is a topic covered in the 5-Minute Clinical Consult
To view the entire topic, please sign in or purchase a subscription.
Medicine Central™ is a quick-consult mobile and web resource that includes diagnosis, treatment, medications, and follow-up information on over 700 diseases and disorders, providing fast answers—anytime, anywhere. Explore these free sample topics:
-- The first section of this topic is shown below --
Mastocytosis is a rare, heterogeneous group of disorders caused by the abnormal clonal proliferation and accumulation of atypical mast cells in one or more organs of the body, most often affecting the skin.
- Two clinical diagnostic categories: cutaneous mastocytosis (CM) or systemic mastocytosis (SM)
- CM only is the most common form, whereas SM constitutes only 10–15% of all the cases.
- CM consistency primarily of skin involvement with characteristic lesions, urticaria pigmentosa (UP)
- Symptoms of mastocytosis are from mast cell degranulation and release of chemical mediators, such as histamine, leukotrienes, and prostaglandins.
- In adults, mastocytosis often is secondary to a gain-of-function point mutation in the proto-oncogene c-kit (D816V in >95% of cases) leading to clonal proliferation of mast cells.
- Childhood mastocytosis is associated with c-kit, D816V in only 40% of cases; majority of cases are limited to the skin and have excellent prognosis with spontaneous resolution around puberty.
- Incidence and prevalence will vary because many cases remain undiagnosed.
- Prevalence estimated 1 in 60,000 people.
- Incidence 0.1 to 1/100,000 people per year in United States
- ~2/3 of reported CM cases are found in children, most diagnosed before the age of 2 years.
- Adults more likely to have systemic disease and onset between 20 and 50 years with diagnosis at 40 to 60 years
- Prevalence equal in males and females
Etiology and PathophysiologyGenetics
The disease is congenital in 15–25% of cases.
- Gain-of-function point mutations in c-kit, in particular D816V
- C-kit (KIT) is a proto-oncogene that encodes for a tyrosine kinase receptor (CD117 transmembrane receptor) located on many hematopoietic stem cells, including mast cells.
- Normally, stem cell factor (SCF) binds to CD117 leading to mast cell growth, migration, survival.
- Autophosphorylation of tyrosine residues in the presence of gain-of-function c-kit mutations leads to unregulated proliferation of mast cells.
- Mutations in other genes may also be pathogenic in some cases.
- There is no known genetic transmission.
Age; c-kit–activating mutations
-- To view the remaining sections of this topic, please sign in or purchase a subscription --