Differentials: leukocytoclastic vasculitis

Differential diagnosis for leukocytoclastic vasculitis

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

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Date Added: 2017-05-27:

Lupus Erythematosus Panniculitis (71 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Cutaneous Small-vessel Vasculitis (71 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Acute Febrile Neutrophilic Dermatosis (65 %) ( Sweets Syndrome,)
Sweets Syndrome (60 %) ( Acute Febrile Neutrophilic Dermatosis,)
Pityriasis Lichenoides Et Varioliformis Acuta (54 %) ( Acute Guttate Parapsoriasis, Acute Parapsoriasis, Acute Pityriasis Lichenoides, Mucha habermann Disease, Parapsoriasis Acuta, Parapsoriasis Lichenoides Et Varioliformis Acuta, Parapsoriasis Varioliformis,)
Pancreatic Panniculitis (52 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Erythema Induratum (52 %) ( Bazin Disease, Nodular Vasculitis,)
Chilblains (52 %) ( Pernio, Perniosis,)
Erythema Elevatum Diutinum (50 %)
Lipodermatosclerosis (48 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
Wells Syndrome (44 %) ( Eosinophilic Cellulitis,)
Eosinophilic Cellulitis (44 %) ( Wells Syndrome,)
Erythema Nodosum (42 %)
Leukemia Cutis (42 %)
Aquarium Granuloma (42 %) ( Fish Tank Granuloma, Swimming Pool Granuloma,)
Familial Mediterranean Fever (42 %)
Eosinophilic Pustular Folliculitis (42 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Livedoid Vasculopathy (42 %) ( Atrophie Blanche, Livedo Reticularis With Summer Ulceration, Livedoid Vasculitis, Purple Syndrome, Segmental Hyalinizing Vasculitis,)
Henoch Schonlein Purpura (42 %)
Pustular (42 %)
Scleroderma (42 %)
Bowel-associated Dermatosis arthritis Syndrome (42 %) ( Bowel Bypass Syndrome, Bowel Bypass Syndrome Without Bowel Bypass, Intestinal Bypass Arthritis dermatitis Syndrome,)
Recurrent Aphthous Stomatitis (42 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Wegener Granulomatosis (40 %)
Sneddon wilkinson Disease (40 %) ( Subcorneal Pustular Dermatosis,)
Cutaneous Lymphoid Hyperplasia (40 %) ( 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,)
Systemic Sarcoidosis (40 %)
Palmoplantar Pustulosis (40 %) ( Persistent Palmoplantar Pustulosis, Pustular Psoriasis Of The Barber Type, Pustular Psoriasis Of The Extremities, Pustulosis Of Palms And Soles, Pustulosis Palmaris Et Plantaris,)
Rosacea (40 %) ( Acne Rosacea,)
Polyarteritis Nodosa (40 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Acne Rosacea (40 %) ( Rosacea,)
Pyoderma Gangrenosum (40 %)
Subcorneal Pustular Dermatosis (40 %) ( Sneddon wilkinson Disease,)
Dermatofibroma (38 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Morphea (38 %)
Geographic Tongue (38 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Kikuchis Disease (38 %) ( Histiocytic Necrotizing Lymphadenitis,)
Borderline Lepromatous Leprosy (38 %)
Histoplasmosis (38 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Neutrophilic Eccrine Hidradenitis (38 %)
Histiocytic Necrotizing Lymphadenitis (38 %) ( Kikuchis Disease,)
Subcutaneous Sarcoidosis (35 %) ( Darier roussy Disease, Darier roussy Sarcoid,)
Septal Panniculitis (35 %)
Necrobiosis Lipoidica Diabeticorum (35 %) ( Necrobiosis Lipoidica,)
Leukemid (35 %) ( Nonspecific Cutaneous Conditions Associated With Leukemia,)
Recurrent Palmoplantar Hidradenitis (35 %) ( Idiopathic Palmoplantar Hidradenitis, Idiopathic Plantar Hidradenitis, Painful Plantar Erythema, Palmoplantar Eccrine Hidradenitis, Plantar Panniculitis,)
Pustular Psoriasis (35 %)
Allergic Granulomatosis (35 %) ( Churg strauss Syndrome,)
Generalized Pustular Psoriasis (35 %) ( Pustular Psoriasis Of Von Zumbusch,)
Necrobiosis Lipoidica (35 %) ( Necrobiosis Lipoidica Diabeticorum,)
Stasis Dermatitis (35 %) ( Congestion Eczema, Gravitational Dermatitis, Gravitational Eczema, Stasis Eczema, Varicose Eczema,)
Lymphomatoid Papulosis (35 %)
