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Maladies du système immunitaire
Maladies du système immunitaire : Questions médicales fréquentes
Termes MeSH sélectionnés :
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"name": "Quels signes indiquent une immunodéficience ?",
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"name": "Quels sont les symptômes d'une maladie auto-immune ?",
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"name": "Quels signes d'immunodéficience sont courants ?",
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"acceptedAnswer": {
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"text": "Infections récurrentes, fatigue persistante et retard de guérison sont des signes d'immunodéficience."
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"name": "Quels symptômes indiquent une maladie inflammatoire ?",
"position": 9,
"acceptedAnswer": {
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"text": "Rougeur, chaleur, gonflement et douleur dans les articulations peuvent signaler une inflammation."
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"name": "Comment reconnaître un choc anaphylactique ?",
"position": 10,
"acceptedAnswer": {
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"text": "Difficultés respiratoires, gonflement du visage et éruption cutanée soudaine sont des signes d'anaphylaxie."
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"name": "Comment prévenir les maladies auto-immunes ?",
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"name": "Quelles mesures pour éviter les allergies ?",
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"name": "Comment réduire le risque d'infections ?",
"position": 13,
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"name": "Quelles vaccinations sont recommandées pour les immunodéficients ?",
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"name": "Comment prévenir les crises d'anaphylaxie ?",
"position": 15,
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"text": "Éviter les allergènes et avoir un auto-injecteur d'épinéphrine à portée de main sont cruciaux."
}
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"@type": "Question",
"name": "Quels traitements existent pour les maladies auto-immunes ?",
"position": 16,
"acceptedAnswer": {
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"text": "Les traitements incluent des immunosuppresseurs, des anti-inflammatoires et des thérapies biologiques."
}
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"@type": "Question",
"name": "Comment traiter une allergie ?",
"position": 17,
"acceptedAnswer": {
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"text": "Les antihistaminiques, les corticostéroïdes et l'immunothérapie sont des options de traitement."
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"@type": "Question",
"name": "Quelles sont les options pour l'immunodéficience ?",
"position": 18,
"acceptedAnswer": {
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"text": "Les traitements peuvent inclure des antibiotiques prophylactiques et des thérapies de remplacement immunitaire."
}
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{
"@type": "Question",
"name": "Comment gérer les symptômes d'une maladie inflammatoire ?",
"position": 19,
"acceptedAnswer": {
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"text": "Des anti-inflammatoires non stéroïdiens (AINS) et des corticostéroïdes peuvent soulager les symptômes."
}
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"@type": "Question",
"name": "Quels traitements sont disponibles pour l'anaphylaxie ?",
"position": 20,
"acceptedAnswer": {
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"text": "L'épinéphrine est le traitement d'urgence principal pour l'anaphylaxie, suivie d'une surveillance médicale."
}
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{
"@type": "Question",
"name": "Quelles complications peuvent survenir avec les maladies auto-immunes ?",
"position": 21,
"acceptedAnswer": {
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"text": "Des complications incluent des dommages aux organes, des infections et des cancers associés."
}
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{
"@type": "Question",
"name": "Quels risques d'infections pour les immunodéficients ?",
"position": 22,
"acceptedAnswer": {
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"text": "Les personnes immunodéficientes sont à risque accru d'infections graves et opportunistes."
}
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"@type": "Question",
"name": "Quelles complications peuvent résulter d'allergies sévères ?",
"position": 23,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les allergies sévères peuvent entraîner un choc anaphylactique, une hospitalisation et des décès."
}
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{
"@type": "Question",
"name": "Comment les maladies inflammatoires affectent-elles la santé ?",
"position": 24,
"acceptedAnswer": {
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"text": "Elles peuvent causer des dommages aux tissus, des douleurs chroniques et des complications systémiques."
}
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{
"@type": "Question",
"name": "Quelles sont les conséquences d'un traitement immunosuppresseur ?",
"position": 25,
"acceptedAnswer": {
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"text": "Les traitements immunosuppresseurs augmentent le risque d'infections et de cancers."
}
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"@type": "Question",
"name": "Quels facteurs augmentent le risque de maladies auto-immunes ?",
"position": 26,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les antécédents familiaux, le sexe féminin et certaines infections virales sont des facteurs de risque."
}
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{
"@type": "Question",
"name": "Comment l'environnement influence-t-il les allergies ?",
"position": 27,
"acceptedAnswer": {
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"text": "L'exposition à des allergènes environnementaux, comme la pollution et les acariens, augmente le risque."
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"@type": "Question",
"name": "Quels sont les facteurs de risque d'immunodéficience ?",
"position": 28,
"acceptedAnswer": {
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"text": "Les maladies chroniques, le vieillissement et certains traitements médicaux peuvent augmenter le risque."
