Concept information
Término preferido
Histiocytosis, Langerhans-Cell
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Tipo
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mesh:Descriptor
Definición
- A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder.
Concepto genérico
Conceptos específicos
Etiquetas alternativas
- Hand-Schueller-Christian Disease
- Hand-Schueller-Christian Syndrome
- Hand-Schüller-Christian Disease
- Hand-Schüller-Christian Syndrome
- Histiocytosis, Generalized
- Histiocytosis X
- Histiocytosis-X
- Langerhans Cell Granulomatosis
- Langerhans Cell Histiocytosis
- Langerhans-Cell Granulomatosis
- Langerhans-Cell Histiocytosis
- Letterer-Siwe Disease
- Non-Lipid Reticuloendotheliosis
- Schueller-Christian Disease
- Systemic Aleukemic Reticuloendotheliosis
- Type 2 Histiocytosis
En otras lenguas
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francés
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Granulomatose à cellules de Langerhans
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Histiocytose des cellules de Langerhans
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Histiocytose langerhansienne
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Histiocytose X
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Maladie de Hand-Schüller-Christian
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Maladie de Letterer-Siwe
URI
http://data.loterre.fr/ark:/67375/JVR-SHWR8G4L-F
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