Differentials: Cutaneous Leukocytoclastic Vasculitis

Differential diagnosis for Cutaneous Leukocytoclastic Vasculitis

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Date Added: 2017-03-19:

Cutaneous Small-vessel Vasculitis (100 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Lupus Erythematosus Panniculitis (47 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Leukocytoclastic Vasculitis (45 %)
Acute Febrile Neutrophilic Dermatosis (43 %) ( Sweets Syndrome,)
Erythema Induratum (43 %) ( Bazin Disease, Nodular Vasculitis,)
Dermatofibroma (42 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Sweets Syndrome (42 %) ( Acute Febrile Neutrophilic Dermatosis,)
Polyarteritis Nodosa (41 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Churg strauss Syndrome (39 %) ( Allergic Granulomatosis,)
Eosinophilic Cellulitis (39 %) ( Wells Syndrome,)
Allergic Granulomatosis (39 %) ( Churg strauss Syndrome,)
Wells Syndrome (39 %) ( Eosinophilic Cellulitis,)
Chilblains (38 %) ( Pernio, Perniosis,)
Interstitial Granulomatous Dermatitis (38 %)
Cutaneous Lymphoid Hyperplasia (37 %) ( Borrelial Lymphocytoma, Lymphadenosis Benigna Cutis, Lymphocytoma Cutis, Pseudolymphoma, Pseudolymphoma Of Spiegler And Fendt, Sarcoidosis Of Spiegler And Fendt, Spiegler fendt Lymphoid Hyperplasia, Spiegler fendt Sarcoid,)
Eosinophilic Pustular Folliculitis (37 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Cutis Laxa (36 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Malignant Mixed Tumor (36 %) ( Malignant Chondroid Syringoma,)
Recurrent Aphthous Stomatitis (36 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Malignant Chondroid Syringoma (36 %) ( Malignant Mixed Tumor,)
Lymphomatoid Papulosis (36 %)
Leukemia Cutis (36 %)
Microscopic Polyangiitis (34 %) ( Microscopic Polyarteritis, Microscopic Polyarteritis Nodosa,)
Epidermal Cyst (34 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Erythema Nodosum (34 %)
Livedoid Vasculopathy (34 %) ( Atrophie Blanche, Livedo Reticularis With Summer Ulceration, Livedoid Vasculitis, Purple Syndrome, Segmental Hyalinizing Vasculitis,)
Pityriasis Lichenoides Et Varioliformis Acuta (34 %) ( Acute Guttate Parapsoriasis, Acute Parapsoriasis, Acute Pityriasis Lichenoides, Mucha habermann Disease, Parapsoriasis Acuta, Parapsoriasis Lichenoides Et Varioliformis Acuta, Parapsoriasis Varioliformis,)
Chromoblastomycosis (33 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Pyoderma Gangrenosum (33 %)
Sj grens Syndrome (33 %) ( Mikulicz Disease, Sicca Syndrome,)
Langerhans Cell Histiocytosis (33 %) ( HistiocytosisX,)
HistiocytosisX (33 %) ( Langerhans Cell Histiocytosis,)
Wegener Granulomatosis (33 %)
Lupus Pernio (32 %)
Systemic Sarcoidosis (32 %)
Rheumatoid Neutrophilic Dermatitis (32 %) ( Rheumatoid Neutrophilic Dermatosis,)
Intravascular LargeB-cell Lymphoma (32 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Miliary Tuberculosis (32 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Panniculitis-likeT-cell Lymphoma (32 %) ( SubcutaneousT-cell Lymphoma,)
Mixed Tumor (32 %) ( Chondroid Syringoma,)
North American Blastomycosis (32 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Chondroid Syringoma (32 %) ( Mixed Tumor,)
Clubbing (32 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
SubcutaneousT-cell Lymphoma (32 %) ( Panniculitis-likeT-cell Lymphoma,)
Pancreatic Panniculitis (30 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Angiolymphoid Hyperplasia With Eosinophilia (30 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Acrodermatitis Chronica Atrophicans (30 %) ( Herxheimer Disease, Primary Diffuse Atrophy,)
Malignant Pilomatricoma (30 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Angiocentric Lymphoma (30 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Cicatricial Pemphigoid (30 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Schwannoma (30 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Urticarial Vasculitis (30 %) ( Chronic Urticaria AsA Manifestation Of Venulitis, Hypocomplementemic Urticarial Vasculitis Syndrome, Hypocomplementemic Vasculitis, Unusual Lupus-like Syndrome,)
