Differentials: Cutaneous Leukocytoclastic Vasculitis

Differential diagnosis for Cutaneous Leukocytoclastic Vasculitis

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Date Added: 2017-06-19:

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

Differentials from Google.

Date Added: 2017-05-15

Cutaneous Leukocytoclastic Vasculitis
Hypersensitivity Angiitis
Hypersensitivity Vasculitis
Leukocytoclastic Vasculitis

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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.

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Bell Raj Eapen
Hamilton, ON
Canada