Differentials: erythema induratum

Differential diagnosis for erythema induratum

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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 erythema induratum.

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Date Added: 2017-12-25:

Cutaneous Small-vessel Vasculitis (50 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Lupus Erythematosus Panniculitis (45 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Chilblains (44 %) ( Pernio, Perniosis,)
Polyarteritis Nodosa (44 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Acute Febrile Neutrophilic Dermatosis (41 %) ( Sweets Syndrome,)
Erythema Nodosum (41 %)
Lipodermatosclerosis (38 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
Sweets Syndrome (38 %) ( Acute Febrile Neutrophilic Dermatosis,)
Leukocytoclastic Vasculitis (38 %)
Pancreatic Panniculitis (36 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Panniculitis-likeT-cell Lymphoma (36 %) ( SubcutaneousT-cell Lymphoma,)
Angiocentric Lymphoma (36 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Epidermal Cyst (36 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
SubcutaneousT-cell Lymphoma (36 %) ( Panniculitis-likeT-cell Lymphoma,)
Mycetoma (35 %) ( Madura Foot, Maduromycosis,)
Lymphomatoid Papulosis (35 %)
Cutaneous Lymphoid Hyperplasia (35 %) ( 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,)
Leukemia Cutis (35 %)
North American Blastomycosis (35 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Eosinophilic Cellulitis (33 %) ( Wells Syndrome,)
Subcutaneous Granuloma Annulare (33 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Dermatofibroma (33 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Wells Syndrome (33 %) ( Eosinophilic Cellulitis,)
Pyoderma Gangrenosum (33 %)
Recurrent Aphthous Stomatitis (33 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Pityriasis Lichenoides Et Varioliformis Acuta (33 %) ( Acute Guttate Parapsoriasis, Acute Parapsoriasis, Acute Pityriasis Lichenoides, Mucha habermann Disease, Parapsoriasis Acuta, Parapsoriasis Lichenoides Et Varioliformis Acuta, Parapsoriasis Varioliformis,)
Eosinophilic Pustular Folliculitis (33 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Lupus Pernio (32 %)
Septal Panniculitis (32 %)
Allergic Granulomatosis (32 %) ( Churg strauss Syndrome,)
Clubbing (32 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Wegener Granulomatosis (32 %)
Subcutaneous Sarcoidosis (32 %) ( Darier roussy Disease, Darier roussy Sarcoid,)
Hidradenitis Suppurativa (32 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Palmoplantar Pustulosis (32 %) ( Persistent Palmoplantar Pustulosis, Pustular Psoriasis Of The Barber Type, Pustular Psoriasis Of The Extremities, Pustulosis Of Palms And Soles, Pustulosis Palmaris Et Plantaris,)
Relapsing Polychondritis (32 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Dyshidrosis (32 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Hyper-ige Syndrome (32 %) ( Buckley Syndrome, Job Syndrome,)
Churg strauss Syndrome (32 %) ( Allergic Granulomatosis,)
Langerhans Cell Histiocytosis (32 %) ( HistiocytosisX,)
HistiocytosisX (32 %) ( Langerhans Cell Histiocytosis,)
Systemic Sarcoidosis (30 %)
Cutis Laxa (30 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Histoplasmosis (30 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Tnf Receptor Associated Periodic Syndrome (30 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Angiolymphoid Hyperplasia With Eosinophilia (30 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Duhring Disease (30 %) ( Dermatitis Herpetiformis,)
