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: 2017-09-25:

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,)
Polyarteritis Nodosa (44 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Chilblains (42 %) ( Pernio, Perniosis,)
Acute Febrile Neutrophilic Dermatosis (41 %) ( Sweets Syndrome,)
Erythema Nodosum (41 %)
Lipodermatosclerosis (38 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
Leukocytoclastic Vasculitis (38 %)
Sweets Syndrome (38 %) ( Acute Febrile Neutrophilic Dermatosis,)
Pancreatic Panniculitis (36 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
SubcutaneousT-cell Lymphoma (36 %) ( Panniculitis-likeT-cell Lymphoma,)
Epidermal Cyst (36 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
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,)
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 %)
Lymphomatoid Papulosis (35 %)
North American Blastomycosis (35 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Mycetoma (35 %) ( Madura Foot, Maduromycosis,)
Eosinophilic Pustular Folliculitis (33 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Wells Syndrome (33 %) ( Eosinophilic Cellulitis,)
Pyoderma Gangrenosum (33 %)
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,)
Subcutaneous Granuloma Annulare (33 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Recurrent Aphthous Stomatitis (33 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Dermatofibroma (33 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Eosinophilic Cellulitis (33 %) ( Wells Syndrome,)
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,)
Hidradenitis Suppurativa (32 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Septal Panniculitis (32 %)
Lupus Pernio (32 %)
Wegener Granulomatosis (32 %)
Relapsing Polychondritis (32 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Hyper-ige Syndrome (32 %) ( Buckley Syndrome, Job Syndrome,)
Clubbing (32 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
HistiocytosisX (32 %) ( Langerhans Cell Histiocytosis,)
Churg strauss Syndrome (32 %) ( Allergic Granulomatosis,)
Allergic Granulomatosis (32 %) ( Churg strauss Syndrome,)
Subcutaneous Sarcoidosis (32 %) ( Darier roussy Disease, Darier roussy Sarcoid,)
Langerhans Cell Histiocytosis (32 %) ( HistiocytosisX,)
Weber christian Disease (30 %) ( Relapsing Febrile Non-suppurative Panniculitis,)
Relapsing Febrile Non-suppurative Panniculitis (30 %) ( Weber christian Disease,)
Systemic Sarcoidosis (30 %)
Cutis Laxa (30 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Urticarial Vasculitis (30 %) ( Chronic Urticaria AsA Manifestation Of Venulitis, Hypocomplementemic Urticarial Vasculitis Syndrome, Hypocomplementemic Vasculitis, Unusual Lupus-like Syndrome,)
Marginal ZoneB-cell Lymphoma (30 %)
Rheumatoid Neutrophilic Dermatitis (30 %) ( Rheumatoid Neutrophilic Dermatosis,)
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,)
Duhring Disease (30 %) ( Dermatitis Herpetiformis,)
Dermatitis Herpetiformis (30 %) ( Duhring Disease,)
Angiolymphoid Hyperplasia With Eosinophilia (30 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Dyshidrosis (30 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Rheumatoid Neutrophilic Dermatosis (29 %) ( Rheumatoid Neutrophilic Dermatitis,)
Familial Cold Autoinflammatory Syndrome (29 %) ( Familial Cold Urticaria,)
Papulonecrotic Tuberculid (29 %)
Callus (29 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Familial Cold Urticaria (29 %) ( Familial Cold Autoinflammatory Syndrome,)
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,)
Miliary Tuberculosis (29 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Sj grens Syndrome (27 %) ( Mikulicz Disease, Sicca Syndrome,)
Pemphigus Herpetiformis (27 %) ( Acantholytic Herpetiform Dermatitis, Herpetiform Pemphigus, Mixed Bullous Disease, Pemphigus Controlled By Sulfapyridine,)
Giant Cell Tumor Of The Tendon Sheath (27 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Livedoid Vasculopathy (27 %) ( Atrophie Blanche, Livedo Reticularis With Summer Ulceration, Livedoid Vasculitis, Purple Syndrome, Segmental Hyalinizing Vasculitis,)
