Structured Summary
Abstract
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.
MeSH Record
Classification
Related Concepts
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MeSH Record
Synonyms
9 entry terms
- Heavy Chain Disease, IgA Type
- IPSID
- Lymphoma, Mediterranean
- alpha-Chain Disease
- Disease, alpha-Chain
- Diseases, alpha-Chain
- Mediterranean Lymphoma
- alpha Chain Disease
- alpha-Chain Diseases
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
87
MeSH Record
Previous Indexing
- Heavy Chain Disease (1966-1986)
- Intestinal Neoplasms (1966-1986)
- Lymphoma (1966-1986)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Immunoproliferative Small Intestinal Disease. Medical Subject Headings (MeSH). 2026. Unique ID D007161. http://id.nlm.nih.gov/mesh/2026/D007161
- Immunoproliferative Small Intestinal Disease. In: Wikidata. https://www.wikidata.org/wiki/Q1916505