Differentials: Chilblains

Differential diagnosis for Chilblains

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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 Chilblains.

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Date Added: 2017-09-14:

Lupus Erythematosus Panniculitis (54 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Cutaneous Small-vessel Vasculitis (51 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Erythema Induratum (49 %) ( Bazin Disease, Nodular Vasculitis,)
Palmoplantar Pustulosis (47 %) ( Persistent Palmoplantar Pustulosis, Pustular Psoriasis Of The Barber Type, Pustular Psoriasis Of The Extremities, Pustulosis Of Palms And Soles, Pustulosis Palmaris Et Plantaris,)
Acute Febrile Neutrophilic Dermatosis (47 %) ( Sweets Syndrome,)
Lupus Pernio (46 %)
Dermatitis Repens (46 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Sweets Syndrome (46 %) ( Acute Febrile Neutrophilic Dermatosis,)
Leukocytoclastic Vasculitis (44 %)
Cutaneous Lymphoid Hyperplasia (42 %) ( 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,)
Recurrent Palmoplantar Hidradenitis (42 %) ( Idiopathic Palmoplantar Hidradenitis, Idiopathic Plantar Hidradenitis, Painful Plantar Erythema, Palmoplantar Eccrine Hidradenitis, Plantar Panniculitis,)
Erythema Nodosum (40 %)
Pyoderma Gangrenosum (40 %)
Eosinophilic Cellulitis (39 %) ( Wells Syndrome,)
Recurrent Aphthous Stomatitis (39 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Pancreatic Panniculitis (39 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Cutis Laxa (39 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Wells Syndrome (39 %) ( Eosinophilic Cellulitis,)
Acne Keloidalis Nuchae (37 %) ( Acne Keloidalis, Dermatitis Papillaris Capillitii, Folliculitis Keloidalis, Folliculitis Keloidis Nuchae, Nuchal Keloid Acne,)
Polyarteritis Nodosa (37 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Lipodermatosclerosis (37 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
Interstitial Granulomatous Dermatitis (37 %)
Relapsing Polychondritis (37 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
North American Blastomycosis (37 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Pityriasis Lichenoides Et Varioliformis Acuta (37 %) ( Acute Guttate Parapsoriasis, Acute Parapsoriasis, Acute Pityriasis Lichenoides, Mucha habermann Disease, Parapsoriasis Acuta, Parapsoriasis Lichenoides Et Varioliformis Acuta, Parapsoriasis Varioliformis,)
Popsicle Panniculitis (37 %) ( Cold Panniculitis,)
Cold Panniculitis (37 %) ( Popsicle Panniculitis,)
Livedoid Vasculopathy (37 %) ( Atrophie Blanche, Livedo Reticularis With Summer Ulceration, Livedoid Vasculitis, Purple Syndrome, Segmental Hyalinizing Vasculitis,)
Septal Panniculitis (37 %)
Nonspecific Cutaneous Conditions Associated With Leukemia (35 %) ( Leukemid,)
Familial Mediterranean Fever (35 %)
Pustular (35 %)
Lepromatous Leprosy (35 %)
Dermatofibroma (35 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Subcutaneous Sarcoidosis (35 %) ( Darier roussy Disease, Darier roussy Sarcoid,)
Churg strauss Syndrome (35 %) ( Allergic Granulomatosis,)
Hidradenitis Suppurativa (35 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Lymphomatoid Papulosis (35 %)
Leukemid (35 %) ( Nonspecific Cutaneous Conditions Associated With Leukemia,)
Allergic Granulomatosis (35 %) ( Churg strauss Syndrome,)
Tnf Receptor Associated Periodic Syndrome (33 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Rheumatoid Neutrophilic Dermatitis (33 %) ( Rheumatoid Neutrophilic Dermatosis,)
Pemphigus Herpetiformis (33 %) ( Acantholytic Herpetiform Dermatitis, Herpetiform Pemphigus, Mixed Bullous Disease, Pemphigus Controlled By Sulfapyridine,)
Id Reaction (33 %) ( Disseminated Eczema, Generalized Eczema, Autoeczematization,)
Mycetoma (33 %) ( Madura Foot, Maduromycosis,)
