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A Case of Cap Polyposis with Epidermal Nevus in an Infant

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,...

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Autores principales: Kim, Soon Chul, Kang, Myoung Jae, Jeong, Yeon Jun, Hwang, Pyoung Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383624/
https://www.ncbi.nlm.nih.gov/pubmed/28378565
http://dx.doi.org/10.3346/jkms.2017.32.5.880
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author Kim, Soon Chul
Kang, Myoung Jae
Jeong, Yeon Jun
Hwang, Pyoung Han
author_facet Kim, Soon Chul
Kang, Myoung Jae
Jeong, Yeon Jun
Hwang, Pyoung Han
author_sort Kim, Soon Chul
collection PubMed
description 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.
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spelling pubmed-53836242017-05-01 A Case of Cap Polyposis with Epidermal Nevus in an Infant Kim, Soon Chul Kang, Myoung Jae Jeong, Yeon Jun Hwang, Pyoung Han J Korean Med Sci Case Report 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. The Korean Academy of Medical Sciences 2017-05 2017-03-03 /pmc/articles/PMC5383624/ /pubmed/28378565 http://dx.doi.org/10.3346/jkms.2017.32.5.880 Text en © 2017 The Korean Academy of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kim, Soon Chul
Kang, Myoung Jae
Jeong, Yeon Jun
Hwang, Pyoung Han
A Case of Cap Polyposis with Epidermal Nevus in an Infant
title A Case of Cap Polyposis with Epidermal Nevus in an Infant
title_full A Case of Cap Polyposis with Epidermal Nevus in an Infant
title_fullStr A Case of Cap Polyposis with Epidermal Nevus in an Infant
title_full_unstemmed A Case of Cap Polyposis with Epidermal Nevus in an Infant
title_short A Case of Cap Polyposis with Epidermal Nevus in an Infant
title_sort case of cap polyposis with epidermal nevus in an infant
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383624/
https://www.ncbi.nlm.nih.gov/pubmed/28378565
http://dx.doi.org/10.3346/jkms.2017.32.5.880
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