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"name": "Quel rôle joue le stress dans les maladies immunitaires ?",
"position": 29,
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"text": "Le stress chronique peut affaiblir le système immunitaire et exacerber les maladies auto-immunes."
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"name": "Comment l'alimentation affecte-t-elle l'immunité ?",
"position": 30,
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"text": "Une alimentation déséquilibrée peut affaiblir le système immunitaire et augmenter le risque de maladies."
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└─
Maladies auto-immunes
Autoimmune Diseases
D001327
-
C20.111
└─
Érythroblastose du nouveau-né
Erythroblastosis, Fetal
D004899
-
C20.306
└─
Glomérulonéphrite membranoproliférative
Glomerulonephritis, Membranoproliferative
D015432
-
C20.425
└─
Maladie du greffon contre l'hôte
Graft vs Host Disease
D006086
-
C20.452
└─
Hypersensibilité
Hypersensitivity
D006967
-
C20.543
└─
Syndrome inflammatoire de restauration immunitaire
Immune Reconstitution Inflammatory Syndrome
D054019
-
C20.608
└─
Déficits immunitaires
Immunologic Deficiency Syndromes
D007153
-
C20.673
└─
Syndromes immunoprolifératifs
Immunoproliferative Disorders
D007160
-
C20.683
└─
Troubles de l'activation mastocytaire
Mast Cell Activation Disorders
D000090362
-
C20.762
└─
Réaction transfusionnelle
Transfusion Reaction
D065227
-
C20.920
└─└─
Maladie d'Addison
Addison Disease
D000224
-
C20.111.163
└─└─
Anémie hémolytique auto-immune
Anemia, Hemolytic, Autoimmune
D000744
-
C20.111.175
└─└─
Maladie des anticorps antimembrane basale glomérulaire
Anti-Glomerular Basement Membrane Disease
D019867
-
C20.111.190
└─└─
Vascularites associées aux anticorps anti-cytoplasme des neutrophiles
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
D056648
-
C20.111.193
└─└─
Syndrome des anticorps antiphospholipides
Antiphospholipid Syndrome
D016736
-
C20.111.197
└─└─
Arthrite juvénile
Arthritis, Juvenile
D001171
-
C20.111.198
└─└─
Polyarthrite rhumatoïde
Arthritis, Rheumatoid
D001172
-
C20.111.199
└─└─
Maladies auto-immunes du système nerveux
Autoimmune Diseases of the Nervous System
D020274
-
C20.111.258
└─└─
Hypophysite auto-immune
Autoimmune Hypophysitis
D000069281
-
C20.111.273
└─└─
Choriorétinopathie de type birdshot
Birdshot Chorioretinopathy
D000080365
-
C20.111.303
└─└─
Dermatite herpétiforme
Dermatitis Herpetiformis
D003874
-
C20.111.318
└─└─
Diabète de type 1
Diabetes Mellitus, Type 1
D003922
-
C20.111.327
└─└─
Glomérulonéphrite à dépôts d'IgA
Glomerulonephritis, IGA
D005922
-
C20.111.525
└─└─
Glomérulonéphrite extra-membraneuse
Glomerulonephritis, Membranous
D015433
-
C20.111.535
└─└─
Maladie de Basedow
Graves Disease
D006111
-
C20.111.555
└─└─
Hépatite auto-immune
Hepatitis, Autoimmune
D019693
-
C20.111.567
└─└─
Maladie associée aux immunoglobulines G4
Immunoglobulin G4-Related Disease
D000077733
-
C20.111.572
└─└─
Diabète auto-immun latent de l'adulte
Latent Autoimmune Diabetes in Adults
D000071698
-
C20.111.576
└─└─
Dermatose bulleuse à IgA linéaire
Linear IgA Bullous Dermatosis
D062027
-
C20.111.585
└─└─
Lupus érythémateux disséminé
Lupus Erythematosus, Systemic
D008180
-
C20.111.590
└─└─
Ophtalmie sympathique
Ophthalmia, Sympathetic
D009879
-
C20.111.709
└─└─
Pemphigoïde bulleuse
Pemphigoid, Bullous
D010391
-
C20.111.730
└─└─
Pemphigus
Pemphigus
D010392
-
C20.111.736
└─└─
