Rare condition guide
Sclerosing mesenteritis: a rare abdominal condition
Sclerosing mesenteritis is a rare inflammatory and scarring condition of the mesentery, the fatty tissue that anchors the small bowel. Many people have no symptoms and it is found by chance on a CT scan, while others have long-standing abdominal pain, bloating or altered bowel habits. No UK patient guide was found when this page was written, so it draws on published medical case reports and reviews and is shorter on detail than most condition pages.
Last checked: 2026-10-04
Key facts
At a glance.
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What it is
A rare, benign, idiopathic inflammatory disorder with fat necrosis and fibrosis in the mesentery of the small bowel, according to a 2022 case report in Cureus.
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Many names
The same review notes it has been called mesenteric panniculitis, retractile mesenteritis, misty mesentery and several other names, with sclerosing mesenteritis used as the overarching term.
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Who gets it
It is more common in men than women (about 2 to 1) and mostly occurs between the fifth and seventh decades of life, with a median age of 65, according to the same report.
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Often silent
Multiple asymptomatic cases have been reported, diagnosed incidentally after scans performed for other reasons.
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Cause unknown
The cause is unknown. Previous abdominal surgery or trauma, autoimmune disease and infection have been suggested, and the link with cancer is unclear.
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No standard treatment
The authors state there is no general agreement on treatment. Asymptomatic people can be managed without medicine, and spontaneous resolution frequently occurs in untreated patients.
What the mesentery is and what goes wrong
The mesentery is a fold of tissue, rich in fat, blood vessels and lymph nodes, that attaches the small intestine to the back of the abdomen. In sclerosing mesenteritis this tissue becomes inflamed, and over time can develop fat necrosis and fibrous scarring. A case report in Cureus calls it a rare benign idiopathic inflammatory disorder, and a second published case series calls it exceedingly rare, resulting in chronic, progressive inflammatory changes.
The name varies with the dominant finding under the microscope. Fat necrosis with foamy immune cells is sometimes called mesenteric lipodystrophy, chronic inflammation is called mesenteric panniculitis and scarring is called retractile mesenteritis, though the Cureus authors note these may not be true stages because they can be present at the same time.
How common it is, and who gets it
The Cureus report cites a figure of 0.6% of more than 7,000 consecutive patients who had abdominal CT scans, which suggests it is found not so rarely when people are scanned, but that figure comes from a single series and should be read cautiously. It describes a male predominance of about two to one and a typical age in the sixties.
Because most information comes from case reports and small series from hospitals, the true frequency and the full range of the condition are uncertain. No UK national guideline or patient charity guide was found for this page.
Symptoms
The reported symptoms are non-specific. The Cureus authors list chronic abdominal pain as the main complaint, with bloating, nausea, vomiting, diarrhoea, constipation, loss of appetite and weight loss. They note that anorexia and weight loss point more towards a neoplastic cause, which is one reason doctors look carefully for other diseases. On examination there may be abdominal tenderness, and sometimes a mass.
The case series in the same journal says patients may also present with complications such as bowel obstruction, obstructive uropathy or reduced blood flow to the bowel (mesenteric ischaemia). Because the symptoms resemble those of common conditions, diagnosis can be delayed; one of the reports describes a patient whose symptoms were first attributed to irritable bowel syndrome.
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Long-standing or recurrent abdominal pain, often in the middle of the abdomen.
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Bloating, nausea or vomiting.
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Diarrhoea, constipation or alternating bowel habit.
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Reduced appetite and weight loss, which always warrant medical review.
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No symptoms at all in some people.
How it is diagnosed
According to the Cureus report, CT is the most convenient diagnostic tool, and the most sensitive imaging is a dual-phase CT showing a fat ring or halo sign and a tumour pseudocapsule. A hazy, misty-looking mesentery is a consistent CT finding but is not specific, as it can also be seen with neoplastic infiltration and portal hypertension. MRI findings are similar, and FDG PET may help to exclude cancer because sclerosing mesenteritis does not usually take up the tracer.
Blood tests are usually normal, although inflammatory markers such as C-reactive protein may be raised. The second case series says a definitive diagnosis is made on histological evaluation, meaning a biopsy examined under the microscope, and warns that scans meant to look for neuroendocrine tumours can give false-positive results in inflammatory conditions.
