Differentials: Pyogenic Granuloma

Differential diagnosis for Pyogenic Granuloma

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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 Pyogenic Granuloma.

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Date Added: 2017-05-24:

Schwannoma (57 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Epidermal Cyst (55 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Fissured Tongue (55 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Wart (53 %) ( Verruca Vulgaris,)
Verruca Vulgaris (53 %) ( Wart,)
Traumatic Neuroma (47 %) ( Amputation Neuroma,)
Dermatofibroma (47 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Amputation Neuroma (47 %) ( Traumatic Neuroma,)
Neurothekeoma (45 %) ( Bizarre Cutaneous Neurofibroma, Cutaneous Lobular Neuromyxoma, Myxoma Of The Nerve Sheath, Myxomatous Perineurioma, Nerve Sheath Myxoma,)
Glomus Tumor (45 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Angiolymphoid Hyperplasia With Eosinophilia (45 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Lipoma (43 %)
Mixed Tumor (43 %) ( Chondroid Syringoma,)
Liposarcoma (43 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Hidrocystoma (43 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Dermoid Cyst (43 %)
Acrospiroma (43 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Chondroid Syringoma (43 %) ( Mixed Tumor,)
Giant Pigmented Nevus (41 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Nevus Of Ota (41 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Epithelioma Cuniculatum (41 %) ( Ackerman Tumor, Carcinoma Cuniculatum,)
Leukoplakia (41 %)
Tufted Angioma (41 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Pilomatricoma (41 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
North American Blastomycosis (41 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Myxoid Cyst (41 %) ( Digital Mucous Cyst, Mucous Cyst,)
Branchial Cleft Cyst (39 %) ( Branchial Cyst,)
Malignant Acrospiroma (39 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Teratoma (39 %)
Actinic Keratosis (39 %) ( Senile Keratosis, Solar Keratosis,)
Malignant Pilomatricoma (39 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Cutaneous Lymphoid Hyperplasia (39 %) ( 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,)
Branchial Cyst (39 %) ( Branchial Cleft Cyst,)
Verrucous Carcinoma (39 %)
Acrochordon (39 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Geographic Tongue (39 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Granular Cell Tumor (37 %) ( Abrikossoffs Tumor, Abrikossovs Tumor, Granular Cell Myoblastoma, Granular Cell Nerve Sheath Tumor, Granular Cell Schwannoma,)
Hamartoma (37 %)
Sj grens Syndrome (37 %) ( Mikulicz Disease, Sicca Syndrome,)
Connective Tissue Nevus (37 %) ( Collagenoma, Elastoma, Shagreen Patch,)
Mucosal Melanoma (37 %)
Thrush (37 %) ( Oral Candidiasis,)
HistiocytosisX (37 %) ( Langerhans Cell Histiocytosis,)
Langerhans Cell Histiocytosis (37 %) ( HistiocytosisX,)
Squamous Cell Carcinoma In Situ (37 %) ( Bowens Disease,)
Oral Candidiasis (37 %) ( Thrush,)
Bowens Disease (37 %) ( Squamous Cell Carcinoma In Situ,)
Spitz Nevus (37 %) ( Benign Juvenile Melanoma, Epithelioid And Spindle Cell Nevus, Spitzs Juvenile Melanoma,)