Amniotic Band Syndrome (33 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Pustular Psoriasis (33 %)
Zoster (32 %) ( Herpes Zoster, Shingles,)
Borderline Lepromatous Leprosy (32 %)
Erythema Elevatum Diutinum (32 %)
Acrodermatitis Chronica Atrophicans (32 %) ( Herxheimer Disease, Primary Diffuse Atrophy,)
Systemic Sarcoidosis (32 %)
Rheumatoid Nodulosis (32 %) ( Accelerated Rheumatoid Nodulosis,)
Accelerated Rheumatoid Nodulosis (32 %) ( Rheumatoid Nodulosis,)
Subcutaneous Granuloma Annulare (32 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Rheumatoid Neutrophilic Dermatosis (32 %) ( Rheumatoid Neutrophilic Dermatitis,)
Dyshidrosis (32 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Common Variable Immunodeficiency (32 %) ( Acquired Hypogammaglobulinemia,)
Histoplasmosis (32 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Cicatricial Pemphigoid (32 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Eosinophilic Pustular Folliculitis (32 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Wegener Granulomatosis (32 %)
Clubbing (32 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Acquired Hypogammaglobulinemia (32 %) ( Common Variable Immunodeficiency,)
Fissured Tongue (32 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Raynaud Phenomenon (30 %)
Plaque Psoriasis (30 %)
Relapsing Febrile Non-suppurative Panniculitis (30 %) ( Weber christian Disease,)
Weber christian Disease (30 %) ( Relapsing Febrile Non-suppurative Panniculitis,)
Callus (30 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Scleroderma (30 %)
Muckle wells Syndrome (30 %)
Sj grens Syndrome (30 %) ( Mikulicz Disease, Sicca Syndrome,)
Nummular Dermatitis (30 %) ( Discoid Eczema, Microbial Eczema, Nummular Eczema, Nummular Neurodermatitis,)
Urticarial Vasculitis (30 %) ( Chronic Urticaria AsA Manifestation Of Venulitis, Hypocomplementemic Urticarial Vasculitis Syndrome, Hypocomplementemic Vasculitis, Unusual Lupus-like Syndrome,)
Acroosteolysis (30 %)
Generalized Pustular Psoriasis (30 %) ( Pustular Psoriasis Of Von Zumbusch,)
Nail Psoriasis (30 %)
Lichen Planopilaris (30 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Lichen Planus (28 %)
Malignant Atrophic Papulosis (28 %) ( Degos Disease,)
Eosinophilic Vasculitis (28 %)
Hyper-ige Syndrome (28 %) ( Buckley Syndrome, Job Syndrome,)
Pustular Psoriasis Of Von Zumbusch (28 %) ( Generalized Pustular Psoriasis,)
Aquarium Granuloma (28 %) ( Fish Tank Granuloma, Swimming Pool Granuloma,)
Pachydermoperiostosis (28 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Lichenoid Keratosis (28 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
L fgren Syndrome (28 %)
Degos Disease (28 %) ( Malignant Atrophic Papulosis,)
Majeed Syndrome (28 %)
Heloderma (28 %) ( Knuckle Pads,)
Knuckle Pads (28 %) ( Heloderma,)
Actinic Keratosis (28 %) ( Senile Keratosis, Solar Keratosis,)
Nevus Flammeus (28 %) ( Capillary Malformation, Port-wine Stain,)
Kerion (28 %)
Pityriasis Rubra Pilaris (28 %) ( Devergies Disease, Lichen Ruber Acuminatus, Lichen Ruber Pilaris,)
Primary Inoculation Tuberculosis (28 %) ( Cutaneous Primary Complex, Primary Tuberculous Complex, Tuberculous Chancre,)
Glomus Tumor (28 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Ulcerative Lichen Planus (28 %)
Leukemia Cutis (28 %)
Neutrophilic Lobular Panniculitis (28 %)
Familial Cold Urticaria (28 %) ( Familial Cold Autoinflammatory Syndrome,)
Geographic Tongue (28 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Juvenile Rheumatoid Arthritis (28 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Familial Cold Autoinflammatory Syndrome (28 %) ( Familial Cold Urticaria,)
Traumatic Neuroma (26 %) ( Amputation Neuroma,)
Neutrophilic Eccrine Hidradenitis (26 %)
Amputation Neuroma (26 %) ( Traumatic Neuroma,)
Coccidioidal Granuloma (26 %) ( Disseminated Coccidioidomycosis,)
Langerhans Cell Histiocytosis (26 %) ( HistiocytosisX,)
