摘要
目的:对3例以腹痛、贫血、便血、肠梗阻为首诊的儿童少见疾病进行确诊。方法:根据患儿家族史、临床观察、肠镜、X线检查、病理检查、手术确诊。结果:儿童色素沉着息肉综合征常以贫血、腹痛、便血、肠梗阻等为主要表现。可有遗传性,可散发。常伴恶性病变。结论:应提高对儿童色素沉着息肉综合征的认识,以利早期诊断,恰当治疗、随访。
Objective. To make a definit diganosis for three children with Peutz- Jelghers syndrome who were first diagnosed to be bellyache, anemia, ileus, and bleed in stool. Methods： Peutz - Jeghers syndrome was diagnosed based on the familial history, clirtie symptoms, X- ray examination, pathology and operation. Results： Bellyache, anemia, ileus, and bleed in stool were the most common symptoms of Peutz- Jeghers of children caused by gastrointestinal polyposis and disorders. Half of the patients had familial history. Most of them would complicated with cancer in their whole life . Conclusion： It is important to diagnose Peutz- Jehgers Syndrome early, and also the disease should be treated early and properly.
出处
《现代预防医学》
CAS
北大核心
2006年第6期1050-1051,共2页
Modern Preventive Medicine
关键词
儿童
色素沉着综合征
息肉
遗传
错构瘤
癌
Children
Peutz-Jegherssyrdrome
Pigmentation
Polyposis
Inheritance
Hamartoma
Cancer
