Immunoproliferative small intestinal disease (IPSID): An overview

Authors

  • Shakil Gani Department of Hepatology, BSMMU, Dhaka
  • Mamun Al-Mahtab Department of Hepatology, BSMMU, Dhaka
  • Salimur Rahman Department of Hepatology, BSMMU, Dhaka

Keywords:

IPSID

Abstract

Immunoproliferative small intestinal disease (IPSID) is a poorly recognized cause of malabsorption syndrome. IPSID shares clinical, morphologic, and molecular features with mucosa-associated lymphoid tissue (MALT) lymphoma, lymphoplasmacyticlymphoma, and plasma cell neoplasms, which involves mainly the proximal small intestine. It is mostly found in young adults of low socioeconomic class and poor sanitation in developing countries. Early-stage IPSID responds to antibiotics. Most untreated IPSID patients progress to lymphoplasmacytic and immunoblastic lymphoma invading the intestinal wall and mesenteric lymph nodes, and may metastasizeto a distant organ. It may be a major public health issue in developing countries.

International Journal of Hepatology Vol.1(3) 2010 pp.31-35

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Abstract
956

Published

2010-11-29

How to Cite

Gani, S., Al-Mahtab, M., & Rahman, S. (2010). Immunoproliferative small intestinal disease (IPSID): An overview. International Journal of Hepatology, 1(3), 31–35. Retrieved from https://www.banglajol.info/index.php/IJH/article/view/6564

Issue

Section

Review Articles