Tuberculosis Verrucosa Cutis (26 %) ( Lupus Verrucosus, Prosectors Wart, Warty Tuberculosis,)
Chronic Granulomatous Disease (26 %) ( Bridges good Syndrome, Chronic Granulomatous Disorder, Quie Syndrome,)
HistiocytosisX (26 %) ( Langerhans Cell Histiocytosis,)
Atrophodermia Vermiculata (26 %) ( 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,)
Pagetoid Reticulosis (26 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Lichen Planus Actinicus (26 %) ( Actinic Lichen Niditus, Actinic Lichen Planus, Lichen Planus Atrophicus Annularis, Lichen Planus Subtropicus, Lichen Planus Tropicus, Lichenoid Melanodermatitis, Lichenoid Melanodermatosis, Summertime Actinic Lichenoid Eruption,)
Disseminated Coccidioidomycosis (26 %) ( Coccidioidal Granuloma,)
SubcutaneousT-cell Lymphoma (26 %) ( Panniculitis-likeT-cell Lymphoma,)
Postinflammatory Hypermelanosis (26 %) ( Postinflammatory Hyperpigmentation,)
Lupus Erythematosus Tumidus (26 %) ( Tumid Lupus Erythematosus,)
Tumid Lupus Erythematosus (26 %) ( Lupus Erythematosus Tumidus,)
Postinflammatory Hyperpigmentation (26 %) ( Postinflammatory Hypermelanosis,)
Chromoblastomycosis (26 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Dermatographism (26 %) ( Dermographism,)
Dermographism (26 %) ( Dermatographism,)
Multicentric Reticulohistiocytosis (26 %)
Papulonecrotic Tuberculid (26 %)
Chickenpox (26 %) ( Varicella,)
Hypohidrosis (26 %) ( Anhidrosis,)
Varicella (26 %) ( Chickenpox,)
Necrobiosis Lipoidica (26 %) ( Necrobiosis Lipoidica Diabeticorum,)
Anhidrosis (26 %) ( Hypohidrosis,)
Pyogenic Granuloma (26 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Panniculitis-likeT-cell Lymphoma (26 %) ( SubcutaneousT-cell Lymphoma,)
Microscopic Polyangiitis (26 %) ( Microscopic Polyarteritis, Microscopic Polyarteritis Nodosa,)
Onycholysis (26 %)
Bowel-associated Dermatosis arthritis Syndrome (26 %) ( Bowel Bypass Syndrome, Bowel Bypass Syndrome Without Bowel Bypass, Intestinal Bypass Arthritis dermatitis Syndrome,)
Necrobiosis Lipoidica Diabeticorum (26 %) ( Necrobiosis Lipoidica,)
Subcorneal Pustular Dermatosis (26 %) ( Sneddon wilkinson Disease,)
Sneddon wilkinson Disease (26 %) ( Subcorneal Pustular Dermatosis,)
Psoriasis Vulgaris (26 %) ( Chronic Stationary Psoriasis, Plaque-like Psoriasis,)
Glossodynia (26 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Henoch Schonlein Purpura (26 %)
Acne Conglobata (25 %)
Kikuchis Disease (25 %) ( Histiocytic Necrotizing Lymphadenitis,)
Sarcoidosis (25 %)
Histiocytic Necrotizing Lymphadenitis (25 %) ( Kikuchis Disease,)
Steatocystoma Multiplex (25 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Necrobiotic Xanthogranuloma (25 %) ( Necrobiotic Xanthogranuloma With Paraproteinemia,)
Acrochordon (25 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Rosacea (25 %) ( Acne Rosacea,)
Necrobiotic Xanthogranuloma With Paraproteinemia (25 %) ( Necrobiotic Xanthogranuloma,)
Balanitis Plasmacellularis (25 %) ( Balanoposthitis Chronica Circumscripta Plasmacellularis, Balanitis Circumscripta Plasmacellularis, Plasma Cell Balanitis, Plasma Cell Vulvitis, Vulvitis Circumscripta Plasmacellularis, Zoons Balanitis, Zoons Erythroplasia, Zoons Vulvitis,)
Wart (25 %) ( Verruca Vulgaris,)
Hansens Disease (25 %) ( Leprosy,)
Inverse Psoriasis (25 %)
Lupus Erythematosus lichen Planus Overlap Syndrome (25 %) ( Lichen Planus lupus Erythematosus Overlap Syndrome,)
Lichen Planus lupus Erythematosus Overlap Syndrome (25 %) ( Lupus Erythematosus lichen Planus Overlap Syndrome,)
Psoriatic Arthritis (25 %)
Acute Generalized Exanthematous Pustulosis (25 %) ( Pustular Drug Eruption, Toxic Pustuloderma,)
Takayasu Arteritis (25 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Morphea (25 %)
Acne Rosacea (25 %) ( Rosacea,)
Livedo Reticularis (25 %)
Perforating Folliculitis (25 %)
Leprosy (25 %) ( Hansens Disease,)
Verruca Vulgaris (25 %) ( Wart,)
