一个患有黑斑息肉综合征的家族中出现的具有加拿大克朗凯特综合征某些成分的病例。

Kang Y W, Park S K, Kim H, Bae O S, Chang E S

Korean J Intern Med. 1988 Jul;3(2):136-41. doi: 10.3904/kjim.1988.3.2.136.

A case with some components of Cronkhite-Canada syndrome such as onycholdystrophy, a large amount of diarrhea, hypoproteinemia and hypoalbuminemia in a 16 year-old man with Peutz-Jeghers syndrome was studied. His family members were conirmed to have Peutz-Jeghers syndrome by biopsy of polyps in the rectum and duodenum. This is the first case report of Peutz-Jeghers syndrome associated with some components of Cronkhite-Canada syndrome.

对一名患有黑斑息肉综合征的16岁男性进行了研究，该患者出现了一些加拿大克朗凯特综合征的症状，如甲营养不良、大量腹泻、低蛋白血症和低白蛋白血症。通过对直肠和十二指肠息肉进行活检，证实其家庭成员患有黑斑息肉综合征。这是首例关于黑斑息肉综合征合并加拿大克朗凯特综合征某些症状的病例报告。