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Sclerosing Mesenteritis.

Christopher J Danford1, Steven C Lin1, Jacqueline L Wolf1

  • 1Division of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.

The American Journal of Gastroenterology
|March 5, 2019
PubMed
Summary
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Sclerosing mesenteritis, a rare condition causing mesenteric fibrosis, is often benign but can cause complications. Treatment involves corticosteroids and tamoxifen, with surgery reserved for severe cases.

Area of Science:

  • Gastroenterology
  • Pathology
  • Radiology

Background:

  • Sclerosing mesenteritis is a rare, non-neoplastic disorder of the small bowel mesentery.
  • Pathogenesis is poorly understood, with potential links to surgery, trauma, autoimmunity, infection, ischemia, and malignancy.
  • Limited understanding is compounded by rarity and inconsistent terminology.

Purpose of the Study:

  • To review the current understanding of sclerosing mesenteritis.
  • To discuss its clinical presentation, diagnosis, and management.
  • To emphasize the importance of clear communication among specialists.

Main Methods:

  • Literature review of sclerosing mesenteritis.
  • Analysis of clinical course and diagnostic findings.

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  • Evaluation of treatment strategies based on case series and fibrosing disorder experience.
  • Main Results:

    • Sclerosing mesenteritis is often incidentally diagnosed on imaging.
    • Symptoms can arise from mass effect, leading to bowel obstruction, chylous ascites, or mesenteric ischemia.
    • First-line treatment for symptomatic patients includes corticosteroids and tamoxifen.

    Conclusions:

    • Sclerosing mesenteritis typically follows a benign course but can be symptomatic.
    • Surgical intervention may be necessary for refractory cases but complete resection is challenging.
    • Standardized terminology and interdisciplinary communication are crucial for advancing the understanding and care of this condition.