Halata M S, Miller J, Stone R K
Department of Pediatrics, New York Medical College, Metropolitan Hospital Center, New York, New York 10029.
Clin Pediatr (Phila). 1989 Nov;28(11):538-40. doi: 10.1177/000992288902801111.
A 14-year-old patient who was eventually found to have Gardner syndrome initially presented at the age of 3 years with a desmoid tumor involving the scalp. A careful review of the family history revealed a high incidence of colonic cancer, which prompted endoscopic evaluation of the patient. The discovery of adenomatous polyps in the colon confirmed the diagnosis of Gardner syndrome. In patients with hard or soft tissue tumors, the possibility of Gardner syndrome should be kept in mind, and a thorough family history taken. Early diagnosis may prevent malignant transformation of colonic polyps.
一名最终被诊断为加德纳综合征的14岁患者,最初在3岁时因头皮硬纤维瘤就诊。仔细回顾家族史发现结肠癌发病率很高,这促使对该患者进行内镜评估。结肠腺瘤性息肉的发现证实了加德纳综合征的诊断。对于有硬组织或软组织肿瘤的患者,应考虑加德纳综合征的可能性,并详细询问家族史。早期诊断可预防结肠息肉恶变。