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Condition

Mastocytosis

Neoplasms

Mastocytosis is a rare disorder, a type of mast cell disease, that can affect both children and adults. It is caused by the accumulation of functionally defective mast cells, also called mastocytes, together with CD34-positive mast cell precursors. Because mast cells store and release histamine and other pro-inflammatory substances, people with the condition are prone to a range of symptoms, including itching, hives and anaphylactic shock. The English Wikipedia lead on which this entry rests is brief, so this description stops at what that lead supports: what the cells are, who is affected and the main symptoms. Its classification into cutaneous and systemic forms, its genetic basis and its treatment are left for later depth work from further sources.

Facts
Classification
Body System
Lymphatic or Immune System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2
Communicable or Non-communicable
Non-Communicable 3
Transmission Route
Non-Transmissible 3
First Described
1869 1
Sources
1. Mastocytosis (Wikipedia)
  • Lead section
    accumulation of functionally defective mast cells
  • Section: History (first-described-year)
    Urticaria pigmentosa was first described in 1869.
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2. World Health Organization ICD-10: ICD-10 Version:2019 - Q80-Q89
World Health Organization ICD-10ICD-10 2019 category Q82.2, Chapter XVII
Quote, ICD-10 2019 category Q82.2, Chapter XVII
Q82.2 Mastocytosis
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3. National Library of Medicine MeSH: Mastocytosis
National Library of Medicine MeSHMeSH tree number C04.557.450.565.465
Quote, MeSH tree number C04.557.450.565.465
<http://id.nlm.nih.gov/mesh/D008415> <http://id.nlm.nih.gov/mesh/vocab#treeNumber> <http://id.nlm.nih.gov/mesh/C04.557.450.565.465> .
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