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Hemic and Lymphatic Diseases > Lymphatic Diseases > Lymphoproliferative Disorders > Lymphoma > Immunoproliferative Small Intestinal Disease
Neoplasms > Neoplasms by Histologic Type > Lymphoma > Immunoproliferative Small Intestinal Disease
Immune System Diseases > Immunoproliferative Disorders > Paraproteinemias > Heavy Chain Disease > Immunoproliferative Small Intestinal Disease

Preferred term

Immunoproliferative Small Intestinal Disease  

Type

  • Topical Descriptor

Entry terms

  • alpha Chain Disease
  • alpha-Chain Disease
  • alpha-Chain Diseases
  • Disease, alpha-Chain
  • Diseases, alpha-Chain
  • Heavy Chain Disease, IgA Type
  • IPSID
  • Lymphoma, Mediterranean
  • Mediterranean Lymphoma

Scope note

  • A condition that is caused by HYPERPLASIA of LYMPHOCYTES in the small intestine (INTESTINE, SMALL) and the mesenteric LYMPH NODES. These lymphocytes produce an anomalous alpha heavy chain protein. Generally, these IPSID patients have either concurrent LYMPHOMA or develop lymphoma within a few years. The disease was first described in the Mediterranean region and is characterized by malabsorption; WEIGHT LOSS; DIARRHEA; and STEATORRHEA.

History note

  • 87

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URI

http://www.yso.fi/onto/mesh/D007161

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