Overview
Solitary rectal ulcer syndrome (SRUS), also known as solitary ulcer of the rectum or mucosal prolapse syndrome of the rectum, is an uncommon benign chronic disorder affecting the rectum. Despite its name, the condition does not always present as a single ulcer — patients may have multiple ulcers, a polypoid lesion, or simply a patch of reddened rectal mucosa without a discrete ulcer. The condition is thought to arise primarily from chronic straining during defecation, internal rectal prolapse (intussusception), and direct trauma to the rectal mucosa. Paradoxical contraction of the pelvic floor muscles during defecation may also play a role, leading to high intrarectal pressures and ischemic injury to the rectal wall. The hallmark symptoms include rectal bleeding (often with passage of mucus), straining at stool, a sensation of incomplete evacuation, and rectal pain or discomfort. Some patients experience constipation, while others may have diarrhea. In more advanced cases, rectal prolapse may be evident. The ulcers are most commonly found on the anterior rectal wall, typically 5 to 10 centimeters from the anal verge. Diagnosis is confirmed by endoscopy and characteristic histopathological findings, which include fibromuscular obliteration of the lamina propria, thickening of the muscularis mucosae, and surface ulceration or erosion. These histological features are important because SRUS can be misdiagnosed as inflammatory bowel disease or even rectal malignancy. Treatment is primarily conservative and includes behavioral modifications such as increasing dietary fiber intake, adequate hydration, avoidance of excessive straining, and biofeedback therapy to retrain pelvic floor muscles. Topical treatments including sucralfate enemas and corticosteroid preparations have been used with variable success. In refractory cases, particularly those associated with significant rectal prolapse, surgical intervention such as rectopexy may be considered. The condition tends to be chronic and relapsing, and complete resolution can be difficult to achieve. A multidisciplinary approach involving gastroenterologists, colorectal surgeons, and pelvic floor physiotherapists often yields the best outcomes.
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Variable
Can begin at different ages, from infancy through adulthood
Treatments
No FDA-approved treatments are currently listed for Solitary rectal ulcer syndrome.
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Specialists
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Treatment Centers
8 centersBaylor College of Medicine Rare Disease Center ↗
Baylor College of Medicine
📍 Houston, TX
🏥 NORDStanford Medicine Rare Disease Center ↗
Stanford Medicine
📍 Stanford, CA
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
🔬 UDNUCLA UDN Clinical Site ↗
UCLA Health
📍 Los Angeles, CA
🔬 UDNBaylor College of Medicine UDN Clinical Site ↗
Baylor College of Medicine
📍 Houston, TX
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDMayo Clinic Center for Individualized Medicine ↗
Mayo Clinic
📍 Rochester, MN
👤 Mayo Clinic Center for Individualized Medicine
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
Travel Grants
No travel grants are currently matched to Solitary rectal ulcer syndrome.
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Common questions about Solitary rectal ulcer syndrome
What is Solitary rectal ulcer syndrome?
Solitary rectal ulcer syndrome (SRUS), also known as solitary ulcer of the rectum or mucosal prolapse syndrome of the rectum, is an uncommon benign chronic disorder affecting the rectum. Despite its name, the condition does not always present as a single ulcer — patients may have multiple ulcers, a polypoid lesion, or simply a patch of reddened rectal mucosa without a discrete ulcer. The condition is thought to arise primarily from chronic straining during defecation, internal rectal prolapse (intussusception), and direct trauma to the rectal mucosa. Paradoxical contraction of the pelvic floor