Descriptor English: | Mastocytosis, Systemic | ||||||
Descriptor Spanish: |
Mastocitosis Sistémica
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Descriptor Portuguese: | Mastocitose Sistêmica | ||||||
Descriptor French: | Mastocytose généralisée | ||||||
Entry term(s): |
Aggressive Systemic Mastocytoses Aggressive Systemic Mastocytosis Indolent Systemic Mastocytoses Indolent Systemic Mastocytosis Mast-Cell Disease, Systemic Mast-Cell Diseases, Systemic Mastocytoses, Aggressive Systemic Mastocytoses, Indolent Systemic Mastocytoses, Systemic Mastocytosis, Aggressive Systemic Mastocytosis, Indolent Systemic Systemic Mast Cell Disease Systemic Mast-Cell Disease Systemic Mast-Cell Diseases Systemic Mastocytoses Systemic Mastocytoses, Aggressive Systemic Mastocytoses, Indolent Systemic Mastocytosis Systemic Mastocytosis, Aggressive Systemic Mastocytosis, Indolent |
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Tree number(s): |
C04.557.450.565.465.750 C20.762.750.750 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D034721 | ||||||
Scope note: | A group of disorders caused by the abnormal proliferation of MAST CELLS in a variety of extracutaneous tissues including bone marrow, liver, spleen, lymph nodes, and gastrointestinal tract. Systemic mastocytosis is commonly seen in adults. These diseases are categorized on the basis of clinical features, pathologic findings, and prognosis. |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Previous Indexing: |
Bone Marrow Diseases (1965-2002) Mast Cells (1965-2002) |
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Public MeSH Note: | 2003 |
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History Note: | 2003 |
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DeCS ID: | 37263 | ||||||
Unique ID: | D034721 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 2003/01/01 | ||||||
Date of Entry: | 2002/07/02 | ||||||
Revision Date: | 2017/06/20 |
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DISEASES
Neoplasms [C04]Neoplasms
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Mastocytosis, Systemic
- Preferred
Aggressive Systemic Mastocytosis
- Narrower
Indolent Systemic Mastocytosis
- Narrower
Concept UI |
M0405932 |
Scope note | A group of disorders caused by the abnormal proliferation of MAST CELLS in a variety of extracutaneous tissues including bone marrow, liver, spleen, lymph nodes, and gastrointestinal tract. Systemic mastocytosis is commonly seen in adults. These diseases are categorized on the basis of clinical features, pathologic findings, and prognosis. |
Preferred term | Mastocytosis, Systemic |
Entry term(s) |
Mast-Cell Disease, Systemic Mast-Cell Diseases, Systemic Mastocytoses, Systemic Systemic Mast Cell Disease Systemic Mast-Cell Disease Systemic Mast-Cell Diseases Systemic Mastocytoses Systemic Mastocytosis |
Concept UI |
M0406102 |
Scope note | A form of systemic mastocytosis in which patients have impaired organ functions due to multifocal infiltrates of pathological MAST CELLS in bone marrow, liver, spleen, gastrointestinal tract, or skeletal system. The cytomorphology shows a low to high grade. |
Preferred term | Aggressive Systemic Mastocytosis |
Entry term(s) |
Aggressive Systemic Mastocytoses Mastocytoses, Aggressive Systemic Mastocytosis, Aggressive Systemic Systemic Mastocytoses, Aggressive Systemic Mastocytosis, Aggressive |
Concept UI |
M0406103 |
Scope note | A form of systemic mastocytosis in which patients experience no pain. It is characterized by the multifocal mast cell filtrates, mostly in skin and bone marrow (<20% MAST CELLS). It has a low cytomorphological grade. |
Preferred term | Indolent Systemic Mastocytosis |
Entry term(s) |
Indolent Systemic Mastocytoses Mastocytoses, Indolent Systemic Mastocytosis, Indolent Systemic Systemic Mastocytoses, Indolent Systemic Mastocytosis, Indolent |
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