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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Main Authors: Deepak V Gopal, Christopher Young, Ronald M Katon
Format: Article
Language:English
Published: Hindawi Limited 2001-01-01
Series:Canadian Journal of Gastroenterology
Online Access:http://dx.doi.org/10.1155/2001/145041
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spelling 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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