Cicatricial Pemphigoid (37 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Nodular Fasciitis (37 %) ( Nodular Pseudosarcomatous Fasciits, Pseudosarcomatous Fasciitis, Subcutaneous Pseudosarcomatous Fibromatosis,)
Lymphomatoid Papulosis (35 %)
Subungual Keratoacanthoma (35 %) ( Solitary Keratoacanthoma,)
Plasma Cell Cheilitis (35 %) ( Plasma Cell Gingivitis, Plasma Cell Orificial Mucositi,)
Disseminated Coccidioidomycosis (35 %) ( Coccidioidal Granuloma,)
Solitary Neurofibroma (35 %) ( Plexiform Neurofibroma, Solitary Nerve Sheath Tumor, Sporadic Neurofibroma,)
Cutaneous Small-vessel Vasculitis (35 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Angiocentric Lymphoma (35 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Basal Cell Carcinoma (35 %)
Blue Nevus (35 %) ( Blue Neuronevus, Dermal Melanocytoma, Nevus Bleu,)
Coccidioidal Granuloma (35 %) ( Disseminated Coccidioidomycosis,)
Mucocele (35 %) ( Mucous Cyst Of The Oral Mucosa,)
Nevoid Basal Cell Carcinoma Syndrome (35 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Mucous Cyst Of The Oral Mucosa (35 %) ( Mucocele,)
Solitary Keratoacanthoma (35 %) ( Subungual Keratoacanthoma,)
Rhinosporidiosis (35 %)
Panniculitis-likeT-cell Lymphoma (33 %) ( SubcutaneousT-cell Lymphoma,)
Mucosal Squamous Cell Carcinoma (33 %)
Erythroplakia (33 %) ( Erythroplasia,)
Spindle Cell Lipoma (33 %)
Desmoplastic Melanoma (33 %) ( Neurotropic Melanoma, Spindled Melanoma,)
Benign Melanocytic Nevus (33 %) ( Banal Nevus, Common Acquired Melanocytic Nevus, Mole, Nevocellular Nevus, Nevocytic Nevus,)
Recurrent Aphthous Stomatitis (33 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Epulis (33 %)
Erythroplasia (33 %) ( Erythroplakia,)
SubcutaneousT-cell Lymphoma (33 %) ( Panniculitis-likeT-cell Lymphoma,)
Malignant Chondroid Syringoma (33 %) ( Malignant Mixed Tumor,)
Kimura Disease (33 %)
Hidradenoma (33 %)
Malignant Mixed Tumor (33 %) ( Malignant Chondroid Syringoma,)
Proliferating Trichilemmal Cyst (33 %) ( Pilar Tumor, Proliferating Follicular Cystic Neoplasm, Proliferating Pilar Tumor, Proliferating Trichilemmal Tumor,)
Sebaceous Carcinoma (33 %)
Apocrine Hidrocystoma (33 %)
Giant Cell Tumor Of The Tendon Sheath (33 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Mucosa-associated Lymphoid Tissue Lymphoma (33 %)
Acne Rosacea (31 %) ( Rosacea,)
Rosacea (31 %) ( Acne Rosacea,)
Nevus Flammeus (31 %) ( Capillary Malformation, Port-wine Stain,)
Histoplasmosis (31 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Systemic Sarcoidosis (31 %)
Subcutaneous Granuloma Annulare (31 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Cylindroma (31 %) ( Dermal Eccrine Cylindroma,)
Acute Febrile Neutrophilic Dermatosis (31 %) ( Sweets Syndrome,)
Intravascular Papillary Endothelial Hyperplasia (31 %) ( Massons Hemangio-endotheliome Vegetant Intravasculaire, Massons Lesion, Massons Pseudoangiosarcoma, Massons Tumor, Papillary Endothelial Hyperplasia,)
Dermatofibrosarcoma Protuberans (31 %)
Granulocytic Sarcoma (31 %) ( Chloroma, Myeloid Sarcoma,)
Focal Epithelial Hyperplasia (31 %) ( Hecks Disease,)
Hecks Disease (31 %) ( Focal Epithelial Hyperplasia,)