Acrodermatitis Chronica Atrophicans (27 %) ( Herxheimer Disease, Primary Diffuse Atrophy,)
Juvenile Rheumatoid Arthritis (27 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Recurrent Palmoplantar Hidradenitis (27 %) ( Idiopathic Palmoplantar Hidradenitis, Idiopathic Plantar Hidradenitis, Painful Plantar Erythema, Palmoplantar Eccrine Hidradenitis, Plantar Panniculitis,)
Tuberculous Gumma (27 %) ( Metastatic Tuberculous Abscess, Metastatic Tuberculous Ulcer,)
Cold Panniculitis (27 %) ( Popsicle Panniculitis,)
Acquired Hypogammaglobulinemia (27 %) ( Common Variable Immunodeficiency,)
Sinus Histiocytosis With Massive Lymphadenopathy (27 %) ( Rosai dorfman Disease,)
Rosai dorfman Disease (27 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Popsicle Panniculitis (27 %) ( Cold Panniculitis,)
Cicatricial Pemphigoid (27 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Common Variable Immunodeficiency (27 %) ( Acquired Hypogammaglobulinemia,)
Familial Mediterranean Fever (27 %)
Leukemid (27 %) ( Nonspecific Cutaneous Conditions Associated With Leukemia,)
Nonspecific Cutaneous Conditions Associated With Leukemia (27 %) ( Leukemid,)
L fgren Syndrome (27 %)
Generalized Pustular Psoriasis (27 %) ( Pustular Psoriasis Of Von Zumbusch,)
Erythema Elevatum Diutinum (27 %)
Sarcoidosis (26 %)
Cytophagic Histiocytic Panniculitis (26 %)
Amniotic Band Syndrome (26 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Bowel-associated Dermatosis arthritis Syndrome (26 %) ( Bowel Bypass Syndrome, Bowel Bypass Syndrome Without Bowel Bypass, Intestinal Bypass Arthritis dermatitis Syndrome,)
Id Reaction (26 %) ( Disseminated Eczema, Generalized Eczema, Autoeczematization,)
Neutrophilic Lobular Panniculitis (26 %)
Necrobiotic Xanthogranuloma (26 %) ( Necrobiotic Xanthogranuloma With Paraproteinemia,)
Necrobiotic Xanthogranuloma With Paraproteinemia (26 %) ( Necrobiotic Xanthogranuloma,)
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,)
Muckle wells Syndrome (26 %)
Scrofuloderma (26 %) ( Tuberculosis Cutis Colliquativa,)
Zoster (26 %) ( Herpes Zoster, Shingles,)
Majeed Syndrome (26 %)
Lichenoid Keratosis (26 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Chromoblastomycosis (26 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Tuberculosis Cutis Colliquativa (26 %) ( Scrofuloderma,)
Pustular Psoriasis Of Von Zumbusch (26 %) ( Generalized Pustular Psoriasis,)
Mycobacterium Kansasii Infection (26 %)
Glomus Tumor (26 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Pustular (26 %)
Chickenpox (24 %) ( Varicella,)
Granulocytic Sarcoma (24 %) ( Chloroma, Myeloid Sarcoma,)
Pustular Psoriasis (24 %)
Amputation Neuroma (24 %) ( Traumatic Neuroma,)
Flesh-eating Bacteria Syndrome (24 %) ( Necrotizing Fasciitis,)
Henoch Schonlein Purpura (24 %)
Necrotizing Fasciitis (24 %) ( Flesh-eating Bacteria Syndrome,)
Varicella (24 %) ( Chickenpox,)
Lichen Planus Verrucosus (24 %) ( Hypertrophic Lichen Planus,)
Interstitial Granulomatous Dermatitis (24 %)
Traumatic Neuroma (24 %) ( Amputation Neuroma,)
Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome (24 %) ( Sapho Syndrome,)
Acrochordon (24 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
South American Blastomycosis (24 %) ( Brazilian Blastomycosis, Paracoccidioidal Granuloma, Paracoccidioidomycosis,)
Ehlers danlos Syndrome (24 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Shulmans Syndrome (24 %) ( Eosinophilic Fasciitis,)
Cd30+ CutaneousT-cell Lymphoma (24 %) ( Primary Cutaneous Anaplastic Large Cell Lymphoma,)
Eosinophilic Fasciitis (24 %) ( Shulmans Syndrome,)
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,)
Hypertrophic Lichen Planus (24 %) ( Lichen Planus Verrucosus,)
Kimura Disease (24 %)
Sapho Syndrome (24 %) ( Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome,)
Aquarium Granuloma (24 %) ( Fish Tank Granuloma, Swimming Pool Granuloma,)
