AI Article Synopsis

  • A 36-year-old woman was diagnosed with solitary rectal ulcer syndrome, characterized by severe mucorrhea and multiple small whitish polypoid lesions in her rectum.
  • Initially, these lesions were misdiagnosed as different conditions like adenoma or polyp syndrome before being treated with argon plasma coagulation, which led to resolution but resulted in a solitary rectal ulcer.
  • The case is notable for its unique presentation of severe mucorrhea and the presence of polypoid lesions that were histologically identified as eroded polypoid hyperplasia.

Article Abstract

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.

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http://dx.doi.org/10.1155/2001/145041DOI Listing

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