CASE REPORT
An unusual aetiology of solitary rectal ulcer syndrome
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Student Scientific Group at the Department of Paediatric Gastroenterology and Nutrition, Medical University of Warsaw, Poland 2Department of Paediatric Gastroenterology and Nutrition, Medical University of Warsaw, Poland
Submission date: 2022-02-07
Final revision date: 2022-03-17
Acceptance date: 2022-03-25
Publication date: 2022-06-10
Pediatr Pol 2022;97(2):156-158
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ABSTRACT
Solitary rectal ulcer syndrome (SRUS) is a rare condition, usually affecting young adults, with few cases in children. Solitary rectal ulcer syndrome appears in the mucosa of the large intestine, typically the rectum, and has the form of singular or multiple lesions – most commonly ulcerations. Its aetiology remains unclear. However, there are some theories explaining its onset. The disease can manifest, e.g., as a rectal bleeding, mucoid discharge or abdominal pain. There is a particular constellation of features in the histopathological examination that confirms the diagnosis of SRUS. In spite of the fact that there are many pharmacological and non-pharmacological forms of treatment, managing SRUS remains unsatisfactory.
The paper describes a case of a patient with a very unusual cause of SRUS – tailgut cyst. It is reported to raise the awareness of such a disease and emphasize the importance of further testing when the treatment fails.
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