Polyendocrinopathies auto-immunes
Polyendocrinopathies, Autoimmune
D016884
-
C20.111.750
└─└─
Thyroïdite auto-immune
Thyroiditis, Autoimmune
D013967
-
C20.111.809
└─└─
Connectivites indifférenciées
Undifferentiated Connective Tissue Diseases
D000074079
-
C20.111.904
└─└─
Syndrome de bronchiolite oblitérante
Bronchiolitis Obliterans Syndrome
D000092122
-
C20.452.500
└─└─
Hypersensibilité retardée
Hypersensitivity, Delayed
D006968
-
C20.543.418
└─└─
Hypersensibilité immédiate
Hypersensitivity, Immediate
D006969
-
C20.543.480
└─└─
Maladies à complexes immuns
Immune Complex Diseases
D007105
-
C20.543.520
└─└─
Syndrome de Kounis
Kounis Syndrome
D000074962
-
C20.543.560
└─└─
Hypersensibilité au latex
Latex Hypersensitivity
D020315
-
C20.543.764
└─└─
Syndrome de Wissler-Fanconi
Wissler's Syndrome
D014924
-
C20.543.928
└─└─
Agammaglobulinémie
Agammaglobulinemia
D000361
-
C20.673.088
└─└─
Déficit immunitaire commun variable
Common Variable Immunodeficiency
D017074
-
C20.673.330
└─└─
Dysgammaglobulinémie
Dysgammaglobulinemia
D004406
-
C20.673.430
└─└─
Infections à VIH
HIV Infections
D015658
-
C20.673.480
└─└─
Infections à deltarétrovirus
Deltaretrovirus Infections
D006800
-
C20.673.483
└─└─
Lymphopénie
Lymphopenia
D008231
-
C20.673.627
└─└─
Dysfonctionnement de l'activité bactéricide phagocytaire
Phagocyte Bactericidal Dysfunction
D010585
-
C20.673.774
└─└─
Maladies d'immunodéficience primaire
Primary Immunodeficiency Diseases
D000081207
-
C20.673.795
└─└─
Syndromes lymphoprolifératifs
Lymphoproliferative Disorders
D008232
-
C20.683.515
└─└─
Paraprotéinémies
Paraproteinemias
D010265
-
C20.683.780
└─└─
Syndrome d'activation mastocytaire
Mast Cell Activation Syndrome
D000090267
-
C20.762.500
└─└─
Mastocytose
Mastocytosis
D008415
-
C20.762.750
└─└─
Oedème pulmonaire lésionnel aigu post-transfusionnel
Transfusion-Related Acute Lung Injury
D000073617
-
C20.920.500
└─└─└─
Syndrome de Churg-Strauss
Churg-Strauss Syndrome
D015267
-
C20.111.193.500
└─└─└─
Polyangéite microscopique
Microscopic Polyangiitis
D055953
-
C20.111.193.750
└─└─└─
Granulomatose avec polyangéite
Granulomatosis with Polyangiitis
D014890
-
C20.111.193.875
└─└─└─
Syndrome de Felty
Felty Syndrome
D005258
-
C20.111.199.389
└─└─└─
Vascularite rhumatoïde
Rheumatoid Vasculitis
D056653
-
C20.111.199.581
└─└─└─
Syndrome de Gougerot-Sjögren
Sjogren's Syndrome
D012859
-
C20.111.199.774
└─└─└─
Maladie de Still débutant à l'âge adulte
Still's Disease, Adult-Onset
D016706
-
C20.111.199.870
└─└─└─
Encéphalite à anticorps anti-récepteur N-méthyl-D-aspartate
Anti-N-Methyl-D-Aspartate Receptor Encephalitis
D060426
-
C20.111.258.124
└─└─└─
Maladies démyélinisantes auto-immunes du SNC
Demyelinating Autoimmune Diseases, CNS
D020278
-
C20.111.258.250
└─└─└─
Myasthénie
Myasthenia Gravis
D009157
-
C20.111.258.500
└─└─└─
Polyradiculoneuropathie
Polyradiculoneuropathy
D011129
-
C20.111.258.750
└─└─└─
Syndrome de l'homme raide
Stiff-Person Syndrome
D016750
-
C20.111.258.850
└─└─└─
Syndrome uvéo-méningo-encéphalique
Uveomeningoencephalitic Syndrome
D014607
-
C20.111.258.925
└─└─└─
Vascularite du système nerveux central
Vasculitis, Central Nervous System
D020293
-
C20.111.258.962
└─└─└─
Ophtalmopathie basedowienne
Graves Ophthalmopathy
D049970
-
C20.111.555.500
└─└─└─
Glomérulonéphrite lupique
Lupus Nephritis
D008181
-
C20.111.590.560
└─└─└─
Vascularite lupique du système nerveux central
Lupus Vasculitis, Central Nervous System
D020945
-
C20.111.590.750
└─└─└─