Nonspecific Cutaneous Conditions Associated With Leukemia (35 %) ( Leukemid,)
Churg strauss Syndrome (35 %) ( Allergic Granulomatosis,)
Rheumatoid Neutrophilic Dermatitis (35 %) ( Rheumatoid Neutrophilic Dermatosis,)
Tufted Angioma (35 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Microscopic Polyangiitis (35 %) ( Microscopic Polyarteritis, Microscopic Polyarteritis Nodosa,)
Lichen Planopilaris (35 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Urticarial Vasculitis (35 %) ( Chronic Urticaria AsA Manifestation Of Venulitis, Hypocomplementemic Urticarial Vasculitis Syndrome, Hypocomplementemic Vasculitis, Unusual Lupus-like Syndrome,)
Epidermal Cyst (35 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Pityriasis Rosea Gibert (33 %) ( Pityriasis Rosea,)
Rheumatoid Neutrophilic Dermatosis (33 %) ( Rheumatoid Neutrophilic Dermatitis,)
SubcutaneousT-cell Lymphoma (33 %) ( Panniculitis-likeT-cell Lymphoma,)
Panniculitis-likeT-cell Lymphoma (33 %) ( SubcutaneousT-cell Lymphoma,)
Interstitial Granulomatous Dermatitis (33 %)
Acute Necrotizing Ulcerative Gingivitis (33 %) ( 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,)
Lupus Pernio (33 %)
Familial Cold Urticaria (33 %) ( Familial Cold Autoinflammatory Syndrome,)
Pityriasis Rosea (33 %) ( Pityriasis Rosea Gibert,)
Iga Pemphigus (33 %)
Amniotic Band Syndrome (33 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Familial Cold Autoinflammatory Syndrome (33 %) ( Familial Cold Urticaria,)
Tnf Receptor Associated Periodic Syndrome (33 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Pemphigus Herpetiformis (33 %) ( Acantholytic Herpetiform Dermatitis, Herpetiform Pemphigus, Mixed Bullous Disease, Pemphigus Controlled By Sulfapyridine,)
Hidradenitis Suppurativa (33 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Lepromatous Leprosy (33 %)
Dermatitis Repens (33 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Takayasu Arteritis (33 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Chromoblastomycosis (33 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Acquired Ichthyosis (31 %) ( Ichthyosis Acquisita,)
Hyper-ige Syndrome (31 %) ( Buckley Syndrome, Job Syndrome,)
Cicatricial Pemphigoid (31 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Ichthyosis Acquisita (31 %) ( Acquired Ichthyosis,)
Flesh-eating Bacteria Syndrome (31 %) ( Necrotizing Fasciitis,)
Sparganosis (31 %)
Papular Purpuric Gloves And Socks Syndrome (31 %)
Relapsing Polychondritis (31 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Necrotizing Fasciitis (31 %) ( Flesh-eating Bacteria Syndrome,)
Klippel trenaunay Syndrome (31 %) ( Angioosteohypertrophy Syndrome, Hemangiectatic Hypertrophy,)
Erythema Annulare Centrifugum (31 %) ( Deep Gyrate Erythema, Erythema Perstans, Palpable Migrating Erythema, Superficial Gyrate Erythema,)
Acrodermatitis Chronica Atrophicans (31 %) ( Herxheimer Disease, Primary Diffuse Atrophy,)
Pyoderma Faciale (31 %) ( Rosacea Fulminans,)
Juvenile Rheumatoid Arthritis (31 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Pustular Psoriasis Of Von Zumbusch (31 %) ( Generalized Pustular Psoriasis,)
Kerion (31 %)
Rosacea Fulminans (31 %) ( Pyoderma Faciale,)
Ecthyma Gangrenosum (31 %)
Zoster (29 %) ( Herpes Zoster, Shingles,)
Mycetoma (29 %) ( Madura Foot, Maduromycosis,)
Blastomycosis-like Pyoderma (29 %) ( Pyoderma Vegetans,)
Id Reaction (29 %) ( Disseminated Eczema, Generalized Eczema, Autoeczematization,)
Pyoderma Vegetans (29 %) ( Blastomycosis-like Pyoderma,)
Dyshidrosis (29 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Pseudopelade Of Brocq (29 %) ( Alopecia Cicatrisata,)
Rheumatoid Vasculitis (29 %)
Heloderma (29 %) ( Knuckle Pads,)
Pruritic Urticarial Papules And Plaques Of Pregnancy (29 %) ( Late-onset Prurigo Of Pregnancy, Polymorphic Eruption Of Pregnancy, Puppp Syndrome, Toxemic Rash Of Pregnancy, Toxic Erythema Of Pregnancy,)