Metastatic Carcinoma (24 %)
Intravascular LargeB-cell Lymphoma (24 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Coccidioidal Granuloma (24 %) ( Disseminated Coccidioidomycosis,)
Primary Cutaneous Anaplastic Large Cell Lymphoma (24 %) ( Cd30+ CutaneousT-cell Lymphoma,)
Disseminated Coccidioidomycosis (24 %) ( Coccidioidal Granuloma,)
Phycomycosis (24 %) ( Zygomycosis,)
Factitial Panniculitis (24 %)
Pagetoid Reticulosis (24 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Zygomycosis (24 %) ( Phycomycosis,)
Tuberculosis Verrucosa Cutis (24 %) ( Lupus Verrucosus, Prosectors Wart, Warty Tuberculosis,)
Alpha-1 Antitrypsin Deficiency Panniculitis (24 %) ( Alpha1-protease Deficiency Panniculitis, Alpha1-proteinase Deficiency Panniculitis,)
Pachydermoperiostosis (23 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Coccidioidomycosis (23 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Microscopic Polyangiitis (23 %) ( Microscopic Polyarteritis, Microscopic Polyarteritis Nodosa,)
Pilomatricoma (23 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Glandular Fever (23 %) ( Infectious Mononucleosis,)
Lichenoid Dermatitis (23 %)
Plaque-type Porokeratosis (23 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Superficial Granulomatous Pyoderma (23 %)
Klippel trenaunay Syndrome (23 %) ( Angioosteohypertrophy Syndrome, Hemangiectatic Hypertrophy,)
Eumycetoma (23 %) ( Fungal Mycetoma,)
Malignant Acrospiroma (23 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Foreign Body Reaction (23 %)
Fox fordyce Disease (23 %)
Mucosa-associated Lymphoid Tissue Lymphoma (23 %)
Multicentric Reticulohistiocytosis (23 %)
Fungal Mycetoma (23 %) ( Eumycetoma,)
Infectious Mononucleosis (23 %) ( Glandular Fever,)
Eosinophilic Vasculitis (23 %)
Lepromatous Leprosy (23 %)
Eosinophilic Granuloma (23 %)
Knuckle Pads (23 %) ( Heloderma,)
Heloderma (23 %) ( Knuckle Pads,)
Scleroderma (23 %)
Tufted Angioma (23 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Subcorneal Pustular Dermatosis (23 %) ( Sneddon wilkinson Disease,)
Sneddon wilkinson Disease (23 %) ( Subcorneal Pustular Dermatosis,)
Actinic Keratosis (23 %) ( Senile Keratosis, Solar Keratosis,)
Acne Necrotica (23 %)
Traumatic Panniculitis (23 %)
Plasma Cell Cheilitis (23 %) ( Plasma Cell Gingivitis, Plasma Cell Orificial Mucositi,)
Schwannoma (23 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Generalized Eruptive Histiocytoma (21 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Rheumatoid Arthritis (21 %)
Gas Gangrene (21 %) ( Clostridial Myonecrosis, Myonecrosis,)
Follicular Mucinosis (21 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Malignant Mixed Tumor (21 %) ( Malignant Chondroid Syringoma,)
Acrospiroma (21 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Pyogenic Granuloma (21 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Primary Cutaneous Follicular Lymphoma (21 %) ( Follicular Center Cell Lymphoma, Follicular Center Lymphoma,)
Gouty Panniculitis (21 %)
Fissured Tongue (21 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Leiomyosarcoma (21 %)
Carney Complex (21 %) ( Lamb Syndrome, Name Syndrome,)
Lichen Sclerosus (21 %) ( Lichen Sclerosus Et Atrophicus,)
Lichen Sclerosus Et Atrophicus (21 %) ( Lichen Sclerosus,)
Primary Cutaneous LargeB-cell Lymphoma (21 %) ( Diffuse LargeB-cell Lymphoma,)
Accelerated Rheumatoid Nodulosis (21 %) ( Rheumatoid Nodulosis,)
Malignant Chondroid Syringoma (21 %) ( Malignant Mixed Tumor,)
Lipoma (21 %)
Cat Scratch Disease (21 %) ( Cat Scratch Fever, English wear Infection, Inoculation Lymphoreticulosis, Subacute Regional Lymphadenitis,)
Tripe Palms (21 %)
Lymphangioma (21 %) ( Lymphangiectasis,)
Verrucous Lupus Erythematosus (21 %) ( Hypertrophic Lupus Erythematosus,)
Complex Regional Pain Syndrome (21 %) ( Reflex Sympathetic Dystrophy,)
Reflex Sympathetic Dystrophy (21 %) ( Complex Regional Pain Syndrome,)
Epithelioma Cuniculatum (21 %) ( Ackerman Tumor, Carcinoma Cuniculatum,)
