's syndrome. A germline mutation of the APC (adenomatous polyposis coli) gene was identified. Our case illustrates the association between prolactinoma and FAP, which may represent a rare subtype of Gardner's and BTP syndromes.
家族性腺瘤性息肉病(FAP)是一种遗传性疾病,可导致大量腺瘤性结肠息肉,并显著增加患结肠癌的风险。FAP可能与各种结肠外表现相关,如硬纤维瘤病和骨瘤(称为加德纳综合征)以及脑肿瘤,通常是髓母细胞瘤或胶质瘤[称为脑肿瘤息肉病(BTP)综合征2型]。我们描述了一名儿科患者,最初表现为催乳素瘤,后来被发现患有加德纳综合征。鉴定出APC(腺瘤性息肉病 coli)基因的种系突变。我们的病例说明了催乳素瘤与FAP之间的关联,这可能代表加德纳综合征和BTP综合征的一种罕见亚型。