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: 2017-12-15:

Lupus Erythematosus Panniculitis (53 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Erythema Induratum (50 %) ( Bazin Disease, Nodular Vasculitis,)
Cutaneous Small-vessel Vasculitis (50 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
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,)
Dermatitis Repens (47 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Acute Febrile Neutrophilic Dermatosis (47 %) ( Sweets Syndrome,)
Lupus Pernio (45 %)
Sweets Syndrome (45 %) ( Acute Febrile Neutrophilic Dermatosis,)
Leukocytoclastic Vasculitis (43 %)
Recurrent Palmoplantar Hidradenitis (43 %) ( Idiopathic Palmoplantar Hidradenitis, Idiopathic Plantar Hidradenitis, Painful Plantar Erythema, Palmoplantar Eccrine Hidradenitis, Plantar Panniculitis,)
Cutaneous Lymphoid Hyperplasia (41 %) ( 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,)
Erythema Nodosum (40 %)
Pyoderma Gangrenosum (40 %)
Cold Panniculitis (38 %) ( Popsicle Panniculitis,)
Wells Syndrome (38 %) ( Eosinophilic Cellulitis,)
Eosinophilic Cellulitis (38 %) ( Wells Syndrome,)
Popsicle Panniculitis (38 %) ( Cold Panniculitis,)
Recurrent Aphthous Stomatitis (38 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Pancreatic Panniculitis (38 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Cutis Laxa (38 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Septal Panniculitis (36 %)
Relapsing Polychondritis (36 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
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,)
Polyarteritis Nodosa (36 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Lipodermatosclerosis (36 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
North American Blastomycosis (36 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Interstitial Granulomatous Dermatitis (36 %)
Acne Keloidalis Nuchae (36 %) ( Acne Keloidalis, Dermatitis Papillaris Capillitii, Folliculitis Keloidalis, Folliculitis Keloidis Nuchae, Nuchal Keloid Acne,)
Livedoid Vasculopathy (36 %) ( Atrophie Blanche, Livedo Reticularis With Summer Ulceration, Livedoid Vasculitis, Purple Syndrome, Segmental Hyalinizing Vasculitis,)
Pustular (34 %)
Lymphomatoid Papulosis (34 %)
Amniotic Band Syndrome (34 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Leukemid (34 %) ( Nonspecific Cutaneous Conditions Associated With Leukemia,)
Subcutaneous Sarcoidosis (34 %) ( Darier roussy Disease, Darier roussy Sarcoid,)
Nonspecific Cutaneous Conditions Associated With Leukemia (34 %) ( Leukemid,)
Hidradenitis Suppurativa (34 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Allergic Granulomatosis (34 %) ( Churg strauss Syndrome,)
Churg strauss Syndrome (34 %) ( Allergic Granulomatosis,)
Dermatofibroma (34 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Lepromatous Leprosy (34 %)
Familial Mediterranean Fever (34 %)
Id Reaction (33 %) ( Disseminated Eczema, Generalized Eczema, Autoeczematization,)
Mycetoma (33 %) ( Madura Foot, Maduromycosis,)
Zoster (33 %) ( Herpes Zoster, Shingles,)
Pustular Psoriasis (33 %)
Tnf Receptor Associated Periodic Syndrome (33 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Dyshidrosis (33 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Pemphigus Herpetiformis (33 %) ( Acantholytic Herpetiform Dermatitis, Herpetiform Pemphigus, Mixed Bullous Disease, Pemphigus Controlled By Sulfapyridine,)
Clubbing (33 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Rheumatoid Neutrophilic Dermatitis (33 %) ( Rheumatoid Neutrophilic Dermatosis,)
Accelerated Rheumatoid Nodulosis (31 %) ( Rheumatoid Nodulosis,)
Cicatricial Pemphigoid (31 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Erythema Elevatum Diutinum (31 %)
Rheumatoid Nodulosis (31 %) ( Accelerated Rheumatoid Nodulosis,)
Acroosteolysis (31 %)