Majeed Syndrome (30 %)
Mucosa-associated Lymphoid Tissue Lymphoma (30 %)
Lipodermatosclerosis (30 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
Amputation Neuroma (30 %) ( Traumatic Neuroma,)
Traumatic Neuroma (30 %) ( Amputation Neuroma,)
Bowel-associated Dermatosis arthritis Syndrome (30 %) ( Bowel Bypass Syndrome, Bowel Bypass Syndrome Without Bowel Bypass, Intestinal Bypass Arthritis dermatitis Syndrome,)
Pilomatricoma (29 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Eosinophilic Granuloma (29 %)
Rheumatoid Neutrophilic Dermatosis (29 %) ( Rheumatoid Neutrophilic Dermatitis,)
Glomus Tumor (29 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Zoster (29 %) ( Herpes Zoster, Shingles,)
Hyper-ige Syndrome (29 %) ( Buckley Syndrome, Job Syndrome,)
Palmoplantar Pustulosis (29 %) ( Persistent Palmoplantar Pustulosis, Pustular Psoriasis Of The Barber Type, Pustular Psoriasis Of The Extremities, Pustulosis Of Palms And Soles, Pustulosis Palmaris Et Plantaris,)
Henoch Schonlein Purpura (29 %)
Scleroderma (29 %)
Cryoglobulinemic Vasculitis (28 %)
Stasis Dermatitis (28 %) ( Congestion Eczema, Gravitational Dermatitis, Gravitational Eczema, Stasis Eczema, Varicose Eczema,)
Papular Mucinosis (28 %) ( Generalized Lichen Myxedematosus, Sclerodermoid Lichen Myxedematosus, Scleromyxedema,)
Lichen Planopilaris (28 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Generalized Pustular Psoriasis (28 %) ( Pustular Psoriasis Of Von Zumbusch,)
Merkel Cell Carcinoma (28 %) ( Cutaneous Apudoma, Primary Neuroendocrine Carcinoma Of The Skin, Primary Small Cell Carcinoma Of The Skin, Trabecular Carcinoma Of The Skin,)
Pemphigus Vulgaris (28 %)
Pustular Psoriasis Of Von Zumbusch (28 %) ( Generalized Pustular Psoriasis,)
Mycetoma (28 %) ( Madura Foot, Maduromycosis,)
Waldenstr m Macroglobulinemia (28 %)
Pemphigus Herpetiformis (28 %) ( Acantholytic Herpetiform Dermatitis, Herpetiform Pemphigus, Mixed Bullous Disease, Pemphigus Controlled By Sulfapyridine,)
Rosacea (28 %) ( Acne Rosacea,)
Blau Syndrome (28 %)
Perforating Folliculitis (28 %)
Acne Rosacea (28 %) ( Rosacea,)
Eosinophilic Vasculitis (28 %)
Coccidioidomycosis (28 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Hypereosinophilic Syndrome (26 %)
Multicentric Reticulohistiocytosis (26 %)
Psoriatic Erythroderma (26 %) ( Erythrodermic Psoriasis,)
Hidradenitis Suppurativa (26 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Histoplasmosis (26 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Epithelioma Cuniculatum (26 %) ( Ackerman Tumor, Carcinoma Cuniculatum,)
Sarcoidosis (26 %)
Sclerotic Fibroma (26 %)
Verruca Vulgaris (26 %) ( Wart,)
Kaposi Sarcoma (26 %)
Necrobiotic Xanthogranuloma (26 %) ( Necrobiotic Xanthogranuloma With Paraproteinemia,)
Hydroa Vacciniforme (26 %) ( Bazins Hydroa Vacciniforme,)
Wart (26 %) ( Verruca Vulgaris,)
Giant Pigmented Nevus (26 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Necrobiotic Xanthogranuloma With Paraproteinemia (26 %) ( Necrobiotic Xanthogranuloma,)
Follicular Mucinosis (26 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Erythrodermic Psoriasis (26 %) ( Psoriatic Erythroderma,)
Connective Tissue Nevus (26 %) ( Collagenoma, Elastoma, Shagreen Patch,)
Eosinophilic Fasciitis (26 %) ( Shulmans Syndrome,)
Neurothekeoma (26 %) ( Bizarre Cutaneous Neurofibroma, Cutaneous Lobular Neuromyxoma, Myxoma Of The Nerve Sheath, Myxomatous Perineurioma, Nerve Sheath Myxoma,)
Callus (26 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Sparganosis (26 %)
Rheumatoid Arthritis (26 %)
Papulonecrotic Tuberculid (26 %)
Mycosis Fungoides (26 %)
Shulmans Syndrome (26 %) ( Eosinophilic Fasciitis,)
