Janneck C
Kinderkrankenhaus Walddörfer, Abteilung des Kinderkrankenhauses Wilhelmstift, Hamburg.
Z Kinderchir. 1988 Oct;43(5):353-4. doi: 10.1055/s-2008-1043484.
Case report of an extremely rare retrorectal duplication, containing gastric mucosa folds with a fistula to the rectum in a 10-year-old boy with myelodysplasia syndrome, anal stenosis and a sacral defect. Persistent tar-like stools prompted detailed investigations, followed by extirpation of the doubling. The combination of anorectal malformations, presacral masses and sacrococcygeal defect may point to a Currarino triad, an autosomal dominant hereditary syndrome which can be simply detected or identified by x-ray examination of the os sacrum.
一名患有脊髓发育不良综合征、肛门狭窄和骶骨缺损的10岁男孩,出现极为罕见的直肠后重复畸形病例报告,该重复畸形内含有胃黏膜皱襞且与直肠形成瘘管。持续的柏油样便促使进行详细检查,随后切除该重复畸形。肛门直肠畸形、骶前肿物和骶尾骨缺损的组合可能提示库拉里诺三联征,这是一种常染色体显性遗传综合征,可通过骶骨的X线检查简单检测或识别。