Annular Elastolytic Giant Cell Granuloma (25 %) ( Giant Cell Elastophagocytosis, Meischers Granuloma, Mieschers Granuloma Of The Face,)
Psoriasis (25 %)
Pseudopelade Of Brocq (23 %) ( Alopecia Cicatrisata,)
Blau Syndrome (23 %)
Molluscum Contagiosum (23 %)
Stasis Dermatitis (23 %) ( Congestion Eczema, Gravitational Dermatitis, Gravitational Eczema, Stasis Eczema, Varicose Eczema,)
Erythrodermic Psoriasis (23 %) ( Psoriatic Erythroderma,)
Psoriatic Erythroderma (23 %) ( Erythrodermic Psoriasis,)
Pyoderma Vegetans (23 %) ( Blastomycosis-like Pyoderma,)
Sciatic Nerve Injury (23 %)
Reflex Sympathetic Dystrophy (23 %) ( Complex Regional Pain Syndrome,)
Protothecosis (23 %)
Blastomycosis-like Pyoderma (23 %) ( Pyoderma Vegetans,)
Sparganosis (23 %)
Alopecia Cicatrisata (23 %) ( Pseudopelade Of Brocq,)
Perifolliculitis Capitis Abscedens Et Suffodiens (23 %) ( Dissecting Cellulitis Of The Scalp, Dissecting Folliculitis, Perifolliculitis Capitis Abscedens Et Suffodiens Of Hoffman,)
Solar Purpura (23 %) ( Actinic Purpura, Senile Purpura,)
Inflammatory Rosacea (23 %) ( Papulopustular Rosacea,)
Zygomycosis (23 %) ( Phycomycosis,)
Lichenoid Dermatitis (23 %)
Iga Pemphigus (23 %)
Complex Regional Pain Syndrome (23 %) ( Reflex Sympathetic Dystrophy,)
Plasma Cell Cheilitis (23 %) ( Plasma Cell Gingivitis, Plasma Cell Orificial Mucositi,)
Keloidal Scar (23 %) ( Keloid,)
Beh ets Disease (23 %) ( Beh ets Syndrome, Oculo-oral-genital Syndrome,)
Tuberculosis Luposa (23 %) ( Lupus Vulgaris,)
Dermatitis Herpetiformis (23 %) ( Duhring Disease,)
Keloid (23 %) ( Keloidal Scar,)
Duhring Disease (23 %) ( Dermatitis Herpetiformis,)
Erosive Lichen Planus (23 %)
Cartilage hair Hypoplasia (23 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Necrolytic Acral Erythema (23 %)
Oral Lichen Planus (23 %)
Alpha-1 Antitrypsin Deficiency Panniculitis (23 %) ( Alpha1-protease Deficiency Panniculitis, Alpha1-proteinase Deficiency Panniculitis,)
Lupus Vulgaris (23 %) ( Tuberculosis Luposa,)
Mckusick Type Metaphyseal Chondrodysplasia (23 %) ( Cartilage hair Hypoplasia,)
X-linked Agammaglobulinemia (23 %) ( Bruton Syndrome, Sex-linked Agammaglobulinemia,)
Phycomycosis (23 %) ( Zygomycosis,)
Hypertrophic Lupus Erythematosus (23 %) ( Verrucous Lupus Erythematosus,)
Lupoid Rosacea (23 %) ( Granulomatous Rosacea, Micropapular Tuberculid, Rosacea-like Tuberculid Of Lewandowsky,)
Discoid Lupus Erythematosus (23 %)
Angiocentric Lymphoma (23 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Piloleiomyoma (23 %)
Papulopustular Rosacea (23 %) ( Inflammatory Rosacea,)
Mixed Tumor (23 %) ( Chondroid Syringoma,)
Erythema Annulare Centrifugum (23 %) ( Deep Gyrate Erythema, Erythema Perstans, Palpable Migrating Erythema, Superficial Gyrate Erythema,)
Angiolymphoid Hyperplasia With Eosinophilia (23 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Papular Mucinosis (23 %) ( Generalized Lichen Myxedematosus, Sclerodermoid Lichen Myxedematosus, Scleromyxedema,)
Acrocyanosis (23 %)
Acral Fibrokeratoma (23 %) ( Acquired Digital Fibrokeratoma, Acquired Periungual Fibrokeratoma,)
Leiomyoma (23 %)
Factitious Dermatitis (23 %) ( Dermatitis Artefacta, Factitial Dermatitis,)
Giant Cell Tumor Of The Tendon Sheath (23 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Nevus Of Ota (23 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Rheumatoid Arthritis (23 %)
Pemphigoid Gestationis (23 %) ( Gestational Pemphigoid, Herpes Gestationis,)
Palmoplantar Keratoderma (23 %)
Verrucous Lupus Erythematosus (23 %) ( Hypertrophic Lupus Erythematosus,)
Chondroid Syringoma (23 %) ( Mixed Tumor,)
Papular Purpuric Gloves And Socks Syndrome (23 %)
Traumatic Panniculitis (23 %)

Differentials from Google.

Date Added: 2017-08-14

Chilblains
Discoid Lupus Erythematosus
Lupus Erythematosus
Pernio
Perniosis
Trench Foot

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