Eczéma de contact allergique
Dermatitis, Allergic Contact
D017449
-
C20.543.418.150
└─└─└─
Sarcoïdose
Sarcoidosis
D012507
-
C20.543.418.575
└─└─└─
Anaphylaxie
Anaphylaxis
D000707
-
C20.543.480.099
└─└─└─
Conjonctivite allergique
Conjunctivitis, Allergic
D003233
-
C20.543.480.200
└─└─└─
Eczéma atopique
Dermatitis, Atopic
D003876
-
C20.543.480.343
└─└─└─
Oesophagite à éosinophiles
Eosinophilic Esophagitis
D057765
-
C20.543.480.356
└─└─└─
Allergies induites par l'exercice physique
Exercise-Induced Allergies
D000092202
-
C20.543.480.363
└─└─└─
Hypersensibilité alimentaire
Food Hypersensitivity
D005512
-
C20.543.480.370
└─└─└─
Hypersensibilité respiratoire
Respiratory Hypersensitivity
D012130
-
C20.543.480.680
└─└─└─
Urticaire
Urticaria
D014581
-
C20.543.480.904
└─└─└─
Hypersensibilité au venin
Venom Hypersensitivity
D000092422
-
C20.543.480.952
└─└─└─
Phénomène d'Arthus
Arthus Reaction
D001183
-
C20.543.520.175
└─└─└─
Vascularite leucocytoclasique cutanée
Vasculitis, Leukocytoclastic, Cutaneous
D018366
-
C20.543.520.910
└─└─└─
Déficit en IgA
IgA Deficiency
D017098
-
C20.673.430.500
└─└─└─
Déficit en IgG
IgG Deficiency
D017099
-
C20.673.430.750
└─└─└─
Syndrome d'immunodéficience acquise
Acquired Immunodeficiency Syndrome
D000163
-
C20.673.480.040
└─└─└─
Syndrome rétroviral aigu
Acute Retroviral Syndrome
D000071297
-
C20.673.480.044
└─└─└─
Artérite du système nerveux central associée au SIDA
AIDS Arteritis, Central Nervous System
D020943
-
C20.673.480.048
└─└─└─
Néphropathie associée au SIDA
AIDS-Associated Nephropathy
D016263
-
C20.673.480.050
└─└─└─
Syndrome pré-SIDA
AIDS-Related Complex
D000386
-
C20.673.480.080
└─└─└─
Infections opportunistes liées au SIDA
AIDS-Related Opportunistic Infections
D017088
-
C20.673.480.100
└─└─└─
Lipodystrophie associée au VIH
HIV-Associated Lipodystrophy Syndrome
D039682
-
C20.673.480.400
└─└─└─
Entéropathie associée au SIDA
HIV Enteropathy
D019053
-
C20.673.480.480
└─└─└─
Séropositivité VIH
HIV Seropositivity
D006679
-
C20.673.480.500
└─└─└─
Syndrome cachectique lié au VIH
HIV Wasting Syndrome
D019247
-
C20.673.480.520
└─└─└─
Infections à HTLV-I
HTLV-I Infections
D015490
-
C20.673.483.470
└─└─└─
Infections à HTLV-II
HTLV-II Infections
D015491
-
C20.673.483.480
└─└─└─
Lymphocytopénie idiopathique T CD4-positif
T-Lymphocytopenia, Idiopathic CD4-Positive
D018344
-
C20.673.627.800
└─└─└─
Ataxie-télangiectasie
Ataxia Telangiectasia
D001260
-
C20.673.795.250
└─└─└─
Syndrome de Bloom
Bloom Syndrome
D001816
-
C20.673.795.313
└─└─└─
Syndrome de Chediak-Higashi
Chediak-Higashi Syndrome
D002609
-
C20.673.795.375
└─└─└─
Déficits héréditaires en complément
Hereditary Complement Deficiency Diseases
D000081208
-
C20.673.795.500
└─└─└─
Syndrome d'hyper-IgM
Hyper-IgM Immunodeficiency Syndrome
D053306
-
C20.673.795.625
└─└─└─
Syndrome de Job
Job Syndrome
D007589
-
C20.673.795.688
└─└─└─
Déficit d'adhérence leucocytaire
Leukocyte-Adhesion Deficiency Syndrome
D018370
-
C20.673.795.719
└─└─└─
Immunodéficience combinée grave
Severe Combined Immunodeficiency
D016511
-
C20.673.795.750
└─└─└─
Syndrome de Wiskott-Aldrich
Wiskott-Aldrich Syndrome
D014923
-
C20.673.795.875
└─└─└─
Déficit en mévalonate kinase
Mevalonate Kinase Deficiency
D054078
-
C20.683.460.319
└─└─└─
Syndrome lymphoprolifératif avec auto-immunité
Autoimmune Lymphoproliferative Syndrome
D056735
-
C20.683.515.124
└─└─└─
Hyperplasie lymphoïde angiofolliculaire
Castleman Disease
D005871
-
C20.683.515.250
└─└─└─