Acute Necrotizing Ulcerative Gingivitis (31 %) ( 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,)
Lymphangiectasis (31 %) ( Lymphangioma,)
Lymphangioma (31 %) ( Lymphangiectasis,)
Leiomyosarcoma (31 %)
Sinus Histiocytosis With Massive Lymphadenopathy (31 %) ( Rosai dorfman Disease,)
Hidradenocarcinoma (31 %)
Dermal Eccrine Cylindroma (31 %) ( Cylindroma,)
Lupus Erythematosus Panniculitis (31 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Malignant Peripheral Nerve Sheath Tumor (31 %) ( Malignant Schwannoma, Neurofibrosarcoma, Neurosarcoma,)
Multiple Familial Trichoepithelioma (31 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Lichen Sclerosus Et Atrophicus (31 %) ( Lichen Sclerosus,)
Rosai dorfman Disease (31 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Pilonidal Sinus (31 %) ( Barbers Interdigital Pilonidal Sinus, Pilonidal Cyst, Pilonidal Disease,)
Lichen Sclerosus (31 %) ( Lichen Sclerosus Et Atrophicus,)
Atypical Fibroxanthoma (31 %)
Oral Lichen Planus (31 %)
Cornu Cutaneum (31 %) ( Cutaneous Horn,)
Vascular Leiomyoma (31 %) ( Angioleiomyoma,)
Cutaneous Horn (31 %) ( Cornu Cutaneum,)
Angioleiomyoma (31 %) ( Vascular Leiomyoma,)
Chondrodermatitis Nodularis Chronica Helicis (31 %) ( Chondrodermatitis Nodularis Helicis,)
Chondrodermatitis Nodularis Helicis (31 %) ( Chondrodermatitis Nodularis Chronica Helicis,)
Eosinophilic Granuloma (29 %)
Sarcoidosis (29 %)
Multiple Endocrine Neoplasia Type2 (29 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Spiradenoma (29 %)
Hypertrophic Lupus Erythematosus (29 %) ( Verrucous Lupus Erythematosus,)
Chilblains (29 %) ( Pernio, Perniosis,)
Verrucous Lupus Erythematosus (29 %) ( Hypertrophic Lupus Erythematosus,)
Mycetoma (29 %) ( Madura Foot, Maduromycosis,)
Clubbing (29 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
South American Blastomycosis (29 %) ( Brazilian Blastomycosis, Paracoccidioidal Granuloma, Paracoccidioidomycosis,)
Rhinophyma (29 %)
Capillary Hemangioma (29 %) ( Infantile Hemangioma, Nevus Maternus, Strawberry Hemangioma Strawberry Nevus,)
Cutis Laxa (29 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Foreign Body Reaction (29 %)
Juvenile Hyaline Fibromatosis (29 %) ( Fibromatosis Hyalinica Multiplex Juvenilis, Murray puretic drescher Syndrome,)
Juvenile Xanthogranuloma (29 %)
Cutaneous Focal Mucinosis (29 %)
Actinomycosis (29 %)
Leiomyoma (29 %)
Wells Syndrome (29 %) ( Eosinophilic Cellulitis,)
Eosinophilic Cellulitis (29 %) ( Wells Syndrome,)
Congenital Melanocytic Nevus (29 %)
Marginal ZoneB-cell Lymphoma (29 %)
Keratoacanthoma (29 %)
Peripheral Giant Cell Granuloma (29 %)
Glossodynia (29 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Smooth Tongue (29 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Pemphigus Vulgaris (29 %)
Sclerotic Fibroma (29 %)
Basaloid Squamous Cell Carcinoma (29 %)
Congenital Self-healing Reticulohistiocytosis (29 %) ( Hashimoto pritzker Disease, Hashimoto pritzker Syndrome,)
Halo Nevus (29 %) ( Leukoderma Acquisitum Centrifugum, Perinevoid Vitiligo, Sutton Nevus,)
Carcinoid (29 %)
Primary Cutaneous Anaplastic Large Cell Lymphoma (29 %) ( Cd30+ CutaneousT-cell Lymphoma,)
Cd30+ CutaneousT-cell Lymphoma (29 %) ( Primary Cutaneous Anaplastic Large Cell Lymphoma,)
