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type
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sameAs
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notation
| - C04.557.450.565.465.750
- C20.762.750.750
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alternative label
| - Mastocytose généralisée agressive
- Mastocytose systémique agressive
- Indolent Systemic Mastocytosis
- Mast-Cell Diseases, Systemic
- Mastocytoses, Systemic
- Mastocytosis, Aggressive Systemic
- Systemic Mast Cell Disease
- Aggressive Systemic Mastocytoses
- Mast-Cell Disease, Systemic
- Mastocytose systémique indolore
- Mastocytoses, Aggressive Systemic
- Mastocytosis, Systemic
- Systemic Mastocytoses
- Systemic Mastocytosis
- Systemic Mastocytosis, Aggressive
- Indolent Systemic Mastocytoses
- Mastocytose diffuse indolore
- Mastocytose systémique
- Mastocytose systémique indolente
- Mastocytoses, Indolent Systemic
- Mastocytosis, Indolent Systemic
- Systemic Mast-Cell Diseases
- Systemic Mastocytoses, Aggressive
- Systemic Mastocytosis, Indolent
- Aggressive Systemic Mastocytosis
- Systemic Mast-Cell Disease
- Systemic Mastocytoses, Indolent
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preferred label
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is in scheme
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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
- 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
- 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
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