Subcutaneous Granuloma Annulare (31 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Histoplasmosis (31 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Acquired Hypogammaglobulinemia (31 %) ( Common Variable Immunodeficiency,)
Borderline Lepromatous Leprosy (31 %)
Acrodermatitis Chronica Atrophicans (31 %) ( Herxheimer Disease, Primary Diffuse Atrophy,)
Fissured Tongue (31 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Wegener Granulomatosis (31 %)
Eosinophilic Pustular Folliculitis (31 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Rheumatoid Neutrophilic Dermatosis (31 %) ( Rheumatoid Neutrophilic Dermatitis,)
Systemic Sarcoidosis (31 %)
Common Variable Immunodeficiency (31 %) ( Acquired Hypogammaglobulinemia,)
Generalized Pustular Psoriasis (29 %) ( Pustular Psoriasis Of Von Zumbusch,)
Plaque Psoriasis (29 %)
Sj grens Syndrome (29 %) ( Mikulicz Disease, Sicca Syndrome,)
Raynaud Phenomenon (29 %)
Nummular Dermatitis (29 %) ( Discoid Eczema, Microbial Eczema, Nummular Eczema, Nummular Neurodermatitis,)
Nail Psoriasis (29 %)
Pachydermoperiostosis (29 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Lichen Planopilaris (29 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Relapsing Febrile Non-suppurative Panniculitis (29 %) ( Weber christian Disease,)
Callus (29 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Urticarial Vasculitis (29 %) ( Chronic Urticaria AsA Manifestation Of Venulitis, Hypocomplementemic Urticarial Vasculitis Syndrome, Hypocomplementemic Vasculitis, Unusual Lupus-like Syndrome,)
Weber christian Disease (29 %) ( Relapsing Febrile Non-suppurative Panniculitis,)
Muckle wells Syndrome (29 %)
Heloderma (29 %) ( Knuckle Pads,)
Knuckle Pads (29 %) ( Heloderma,)
Scleroderma (29 %)
Primary Inoculation Tuberculosis (28 %) ( Cutaneous Primary Complex, Primary Tuberculous Complex, Tuberculous Chancre,)
Lichenoid Keratosis (28 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Kerion (28 %)
Eosinophilic Vasculitis (28 %)
Glomus Tumor (28 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Pustular Psoriasis Of Von Zumbusch (28 %) ( Generalized Pustular Psoriasis,)
Pityriasis Rubra Pilaris (28 %) ( Devergies Disease, Lichen Ruber Acuminatus, Lichen Ruber Pilaris,)
Lichen Planus (28 %)
L fgren Syndrome (28 %)
Majeed Syndrome (28 %)
Actinic Keratosis (28 %) ( Senile Keratosis, Solar Keratosis,)
Degos Disease (28 %) ( Malignant Atrophic Papulosis,)
Malignant Atrophic Papulosis (28 %) ( Degos Disease,)
Nevus Flammeus (28 %) ( Capillary Malformation, Port-wine Stain,)
Aquarium Granuloma (28 %) ( Fish Tank Granuloma, Swimming Pool Granuloma,)
Hyper-ige Syndrome (28 %) ( Buckley Syndrome, Job Syndrome,)
Ulcerative Lichen Planus (28 %)
Onycholysis (28 %)
Leukemia Cutis (28 %)
Juvenile Rheumatoid Arthritis (28 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Neutrophilic Lobular Panniculitis (28 %)
Familial Cold Autoinflammatory Syndrome (28 %) ( Familial Cold Urticaria,)
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,)
Familial Cold Urticaria (28 %) ( Familial Cold Autoinflammatory Syndrome,)
Glossodynia (26 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Chronic Granulomatous Disease (26 %) ( Bridges good Syndrome, Chronic Granulomatous Disorder, Quie Syndrome,)
Microscopic Polyangiitis (26 %) ( Microscopic Polyarteritis, Microscopic Polyarteritis Nodosa,)
Postinflammatory Hypermelanosis (26 %) ( Postinflammatory Hyperpigmentation,)
Tuberculosis Verrucosa Cutis (26 %) ( Lupus Verrucosus, Prosectors Wart, Warty Tuberculosis,)
Papulonecrotic Tuberculid (26 %)
Bowel-associated Dermatosis arthritis Syndrome (26 %) ( Bowel Bypass Syndrome, Bowel Bypass Syndrome Without Bowel Bypass, Intestinal Bypass Arthritis dermatitis Syndrome,)
