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Updated: May 20, 2026

Multimodality Diagnosis of Mesenteric Ischemia
Published on: July 21, 2023
[Mesenteric panniculitis: variable presentations]
Debbie G J Robbrecht1, Fazil Alidjan, Bob Eikemans
1Amphia Ziekenhuis, Breda, Afd. Interne geneeskunde, the Netherlands. debbie_robbrecht@hotmail.com
Abstract:
Mesenteric panniculitis is a non-specific inflammation of the mesenteric adipose tissue, with varying degrees of fibrosis and fat necrosis. It can be associated with varying diseases and conditions, such as autoimmune disease and cancer. Many doctors are not familiar with this disease or do not know how to interpret the signs and symptoms. Here, we describe three patients illustrating the variety of clinical course, diagnostics, prognosis and treatment. A 44-year-old woman suffering from episodic abdominal pain was diagnosed with uncomplicated mesenteric panniculitis. The disease was stable while maintaining a conservative approach. In a 43-year-old woman, mesenteric panniculitis was complicated by autoimmune haemolytic anaemia. After treatment with corticosteroids, she made a full recovery from both disorders. Finally, a 73-year-old man was diagnosed with mesenteric panniculitis and auto-immune haemolytic anaemia, which both appeared to be consequences of an angioimmunoblastic T-cell lymphoma.
Insights
Mesenteric panniculitis, an inflammation of abdominal fat, presents varied clinical courses. This review highlights its diverse associations, including autoimmune conditions and lymphoma, emphasizing diagnostic and treatment challenges.
Area of Science:
- Gastroenterology
- Oncology
- Immunology
Background:
- Mesenteric panniculitis involves inflammation, fibrosis, and fat necrosis of mesenteric adipose tissue.
- It often presents non-specifically and can be linked to various systemic diseases.
- Physician familiarity with this condition and its varied presentations is limited.
Observation:
- Case 1: A 44-year-old woman with episodic abdominal pain had uncomplicated mesenteric panniculitis, managed conservatively with stable disease.
- Case 2: A 43-year-old woman experienced mesenteric panniculitis complicated by autoimmune hemolytic anemia, resolving with corticosteroid therapy.
- Case 3: A 73-year-old man presented with mesenteric panniculitis and autoimmune hemolytic anemia, both attributed to underlying angioimmunoblastic T-cell lymphoma.
Findings:
- Mesenteric panniculitis exhibits a wide spectrum of clinical manifestations, diagnostic challenges, and prognoses.
- The condition can occur independently or be associated with autoimmune disorders and malignancies.
- Successful management depends on accurate diagnosis and tailored treatment strategies.
Implications:
- Increased awareness of mesenteric panniculitis and its potential associations is crucial for timely diagnosis.
- Understanding the diverse clinical pathways can guide appropriate patient management and improve outcomes.
- Further research into the pathogenesis and treatment of mesenteric panniculitis is warranted.
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