Roza-Molnar I, Juhas M, Tot T, Balint Z
Zdravstveni centar Dr Gere Istvan, Senta.
Med Pregl. 1991;44(7-8):313-5.
A case of a ten year old adopted girl is presented, who had gastrointestinal disturbances, anal pruritus and relapses of urticaria from her fourth year of age. By means of radiological and endoscopis analysis, multiple gastrointestinal polyposis was established. Pathohistological examination of the polyp indicated that tubular adenomas were in question, therefore in the case of this girl it can be stated that she has diffuse tubular gastrointestinal adenomatous polyposis, which is a characteristic of Gardner's syndrome. At the moment of the setting of the diagnosis, the girl had no skin changes nor did she have any radiological changes on the bones of her skull. The first skin changes appeared one year after the diagnosis was set, and they were in the form of maculopapular nodules, comedos of the closed and open type on the forehead and chin.
本文介绍了一例十岁的领养女孩，自四岁起就出现胃肠道紊乱、肛门瘙痒和荨麻疹复发的症状。通过放射学和内镜分析，确诊为多发性胃肠道息肉病。对息肉进行病理组织学检查表明，所涉及的是管状腺瘤，因此可以说，这个女孩患有弥漫性管状胃肠道腺瘤性息肉病，这是加德纳综合征的一个特征。在确诊时，该女孩没有皮肤变化，颅骨骨骼也没有任何放射学改变。确诊一年后首次出现皮肤变化，表现为斑丘疹结节，前额和下巴有闭合性和开放性粉刺。
