serw-MX  [xml]  
 


    
 DeCS Categories

A11 Cells .
A11.329 Connective Tissue Cells .
A11.329.372 Macrophages .
A11.329.372.385 Histiocytes .
A11.627 Myeloid Cells .
A11.627.482 Macrophages .
A11.627.482.385 Histiocytes .
A11.733 Phagocytes .
A11.733.397 Macrophages .
A11.733.397.385 Histiocytes .
A15 Hemic and Immune Systems .
A15.382 Immune System .
A15.382.680 Phagocytes .
A15.382.680.397 Macrophages .
A15.382.680.397.385 Histiocytes .
A15.382.812 Mononuclear Phagocyte System .
A15.382.812.522 Macrophages .
A15.382.812.522.385 Histiocytes .
C04 Neoplasms .
C04.557 Neoplasms by Histologic Type .
C04.557.450 Neoplasms, Connective and Soft Tissue .
C04.557.450.565 Neoplasms, Connective Tissue .
C04.557.450.565.590 Neoplasms, Fibrous Tissue .
C04.557.450.565.590.425 Histiocytoma .
C08 Respiratory Tract Diseases .
C08.381 Lung Diseases .
C08.381.483 Lung Diseases, Interstitial .
C08.381.483.375 Histiocytosis, Langerhans-Cell .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.825 Sphingolipidoses .
C10.228.140.163.100.435.825.700 Niemann-Pick Diseases .
C15 Hemic and Lymphatic Diseases .
C15.604 Lymphatic Diseases .
C15.604.250 Histiocytosis .
C15.604.250.400 Histiocytosis, Langerhans-Cell .
C15.604.250.410 Histiocytosis, Non-Langerhans-Cell .
C15.604.250.410.450 Histiocytosis, Sinus .
C15.604.250.410.625 Niemann-Pick Diseases .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.825 Sphingolipidoses .
C16.320.565.189.435.825.700 Niemann-Pick Diseases .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.730 Niemann-Pick Diseases .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.700 Niemann-Pick Diseases .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.825 Sphingolipidoses .
C18.452.132.100.435.825.700 Niemann-Pick Diseases .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.730 Niemann-Pick Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.825 Sphingolipidoses .
C18.452.648.189.435.825.700 Niemann-Pick Diseases .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.730 Niemann-Pick Diseases .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.700 Niemann-Pick Diseases .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Histiocytosis .
Histiocytoses .
General term for the abnormal appearance of histiocytes in the blood. Based on the pathological features of the cells involved rather than on clinical findings, the histiocytic diseases are subdivided into three groups: HISTIOCYTOSIS, LANGERHANS CELL; HISTIOCYTOSIS, NON-LANGERHANS-CELL; and HISTIOCYTIC DISORDERS, MALIGNANT. .
1.00
61696
 
Histiocytoma .
Histiocytomas .
A neoplasm containing HISTIOCYTES. Important forms include BENIGN FIBROUS HISTIOCYTOMA; and MALIGNANT FIBROUS HISTIOCYTOMA. .
0.83
266
 
Histiocytes .
Histiocyte .
Macrophages found in the TISSUES, as opposed to those found in the blood (MONOCYTES) or serous cavities (SEROUS MEMBRANE). .
0.81
364519
 
Histiocytosis, Sinus .
Sinus Histiocytosis with Massive Lymphadenopathy .
Destombes Rosai Dorfman Syndrome .
Disease, Rosai-Dorfman .
Histiocytoses, Sinus .
Rosai Dorfman Disease .
Sinus Histiocytoses .
Sinus Histiocytosis .
Syndrome, Destombes-Rosai-Dorfman .
Destombes-Rosai-Dorfman Syndrome .
Rosai-Dorfman Disease .
Benign, non-Langerhans-cell, histiocytic proliferative disorder that primarily affects the lymph nodes. It is often referred to as sinus histiocytosis with massive lymphadenopathy. .
0.80
441000
 
Histiocytosis, Langerhans-Cell .
Hand-Schueller-Christian Disease .
Hand-Schueller-Christian Syndrome .
Hand-Schüller-Christian Disease .
Hand-Schüller-Christian Syndrome .
Hashimoto-Pritzger Disease .
Histiocytosis, Generalized .
Histiocytosis-X .
Langerhans Cell Granulomatosis .
Langerhans Cell Granulomatosis, Pulmonary .
Langerhans Cell Histiocytosis .
Letterer-Siwe Disease .
Non-Lipid Reticuloendotheliosis .
Pulmonary Histiocytosis X .
Pulmonary Langerhans Cell Granulomatosis .
Schueller-Christian Disease .
Systemic Aleukemic Reticuloendotheliosis .
Type 2 Histiocytosis .
Aleukemic Reticuloendothelioses, Systemic .
Aleukemic Reticuloendotheliosis, Systemic .
Cell Granulomatoses, Langerhans .
Cell Granulomatosis, Langerhans .
Cell Histiocytoses, Langerhans .
Cell Histiocytosis, Langerhans .
Disease, Hand-Schueller-Christian .
Disease, Hand-Schüller-Christian .
Disease, Letterer-Siwe .
Disease, Schueller-Christian .
Generalized Histiocytoses .
Generalized Histiocytosis .
Granulomatoses, Langerhans Cell .
Granulomatosis, Langerhans Cell .
Granulomatosis, Langerhans-Cell .
Hand Schueller Christian Disease .
Hand Schueller Christian Syndrome .
Hand Schüller Christian Disease .
Hand Schüller Christian Syndrome .
Histiocytoses, Generalized .
Histiocytoses, Langerhans Cell .
Histiocytoses, Type 2 .
Histiocytosis X, Pulmonary .
Histiocytosis, Langerhans Cell .
Histiocytosis, Type 2 .
Langerhans Cell Granulomatoses .
Langerhans Cell Histiocytoses .
Letterer Siwe Disease .
Non Lipid Reticuloendotheliosis .
Non-Lipid Reticuloendothelioses .
Reticuloendothelioses, Non-Lipid .
Reticuloendothelioses, Systemic Aleukemic .
Reticuloendotheliosis, Non-Lipid .
Reticuloendotheliosis, Systemic Aleukemic .
Schueller Christian Disease .
Syndrome, Hand-Schueller-Christian .
Syndrome, Hand-Schüller-Christian .
Systemic Aleukemic Reticuloendothelioses .
Type 2 Histiocytoses .
Histiocytosis X .
Langerhans-Cell Granulomatosis .
Langerhans-Cell Histiocytosis .
Hand-Schueller-Christian Syndrome .
Schueller-Christian Disease .
Letterer-Siwe Disease .
Histiocytosis, Generalized .
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. .
0.79
2144771
 
Niemann-Pick Diseases .
Niemann Pick Disease .
Niemann Pick Diseases .
Niemann-Pick Disease .
Lipidosis, Neuronal Cholesterol .
Ophthalmoplegia, Supraoptic Vertical .
HISTIOCYTOSIS, LIPID .
A group of autosomal recessive disorders in which harmful quantities of lipids accumulate in the viscera and the central nervous system. They can be caused by deficiencies of enzyme activities (SPHINGOMYELIN PHOSPHODIESTERASE) or defects in intracellular transport, resulting in the accumulation of SPHINGOMYELINS and CHOLESTEROL. There are various subtypes based on their clinical and genetic differences. .
0.78
181525