Pyogenic Granuloma (26 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Lupus Erythematosus Tumidus (26 %) ( Tumid Lupus Erythematosus,)
Lichen Planus lupus Erythematosus Overlap Syndrome (26 %) ( Lupus Erythematosus lichen Planus Overlap Syndrome,)
Lupus Erythematosus lichen Planus Overlap Syndrome (26 %) ( Lichen Planus lupus Erythematosus Overlap Syndrome,)
Chickenpox (26 %) ( Varicella,)
SubcutaneousT-cell Lymphoma (26 %) ( Panniculitis-likeT-cell Lymphoma,)
Chromoblastomycosis (26 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Psoriasis Vulgaris (26 %) ( Chronic Stationary Psoriasis, Plaque-like Psoriasis,)
Tumid Lupus Erythematosus (26 %) ( Lupus Erythematosus Tumidus,)
Multicentric Reticulohistiocytosis (26 %)
Panniculitis-likeT-cell Lymphoma (26 %) ( SubcutaneousT-cell Lymphoma,)
Disseminated Coccidioidomycosis (26 %) ( Coccidioidal Granuloma,)
Pagetoid Reticulosis (26 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
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,)
HistiocytosisX (26 %) ( Langerhans Cell Histiocytosis,)
Langerhans Cell Histiocytosis (26 %) ( HistiocytosisX,)
Neutrophilic Eccrine Hidradenitis (26 %)
Dermographism (26 %) ( Dermatographism,)
Dermatographism (26 %) ( Dermographism,)
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,)
Anhidrosis (26 %) ( Hypohidrosis,)
Hypohidrosis (26 %) ( Anhidrosis,)
Amputation Neuroma (26 %) ( Traumatic Neuroma,)
Coccidioidal Granuloma (26 %) ( Disseminated Coccidioidomycosis,)
Varicella (26 %) ( Chickenpox,)
Traumatic Neuroma (26 %) ( Amputation Neuroma,)
Subcorneal Pustular Dermatosis (26 %) ( Sneddon wilkinson Disease,)
Necrobiosis Lipoidica Diabeticorum (26 %) ( Necrobiosis Lipoidica,)
Necrobiosis Lipoidica (26 %) ( Necrobiosis Lipoidica Diabeticorum,)
Sneddon wilkinson Disease (26 %) ( Subcorneal Pustular Dermatosis,)
Henoch Schonlein Purpura (26 %)
Postinflammatory Hyperpigmentation (26 %) ( Postinflammatory Hypermelanosis,)
Livedo Reticularis (24 %)
Steatocystoma Multiplex (24 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Reflex Sympathetic Dystrophy (24 %) ( Complex Regional Pain Syndrome,)
Complex Regional Pain Syndrome (24 %) ( Reflex Sympathetic Dystrophy,)
Acne Rosacea (24 %) ( Rosacea,)
Rosacea (24 %) ( Acne Rosacea,)
Verruca Vulgaris (24 %) ( Wart,)
Psoriasis (24 %)
Perforating Folliculitis (24 %)
Sarcoidosis (24 %)
Inverse Psoriasis (24 %)
Necrobiotic Xanthogranuloma (24 %) ( Necrobiotic Xanthogranuloma With Paraproteinemia,)
Acute Generalized Exanthematous Pustulosis (24 %) ( Pustular Drug Eruption, Toxic Pustuloderma,)
Psoriatic Arthritis (24 %)
Necrobiotic Xanthogranuloma With Paraproteinemia (24 %) ( Necrobiotic Xanthogranuloma,)
Hansens Disease (24 %) ( Leprosy,)
Acne Conglobata (24 %)
Histiocytic Necrotizing Lymphadenitis (24 %) ( Kikuchis Disease,)
Annular Elastolytic Giant Cell Granuloma (24 %) ( Giant Cell Elastophagocytosis, Meischers Granuloma, Mieschers Granuloma Of The Face,)
Wart (24 %) ( Verruca Vulgaris,)
Acrochordon (24 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Kikuchis Disease (24 %) ( Histiocytic Necrotizing Lymphadenitis,)
Takayasu Arteritis (24 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Leprosy (24 %) ( Hansens Disease,)
Giant Cell Tumor Of The Tendon Sheath (24 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Balanitis Plasmacellularis (24 %) ( Balanoposthitis Chronica Circumscripta Plasmacellularis, Balanitis Circumscripta Plasmacellularis, Plasma Cell Balanitis, Plasma Cell Vulvitis, Vulvitis Circumscripta Plasmacellularis, Zoons Balanitis, Zoons Erythroplasia, Zoons Vulvitis,)
Morphea (24 %)
Onychomadesis (22 %)
Pseudopelade Of Brocq (22 %) ( Alopecia Cicatrisata,)
Blau Syndrome (22 %)
Ehlers danlos Syndrome (22 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Sparganosis (22 %)
Piloleiomyoma (22 %)
Mixed Tumor (22 %) ( Chondroid Syringoma,)