Dermatitis Herpetiformis (30 %) ( Duhring Disease,)
Urticarial Vasculitis (30 %) ( Chronic Urticaria AsA Manifestation Of Venulitis, Hypocomplementemic Urticarial Vasculitis Syndrome, Hypocomplementemic Vasculitis, Unusual Lupus-like Syndrome,)
Marginal ZoneB-cell Lymphoma (30 %)
Weber christian Disease (30 %) ( Relapsing Febrile Non-suppurative Panniculitis,)
Rheumatoid Neutrophilic Dermatitis (30 %) ( Rheumatoid Neutrophilic Dermatosis,)
Relapsing Febrile Non-suppurative Panniculitis (30 %) ( Weber christian Disease,)
Familial Cold Autoinflammatory Syndrome (29 %) ( Familial Cold Urticaria,)
Familial Cold Urticaria (29 %) ( Familial Cold Autoinflammatory Syndrome,)
Rheumatoid Neutrophilic Dermatosis (29 %) ( Rheumatoid Neutrophilic Dermatitis,)
Miliary Tuberculosis (29 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Recurrent Palmoplantar Hidradenitis (29 %) ( Idiopathic Palmoplantar Hidradenitis, Idiopathic Plantar Hidradenitis, Painful Plantar Erythema, Palmoplantar Eccrine Hidradenitis, Plantar Panniculitis,)
Callus (29 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Papulonecrotic Tuberculid (29 %)
Acute Necrotizing Ulcerative Gingivitis (29 %) ( 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,)
Sj grens Syndrome (27 %) ( Mikulicz Disease, Sicca Syndrome,)
Cold Panniculitis (27 %) ( Popsicle Panniculitis,)
Nonspecific Cutaneous Conditions Associated With Leukemia (27 %) ( Leukemid,)
Juvenile Rheumatoid Arthritis (27 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Cicatricial Pemphigoid (27 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Zoster (27 %) ( Herpes Zoster, Shingles,)
Giant Cell Tumor Of The Tendon Sheath (27 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Leukemid (27 %) ( Nonspecific Cutaneous Conditions Associated With Leukemia,)
Acrodermatitis Chronica Atrophicans (27 %) ( Herxheimer Disease, Primary Diffuse Atrophy,)
Pemphigus Herpetiformis (27 %) ( Acantholytic Herpetiform Dermatitis, Herpetiform Pemphigus, Mixed Bullous Disease, Pemphigus Controlled By Sulfapyridine,)
Rosai dorfman Disease (27 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Livedoid Vasculopathy (27 %) ( Atrophie Blanche, Livedo Reticularis With Summer Ulceration, Livedoid Vasculitis, Purple Syndrome, Segmental Hyalinizing Vasculitis,)
Generalized Pustular Psoriasis (27 %) ( Pustular Psoriasis Of Von Zumbusch,)
Popsicle Panniculitis (27 %) ( Cold Panniculitis,)
Acquired Hypogammaglobulinemia (27 %) ( Common Variable Immunodeficiency,)
Tuberculous Gumma (27 %) ( Metastatic Tuberculous Abscess, Metastatic Tuberculous Ulcer,)
L fgren Syndrome (27 %)
Common Variable Immunodeficiency (27 %) ( Acquired Hypogammaglobulinemia,)
Erythema Elevatum Diutinum (27 %)
Sinus Histiocytosis With Massive Lymphadenopathy (27 %) ( Rosai dorfman Disease,)
Familial Mediterranean Fever (27 %)
Tuberculosis Cutis Colliquativa (26 %) ( Scrofuloderma,)
Chromoblastomycosis (26 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Necrobiotic Xanthogranuloma (26 %) ( Necrobiotic Xanthogranuloma With Paraproteinemia,)
Id Reaction (26 %) ( Disseminated Eczema, Generalized Eczema, Autoeczematization,)
Pustular Psoriasis Of Von Zumbusch (26 %) ( Generalized Pustular Psoriasis,)