Lymphadénopathie angio-immunoblastique
Immunoblastic Lymphadenopathy
D007119
-
C20.683.515.501
└─└─└─
Mononucléose infectieuse
Infectious Mononucleosis
D007244
-
C20.683.515.515
└─└─└─
Leucémie à tricholeucocytes
Leukemia, Hairy Cell
D007943
-
C20.683.515.517
└─└─└─
Leucémie lymphoïde
Leukemia, Lymphoid
D007945
-
C20.683.515.528
└─└─└─
Lymphangiomyome
Lymphangiomyoma
D008203
-
C20.683.515.710
└─└─└─
Lymphomes
Lymphoma
D008223
-
C20.683.515.761
└─└─└─
Syndrome d'activation macrophagique
Macrophage Activation Syndrome
D055501
-
C20.683.515.800
└─└─└─
Plasmocytome
Plasmacytoma
D010954
-
C20.683.515.880
└─└─└─
Syndrome de Sézary
Sezary Syndrome
D012751
-
C20.683.515.920
└─└─└─
Syndrome de lyse tumorale
Tumor Lysis Syndrome
D015275
-
C20.683.515.950
└─└─└─
Cryoglobulinémie
Cryoglobulinemia
D003449
-
C20.683.780.250
└─└─└─
Maladie des chaines lourdes
Heavy Chain Disease
D006362
-
C20.683.780.490
└─└─└─
Amylose à chaine légère d'immunoglobuline
Immunoglobulin Light-chain Amyloidosis
D000075363
-
C20.683.780.565
└─└─└─
Gammapathie monoclonale de signification indéterminée
Monoclonal Gammopathy of Undetermined Significance
D008998
-
C20.683.780.640
└─└─└─
Myélome multiple
Multiple Myeloma
D009101
-
C20.683.780.650
└─└─└─
Syndrome POEMS
POEMS Syndrome
D016878
-
C20.683.780.750
└─└─└─
Myélome multiple indolent
Smoldering Multiple Myeloma
D000075122
-
C20.683.780.838
└─└─└─
Macroglobulinémie de Waldenström
Waldenstrom Macroglobulinemia
D008258
-
C20.683.780.925
└─└─└─
Sarcome à mastocytes
Mast-Cell Sarcoma
D012515
-
C20.762.750.375
└─└─└─
Mastocytome
Mastocytoma
D034801
-
C20.762.750.469
└─└─└─
Mastocytose cutanée
Mastocytosis, Cutaneous
D034701
-
C20.762.750.563
└─└─└─
Mastocytose généralisée
Mastocytosis, Systemic
D034721
-
C20.762.750.750
└─└─└─└─
Sclérose cérébrale diffuse de Schilder
Diffuse Cerebral Sclerosis of Schilder
D002549
-
C20.111.258.250.175
└─└─└─└─
Sclérose en plaques
Multiple Sclerosis
D009103
-
C20.111.258.250.500
└─└─└─└─
Myélite transverse
Myelitis, Transverse
D009188
-
C20.111.258.250.550
└─└─└─└─
Neuromyélite optique
Neuromyelitis Optica
D009471
-
C20.111.258.250.775
└─└─└─└─
Syndrome myasthénique de Lambert-Eaton
Lambert-Eaton Myasthenic Syndrome
D015624
-
C20.111.258.500.150
└─└─└─└─
Myasthénie congénitale
Myasthenia Gravis, Neonatal
D020941
-
C20.111.258.500.650
└─└─└─└─
Artérite à cellules géantes
Giant Cell Arteritis
D013700
-
C20.111.258.962.800
└─└─└─└─
Dermatite photoallergique
Dermatitis, Photoallergic
D017454
-
C20.543.418.150.600
└─└─└─└─
Dermatite de contact au Rhus toxicodendron
Dermatitis, Toxicodendron
D011040
-
C20.543.418.150.700
└─└─└─└─
Sarcoïdose pulmonaire
Sarcoidosis, Pulmonary
D017565
-
C20.543.418.575.725
└─└─└─└─
Uvéoparotidite
Uveoparotid Fever
D014608
-
C20.543.418.575.865
└─└─└─└─
Hypersensibilité à l'oeuf
Egg Hypersensitivity
D021181
-
C20.543.480.370.150
└─└─└─└─
Hypersensibilité au lait
Milk Hypersensitivity
D016269
-
C20.543.480.370.500
└─└─└─└─
Hypersensibilité aux noix et aux arachides
Nut and Peanut Hypersensitivity
D000074924
-
C20.543.480.370.572
└─└─└─└─
Hypersensibilité aux fruits de mer
Shellfish Hypersensitivity
D000067208
-
C20.543.480.370.763
└─└─└─└─
Hypersensibilité au blé
Wheat Hypersensitivity
D021182
-
C20.543.480.370.850
└─└─└─└─
Sinusite fongique allergique
Allergic Fungal Sinusitis
D000092562
-
C20.543.480.680.038
└─└─└─└─
Alvéolite allergique extrinsèque
Alveolitis, Extrinsic Allergic
D000542
-
C20.543.480.680.075
└─└─└─└─