Discoid Lupus Erythematosus (22 %)
Erosive Lichen Planus (22 %)
X-linked Agammaglobulinemia (22 %) ( Bruton Syndrome, Sex-linked Agammaglobulinemia,)
Blastomycosis-like Pyoderma (22 %) ( Pyoderma Vegetans,)
Sciatic Nerve Injury (22 %)
Molluscum Contagiosum (22 %)
Protothecosis (22 %)
Chondroid Syringoma (22 %) ( Mixed Tumor,)
Necrolytic Acral Erythema (22 %)
Hypertrophic Lupus Erythematosus (22 %) ( Verrucous Lupus Erythematosus,)
Alopecia Cicatrisata (22 %) ( Pseudopelade Of Brocq,)
Pemphigoid Gestationis (22 %) ( Gestational Pemphigoid, Herpes Gestationis,)
Olmsted Syndrome (22 %) ( Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Mutilating Palmoplantar Keratoderma With Periorificial Plaques, Polykeratosis Of Touraine,)
Lichenoid Dermatitis (22 %)
Dermatitis Herpetiformis (22 %) ( Duhring Disease,)
Acrocyanosis (22 %)
Yellow Nail Syndrome (22 %) ( Primary Lymphedema Associated With Yellow Nails And Pleural Effusion,)
Lupoid Rosacea (22 %) ( Granulomatous Rosacea, Micropapular Tuberculid, Rosacea-like Tuberculid Of Lewandowsky,)
Stasis Dermatitis (22 %) ( Congestion Eczema, Gravitational Dermatitis, Gravitational Eczema, Stasis Eczema, Varicose Eczema,)
Primary Lymphedema Associated With Yellow Nails And Pleural Effusion (22 %) ( Yellow Nail Syndrome,)
Duhring Disease (22 %) ( Dermatitis Herpetiformis,)
Tufted Angioma (22 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Phycomycosis (22 %) ( Zygomycosis,)
Alpha-1 Antitrypsin Deficiency Panniculitis (22 %) ( Alpha1-protease Deficiency Panniculitis, Alpha1-proteinase Deficiency Panniculitis,)
Zygomycosis (22 %) ( Phycomycosis,)
Cartilage hair Hypoplasia (22 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Mckusick Type Metaphyseal Chondrodysplasia (22 %) ( Cartilage hair Hypoplasia,)
Factitious Dermatitis (22 %) ( Dermatitis Artefacta, Factitial Dermatitis,)
Oral Lichen Planus (22 %)
Angiocentric Lymphoma (22 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Inflammatory Rosacea (22 %) ( Papulopustular Rosacea,)
Iga Pemphigus (22 %)
Keloid (22 %) ( Keloidal Scar,)
Tuberculosis Luposa (22 %) ( Lupus Vulgaris,)
Keloidal Scar (22 %) ( Keloid,)
Papular Mucinosis (22 %) ( Generalized Lichen Myxedematosus, Sclerodermoid Lichen Myxedematosus, Scleromyxedema,)
Psoriatic Erythroderma (22 %) ( Erythrodermic Psoriasis,)
Erythrodermic Psoriasis (22 %) ( Psoriatic Erythroderma,)
Lupus Vulgaris (22 %) ( Tuberculosis Luposa,)
Traumatic Panniculitis (22 %)
Perifolliculitis Capitis Abscedens Et Suffodiens (22 %) ( Dissecting Cellulitis Of The Scalp, Dissecting Folliculitis, Perifolliculitis Capitis Abscedens Et Suffodiens Of Hoffman,)
Beh ets Disease (22 %) ( Beh ets Syndrome, Oculo-oral-genital Syndrome,)
Nevus Of Ota (22 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Plasma Cell Cheilitis (22 %) ( Plasma Cell Gingivitis, Plasma Cell Orificial Mucositi,)
Papular Purpuric Gloves And Socks Syndrome (22 %)
Solar Purpura (22 %) ( Actinic Purpura, Senile Purpura,)
Epidermal Cyst (22 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Pyoderma Vegetans (22 %) ( Blastomycosis-like Pyoderma,)
Leiomyoma (22 %)
Rheumatoid Arthritis (22 %)
Verrucous Lupus Erythematosus (22 %) ( Hypertrophic Lupus Erythematosus,)
Papulopustular Rosacea (22 %) ( Inflammatory Rosacea,)
Erythema Annulare Centrifugum (22 %) ( Deep Gyrate Erythema, Erythema Perstans, Palpable Migrating Erythema, Superficial Gyrate Erythema,)
Angiolymphoid Hyperplasia With Eosinophilia (22 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Acral Fibrokeratoma (22 %) ( Acquired Digital Fibrokeratoma, Acquired Periungual Fibrokeratoma,)
Palmoplantar Keratoderma (22 %)

Differentials from Google.

Date Added: 2017-11-22

Chilblains
Discoid Lupus Erythematosus
Lupus Erythematosus
Pernio
Perniosis

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