Malakoplakia (29 %) ( Malacoplakia,)
Malacoplakia (29 %) ( Malakoplakia,)
Lupus Pernio (29 %)
Nodular Melanoma (27 %)
Mucinous Carcinoma (27 %)
Lentigo (27 %)
Lentigo Maligna Melanoma (27 %)
Verruca Plana (27 %) ( Flat Warts,)
Flat Warts (27 %) ( Verruca Plana,)
Syringoma (27 %)
Melanocytic Nevi (27 %)
Gingival Hypertrophy (27 %)
Central Papillary Atrophy (27 %) ( Median Rhomboid Glossitis,)
Multiple Endocrine Neoplasia Type3 (27 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
Aggressive Digital Papillary Adenocarcinoma (27 %) ( Digital Papillary Adenocarcinoma, Papillary Adenoma,)
Eosinophilic Ulcer (27 %)
Histiocytic Medullary Reticulosis (27 %) ( Malignant Histiocytosis,)
White Nails (27 %) ( Leukonychia,)
Keloidal Scar (27 %) ( Keloid,)
Spindle Cell Squamous Cell Carcinoma (27 %) ( Spindle Cell Carcinoma,)
Cutaneous Melanoma (27 %)
Keloid (27 %) ( Keloidal Scar,)
Proliferative Verrucous Leukoplakia (27 %)
Keratocyst (27 %)
Angiolipoma (27 %)
Pleomorphic Fibroma (27 %)
Pityriasis Lichenoides Et Varioliformis Acuta (27 %) ( Acute Guttate Parapsoriasis, Acute Parapsoriasis, Acute Pityriasis Lichenoides, Mucha habermann Disease, Parapsoriasis Acuta, Parapsoriasis Lichenoides Et Varioliformis Acuta, Parapsoriasis Varioliformis,)
Melanonychia (27 %)
Acral Fibrokeratoma (27 %) ( Acquired Digital Fibrokeratoma, Acquired Periungual Fibrokeratoma,)
Paraneoplastic Syndrome (27 %)
Hairy Leukoplakia (27 %) ( Oral Hairy Leukoplakia,)
Oral Hairy Leukoplakia (27 %) ( Hairy Leukoplakia,)
Actinic Elastosis (27 %) ( Solar Elastosis,)
Hidradenitis Suppurativa (27 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Solar Elastosis (27 %) ( Actinic Elastosis,)
Microcystic Adnexal Carcinoma (27 %) ( Sclerosing Sweat Duct Carcinoma,)
Pagetoid Reticulosis (27 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Spindle Cell Carcinoma (27 %) ( Spindle Cell Squamous Cell Carcinoma,)
Reticulohistiocytoma (27 %)
Leukonychia (27 %) ( White Nails,)
Hyperparathyroidism (27 %)
Mucosal Lentigines (27 %) ( Labial And Penile And Vulvar Melanosis, Melanotic Macules,)
Stomatitis Nicotina (27 %) ( Nicotine Stomatitis, Smokers Keratosis, Smokers Patches,)
Infantile Myofibromatosis (27 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Sclerosing Sweat Duct Carcinoma (27 %) ( Microcystic Adnexal Carcinoma,)
Median Rhomboid Glossitis (27 %) ( Central Papillary Atrophy,)
Hypohidrosis (27 %) ( Anhidrosis,)
Blau Syndrome (27 %)
Erythema Induratum (27 %) ( Bazin Disease, Nodular Vasculitis,)
Cheilitis Granulomatosa (27 %) ( Granulomatous Cheilitis, Orofacial Granulomatosis,)
Follicular Mucinosis (27 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Anhidrosis (27 %) ( Hypohidrosis,)
Sparganosis (27 %)
Verruciform Xanthoma (27 %)
Relapsing Polychondritis (27 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Lentigo Maligna (27 %) ( Lentiginous Melanoma On Sun-damaged Skin,)
Callus (27 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Lentiginous Melanoma On Sun-damaged Skin (27 %) ( Lentigo Maligna,)
Sweets Syndrome (27 %) ( Acute Febrile Neutrophilic Dermatosis,)
Acral Lentiginous Melanoma (27 %)
Malignant Histiocytosis (27 %) ( Histiocytic Medullary Reticulosis,)
Linea Alba (25 %)
Encephalocele (25 %)