Aspergillose bronchopulmonaire allergique
Aspergillosis, Allergic Bronchopulmonary
D001229
-
C20.543.480.680.085
└─└─└─└─
Asthme
Asthma
D001249
-
C20.543.480.680.095
└─└─└─└─
Rhinite allergique
Rhinitis, Allergic
D065631
-
C20.543.480.680.443
└─└─└─└─
Angioedème
Angioedema
D000799
-
C20.543.480.904.066
└─└─└─└─
Angio-oedèmes héréditaires
Angioedemas, Hereditary
D054179
-
C20.673.795.500.500
└─└─└─└─
Syndrome d'hyper-IgM lié à l'X
Hyper-IgM Immunodeficiency Syndrome, Type 1
D053307
-
C20.673.795.625.500
└─└─└─└─
Immunodéficiences combinées graves liées à l'X
X-Linked Combined Immunodeficiency Diseases
D053632
-
C20.673.795.750.500
└─└─└─└─
Leucémie B
Leukemia, B-Cell
D015448
-
C20.683.515.528.080
└─└─└─└─
Leucémie aigüe biphénotypique
Leukemia, Biphenotypic, Acute
D015456
-
C20.683.515.528.100
└─└─└─└─
Leucémie prolymphocytaire
Leukemia, Prolymphocytic
D015463
-
C20.683.515.528.565
└─└─└─└─
Leucémie à cellules T
Leukemia, T-Cell
D015458
-
C20.683.515.528.582
└─└─└─└─
Leucémie-lymphome lymphoblastique à précurseurs B et T
Precursor Cell Lymphoblastic Leukemia-Lymphoma
D054198
-
C20.683.515.528.600
└─└─└─└─
Lymphangioléiomyomatose
Lymphangioleiomyomatosis
D018192
-
C20.683.515.710.465
└─└─└─└─
Lymphome composite
Composite Lymphoma
D058617
-
C20.683.515.761.150
└─└─└─└─
Maladie de Hodgkin
Hodgkin Disease
D006689
-
C20.683.515.761.355
└─└─└─└─
Lymphome intraoculaire
Intraocular Lymphoma
D064090
-
C20.683.515.761.417
└─└─└─└─
Lymphome malin non hodgkinien
Lymphoma, Non-Hodgkin
D008228
-
C20.683.515.761.480
└─└─└─└─
Leucémie à plasmocytes
Leukemia, Plasma Cell
D007952
-
C20.683.515.845.500
└─└─└─└─
Maladie immunoproliférative de l'intestin grêle
Immunoproliferative Small Intestinal Disease
D007161
-
C20.683.780.490.512
└─└─└─└─
Syndrome de Schnitzler
Schnitzler Syndrome
D019873
-
C20.683.780.640.700
└─└─└─└─
Mastocytome cutané
Mastocytoma, Skin
D054705
-
C20.762.750.563.500
└─└─└─└─
Urticaire pigmentaire
Urticaria Pigmentosa
D014582
-
C20.762.750.563.850
└─└─└─└─
Leucémie à mastocytes
Leukemia, Mast-Cell
D007946
-
C20.762.750.750.500
└─└─└─└─└─
Leucoencéphalite aigüe hémorragique
Leukoencephalitis, Acute Hemorrhagic
D004684
-
C20.111.258.250.350.500
└─└─└─└─└─
Sclérose en plaques récurrente-rémittente
Multiple Sclerosis, Relapsing-Remitting
D020529
-
C20.111.258.250.500.600
└─└─└─└─└─
Syndrome de Miller-Fisher
Miller Fisher Syndrome
D019846
-
C20.111.258.750.400.500
└─└─└─└─└─
Hypersensibilité aux noix
Nut Hypersensitivity
D021184
-
C20.543.480.370.572.500
└─└─└─└─└─
Hypersensibilité aux arachides
Peanut Hypersensitivity
D021183
-
C20.543.480.370.572.750
└─└─└─└─└─
Trichosporonose
Trichosporonosis
D060586
-
C20.543.480.680.075.682
└─└─└─└─└─
Asthme à l'effort
Asthma, Exercise-Induced
D001250
-
C20.543.480.680.095.110
└─└─└─└─└─
État de mal asthmatique
Status Asthmaticus
D013224
-
C20.543.480.680.095.880
└─└─└─└─└─
Rhinite spasmodique apériodique
Rhinitis, Allergic, Perennial
D012221
-
C20.543.480.680.443.500
└─└─└─└─└─
Rhinite allergique saisonnière
Rhinitis, Allergic, Seasonal
D006255
-
C20.543.480.680.443.750
└─└─└─└─└─
Leucémie prolymphocytaire à cellules B
Leukemia, Prolymphocytic, B-Cell
D054403
-
C20.683.515.528.565.745
└─└─└─└─└─
Leucémie à grands lymphocytes granuleux
Leukemia, Large Granular Lymphocytic
D054066
-
C20.683.515.528.582.049
└─└─└─└─└─
Leucémie-lymphome à cellules T de l'adulte
Leukemia-Lymphoma, Adult T-Cell
D015459
-
C20.683.515.528.582.100
└─└─└─└─└─
Leucémie prolymphocytaire à cellules T
