JGH Open (Dec 2022)

A rare cause of jejunal perforation: Monomorphic epitheliotropic intestinal T‐cell lymphoma

  • Masahiro Yanagi,
  • Takuya Komura,
  • Takashi Kagaya

DOI
https://doi.org/10.1002/jgh3.12844
Journal volume & issue
Vol. 6, no. 12
pp. 915 – 917

Abstract

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Abstract Monomorphic epitheliotropic intestinal T‐cell lymphoma (MEITL) is a very rare intestinal T‐cell lymphoma which is observed most frequently in the jejunum. MEITL is prone to cause intestinal perforation and the prognosis is very poor when it occurs. Here we report a fatal case of MEITL causing jejunal perforation at the time of diagnosis in a 79‐year‐old man. The patient underwent emergency surgery for jejunal perforation caused by MEITL but died 3 months after the initial visit due to prolonged peritonitis. It is desirable to establish a method to predict cases with intestinal perforation, and systematize the treatment strategies to avoid perforation.

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