Differentials: Thrombotic Thrombocytopenic Purpura

Differential diagnosis for Thrombotic Thrombocytopenic Purpura

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This list is calculated based on an algorithm and may be inaccurate. Google search based on different algorithm is also displayed. Please interpret with caution. Click here to search for differential diagnosis for a set of clinical findings or a short case summary. The images are provided by Bing Image Search. The images may not be related to Thrombotic Thrombocytopenic Purpura.

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Date Added: 2018-03-04:

Moschcowitz Syndrome (100 %) ( Thrombotic Thrombocytopenic Purpura,)
Paroxysmal Nocturnal Hemoglobinuria (69 %)
Urticarial Vasculitis (59 %) ( Chronic Urticaria AsA Manifestation Of Venulitis, Hypocomplementemic Urticarial Vasculitis Syndrome, Hypocomplementemic Vasculitis, Unusual Lupus-like Syndrome,)
Clubbing (59 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Acquired Hypogammaglobulinemia (56 %) ( Common Variable Immunodeficiency,)
Cutaneous Small-vessel Vasculitis (56 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Common Variable Immunodeficiency (56 %) ( Acquired Hypogammaglobulinemia,)
Zoster (56 %) ( Herpes Zoster, Shingles,)
Cutis Laxa (56 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Hyperparathyroidism (56 %)
Idiopathic Thrombocytopenic Purpura (56 %) ( Autoimmune Thrombocytopenic Purpura, Werlhofs Disease,)
Waldenstr m Macroglobulinemia (56 %)
Recurrent Aphthous Stomatitis (53 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Iron Deficiency (53 %)
Fibrinolysis Syndrome (53 %) ( Defibrinating Syndrome, Hypofibrinogenemia,)
Coccidioidomycosis (53 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Granulocytic Sarcoma (53 %) ( Chloroma, Myeloid Sarcoma,)
Hemochromatosis (50 %) ( Bronze Diabetes,)
Nail patella Syndrome (50 %) ( Fong Syndrome, Hereditary Osteoonychodysplasia, Hood Syndrome,)
Intravascular LargeB-cell Lymphoma (50 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Cyclic Neutropenia (50 %)
Bronze Diabetes (50 %) ( Hemochromatosis,)
Fanconi Syndrome (50 %) ( Familial Pancytopenia, Familial Panmyelophthisis,)
Angioimmunoblastic Lymphadenopathy With Dysproteinemia (50 %) ( AngioimmunoblasticT-cell Lymphoma,)
Familial Mediterranean Fever (50 %)
Hypoparathyroidism (50 %)
Polyarteritis Nodosa (50 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Disseminated Intravascular Coagulation (50 %)
Gingival Hypertrophy (50 %)
Mixed Connective Tissue Disease (50 %) ( Sharps Syndrome, Undifferentiated Connective Tissue Disease,)
Amniotic Band Syndrome (50 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Tuberous Sclerosis (50 %) ( Bourneville Disease, Epiloia,)
AngioimmunoblasticT-cell Lymphoma (50 %) ( Angioimmunoblastic Lymphadenopathy With Dysproteinemia,)
HistiocytosisX (50 %) ( Langerhans Cell Histiocytosis,)
Langerhans Cell Histiocytosis (50 %) ( HistiocytosisX,)
Miliary Tuberculosis (47 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
VitaminK Deficiency (47 %)
Angiocentric Lymphoma (47 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Hyper-ige Syndrome (47 %) ( Buckley Syndrome, Job Syndrome,)
Roseola Infantum (47 %) ( Exanthem Subitum, Exanthema Subitum, Sixth Disease,)
Duhring Disease (47 %) ( Dermatitis Herpetiformis,)
Juvenile Rheumatoid Arthritis (47 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Glandular Fever (47 %) ( Infectious Mononucleosis,)
Infectious Mononucleosis (47 %) ( Glandular Fever,)
Churg strauss Syndrome (47 %) ( Allergic Granulomatosis,)
Dermatitis Herpetiformis (47 %) ( Duhring Disease,)
Allergic Granulomatosis (47 %) ( Churg strauss Syndrome,)
Ehlers-danlos Syndrome (44 %)
Systemic Lupus Erythematosus (44 %)
Sinus Histiocytosis With Massive Lymphadenopathy (44 %) ( Rosai dorfman Disease,)
VitaminB12 Deficiency (44 %) ( Cyanocobalamin Deficiency,)
Schwannoma (44 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Rosai dorfman Disease (44 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Cyanocobalamin Deficiency (44 %) ( VitaminB12 Deficiency,)
Callus (44 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Rheumatoid Arthritis (44 %)
Majeed Syndrome (44 %)
Merkel Cell Carcinoma (44 %) ( Cutaneous Apudoma, Primary Neuroendocrine Carcinoma Of The Skin, Primary Small Cell Carcinoma Of The Skin, Trabecular Carcinoma Of The Skin,)
Anhidrosis (44 %) ( Hypohidrosis,)
Diffuse LargeB-cell Lymphoma (44 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Hypereosinophilic Syndrome (44 %)
Acrochordon (44 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Hypohidrosis (44 %) ( Anhidrosis,)
Sj grens Syndrome (44 %) ( Mikulicz Disease, Sicca Syndrome,)
Primary Cutaneous LargeB-cell Lymphoma (44 %) ( Diffuse LargeB-cell Lymphoma,)
Dermatofibroma (44 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Tumor Lysis Syndrome (44 %)
Juvenile Myelomonocytic Leukemia (44 %)
Henoch Schonlein Purpura (44 %)
Tnf Receptor Associated Periodic Syndrome (41 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Johanson blizzard Syndrome (41 %)
Takayasu Arteritis (41 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Digeorge Syndrome (41 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Growth Hormone Deficiency (41 %)
Angioedema (41 %)
Ehlers danlos Syndrome (41 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Hairy-cell Leukemia (41 %)
Mckusick Type Metaphyseal Chondrodysplasia (41 %) ( Cartilage hair Hypoplasia,)
Cartilage hair Hypoplasia (41 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Smooth Tongue (41 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Angiokeratoma (41 %)
Solar Purpura (41 %) ( Actinic Purpura, Senile Purpura,)
North American Blastomycosis (41 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Human Herpesvirus6 (41 %)
Alternariosis (41 %)
Echinococcosis (41 %) ( Hydatid Disease,)
Liposarcoma (41 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Folic Acid Deficiency (41 %)
Hydatid Disease (41 %) ( Echinococcosis,)
Virus-related (41 %)
Lymphangioma (41 %) ( Lymphangiectasis,)
Lymphangiectasis (41 %) ( Lymphangioma,)
Disease (41 %)
Encephalocele (41 %)
Paraneoplastic Syndrome (41 %)
Turner Syndrome (41 %)

Differentials from Google.

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Thrombotic Thrombocytopenic Purpura

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