Scrofuloderma (26 %) ( Tuberculosis Cutis Colliquativa,)
Sarcoidosis (26 %)
Neutrophilic Lobular Panniculitis (26 %)
Glomus Tumor (26 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Necrobiotic Xanthogranuloma With Paraproteinemia (26 %) ( Necrobiotic Xanthogranuloma,)
Amniotic Band Syndrome (26 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Lichenoid Keratosis (26 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Muckle wells Syndrome (26 %)
Bowel-associated Dermatosis arthritis Syndrome (26 %) ( Bowel Bypass Syndrome, Bowel Bypass Syndrome Without Bowel Bypass, Intestinal Bypass Arthritis dermatitis Syndrome,)
Mycobacterium Kansasii Infection (26 %)
Majeed Syndrome (26 %)
Cytophagic Histiocytic Panniculitis (26 %)
Dermatitis Repens (26 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Pustular (26 %)
Varicella (24 %) ( Chickenpox,)
Intravascular LargeB-cell Lymphoma (24 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Lichen Planus Verrucosus (24 %) ( Hypertrophic Lichen Planus,)
Primary Cutaneous Anaplastic Large Cell Lymphoma (24 %) ( Cd30+ CutaneousT-cell Lymphoma,)
Chickenpox (24 %) ( Varicella,)
Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome (24 %) ( Sapho Syndrome,)
Traumatic Neuroma (24 %) ( Amputation Neuroma,)
Amputation Neuroma (24 %) ( Traumatic Neuroma,)
Eosinophilic Fasciitis (24 %) ( Shulmans Syndrome,)
Interstitial Granulomatous Dermatitis (24 %)
Metastatic Carcinoma (24 %)
Necrotizing Fasciitis (24 %) ( Flesh-eating Bacteria Syndrome,)
Kimura Disease (24 %)
Coccidioidal Granuloma (24 %) ( Disseminated Coccidioidomycosis,)
Ehlers danlos Syndrome (24 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Tuberculosis Verrucosa Cutis (24 %) ( Lupus Verrucosus, Prosectors Wart, Warty Tuberculosis,)
South American Blastomycosis (24 %) ( Brazilian Blastomycosis, Paracoccidioidal Granuloma, Paracoccidioidomycosis,)
Zygomycosis (24 %) ( Phycomycosis,)
Flesh-eating Bacteria Syndrome (24 %) ( Necrotizing Fasciitis,)
Aquarium Granuloma (24 %) ( Fish Tank Granuloma, Swimming Pool Granuloma,)
Disseminated Coccidioidomycosis (24 %) ( Coccidioidal Granuloma,)
Acrochordon (24 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Henoch Schonlein Purpura (24 %)
Shulmans Syndrome (24 %) ( Eosinophilic Fasciitis,)
Pustular Psoriasis (24 %)
Granulocytic Sarcoma (24 %) ( Chloroma, Myeloid Sarcoma,)
Factitial Panniculitis (24 %)
Alpha-1 Antitrypsin Deficiency Panniculitis (24 %) ( Alpha1-protease Deficiency Panniculitis, Alpha1-proteinase Deficiency Panniculitis,)
Geographic Tongue (24 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Sapho Syndrome (24 %) ( Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome,)
Hypertrophic Lichen Planus (24 %) ( Lichen Planus Verrucosus,)
Cd30+ CutaneousT-cell Lymphoma (24 %) ( Primary Cutaneous Anaplastic Large Cell Lymphoma,)
Pagetoid Reticulosis (24 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Phycomycosis (24 %) ( Zygomycosis,)
Mucosa-associated Lymphoid Tissue Lymphoma (23 %)
Plasma Cell Cheilitis (23 %) ( Plasma Cell Gingivitis, Plasma Cell Orificial Mucositi,)
Eosinophilic Vasculitis (23 %)
Eumycetoma (23 %) ( Fungal Mycetoma,)
Actinic Keratosis (23 %) ( Senile Keratosis, Solar Keratosis,)
Lichenoid Dermatitis (23 %)
Heloderma (23 %) ( Knuckle Pads,)
Knuckle Pads (23 %) ( Heloderma,)