Nasal Glioma (25 %) ( Brain-like Heterotopia, Cephalic Brain-like Heterotopia, Glial Hamartoma, Heterotopic Neuroglial Tissue, Nasal Cerebral Heterotopia, Nasal Heterotopic Brain Tissue,)
Metastatic Carcinoma (25 %)
Pseudomelanoma (25 %) ( Recurrent Melanocytic Nevus, Recurrent Nevus,)
Longitudinal Erythronychia (25 %)
Actinic Cheilitis (25 %) ( Actinic Cheilosis,)
Omphalomesenteric Duct Cyst (25 %) ( Omphalomesenteric Duct Remnant, Vitelline Cyst,)
Longitudinal Melanonychia (25 %)
Brunsting perry Cicatricial Pemphigoid (25 %) ( Localized Cicatricial Pemphigoid,)
Onychocryptosis (25 %) ( Ingrown Nail, Unguis Incarnatus,)
Localized Cicatricial Pemphigoid (25 %) ( Brunsting perry Cicatricial Pemphigoid,)
Oral Submucous Fibrosis (25 %)
Plantar Fibromatosis (25 %) ( Ledderhoses Disease,)
Freckle (25 %) ( Ephelis,)
Lichen Planus (25 %)
Steatocystoma Multiplex (25 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Carney Complex (25 %) ( Lamb Syndrome, Name Syndrome,)
Subcutaneous Sarcoidosis (25 %) ( Darier roussy Disease, Darier roussy Sarcoid,)
Neuroblastoma (25 %) ( Infantile Neuroblastoma, Neuroepithelioma,)
Pleomorphic Lipoma (25 %)
Plexiform Fibrohistiocytic Tumor (25 %)
Plaque-type Porokeratosis (25 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Thyroglossal Duct Cyst (25 %)
Ledderhoses Disease (25 %) ( Plantar Fibromatosis,)
Trichoepithelioma (25 %)
Lichenoid Keratosis (25 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Acanthosis Nigricans (25 %)
Isthmicoma (25 %) ( Infundibuloma, Tumor Of The Follicular Infundibulum,)
Peutz jeghers Syndrome (25 %)
Hemangiopericytoma (25 %)
Actinic Cheilosis (25 %) ( Actinic Cheilitis,)
Coccidioidomycosis (25 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Soft-tissue Melanoma (25 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Ehlers danlos Syndrome (25 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Sebaceous Epithelioma (25 %) ( Sebaceoma,)
Eosinophilic Pustular Folliculitis (25 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Nevus Sebaceous (25 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Chromoblastomycosis (25 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Kindler Syndrome (25 %) ( Acrokeratotic Poikiloderma, Bullous Acrokeratotic Poikiloderma Of Kindler And Weary, Congenital Poikiloderma With Blisters And Keratoses, Congenital Poikiloderma With Bullae And Progressive Cutaneous Atrophy, Hereditary Acrokeratotic Poikiloderma, Hyperkeratosis hyperpigmentation Syndrome, Weary kindler Syndrome,)
Sebaceoma (25 %) ( Sebaceous Epithelioma,)
Blue Nevi (25 %)
Ephelis (25 %) ( Freckle,)
L fgren Syndrome (25 %)
Von Recklinghausens Disease (25 %) ( Neurofibromatosis Type1,)
Erythema Multiforme (25 %)
Erosive Lichen Planus (25 %)
Pigmented Basal Cell Carcinoma (25 %)
Neurofibromatosis Type1 (25 %) ( Von Recklinghausens Disease,)
Familial Mediterranean Fever (25 %)
Rhinoscleroma (25 %)
Tnf Receptor Associated Periodic Syndrome (25 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)

Differentials from Google.

Date Added: 2017-05-27

Capillary Hemangioma
Lobular Capillary Hemangioma
Peripheral Giant Cell Granuloma
Pyogenic Granuloma

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