Klippel trenaunay Syndrome (26 %) ( Angioosteohypertrophy Syndrome, Hemangiectatic Hypertrophy,)
Bazins Hydroa Vacciniforme (26 %) ( Hydroa Vacciniforme,)
Polyneuropathy organomegaly endocrinopathy monoclonal Gammopathy skin Changes Syndrome (26 %) ( Crow fukase Syndrome, Poems Syndrome,)
Solar Purpura (26 %) ( Actinic Purpura, Senile Purpura,)
Mixed Connective Tissue Disease (26 %) ( Sharps Syndrome, Undifferentiated Connective Tissue Disease,)
Juvenile Rheumatoid Arthritis (26 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Pustular (26 %)
Erythema Annulare Centrifugum (26 %) ( Deep Gyrate Erythema, Erythema Perstans, Palpable Migrating Erythema, Superficial Gyrate Erythema,)
Lichen Planus Verrucosus (25 %) ( Hypertrophic Lichen Planus,)
Acroosteolysis (25 %)
Gianotti crosti Syndrome (25 %) ( Infantile Papular Acrodermatitis, Papular Acrodermatitis Of Childhood, Papulovesicular Acrolocated Syndrome,)
Nonspecific Cutaneous Conditions Associated With Leukemia (25 %) ( Leukemid,)
Marginal ZoneB-cell Lymphoma (25 %)
Linear Iga Bullous Dermatosis (25 %) ( Linear Iga Dermatosis,)
Tnf Receptor Associated Periodic Syndrome (25 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Fissured Tongue (25 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Geographic Tongue (25 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Subcutaneous Granuloma Annulare (25 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Acute Necrotizing Ulcerative Gingivitis (25 %) ( Acute Membranous Gingivitis, Acute Necrotizing Ulcerative Gingivostomatitis, Fusospirillary Gingivitis, Fusospirillosis, Fusospirochetal Gingivitis, Necrotizing Gingivitis, Phagedenic Gingivitis, Trench Mouth, Ulcerative Gingivitis, Vincent Gingivitis, Vincent Infection, Vincent Stomatitis, Vincents Disease,)
Folliculitis (25 %)
Immune Reconstitution Inflammatory Syndrome (25 %) ( Immune Recovery Syndrome,)
Acrospiroma (25 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Aquarium Granuloma (25 %) ( Fish Tank Granuloma, Swimming Pool Granuloma,)
Immune Recovery Syndrome (25 %) ( Immune Reconstitution Inflammatory Syndrome,)
Rheumatoid Nodulosis (25 %) ( Accelerated Rheumatoid Nodulosis,)
Linear Iga Dermatosis (25 %) ( Linear Iga Bullous Dermatosis,)
Leukemid (25 %) ( Nonspecific Cutaneous Conditions Associated With Leukemia,)
Accelerated Rheumatoid Nodulosis (25 %) ( Rheumatoid Nodulosis,)
Necrotizing Fasciitis (25 %) ( Flesh-eating Bacteria Syndrome,)
Lymphangioma (25 %) ( Lymphangiectasis,)
Flesh-eating Bacteria Syndrome (25 %) ( Necrotizing Fasciitis,)
Gingival Hypertrophy (25 %)
Malignant Acrospiroma (25 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Lymphangiectasis (25 %) ( Lymphangioma,)
Carcinoid (25 %)
Acquired Hypogammaglobulinemia (25 %) ( Common Variable Immunodeficiency,)
Common Variable Immunodeficiency (25 %) ( Acquired Hypogammaglobulinemia,)
Hypertrophic Lichen Planus (25 %) ( Lichen Planus Verrucosus,)
Superficial Granulomatous Pyoderma (25 %)
Sneddon wilkinson Disease (25 %) ( Subcorneal Pustular Dermatosis,)
South American Blastomycosis (25 %) ( Brazilian Blastomycosis, Paracoccidioidal Granuloma, Paracoccidioidomycosis,)
Subcorneal Pustular Dermatosis (25 %) ( Sneddon wilkinson Disease,)
Carney Complex (25 %) ( Lamb Syndrome, Name Syndrome,)
Granulocytic Sarcoma (24 %) ( Chloroma, Myeloid Sarcoma,)
Hyperhidrosis (24 %)
Syringoma (24 %)
Livedo Racemosa (24 %)
Lymphomatoid Granulomatosis (24 %)
Primary Cutaneous Anaplastic Large Cell Lymphoma (24 %) ( Cd30+ CutaneousT-cell Lymphoma,)
Cd30+ CutaneousT-cell Lymphoma (24 %) ( Primary Cutaneous Anaplastic Large Cell Lymphoma,)
L fgren Syndrome (24 %)
Duhring Disease (24 %) ( Dermatitis Herpetiformis,)
Gouty Panniculitis (24 %)
Lepromatous Leprosy (24 %)
Congenital Self-healing Reticulohistiocytosis (24 %) ( Hashimoto pritzker Disease, Hashimoto pritzker Syndrome,)
Giant Cell Tumor Of The Tendon Sheath (24 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Lichenoid Dermatitis (24 %)