Hypertrophic Lupus Erythematosus (21 %) ( Verrucous Lupus Erythematosus,)
Lymphangiectasis (21 %) ( Lymphangioma,)
Rheumatoid Nodulosis (21 %) ( Accelerated Rheumatoid Nodulosis,)
Non-mycosis Fungoides Cd30- Pleomorphic Small/medium Sized CutaneousT-cell Lymphoma (21 %) ( PleomorphicT-cell Lymphoma,)
Diffuse LargeB-cell Lymphoma (21 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
PleomorphicT-cell Lymphoma (21 %) ( Non-mycosis Fungoides Cd30- Pleomorphic Small/medium Sized CutaneousT-cell Lymphoma,)
Malignant Pilomatricoma (21 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Malignant Fibrous Histiocytoma (21 %)
Toxic Shock Syndrome (21 %) ( Streptococcal Toxic Shock Syndrome, Streptococcal Toxic Shock-like Syndrome, Toxic Streptococcal Syndrome,)
Schnitzler Syndrome (21 %)
Acne Fulminans (21 %) ( Acute Febrile Ulcerative Acne,)
Solar Purpura (21 %) ( Actinic Purpura, Senile Purpura,)
Hypoparathyroidism (21 %)
Acute Febrile Ulcerative Acne (21 %) ( Acne Fulminans,)
Histiocytic Necrotizing Lymphadenitis (21 %) ( Kikuchis Disease,)
Kikuchis Disease (21 %) ( Histiocytic Necrotizing Lymphadenitis,)
Acne Conglobata (21 %)
Alopecia Neoplastica (21 %)
Borderline Lepromatous Leprosy (21 %)
Botryomycosis (21 %)
Subungual Exostosis (20 %)
Lichen Planus lupus Erythematosus Overlap Syndrome (20 %) ( Lupus Erythematosus lichen Planus Overlap Syndrome,)
Olmsted Syndrome (20 %) ( Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Mutilating Palmoplantar Keratoderma With Periorificial Plaques, Polykeratosis Of Touraine,)
Neutrophilic Eccrine Hidradenitis (20 %)
Cartilage hair Hypoplasia (20 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Verrucous Carcinoma (20 %)
Lupus Erythematosus lichen Planus Overlap Syndrome (20 %) ( Lichen Planus lupus Erythematosus Overlap Syndrome,)
Pityriasis Rosea (20 %) ( Pityriasis Rosea Gibert,)
Mckusick Type Metaphyseal Chondrodysplasia (20 %) ( Cartilage hair Hypoplasia,)
Steatocystoma Multiplex (20 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Tuberculosis Cutis Lichenoides (20 %) ( Lichen Scrofulosorum,)
Stevens johnson Syndrome (20 %)
Lichen Scrofulosorum (20 %) ( Tuberculosis Cutis Lichenoides,)
Clear Cell Acanthoma (20 %) ( Acanthome Cellules Claires Of Degos And Civatte, Degos Acanthoma, Pale Cell Acanthoma,)
Silicone Granuloma (20 %)
Liposarcoma (20 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Morphea (20 %)
Pyoderma Vegetans (20 %) ( Blastomycosis-like Pyoderma,)
Nocardiosis (20 %)
Kerion (20 %)
Blau Syndrome (20 %)
Acne Keloidalis Nuchae (20 %) ( Acne Keloidalis, Dermatitis Papillaris Capillitii, Folliculitis Keloidalis, Folliculitis Keloidis Nuchae, Nuchal Keloid Acne,)
Nevus Of Ota (20 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Mixed Tumor (20 %) ( Chondroid Syringoma,)
Giant Pigmented Nevus (20 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Pityriasis Rosea Gibert (20 %) ( Pityriasis Rosea,)
Fox-fordyce Disease (20 %)
Nevus Spilus (20 %) ( Speckled Lentiginous Nevus, Zosteriform Lentiginous Nevus,)
Molluscum Contagiosum (20 %)
Ainhum (20 %) ( Bankokerend, Dactylolysis Spontanea, Sukhapakla,)
Chondroid Syringoma (20 %) ( Mixed Tumor,)
Giant-cell Arteritis (20 %)
Adiposis Dolorosa (20 %) ( Dercums Disease,)
Takayasu Arteritis (20 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Phaeohyphomycosis (20 %)
Blastomycosis-like Pyoderma (20 %) ( Pyoderma Vegetans,)
Dercums Disease (20 %) ( Adiposis Dolorosa,)
Thrombophlebitis (20 %)
Papular Mucinosis (20 %) ( Generalized Lichen Myxedematosus, Sclerodermoid Lichen Myxedematosus, Scleromyxedema,)
Soft-tissue Melanoma (20 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Temporal Arteritis (20 %) ( Cranial Arteritis, Hortons Disease,)

Differentials from Google.

Date Added: 2017-10-09

Acute Urticaria

Erysipelas
Erythema Induratum
Erythema Nodosum
Nodular Vasculitis

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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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