Systemic mastocytosis

Umaprasanna S. Karnam, Arvey I. Rogers

Research output: Contribution to journalReview article

6 Scopus citations

Abstract

Mastocytosis is a disease characterized by an abnormal increase in mast cells. Rare in occurrence, protean in its manifestations, it is a disease which is very seldom thought of and hence, possibly even overlooked. The last few decades have witnessed an upsurge in the understanding of the physiology and pathobiology of mast cells. Better means for diagnosis and follow-up have become available. Once a diagnosis is established histamine antagonists remain the mainstay of treatment. Most patients live and die with the disease rather than of it. The objective of this review is to discuss this entity with a special focus on diagnosis and treatment. Copyright (C) 2000 S. Karger AG, Basel.

Original languageEnglish (US)
Pages (from-to)299-307
Number of pages9
JournalDigestive Diseases
Volume17
Issue number5-6
DOIs
StatePublished - Jan 1 1999

Keywords

  • Cromolyn
  • Histamine
  • Histamine antagonists
  • Mast cell
  • Mediators
  • PGD
  • Steroids
  • Tryptase
  • Urticaria pigmentosa

ASJC Scopus subject areas

  • Gastroenterology

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  • Cite this

    Karnam, U. S., & Rogers, A. I. (1999). Systemic mastocytosis. Digestive Diseases, 17(5-6), 299-307. https://doi.org/10.1159/000016955