Solitary Rectal Ulcer Syndrome Presenting with Rectal Prolapse, Severe Mucorrhea and Eroded Polypoid Hyperplasia: Case Report and Review of the Literature
A case of solitary rectal ulcer syndrome in a 36-year-old woman presenting with severe, persistent mucorrhea and eroded polypoid hyperplasia as the predominant clinical features, who was ultimately noted to have symptoms of rectal prolapse, is presented. Endoscopically, she had multiple (50 to 60) s...
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Hindawi Limited
2001-01-01
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Series: | Canadian Journal of Gastroenterology |
Online Access: | http://dx.doi.org/10.1155/2001/145041 |
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doaj-55ea02cb2c3b4586996e1903e480e33e2020-11-24T22:51:54ZengHindawi LimitedCanadian Journal of Gastroenterology0835-79002001-01-0115747948310.1155/2001/145041Solitary Rectal Ulcer Syndrome Presenting with Rectal Prolapse, Severe Mucorrhea and Eroded Polypoid Hyperplasia: Case Report and Review of the LiteratureDeepak V Gopal0Christopher Young1Ronald M Katon2Division of Gastroenterology, Oregon Health Sciences University, Portland, Oregon, USADepartment of Pathology, Oregon Health Sciences University, Portland, Oregon, USADivision of Gastroenterology, Oregon Health Sciences University, Portland, Oregon, USAA case of solitary rectal ulcer syndrome in a 36-year-old woman presenting with severe, persistent mucorrhea and eroded polypoid hyperplasia as the predominant clinical features, who was ultimately noted to have symptoms of rectal prolapse, is presented. Endoscopically, she had multiple (50 to 60) small, whitish polypoid lesions in the rectum that were initially misinterpreted as being a carpeted villous adenoma, juvenile polyposis or atypical proctitis. The lesions were treated with argon plasma coagulation with resolution, but a solitary rectal ulcer developed. The patient then admitted to a history of massive rectal prolapse over the preceding six months and underwent surgical treatment. Severe mucorrhea as the presenting feature and the presence of multiple polypoid lesions consistent with a histological diagnosis of eroded polypoid hyperplasia make the present case unique.http://dx.doi.org/10.1155/2001/145041 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Deepak V Gopal Christopher Young Ronald M Katon |
spellingShingle |
Deepak V Gopal Christopher Young Ronald M Katon Solitary Rectal Ulcer Syndrome Presenting with Rectal Prolapse, Severe Mucorrhea and Eroded Polypoid Hyperplasia: Case Report and Review of the Literature Canadian Journal of Gastroenterology |
author_facet |
Deepak V Gopal Christopher Young Ronald M Katon |
author_sort |
Deepak V Gopal |
title |
Solitary Rectal Ulcer Syndrome Presenting with Rectal Prolapse, Severe Mucorrhea and Eroded Polypoid Hyperplasia: Case Report and Review of the Literature |
title_short |
Solitary Rectal Ulcer Syndrome Presenting with Rectal Prolapse, Severe Mucorrhea and Eroded Polypoid Hyperplasia: Case Report and Review of the Literature |
title_full |
Solitary Rectal Ulcer Syndrome Presenting with Rectal Prolapse, Severe Mucorrhea and Eroded Polypoid Hyperplasia: Case Report and Review of the Literature |
title_fullStr |
Solitary Rectal Ulcer Syndrome Presenting with Rectal Prolapse, Severe Mucorrhea and Eroded Polypoid Hyperplasia: Case Report and Review of the Literature |
title_full_unstemmed |
Solitary Rectal Ulcer Syndrome Presenting with Rectal Prolapse, Severe Mucorrhea and Eroded Polypoid Hyperplasia: Case Report and Review of the Literature |
title_sort |
solitary rectal ulcer syndrome presenting with rectal prolapse, severe mucorrhea and eroded polypoid hyperplasia: case report and review of the literature |
publisher |
Hindawi Limited |
series |
Canadian Journal of Gastroenterology |
issn |
0835-7900 |
publishDate |
2001-01-01 |
description |
A case of solitary rectal ulcer syndrome in a 36-year-old woman presenting with severe, persistent mucorrhea and eroded polypoid hyperplasia as the predominant clinical features, who was ultimately noted to have symptoms of rectal prolapse, is presented. Endoscopically, she had multiple (50 to 60) small, whitish polypoid lesions in the rectum that were initially misinterpreted as being a carpeted villous adenoma, juvenile polyposis or atypical proctitis. The lesions were treated with argon plasma coagulation with resolution, but a solitary rectal ulcer developed. The patient then admitted to a history of massive rectal prolapse over the preceding six months and underwent surgical treatment. Severe mucorrhea as the presenting feature and the presence of multiple polypoid lesions consistent with a histological diagnosis of eroded polypoid hyperplasia make the present case unique. |
url |
http://dx.doi.org/10.1155/2001/145041 |
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