Idiopathic Mesenteric Phlebosclerosis: A Single-Institute Experience in Taiwan

Jen-Wei Chou1, Chia-Hsi Chang2, Yi-Hua Wu3

  • 1China Medical University Faculty of Medicine, Taichung, Taiwan; Department of Internal Medicine, Center for Digestive Medicine, China Medical University Hospital, Taichung, Taiwan; Taiwan Association for the Study of Small Intestinal Diseases (TASSID), Touyuan, Taiwan.

Abstract

Insights

Idiopathic mesenteric phlebosclerosis is a rare condition. Most patients recover with conservative treatment, but severe cases may require surgery. Diagnosis is aided by imaging like CT scans.

Area of Science:

  • Gastroenterology
  • Radiology
  • Vascular Medicine

Background:

  • Idiopathic mesenteric phlebosclerosis is a rare condition with an unknown cause.
  • This study focuses on patients in Taiwan.

Purpose of the Study:

  • To investigate the clinical features, diagnostic methods, treatments, and outcomes of idiopathic mesenteric phlebosclerosis.
  • To provide insights into this rare vascular condition.

Main Methods:

  • Retrospective analysis of 36 patients diagnosed between 1992 and 2021.
  • Diagnosis confirmed by tree-like mesenteric venous calcifications on radiography or CT scans.

Main Results:

  • Most patients (72.2%) were symptomatic, with abdominal pain being the most common symptom.
  • Common comorbidities included cardiovascular disease (36.1%) and chronic renal disease (44.4%).
  • Diagnosis was primarily achieved through abdominal CT and radiography (94.4%).
  • Over 91.6% of patients had good recovery with conservative treatment; 8.3% required colectomy.

Conclusions:

  • Idiopathic mesenteric phlebosclerosis is rare in Taiwan.
  • Plain abdominal radiography and CT scans are effective diagnostic tools.
  • Conservative management is typically sufficient, with surgery reserved for severe cases.

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