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Cap polyposis is extremely rare in children. We report a case of an 11-month-old male infant who visited our hospital because of rectal prolapse and small amount of hematochezia lasting several days. He also had an epidermal nevus in the sacral area. Colonoscopy showed erythematous, multilobulated, circumferential, polypoid lesions with mucoid discharge from the rectum. He was diagnosed with cap polyposis by endoscopy and histologic examination. He was treated with surgical resection, and was closely followed up. In the relevant literature, there is no report of cap polyposis in an infant. We report the first case of cap polyposis in the youngest infant.

作者:Soon Chul, Kim;Myoung Jae, Kang;Yeon Jun, Jeong;Pyoung Han, Hwang

来源:Journal of Korean medical science 2017 年 32卷 5期

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作者:
Soon Chul, Kim;Myoung Jae, Kang;Yeon Jun, Jeong;Pyoung Han, Hwang
来源:
Journal of Korean medical science 2017 年 32卷 5期
标签:
Cap Polyposis Epidermal Nevus Hematochezia
Cap polyposis is extremely rare in children. We report a case of an 11-month-old male infant who visited our hospital because of rectal prolapse and small amount of hematochezia lasting several days. He also had an epidermal nevus in the sacral area. Colonoscopy showed erythematous, multilobulated, circumferential, polypoid lesions with mucoid discharge from the rectum. He was diagnosed with cap polyposis by endoscopy and histologic examination. He was treated with surgical resection, and was closely followed up. In the relevant literature, there is no report of cap polyposis in an infant. We report the first case of cap polyposis in the youngest infant.