Sinus Histiocytosis With Massive Lymphadenopathy (24 %) ( Rosai dorfman Disease,)
Rosai dorfman Disease (24 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Borderline Lepromatous Leprosy (24 %)
Actinic Keratosis (24 %) ( Senile Keratosis, Solar Keratosis,)
Kimura Disease (24 %)
Takayasu Arteritis (24 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Generalized Eruptive Histiocytoma (24 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Thrombotic Thrombocytopenic Purpura (24 %) ( Moschcowitz Syndrome,)
Subcutaneous Sarcoidosis (24 %) ( Darier roussy Disease, Darier roussy Sarcoid,)
Juvenile Systemic Hyalinosis (24 %) ( Infantile Systemic Hyalinosis,)
Paraneoplastic Pemphigus (24 %)
Acrochordon (24 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Familial Mediterranean Fever (24 %)
Erythema Elevatum Diutinum (24 %)
Paraneoplastic Syndrome (24 %)
Infantile Systemic Hyalinosis (24 %) ( Juvenile Systemic Hyalinosis,)
Pyogenic Granuloma (24 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Dermatitis Herpetiformis (24 %) ( Duhring Disease,)
Moschcowitz Syndrome (24 %) ( Thrombotic Thrombocytopenic Purpura,)
Tuberous Sclerosis (22 %) ( Bourneville Disease, Epiloia,)
Blastomycosis-like Pyoderma (22 %) ( Pyoderma Vegetans,)
Relapsing Polychondritis (22 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Reflex Sympathetic Dystrophy (22 %) ( Complex Regional Pain Syndrome,)
Metastatic Carcinoma (22 %)
Pustular Psoriasis (22 %)
Primary Cutaneous LargeB-cell Lymphoma (22 %) ( Diffuse LargeB-cell Lymphoma,)
Pachydermoperiostosis (22 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Cylindroma (22 %) ( Dermal Eccrine Cylindroma,)
Tuberculosis Luposa (22 %) ( Lupus Vulgaris,)
Necrobiosis Lipoidica Diabeticorum (22 %) ( Necrobiosis Lipoidica,)
Livedo Reticularis (22 %)
Amniotic Band Syndrome (22 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Necrobiosis Lipoidica (22 %) ( Necrobiosis Lipoidica Diabeticorum,)
Hydatid Disease (22 %) ( Echinococcosis,)
Pyoderma Vegetans (22 %) ( Blastomycosis-like Pyoderma,)
Dermal Eccrine Cylindroma (22 %) ( Cylindroma,)
Echinococcosis (22 %) ( Hydatid Disease,)
Hyperparathyroidism (22 %)
Rosacea Fulminans (22 %) ( Pyoderma Faciale,)
Id Reaction (22 %) ( Disseminated Eczema, Generalized Eczema, Autoeczematization,)
Pyoderma Faciale (22 %) ( Rosacea Fulminans,)
Congenital Melanocytic Nevus (22 %)
Cutaneous Focal Mucinosis (22 %)
Juvenile Hyaline Fibromatosis (22 %) ( Fibromatosis Hyalinica Multiplex Juvenilis, Murray puretic drescher Syndrome,)
Reticulohistiocytoma (22 %)
Lupus Vulgaris (22 %) ( Tuberculosis Luposa,)
Liposarcoma (22 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Spitz Nevus (22 %) ( Benign Juvenile Melanoma, Epithelioid And Spindle Cell Nevus, Spitzs Juvenile Melanoma,)
Familial Cold Urticaria (22 %) ( Familial Cold Autoinflammatory Syndrome,)
Soft-tissue Melanoma (22 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Diffuse LargeB-cell Lymphoma (22 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Complex Regional Pain Syndrome (22 %) ( Reflex Sympathetic Dystrophy,)
Familial Cold Autoinflammatory Syndrome (22 %) ( Familial Cold Urticaria,)
Nodular Fasciitis (22 %) ( Nodular Pseudosarcomatous Fasciits, Pseudosarcomatous Fasciitis, Subcutaneous Pseudosarcomatous Fibromatosis,)
Erythema Multiforme (22 %)
Alternariosis (22 %)
Mycobacterium Haemophilum Infection (22 %)
Acne Keloidalis Nuchae (21 %) ( Acne Keloidalis, Dermatitis Papillaris Capillitii, Folliculitis Keloidalis, Folliculitis Keloidis Nuchae, Nuchal Keloid Acne,)
Acroangiodermatitis (21 %) ( Acroangiodermatitis Of Mali, Mali Acroangiodermatitis, Pseudo-kaposis Sarcoma, Pseudo-kaposi Sarcoma,)
Dermographism (21 %) ( Dermatographism,)
Hypersensitivity Vasculitis (21 %)
Pityriasis Lichenoides (21 %)
Acne Fulminans (21 %) ( Acute Febrile Ulcerative Acne,)
Mckusick Type Metaphyseal Chondrodysplasia (21 %) ( Cartilage hair Hypoplasia,)
