Differentials: Cutaneous Leukocytoclastic Vasculitis

Differential diagnosis for Cutaneous Leukocytoclastic Vasculitis

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Date Added: 2017-09-18:

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

Differentials from Google.

Date Added: 2017-09-01

Cutaneous Leukocytoclastic Vasculitis
Hepatitis C
Hypersensitivity Vasculitis
Leukocytoclastic Vasculitis

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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