Eosinophilic Colitis that Presented with Subepithelial Tumor-like Lesions

Eosinophilic colitis is a rare disease that is characterized by eosinophilic infiltration in the colon wall in symptomatic patients. Thus far, the epidemiology and pathophysiology of eosinophilic colitis have not been well defined, but the hypersensitivity response is likely to play a role in its pa...

Full description

Saved in:
Bibliographic Details
Published inThe Korean journal of gastroenterology Vol. 77; no. 6; pp. 300 - 304
Main Authors Yun, Jeonghui, Park, Sanggyu, Park, Hojun, Lim, Won, Lee, Taeyeong, Song, Chulsoo
Format Journal Article
LanguageEnglish
Published Jin Publishing & Printing Co 01.06.2021
대한소화기학회
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Eosinophilic colitis is a rare disease that is characterized by eosinophilic infiltration in the colon wall in symptomatic patients. Thus far, the epidemiology and pathophysiology of eosinophilic colitis have not been well defined, but the hypersensitivity response is likely to play a role in its pathogenesis. The clinical presentation of eosinophilic colitis is usually nonspecific and depends on the layer of the intestinal wall affected by the eosinophilic infiltrate. Eosinophilic colitis is diagnosed generally by exclusion, i.e., after all other causes of eosinophilic infiltration have been excluded. Although there is no consensus over its diagnostic criteria, the laboratory results and radiology and endoscopy findings can provide important diagnostic evidence. This paper reports a case of eosinophilic colitis presenting as subepithelial tumor-like lesions in a 41-year-old man with the chief complaints of abdominal pain and loose stools. The patient had no diseases and no food or drug allergies in his medical history. In general, the endoscopic findings of eosinophilic colitis can vary from a normal mucosa to frank ulcerations. In this case, however, endoscopy revealed subepithelial tumor-like lesions. The colon biopsy showed eosinophilic infiltration in the lamina propria. The patient was treated with steroids, and his symptoms regressed with no signs of relapse.
ISSN:1598-9992
2233-6869
DOI:10.4166/kjg.2021.009