Plaque-type Porokeratosis (23 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Tufted Angioma (23 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Coccidioidomycosis (23 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Pilomatricoma (23 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Foreign Body Reaction (23 %)
Fungal Mycetoma (23 %) ( Eumycetoma,)
Sneddon wilkinson Disease (23 %) ( Subcorneal Pustular Dermatosis,)
Fox fordyce Disease (23 %)
Scleroderma (23 %)
Infectious Mononucleosis (23 %) ( Glandular Fever,)
Eosinophilic Granuloma (23 %)
Subcorneal Pustular Dermatosis (23 %) ( Sneddon wilkinson Disease,)
Microscopic Polyangiitis (23 %) ( Microscopic Polyarteritis, Microscopic Polyarteritis Nodosa,)
Traumatic Panniculitis (23 %)
Schwannoma (23 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Malignant Acrospiroma (23 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Superficial Granulomatous Pyoderma (23 %)
Glandular Fever (23 %) ( Infectious Mononucleosis,)
Multicentric Reticulohistiocytosis (23 %)
Acne Necrotica (23 %)
Klippel trenaunay Syndrome (23 %) ( Angioosteohypertrophy Syndrome, Hemangiectatic Hypertrophy,)
Pachydermoperiostosis (23 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Lepromatous Leprosy (23 %)
Fissured Tongue (21 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Carney Complex (21 %) ( Lamb Syndrome, Name Syndrome,)
Rheumatoid Arthritis (21 %)
Hypertrophic Lupus Erythematosus (21 %) ( Verrucous Lupus Erythematosus,)
PleomorphicT-cell Lymphoma (21 %) ( Non-mycosis Fungoides Cd30- Pleomorphic Small/medium Sized CutaneousT-cell Lymphoma,)
Reflex Sympathetic Dystrophy (21 %) ( Complex Regional Pain Syndrome,)
Diffuse LargeB-cell Lymphoma (21 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Pyogenic Granuloma (21 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Malignant Chondroid Syringoma (21 %) ( Malignant Mixed Tumor,)
Complex Regional Pain Syndrome (21 %) ( Reflex Sympathetic Dystrophy,)
Epithelioma Cuniculatum (21 %) ( Ackerman Tumor, Carcinoma Cuniculatum,)
Lipoma (21 %)
Malignant Mixed Tumor (21 %) ( Malignant Chondroid Syringoma,)
Lichen Sclerosus (21 %) ( Lichen Sclerosus Et Atrophicus,)
Non-mycosis Fungoides Cd30- Pleomorphic Small/medium Sized CutaneousT-cell Lymphoma (21 %) ( PleomorphicT-cell Lymphoma,)
Acne Fulminans (21 %) ( Acute Febrile Ulcerative Acne,)
Follicular Mucinosis (21 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Lymphangioma (21 %) ( Lymphangiectasis,)
Verrucous Lupus Erythematosus (21 %) ( Hypertrophic Lupus Erythematosus,)
Primary Cutaneous Follicular Lymphoma (21 %) ( Follicular Center Cell Lymphoma, Follicular Center Lymphoma,)
Lymphangiectasis (21 %) ( Lymphangioma,)
Primary Cutaneous LargeB-cell Lymphoma (21 %) ( Diffuse LargeB-cell Lymphoma,)
Lichen Sclerosus Et Atrophicus (21 %) ( Lichen Sclerosus,)
Cat Scratch Disease (21 %) ( Cat Scratch Fever, English wear Infection, Inoculation Lymphoreticulosis, Subacute Regional Lymphadenitis,)
Generalized Eruptive Histiocytoma (21 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Botryomycosis (21 %)
Acrospiroma (21 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Malignant Pilomatricoma (21 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Schnitzler Syndrome (21 %)
Borderline Lepromatous Leprosy (21 %)
Gas Gangrene (21 %) ( Clostridial Myonecrosis, Myonecrosis,)
Hypoparathyroidism (21 %)
Alopecia Neoplastica (21 %)
Acute Febrile Ulcerative Acne (21 %) ( Acne Fulminans,)
Tripe Palms (21 %)
