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Protein-loosing enteropathy in sclerosing mesenteritis

A Rispo1, M Sica, L Bucci

  • 1Gastroenterology, Colorectal Surgery, Radiology, Pathology; Department of Clinical Medicine and Surgery, University "Federico II" of Naples, Italy. antoniorispo@email.it.

European Review for Medical and Pharmacological Sciences
|February 28, 2015
PubMed

Insights

Sclerosing mesenteritis (SM) is a rare condition causing fibrous inflammation of the mesentery. This report details a fatal case of severe SM complicated by protein-losing enteropathy, highlighting potential severe outcomes.

Area of Science:

  • Gastroenterology
  • Pathology
  • Rare Diseases

Background:

  • Sclerosing mesenteritis (SM) is a rare idiopathic disorder characterized by chronic fibrous inflammation of the mesentery.
  • It presents with non-specific symptoms like abdominal pain and diarrhea, making diagnosis challenging.

Observation:

  • Diagnosis of SM typically requires biopsy, and various treatments show variable success rates.
  • While often self-limiting with a good prognosis, severe cases of SM are documented.

Findings:

  • This case report details a fatal instance of sclerosing mesenteritis.
  • The severe SM was associated with protein-losing enteropathy, a rare complication.

Implications:

  • This case underscores the potential for severe manifestations and fatal outcomes in sclerosing mesenteritis.
  • It highlights the critical association between severe SM and protein-losing enteropathy, necessitating further investigation into this link.

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