Factitious Dermatitis (29 %) ( Dermatitis Artefacta, Factitial Dermatitis,)
Blau Syndrome (29 %)
Knuckle Pads (29 %) ( Heloderma,)
Weber christian Disease (29 %) ( Relapsing Febrile Non-suppurative Panniculitis,)
Lupus Erythematosus lichen Planus Overlap Syndrome (29 %) ( Lichen Planus lupus Erythematosus Overlap Syndrome,)
Lichen Planus lupus Erythematosus Overlap Syndrome (29 %) ( Lupus Erythematosus lichen Planus Overlap Syndrome,)
Perifolliculitis Capitis Abscedens Et Suffodiens (29 %) ( Dissecting Cellulitis Of The Scalp, Dissecting Folliculitis, Perifolliculitis Capitis Abscedens Et Suffodiens Of Hoffman,)
Palmoplantar Keratoderma (29 %)
Relapsing Febrile Non-suppurative Panniculitis (29 %) ( Weber christian Disease,)
Plaque Psoriasis (29 %)
Dermatomyositis (29 %)
Psoriatic Arthritis (29 %)
Madarosis (29 %)
Necrobiotic Xanthogranuloma With Paraproteinemia (29 %) ( Necrobiotic Xanthogranuloma,)
Reflex Sympathetic Dystrophy (29 %) ( Complex Regional Pain Syndrome,)
Complex Regional Pain Syndrome (29 %) ( Reflex Sympathetic Dystrophy,)
Alopecia Cicatrisata (29 %) ( Pseudopelade Of Brocq,)
Stevens johnson Syndrome (29 %)
Chickenpox (29 %) ( Varicella,)
Varicella (29 %) ( Chickenpox,)
Tuberculosis Luposa (29 %) ( Lupus Vulgaris,)
Lupus Vulgaris (29 %) ( Tuberculosis Luposa,)
Necrobiotic Xanthogranuloma (29 %) ( Necrobiotic Xanthogranuloma With Paraproteinemia,)
Papulonecrotic Tuberculid (29 %)
Muckle wells Syndrome (29 %)
Acne Keloidalis Nuchae (29 %) ( Acne Keloidalis, Dermatitis Papillaris Capillitii, Folliculitis Keloidalis, Folliculitis Keloidis Nuchae, Nuchal Keloid Acne,)
Henoch sch nlein Purpura (29 %) ( Anaphylactoid Purpura, Purpura Rheumatica,)
Gianotti crosti Syndrome (29 %) ( Infantile Papular Acrodermatitis, Papular Acrodermatitis Of Childhood, Papulovesicular Acrolocated Syndrome,)
Acne Necrotica (29 %)
Solar Purpura (29 %) ( Actinic Purpura, Senile Purpura,)
Acroangiodermatitis (27 %) ( Acroangiodermatitis Of Mali, Mali Acroangiodermatitis, Pseudo-kaposis Sarcoma, Pseudo-kaposi Sarcoma,)
Nail Psoriasis (27 %)
Erythema Chronicum Migrans (27 %) ( Erythema Migrans,)
Pretibial Myxedema (27 %)
Oral Lichen Planus (27 %)
Livedo Racemosa (27 %)
Immune Reconstitution Inflammatory Syndrome (27 %) ( Immune Recovery Syndrome,)
Immune Recovery Syndrome (27 %) ( Immune Reconstitution Inflammatory Syndrome,)
Pyostomatitis Vegetans (27 %)
Alopecia Neoplastica (27 %)
Eosinophilic Fasciitis (27 %) ( Shulmans Syndrome,)
Malignant Atrophic Papulosis (27 %) ( Degos Disease,)
Erythema Migrans (27 %) ( Erythema Chronicum Migrans,)
Pemphigoid Gestationis (27 %) ( Gestational Pemphigoid, Herpes Gestationis,)
Erosive Lichen Planus (27 %)
Shulmans Syndrome (27 %) ( Eosinophilic Fasciitis,)
Lichenoid Keratosis (27 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Steatocystoma Multiplex (27 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
North American Blastomycosis (27 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Follicular Mucinosis (27 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Mucosa-associated Lymphoid Tissue Lymphoma (27 %)
Callus (27 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Dermographism (27 %) ( Dermatographism,)
Dermatographism (27 %) ( Dermographism,)
Papulopustular Rosacea (27 %) ( Inflammatory Rosacea,)
Degos Disease (27 %) ( Malignant Atrophic Papulosis,)
Popsicle Panniculitis (27 %) ( Cold Panniculitis,)
Mycobacterium Haemophilum Infection (27 %)
Aphthous Stomatitis (27 %)
Inflammatory Rosacea (27 %) ( Papulopustular Rosacea,)
Cold Panniculitis (27 %) ( Popsicle Panniculitis,)
Primary Inoculation Tuberculosis (27 %) ( Cutaneous Primary Complex, Primary Tuberculous Complex, Tuberculous Chancre,)

Differentials from Google.

Date Added: 2017-07-14

Cutaneous Leukocytoclastic Vasculitis

Hypersensitivity Angiitis
Hypersensitivity Vasculitis
Leukocytoclastic Vasculitis
Urticarial Vasculitis

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