Maculopapular cutaneous mastocytosis

What causes maculopapular cutaneous mastocytosis?

Maculopapular cutaneous mastocytosis occurs when there are too many inflammatory cells (called mast cells) in the skin. The underlying reason for this excess of mast cells is not fully understood. While most cases appear to be random (occur sporadically for no apparent reason), familial cases have been reported. These familial cases are thought to be inherited in an autosomal dominant manner and may be caused by mutations in the KIT gene.

Last updated on 05-01-20

What is the prognosis for children with maculopapular cutaneous mastocytosis?

The prognosis for children with maculopapular cutaneous mastocytosis is good. Up to 50% of cases improve and 30% of cases resolve completely by adolescence.

Last updated on 05-01-20

How might maculopapular cutaneous mastocytosis be treated?

Maculopapular cutaneous mastocytosis is generally not serious and many cases do not require treatment. For those cases that do, oral antihistamines, topical steroids, and a photochemotherapy called PUVA may be used. These treatments are aimed at reducing the symptoms of the condition and making patients more comfortable.

Last updated on 05-01-20

Where To Start

National Institute of Allergy and Infectious Diseases

The National Institute of Allergy and Infectious Diseases (NIAID) supports scientists developing better ways to diagnose, treat, and prevent the many infectious, immunologic, and allergic diseases that afflict people worldwide. Click on the link to view information on this topic.

Last updated on 04-27-20

The Mastocytosis Society

The Mastocytosis Society provides information about mast cell diseases, including Maculopapular cutaneous mastocytosis.

Last updated on 04-27-20

Name: The Mastocytosis Society P.O. Box 416
Sterling, MA, 01564, United States
Email: info@tmsforacure.org Url: https://tmsforacure.org/

Connect with other users with Maculopapular cutaneous mastocytosis on the RareGuru app

Do you have information about a disease, disorder, or syndrome? Want to suggest a symptom?
Please send suggestions to RareGuru!

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

People Using the App

Join the RareGuru Community

To connect, share, empower and heal today.

People Using the App