Cutaneous Mastocytoma
Description
Cutaneous mastocytoma is a form of cutaneous mastocytosis (CM, see this term) generally characterized by the presence of a solitary or multiple hyperpigmented macules, plaques or nodules associated with abnormal accumulation of mast cells in the skin.
Clinical Features
Phenotypes and symptoms related to Cutaneous Mastocytoma
- Headache
- Abdominal pain
- Pruritus
- Abnormality of skin pigmentation
- Abnormal blistering of the skin
- Subcutaneous nodule
- Thickened skin
- Urticaria
- Hypermelanotic macule
- Cutaneous mastocytosis
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Cutaneous Mastocytoma Is also known as solitary mastocytoma, cutaneous local mastocytoma, multiple mastocytoma.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Cutaneous Mastocytoma Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
KIT related disorders - KIT Sequencing.
By Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado (United States).
KIT
Specificity
100 %
Genes
100 % |
KIT Mutation Analysis.
By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories (United States).
KIT
Specificity
100 %
Genes
100 % |
MyeloidDx by NGS.
By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories (United States).
RUNX1, SF3B1, SRSF2, BRAF, SMC1A, STAG2, TP53, U2AF1, KDM6A, WT1, IKZF1, CALR, CBL, CBLB, SETBP1, FBXW7, CDKN2A, PHF6, ASXL1, CEBPA , (...)
View the complete list with 32 more genes
Specificity
2 %
Genes
100 % |
MyeloidDx by NGS.
By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories (United States).
RUNX1, SF3B1, SRSF2, BRAF, SMC1A, STAG2, TP53, U2AF1, KDM6A, WT1, IKZF1, CALR, CBL, CBLB, SETBP1, CBLC, FBXW7, CDKN2A, PHF6, CEBPA , (...)
View the complete list with 31 more genes
Specificity
2 %
Genes
100 % |
Hereditary Gastric Cancer Panel.
By Genetic Services Laboratory University of Chicago (United States).
SDHB, SDHC, BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, CDH1, CTNNA1, APC, KIT, SMAD4, MLH1, MSH2, MSH6, PDGFRA, PMS2, PTEN
Specificity
6 %
Genes
100 % |
KIT. Complete sequencing.
By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
KIT
Specificity
100 %
Genes
100 % |
Hereditary Colorectal and Gastrointestinal Cancer Panel.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia (United States).
BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, CDH1, CDK4, CDKN2A, PALB2, APC, KIT, SMAD4, MLH1, MSH2, MSH6, MUTYH, ATM, PMS2, POLD1 , (...)
View the complete list with 2 more genes
Specificity
5 %
Genes
100 % |
CHOP Comprehensive Hereditary Cancer Panel.
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia (United States).
RMRP, RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, SH2D1A, SLC25A13, BRCA1, BRCA2, SMARCA4, SMARCB1, SMARCE1, BUB1B, EPCAM, XPA, IKZF1, CBL , (...)
View the complete list with 85 more genes
Specificity
1 %
Genes
100 % |
You can get up to 113 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
ORPHANET Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like WEILL-MARCHESANI SYNDROME 3; WMS3 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5; SMDP5 MITRAL VALVE PROLAPSE 2; MVP2 PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10; ARCI10 ACID-LABILE SUBUNIT DEFICIENCY; ACLSD