Nasal Glioma (21 %) ( Brain-like Heterotopia, Cephalic Brain-like Heterotopia, Glial Hamartoma, Heterotopic Neuroglial Tissue, Nasal Cerebral Heterotopia, Nasal Heterotopic Brain Tissue,)
Multiple Lentigines Syndrome (21 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Xanthoma Planum (21 %) ( Plane Xanthoma,)
Drug-induced Lichenoid Reaction (21 %) ( Drug-induced Lichen Planus, Lichenoid Drug Eruption,)
Milium (21 %)
Rheumatoid Vasculitis (21 %)
Pruritic Urticarial Papules And Plaques Of Pregnancy (21 %) ( Late-onset Prurigo Of Pregnancy, Polymorphic Eruption Of Pregnancy, Puppp Syndrome, Toxemic Rash Of Pregnancy, Toxic Erythema Of Pregnancy,)
AngioimmunoblasticT-cell Lymphoma (21 %) ( Angioimmunoblastic Lymphadenopathy With Dysproteinemia,)
Cartilage hair Hypoplasia (21 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Leukoplakia (21 %)
Recurrent Palmoplantar Hidradenitis (21 %) ( Idiopathic Palmoplantar Hidradenitis, Idiopathic Plantar Hidradenitis, Painful Plantar Erythema, Palmoplantar Eccrine Hidradenitis, Plantar Panniculitis,)
Disseminated Intravascular Coagulation (21 %)
Phycomycosis (21 %) ( Zygomycosis,)
Acute Febrile Ulcerative Acne (21 %) ( Acne Fulminans,)
Blueberry Muffin Baby (21 %)
Neutrophilic Lobular Panniculitis (21 %)
Scrofuloderma (21 %) ( Tuberculosis Cutis Colliquativa,)
Dermatographism (21 %) ( Dermographism,)
Raynaud Phenomenon (21 %)
Zygomycosis (21 %) ( Phycomycosis,)
Systemic Sclerosis (21 %)
Plane Xanthoma (21 %) ( Xanthoma Planum,)
Tuberculosis Cutis Colliquativa (21 %) ( Scrofuloderma,)
Lipoma (21 %)
Primary Inoculation Tuberculosis (21 %) ( Cutaneous Primary Complex, Primary Tuberculous Complex, Tuberculous Chancre,)
Disseminated Coccidioidomycosis (21 %) ( Coccidioidal Granuloma,)
Angioimmunoblastic Lymphadenopathy With Dysproteinemia (21 %) ( AngioimmunoblasticT-cell Lymphoma,)
Foreign Body Reaction (21 %)
Lichenoid Keratosis (21 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Tufted Angioma (21 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Proliferating Trichilemmal Cyst (21 %) ( Pilar Tumor, Proliferating Follicular Cystic Neoplasm, Proliferating Pilar Tumor, Proliferating Trichilemmal Tumor,)
Relapsing Febrile Non-suppurative Panniculitis (21 %) ( Weber christian Disease,)
Aggressive Digital Papillary Adenocarcinoma (21 %) ( Digital Papillary Adenocarcinoma, Papillary Adenoma,)
Dermatitis Repens (21 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Acral Fibrokeratoma (21 %) ( Acquired Digital Fibrokeratoma, Acquired Periungual Fibrokeratoma,)
Hamartoma (21 %)
Coccidioidal Granuloma (21 %) ( Disseminated Coccidioidomycosis,)
Weber christian Disease (21 %) ( Relapsing Febrile Non-suppurative Panniculitis,)
Psoriasis Vulgaris (20 %) ( Chronic Stationary Psoriasis, Plaque-like Psoriasis,)
Histiocytic Medullary Reticulosis (20 %) ( Malignant Histiocytosis,)
Mucocele (20 %) ( Mucous Cyst Of The Oral Mucosa,)
Paroxysmal Nocturnal Hemoglobinuria (20 %)
Desmoplastic Melanoma (20 %) ( Neurotropic Melanoma, Spindled Melanoma,)
HypovitaminosisA (20 %) ( Phrynoderma,)
Phrynoderma (20 %) ( HypovitaminosisA,)
Nevus Of Ota (20 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Seborrheic Keratosis (20 %) ( Seborrheic Verruca, Senile Wart,)
Nevus Flammeus (20 %) ( Capillary Malformation, Port-wine Stain,)
Sapho Syndrome (20 %) ( Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome,)
Ichthyosis Acquisita (20 %) ( Acquired Ichthyosis,)
Hidrocystoma (20 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Lichen Myxedematosus (20 %)
Multiple Familial Trichoepithelioma (20 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Mucous Cyst Of The Oral Mucosa (20 %) ( Mucocele,)
Kikuchis Disease (20 %) ( Histiocytic Necrotizing Lymphadenitis,)
Infectious Mononucleosis (20 %) ( Glandular Fever,)
Aphthous Stomatitis (20 %)
Malacoplakia (20 %) ( Malakoplakia,)
Verrucous Carcinoma (20 %)
