产后女性克朗凯特-加拿大综合征的自发改善
Spontaneous improvement of Cronkhite-Canada syndrome in a postpartum female.
作者信息
Peart A G, Sivak M V, Rankin G B, Kish L S, Steck W D
出版信息
Dig Dis Sci. 1984 May;29(5):470-4. doi: 10.1007/BF01296227.
PMID:6714066
Abstract
A case report of a 34-year-old female with the Cronkhite-Canada syndrome is presented. The patient developed the characteristic clinical features of intestinal polyposis, skin pigmentation, alopecia, and onychodystrophy which later resolved. An unusual feature was that symptoms developed during the postpartum period. This is the youngest female patient described with the syndrome. The etiology, pathophysiology, clinical manifestations, and management of the Cronkhite-Canada syndrome are reviewed.
摘要
本文报告一例34岁患有克朗凯特-加拿大综合征的女性病例。该患者出现了肠道息肉病、皮肤色素沉着、脱发和甲营养不良等典型临床特征，这些症状后来有所缓解。一个不寻常的特征是症状在产后出现。这是所报道的患该综合征最年轻的女性患者。本文对克朗凯特-加拿大综合征的病因、病理生理学、临床表现及治疗进行了综述。
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Ann Intern Med. 1962 Jun;56:935-40. doi: 10.7326/0003-4819-56-6-935.
2
Generalized gastrointestinal polyposis; an unusual syndrome of polyposis, pigmentation, alopecia and onychotrophia.全身性胃肠道息肉病；一种伴有息肉病、色素沉着、脱发和甲营养障碍的罕见综合征。
N Engl J Med. 1955 Jun 16;252(24):1011-5. doi: 10.1056/NEJM195506162522401.
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Cronkhite-Canada syndrome: report of an unusual case.
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