Olmsted Syndrome (21 %) ( Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Mutilating Palmoplantar Keratoderma With Periorificial Plaques, Polykeratosis Of Touraine,)
Histiocytic Necrotizing Lymphadenitis (21 %) ( Kikuchis Disease,)
Toxic Shock Syndrome (21 %) ( Streptococcal Toxic Shock Syndrome, Streptococcal Toxic Shock-like Syndrome, Toxic Streptococcal Syndrome,)
Solar Purpura (21 %) ( Actinic Purpura, Senile Purpura,)
Acne Conglobata (21 %)
Malignant Fibrous Histiocytoma (21 %)
Kikuchis Disease (21 %) ( Histiocytic Necrotizing Lymphadenitis,)
Gouty Panniculitis (21 %)
Accelerated Rheumatoid Nodulosis (21 %) ( Rheumatoid Nodulosis,)
Leiomyosarcoma (21 %)
Rheumatoid Nodulosis (21 %) ( Accelerated Rheumatoid Nodulosis,)
Kerion (20 %)
Adiposis Dolorosa (20 %) ( Dercums Disease,)
Silicone Granuloma (20 %)
Acne Keloidalis Nuchae (20 %) ( Acne Keloidalis, Dermatitis Papillaris Capillitii, Folliculitis Keloidalis, Folliculitis Keloidis Nuchae, Nuchal Keloid Acne,)
Giant Pigmented Nevus (20 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Verrucous Carcinoma (20 %)
Onycholysis (20 %)
Cartilage hair Hypoplasia (20 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Blastomycosis-like Pyoderma (20 %) ( Pyoderma Vegetans,)
Pityriasis Rosea (20 %) ( Pityriasis Rosea Gibert,)
Nevus Of Ota (20 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Dercums Disease (20 %) ( Adiposis Dolorosa,)
Phaeohyphomycosis (20 %)
Blau Syndrome (20 %)
Lupus Erythematosus lichen Planus Overlap Syndrome (20 %) ( Lichen Planus lupus Erythematosus Overlap Syndrome,)
Clear Cell Acanthoma (20 %) ( Acanthome Cellules Claires Of Degos And Civatte, Degos Acanthoma, Pale Cell Acanthoma,)
Giant-cell Arteritis (20 %)
Molluscum Contagiosum (20 %)
Temporal Arteritis (20 %) ( Cranial Arteritis, Hortons Disease,)
Thrombophlebitis (20 %)
Takayasu Arteritis (20 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Cryoglobulinemic Vasculitis (20 %)
Morphea (20 %)
Mckusick Type Metaphyseal Chondrodysplasia (20 %) ( Cartilage hair Hypoplasia,)
Soft-tissue Melanoma (20 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Nevus Spilus (20 %) ( Speckled Lentiginous Nevus, Zosteriform Lentiginous Nevus,)
Lichen Planus lupus Erythematosus Overlap Syndrome (20 %) ( Lupus Erythematosus lichen Planus Overlap Syndrome,)
Neutrophilic Eccrine Hidradenitis (20 %)
Nocardiosis (20 %)
Fox-fordyce Disease (20 %)
Subungual Exostosis (20 %)
Ainhum (20 %) ( Bankokerend, Dactylolysis Spontanea, Sukhapakla,)
Lichen Scrofulosorum (20 %) ( Tuberculosis Cutis Lichenoides,)
Steatocystoma Multiplex (20 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Pyoderma Vegetans (20 %) ( Blastomycosis-like Pyoderma,)
Pityriasis Rosea Gibert (20 %) ( Pityriasis Rosea,)
Sclerotic Fibroma (20 %)
Stevens johnson Syndrome (20 %)
Liposarcoma (20 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Chondroid Syringoma (20 %) ( Mixed Tumor,)
Tuberculosis Cutis Lichenoides (20 %) ( Lichen Scrofulosorum,)
Papular Mucinosis (20 %) ( Generalized Lichen Myxedematosus, Sclerodermoid Lichen Myxedematosus, Scleromyxedema,)
Mixed Tumor (20 %) ( Chondroid Syringoma,)

Differentials from Google.

Date Added: 2018-01-11


Erythema Induratum
Erythema Nodosum
Id Reaction
Nodular Vasculitis
Periarteritis Nodosa
Pernio
Perniosis
Polyarteritis Nodosa
Sarcoidosis
Thrombophlebitis

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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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