Keratosis Lichenoides Chronica (20 %) ( N kams Disease,)
Lichen Planus Actinicus (20 %) ( Actinic Lichen Niditus, Actinic Lichen Planus, Lichen Planus Atrophicus Annularis, Lichen Planus Subtropicus, Lichen Planus Tropicus, Lichenoid Melanodermatitis, Lichenoid Melanodermatosis, Summertime Actinic Lichenoid Eruption,)
AdultT-cell Leukemia/lymphoma (20 %)
Basal Cell Carcinoma (20 %)
Septal Panniculitis (20 %)
Diabetic Dermopathy (20 %) ( Shin Spots,)
Muckle wells Syndrome (20 %)
Glandular Fever (20 %) ( Infectious Mononucleosis,)
Gas Gangrene (20 %) ( Clostridial Myonecrosis, Myonecrosis,)
Calcinosis Cutis (20 %)
Silicosis (20 %)
N kams Disease (20 %) ( Keratosis Lichenoides Chronica,)
Molluscum Contagiosum (20 %)
Calcinosis raynaud Phenomenon esophageal Dysmotility sclerodactyly telangiectasia Syndrome (20 %) ( Crest Syndrome,)
Isthmicoma (20 %) ( Infundibuloma, Tumor Of The Follicular Infundibulum,)
Lichen Planus (20 %)
PleomorphicT-cell Lymphoma (20 %) ( Non-mycosis Fungoides Cd30- Pleomorphic Small/medium Sized CutaneousT-cell Lymphoma,)
Birt hogg dub Syndrome (20 %)
Acquired Ichthyosis (20 %) ( Ichthyosis Acquisita,)
Histiocytic Necrotizing Lymphadenitis (20 %) ( Kikuchis Disease,)
Malignant Histiocytosis (20 %) ( Histiocytic Medullary Reticulosis,)
Leiomyosarcoma (20 %)
Shin Spots (20 %) ( Diabetic Dermopathy,)
Hypoparathyroidism (20 %)
Varicella (20 %) ( Chickenpox,)
Papular Purpuric Gloves And Socks Syndrome (20 %)
Birt-hogg-dube Syndrome (20 %)
Malakoplakia (20 %) ( Malacoplakia,)
Lymphangiectasia (20 %)
Lupoid Rosacea (20 %) ( Granulomatous Rosacea, Micropapular Tuberculid, Rosacea-like Tuberculid Of Lewandowsky,)
Bullous Pemphigoid (20 %)
Pityriasis Rosea Gibert (20 %) ( Pityriasis Rosea,)
Chickenpox (20 %) ( Varicella,)
Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome (20 %) ( Sapho Syndrome,)
Systemic Lupus Erythematosus (20 %)
Phaeohyphomycosis (20 %)
Iga Pemphigus (20 %)
Crest Syndrome (20 %) ( Calcinosis raynaud Phenomenon esophageal Dysmotility sclerodactyly telangiectasia Syndrome,)
Pretibial Myxedema (20 %)
Steatocystoma Multiplex (20 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Acid-induced (20 %)
Chronic Granulomatous Disease (20 %) ( Bridges good Syndrome, Chronic Granulomatous Disorder, Quie Syndrome,)
Myxoid Cyst (20 %) ( Digital Mucous Cyst, Mucous Cyst,)
Chondrodermatitis Nodularis Helicis (20 %) ( Chondrodermatitis Nodularis Chronica Helicis,)
Good Syndrome (20 %) ( Thymoma With Immunodeficiency,)
Chondrodermatitis Nodularis Chronica Helicis (20 %) ( Chondrodermatitis Nodularis Helicis,)
Dermatomyositis (20 %)
Non-mycosis Fungoides Cd30- Pleomorphic Small/medium Sized CutaneousT-cell Lymphoma (20 %) ( PleomorphicT-cell Lymphoma,)
Toxic Shock Syndrome (20 %) ( Streptococcal Toxic Shock Syndrome, Streptococcal Toxic Shock-like Syndrome, Toxic Streptococcal Syndrome,)
Hemangiosarcoma (20 %)
Colloid Milium (20 %)
Pyostomatitis Vegetans (20 %)
Nevoid Basal Cell Carcinoma Syndrome (20 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Fabry Disease (20 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Thymoma With Immunodeficiency (20 %) ( Good Syndrome,)
Pityriasis Rosea (20 %) ( Pityriasis Rosea Gibert,)
Pityriasis Rubra Pilaris (20 %) ( Devergies Disease, Lichen Ruber Acuminatus, Lichen Ruber Pilaris,)
Keratocyst (20 %)
Papa Syndrome (18 %) ( Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome,)
Tumid Lupus Erythematosus (18 %) ( Lupus Erythematosus Tumidus,)
HepatitisC (18 %)
Congenital Fascial Dystrophy (18 %) ( Stiff Skin Syndrome,)
Neutrophilic Eccrine Hidradenitis (18 %)
Rhinophyma (18 %)
Smooth Tongue (18 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Lupus Erythematosus Tumidus (18 %) ( Tumid Lupus Erythematosus,)
Henoch sch nlein Purpura (18 %) ( Anaphylactoid Purpura, Purpura Rheumatica,)
Irritant Diaper Dermatitis (18 %) ( Diaper Dermatitis, Napkin Dermatitis,)
