[Mesenteric panniculitis: variable presentations]

Debbie G J Robbrecht1, Fazil Alidjan, Bob Eikemans

  • 1Amphia Ziekenhuis, Breda, Afd. Interne geneeskunde, the Netherlands. debbie_robbrecht@hotmail.com

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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