Leukemia, Prolymphocytic, T-Cell
D015461
-
C20.683.515.528.582.125
└─└─└─└─└─
Leucémie-lymphome lymphoblastique à précurseurs B
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
D015452
-
C20.683.515.528.600.600
└─└─└─└─└─
Leucémie-lymphome lymphoblastique à précurseurs T
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
D054218
-
C20.683.515.528.600.620
└─└─└─└─└─
Lymphome B
Lymphoma, B-Cell
D016393
-
C20.683.515.761.480.150
└─└─└─└─└─
Lymphome folliculaire
Lymphoma, Follicular
D008224
-
C20.683.515.761.480.350
└─└─└─└─└─
Lymphome immunoblastique à grandes cellules
Lymphoma, Large-Cell, Immunoblastic
D016400
-
C20.683.515.761.480.487
└─└─└─└─└─
Lymphome à cellules du manteau
Lymphoma, Mantle-Cell
D020522
-
C20.683.515.761.480.525
└─└─└─└─└─
Lymphome T
Lymphoma, T-Cell
D016399
-
C20.683.515.761.480.750
└─└─└─└─└─└─
Allergie aux acariens
Dust Mite Allergy
D000092542
-
C20.543.480.680.443.500.500
└─└─└─└─└─└─
Angioedème héréditaire de type III
Hereditary Angioedema Type III
D056828
-
C20.543.480.904.066.500.500
└─└─└─└─└─└─
Angioedèmes héréditaires de types I et II
Hereditary Angioedema Types I and II
D056829
-
C20.543.480.904.066.500.750
└─└─└─└─└─└─
Lymphome de Burkitt
Burkitt Lymphoma
D002051
-
C20.683.515.761.480.150.165
└─└─└─└─└─└─
Lymphome lié au SIDA
Lymphoma, AIDS-Related
D016483
-
C20.683.515.761.480.150.450
└─└─└─└─└─└─
Lymphome B de la zone marginale
Lymphoma, B-Cell, Marginal Zone
D018442
-
C20.683.515.761.480.150.570
└─└─└─└─└─└─
Lymphome B diffus à grandes cellules
Lymphoma, Large B-Cell, Diffuse
D016403
-
C20.683.515.761.480.150.585
└─└─└─└─└─└─
Lymphome primitif des séreuses
Lymphoma, Primary Effusion
D054685
-
C20.683.515.761.480.150.592
└─└─└─└─└─└─
Granulomatose lymphomatoïde
Lymphomatoid Granulomatosis
D008230
-
C20.683.515.761.480.150.600
└─└─└─└─└─└─
Lymphome T associé à une entéropathie
Enteropathy-Associated T-Cell Lymphoma
D058527
-
C20.683.515.761.480.750.199
└─└─└─└─└─└─
Lymphome à grandes cellules anaplasiques
Lymphoma, Large-Cell, Anaplastic
D017728
-
C20.683.515.761.480.750.399
└─└─└─└─└─└─
Lymphome T cutané
Lymphoma, T-Cell, Cutaneous
D016410
-
C20.683.515.761.480.750.800
└─└─└─└─└─└─
Lymphome T périphérique
Lymphoma, T-Cell, Peripheral
D016411
-
C20.683.515.761.480.750.825
└─└─└─└─└─└─└─
Lymphome plasmoblastique
Plasmablastic Lymphoma
D000069293
-
C20.683.515.761.480.150.585.500
└─└─└─└─└─└─└─
Lymphome cutané primitif à grandes cellules anaplasiques
Lymphoma, Primary Cutaneous Anaplastic Large Cell
D054446
-
C20.683.515.761.480.750.800.507
└─└─└─└─└─└─└─
Papulose lymphomatoïde
Lymphomatoid Papulosis
D017731
-
C20.683.515.761.480.750.800.528
└─└─└─└─└─└─└─
Mycosis fongoïde
Mycosis Fungoides
D009182
-
C20.683.515.761.480.750.800.550
└─└─└─└─└─└─└─└─
Réticulose pagétoïde
Pagetoid Reticulosis
D056267
-
C20.683.515.761.480.750.800.550.600
Fibromuscular dysplasia (FMD) is a rare vasculopathy for which limited data are available particularly from Europe. Our aim was to study the clinical characteristics of a regional cohort of carotid fi...
A retrospective cohort study of all cases of carotid/cerebrovascular FMD presenting to our regional vascular service (catchment population approximately 2 million), between 1998 and 2020. Imaging repo...
Eighty six patients with a diagnosis of cerebrovascular fibromuscular dysplasia were identified on imaging (31 computed tomography angiography, 46 magnetic resonance angiography, and 9 digital subtrac...