Yaws (18 %) ( Bouba, Framb sie, Parangi, Pian,)
Malignant Fibrous Histiocytoma (18 %)
Orf (18 %) ( Contagious Pustular Dermatosis, Ecthyma Contagiosum, Infectious Labial Dermatitis, Sheep Pox,)
Idiopathic Thrombocytopenic Purpura (18 %) ( Autoimmune Thrombocytopenic Purpura, Werlhofs Disease,)
Teratoma (18 %)
Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome (18 %) ( Papa Syndrome,)
Formaldehyde-induced (18 %)
Leiomyoma (18 %)
Cutaneous Sinus Of Dental Origin (18 %) ( Dental Sinus,)
Linear Verrucous Epidermal Nevus (18 %) ( Linear Epidermal Nevus, Verrucous Epidermal Nevus,)
Letterer siwe Disease (18 %)
Nevus Spilus (18 %) ( Speckled Lentiginous Nevus, Zosteriform Lentiginous Nevus,)
Dental Sinus (18 %) ( Cutaneous Sinus Of Dental Origin,)
Botryomycosis (18 %)
Glossodynia (18 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Atrophodermia Vermiculata (18 %) ( Acne Vermoulante, Acne Vermoulanti, Atrophoderma Reticulata Symmetrica Faciei, Atrophoderma Reticulatum, Atrophoderma Vermiculata, Atrophoderma Vermiculatum, Atrophodermia Reticulata Symmetrica Faciei, Atrophodermia Ulerythematosa, Atrophodermie Vermicul e Des Joues AvecK ratoses Folliculaires, Folliculitis Ulerythema Reticulata, Folliculitis Ulerythematous Reticulata, Folliculitis Ulerythemosa, Honeycomb Atrophy, Ulerythema Acneforme, Ulerythema Acneiforme,)
Halo Nevus (18 %) ( Leukoderma Acquisitum Centrifugum, Perinevoid Vitiligo, Sutton Nevus,)
Tumor Lysis Syndrome (18 %)
Dermoid Cyst (18 %)
Squamous Cell Carcinoma In Situ (18 %) ( Bowens Disease,)
Epithelioid Sarcoma (18 %)
Solar Elastosis (18 %) ( Actinic Elastosis,)
Primary Cutaneous Follicular Lymphoma (18 %) ( Follicular Center Cell Lymphoma, Follicular Center Lymphoma,)
Extramammary Paget Disease (18 %)
Actinic Elastosis (18 %) ( Solar Elastosis,)
Thrush (18 %) ( Oral Candidiasis,)
Oral Candidiasis (18 %) ( Thrush,)
Stiff Skin Syndrome (18 %) ( Congenital Fascial Dystrophy,)
Cutaneous Lupus Mucinosis (18 %) ( Papular And Nodular Mucinosis In Lupus Erythematosus, Papular And Nodular Mucinosis Of Gold, Papulonodular Mucinosis In Lupus Erythematosus,)
Dyshidrosis (18 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Juvenile Xanthogranuloma (18 %)
Pagetoid Reticulosis (18 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Blepharophyma (18 %)
Bowens Disease (18 %) ( Squamous Cell Carcinoma In Situ,)
Otophyma (18 %)
Metophyma (18 %)
Plaque-type Porokeratosis (18 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Psoriatic Arthritis (18 %)
Glucagonoma Syndrome (18 %) ( Necrolytic Migratory Erythema,)
Necrolytic Migratory Erythema (18 %) ( Glucagonoma Syndrome,)
Infantile Digital Fibromatosis (18 %) ( Inclusion Body Fibromatosis, Infantile Digital Myofibroblastoma, Reye Tumor,)
Majocchi Granuloma (18 %) ( Fungal Folliculitis,)
Erythema Infectiosum (18 %) ( Fifth Disease, Slapped Cheek Disease,)
Nummular Dermatitis (18 %) ( Discoid Eczema, Microbial Eczema, Nummular Eczema, Nummular Neurodermatitis,)
Fungal Folliculitis (18 %) ( Majocchi Granuloma,)
Acne Necrotica (18 %)
Wiskott aldrich Syndrome (18 %)
Multiple Endocrine Neoplasia Type3 (18 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
Ganglion Cyst (17 %)
Nevus Sebaceous (17 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Dystrophic Epidermolysis Bullosa (17 %)
Hypohidrotic Ectodermal Dysplasia (17 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Morphea (17 %)
Nonne milroy meige Syndrome (17 %) ( Hereditary Lymphedema, Milroy Disease,)
Lentigo Maligna (17 %) ( Lentiginous Melanoma On Sun-damaged Skin,)
Tuberculous Cellulitis (17 %)
Genital Herpes (17 %) ( Herpes Genitalis, Herpes Progenitalis,)
Tubular Apocrine Adenoma (17 %) ( Papillary Eccrine Adenoma,)
Polymorphic Light Eruption (17 %) ( Polymorphous Light Eruption,)
Pilonidal Sinus (17 %) ( Barbers Interdigital Pilonidal Sinus, Pilonidal Cyst, Pilonidal Disease,)
Lymphedema Praecox (17 %)
Keloidal Scar (17 %) ( Keloid,)