The link with cancer
Some reports have suggested that sclerosing mesenteritis may be a paraneoplastic syndrome, but the Cureus authors describe the data as conflicting: some studies found no difference in cancer rates, while others found more cancer, with lymphoma, melanoma, colon and prostate cancers the most often mentioned. They advise a thorough history and physical examination, including a detailed skin examination, and that suspicious lesions are investigated with PET and biopsy.
This does not mean the condition is cancer. It means a doctor will usually want to make sure that nothing else is going on, and will keep up with routine cancer screening.
Treatment and outlook
There is no agreed standard. The Cureus authors say asymptomatic people can be managed without medication, treatment for those with symptoms is usually individualised, and spontaneous resolution frequently occurs without treatment. Corticosteroids helped some people; colchicine, tamoxifen, azathioprine, methotrexate and infliximab have also been tried, but the authors stress that the evidence comes from case series, so the best medical approach remains unclear.
Surgery is sometimes difficult because of the extent of disease and involvement of blood vessels, but is required for complications such as perforation, or vascular or intestinal obstruction. The second case series concludes that early diagnosis matters to prevent serious complications in an otherwise benign disease.
When to seek help
See a GP for abdominal pain that keeps returning, or for unexplained weight loss or a change in bowel habit. Call NHS 111 or seek urgent care for severe or worsening abdominal pain, repeated vomiting, a swollen tummy with inability to pass wind or stool, or blood in vomit or poo. Anyone told after a scan that they have a misty mesentery should ask their doctor what follow-up is advised.
Frequently asked
Questions people ask.
Quick, plain-English answers to the questions we hear most.
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Is sclerosing mesenteritis cancer?
No. It is described as a rare benign inflammatory condition. The link with cancer is uncertain, so doctors usually check carefully for other diseases, but the condition itself is not a cancer.
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What is a misty mesentery?
A descriptive CT term for hazy-looking fat in the mesentery. It is a consistent finding in sclerosing mesenteritis but is not specific, since it can also occur with other conditions, including cancers and portal hypertension.
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What causes it?
Unknown. Previous abdominal surgery or trauma, autoimmune disease, abdominal aortic aneurysm and infection have been suggested as possible factors, but none has been proven.
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Can it be mistaken for irritable bowel syndrome?
Yes. The symptoms of abdominal pain, bloating and altered bowel habit overlap with IBS, and one published case describes a diagnosis delayed for that reason. Worsening or unusual symptoms should prompt further assessment.
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Will I need a biopsy?
Sometimes. A definitive diagnosis is made on histology. A biopsy may be advised if the CT is unclear, if cancer needs to be excluded or if the picture is atypical.
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Does it need treatment?
Not always. Asymptomatic people can often be followed without medicine, and symptoms sometimes settle without treatment. If symptoms are troublesome, medicines such as corticosteroids have been used, and surgery is reserved for complications.
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What complications can happen?
Reported complications include bowel obstruction, perforation, reduced blood flow to the bowel and obstruction of the urinary tract. They are uncommon, but are why persistent or worsening symptoms should be reviewed.
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Is there a UK patient group?
No UK charity or national guideline was found when this page was written. Your gastroenterologist or hospital team is the best source of information for your own case.
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Does it run in families?
None of the sources read describe an inherited pattern. It is generally regarded as idiopathic, meaning without a known cause.
Where this comes from
Sources and checking.
This guide is for information, not medical advice.
Your GP or consultant knows your history and can tell you which parts apply to you. If your symptoms are severe, rapidly worsening, or come with red-flag features, seek urgent medical care. Figures and availability change, so treat them as a guide and confirm with the provider.
Published 2026-10-04, next review 2027-10-04.
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Sharawi S, Graffeo V, Goebel LJ. Sclerosing Mesenteritis: A Rare Cause of Abdominal Pain. Cureus 2022 (https://pmc.ncbi.nlm.nih.gov/articles/PMC9520956/), retrieved October 2026. US case report with literature review; no UK source was found.
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Sclerosing mesenteritis: a case series detailing importance of early diagnosis, PubMed Central (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12253950/), retrieved October 2026. US case series.
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