Carotid FMD patients have a high rate of multisite involvement, extracerebral vascular complications, and evidence of hereditary vasculopathy, requiring careful screening and surveillance....
Breast angiosarcoma is a rare and aggressive disease with a poor prognosis. Two subtypes have been identified: primary angiosarcoma (PBA) and secondary breast angiosarcoma (SBA). In this retrospective...
We included in our analysis 29 patients who received a diagnosis of PBA or SBA between 2006 and 2019....
All patients received surgery as frontline treatment, but only 6 patients underwent to adjuvant treatment. Neoadjuvant chemotherapy was administered 2 patients. The preferred chemotherapeutic regimen ...
In our analysis, we have shown a lower median RFS and OS in patients with PBA compared with those with SBA, and a significantly younger age at diagnosis in patients affected by PBA....
The current study aimed to evaluate rheumatoid arthritis (RA) patients with interstitial lung disease (ILD) in clinical practice and whether disease characteristics are associated with X-ray and high-...
The elderly population, which is more active than before, is increasingly suffering from trauma (loss of reflexes and systemic pathologic conditions). Surgical management may be more controversial due...
In this retrospective study (over a five-year period), we analyzed the causes and management of facial fractures in patients aged over 65 years, and the medical history of each patient was investigate...
One hundred and nineteen patients with 198 facial fractures were included. The main cause of fractures was a fall (50%). The zygomatic region (39.9%) and mandible (27.8%) were the sites of the most fr...
This work is a help to understanding the causes and consequences of facial trauma in the elderly population. The management of these facial fractures requires a multidisciplinary assessment, taking in...
Rhabdomyolysis (RM) refers to a clinical syndrome in which muscle cells are damaged by various causes and the clinical manifestations are mainly muscle pain, weakness, and dark urine. Acute kidney inj...
Analysis of medical records of RM patients admitted to Tianjin Medical University General Hospital from October 2019 to October 2022. Statistical software SPSS 25.0 was used to analyze the data. The r...
Among the 71 patients, the median age of the patients was 53.0 (30.0, 71.0) years and was 2.5 times higher in men than in women. Infection was the most common etiology. History of alcohol consumption,...
Our study revealed the clinical and laboratory characteristics of RM in the population attending the Tianjin Medical University General Hospital in the last three years, which is a reference for futur...
Adolescent and young adult female patients receiving myelosuppressive cancer treatments are at risk of abnormal uterine bleeding (AUB). The frequency with which patients with cancer receive menstrual ...
We established a retrospective cohort of 90 females with a diagnosis of Hodgkin or non-Hodgkin lymphoma (n = 25), AML (n = 46), or sarcoma (n = 19) and treated with chemotherapy between 2008 and 2019 ...
The majority of patients (77.8%) received menstrual suppression. Compared with nonsuppressed patients, suppressed patients had similar rates of packed red blood cell transfusions but higher number of ...
Menstrual suppression was common in our cohort with variability in agents used. Pediatric and adult oncologists demonstrated different practice patterns....
To determine the prevalence of maternal sudden death (MSD) and to compare the characteristics of death between women with explained and unexplained sudden death....
A national retrospective study in France....
Maternal deaths related to an unexpected sudden cardiac arrest were extracted from the French National Confidential Enquiry into Maternal Deaths database for 2007-2012....
Maternal, pregnancy, sudden death characteristics and maternal investigations were compared between women with explained and unexplained cause of death....
A total of 83 maternal sudden deaths and 4 949 890 live births occurred over the period studied, thus accounting for 16% of all maternal deaths (n = 510). Death was explained in 51 (61%) women and une...
Maternal sudden death is a rare event but accounts for a high proportion of all maternal deaths. This highlights the importance of providing training in diagnostic and management strategy for care pro...
IgG4-related hypophysitis (IgG4-RH) is a rare chronic inflammatory condition of the pituitary gland. This study reports the presentation, management and outcomes for patients with histologically prove...
A prospectively maintained electronic database was searched over a 14-year period from 1 January 2007 to 31 December 2020 at a single academic centre to identify all patients with a histological diagn...
A total of 8 patients (5 male) with a median age of 51 years were identified. The most common presenting symptoms were headache (4/8; 50%), fatigue (3/8; 37.5%) and visual impairment (2/8; 25%). Three...
IgG4-RH is an increasingly recognised entity presenting with a variety of symptoms and signs. Clinical presentation is similar to other forms of hypophysitis. It is therefore important to consider IgG...
The purpose of this study was to introduce the surgical process of Sommerlad-Furlow modified (S-F) palatoplasty and compare its surgical and functional outcomes with conventional Sommerlad (S) palatop...
Diabetes mellitus is a highly prevalent disease globally and contributes to significant morbidity and mortality. As a consequence of multiple pathophysiologic changes which are associated with diabete...