Leptospirosis (17 %) ( Fort Bragg Fever, Pretibial Fever, Weils Disease,)
Keloid (17 %) ( Keloidal Scar,)
Blue Nevus (17 %) ( Blue Neuronevus, Dermal Melanocytoma, Nevus Bleu,)
Benign Melanocytic Nevus (17 %) ( Banal Nevus, Common Acquired Melanocytic Nevus, Mole, Nevocellular Nevus, Nevocytic Nevus,)
Bronze Diabetes (17 %) ( Hemochromatosis,)
Ulcerative Sarcoidosis (17 %)
Injection Site Reaction (17 %)
Toxoplasmosis (17 %)
Flat Warts (17 %) ( Verruca Plana,)
Isolated Dyskeratosis Follicularis (17 %) ( Warty Dyskeratoma,)
Thyroglossal Duct Cyst (17 %)
Branchial Cyst (17 %) ( Branchial Cleft Cyst,)
Discoid Lupus Erythematosus (17 %)
Lupus Miliaris Disseminatus Faciei (17 %)
Inflammatory Skin Lesions Following Zoster Infection (17 %) ( Isotopic Response,)
Isotopic Response (17 %) ( Inflammatory Skin Lesions Following Zoster Infection,)
Favre racouchot Syndrome (17 %) ( Favre racouchot Disease, Nodular Cutaneous Elastosis With Cysts And Comedones,)
Multiple Endocrine Neoplasia Type1 (17 %) ( Wermer Syndrome,)
Progressive Systemic Sclerosis (17 %)
Lymphangioma Circumscriptum (17 %) ( Superficial Lymphatic Malformation,)
Subepidermal Calcified Nodule (17 %) ( Solitary Congenital Nodular Calcification, Winers Nodular Calcinosis,)
Wermer Syndrome (17 %) ( Multiple Endocrine Neoplasia Type1,)
Warty Dyskeratoma (17 %) ( Isolated Dyskeratosis Follicularis,)
Necrotizing Sialometaplasia (17 %)
Infantile Myofibromatosis (17 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Basaloid Squamous Cell Carcinoma (17 %)
Lentiginous Melanoma On Sun-damaged Skin (17 %) ( Lentigo Maligna,)
Branchial Cleft Cyst (17 %) ( Branchial Cyst,)
Angiosarcoma (17 %)
Ecthyma Gangrenosum (17 %)
Papillary Eccrine Adenoma (17 %) ( Tubular Apocrine Adenoma,)
Hidradenoma (17 %)
Annular Elastolytic Giant Cell Granuloma (17 %) ( Giant Cell Elastophagocytosis, Meischers Granuloma, Mieschers Granuloma Of The Face,)
Leukonychia (17 %) ( White Nails,)
Fungal Mycetoma (17 %) ( Eumycetoma,)
Self-healing Juvenile Cutaneous Mucinosis (17 %)
Polymorphous Light Eruption (17 %) ( Polymorphic Light Eruption,)
Tripe Palms (17 %)
White Nails (17 %) ( Leukonychia,)
Urticaria-like Follicular Mucinosis (17 %)
Oral Lichen Planus (17 %)
Acral Lentiginous Melanoma (17 %)
Elephantiasis Nostras (17 %)
Cheilitis Granulomatosa (17 %) ( Granulomatous Cheilitis, Orofacial Granulomatosis,)
Histoid Leprosy (17 %)
Mycobacterium Kansasii Infection (17 %)
Eumycetoma (17 %) ( Fungal Mycetoma,)
Temporal Arteritis (17 %) ( Cranial Arteritis, Hortons Disease,)
Desmoplastic Fibroblastoma (17 %) ( Collagenous Fibroma,)
Thrombophlebitis (17 %)
Granuloma Annulare (17 %)
Herpangina (17 %)
Collagenous Fibroma (17 %) ( Desmoplastic Fibroblastoma,)
Rhinosporidiosis (17 %)
Hemochromatosis (17 %) ( Bronze Diabetes,)
Verruca Plana (17 %) ( Flat Warts,)
Telangiectasia (17 %)
Nail patella Syndrome (17 %) ( Fong Syndrome, Hereditary Osteoonychodysplasia, Hood Syndrome,)
Superficial Lymphatic Malformation (17 %) ( Lymphangioma Circumscriptum,)
Giant-cell Arteritis (17 %)
Spiradenoma (17 %)

Differentials from Google.

From Cache (Web service failed):
Cutaneous Leukocytoclastic Vasculitis
Hypersensitivity Angiitis
Hypersensitivity Vasculitis
Leukocytoclastic Vasculitis
Lupus Erythematosus
Systemic Lupus Erythematosus

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This is an experimental application for healthcare professionals. The information presented here is not intended to diagnose, treat, cure or prevent any disease. Read disclaimer.

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About Me

I have varied research interests ranging from eHealth, Health Information Exchange, Clinical Trials and Research, Contact Dermatitis, Bioinformatics, and Cosmetic Dermatology. I have work experience in Canada as an eHealth analyst, and in Dubai and India as a Specialist Dermatologist.

Address

Bell Raj Eapen
Hamilton, ON
Canada