Differentials: Infundibular Cyst

Differential diagnosis for Infundibular Cyst

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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 Infundibular Cyst.

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Date Added: 2017-11-30:

Epidermal Cyst (100 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Dermatofibroma (46 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Schwannoma (44 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Pilomatricoma (40 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Acrochordon (38 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Epithelioma Cuniculatum (36 %) ( Ackerman Tumor, Carcinoma Cuniculatum,)
Lupus Erythematosus Panniculitis (35 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Acrospiroma (35 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Pyogenic Granuloma (35 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Chondroid Syringoma (34 %) ( Mixed Tumor,)
Cutaneous Small-vessel Vasculitis (34 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Hamartoma (34 %)
Giant Pigmented Nevus (34 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Mixed Tumor (34 %) ( Chondroid Syringoma,)
Lichen Planopilaris (33 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Wart (33 %) ( Verruca Vulgaris,)
Traumatic Neuroma (33 %) ( Amputation Neuroma,)
Verruca Vulgaris (33 %) ( Wart,)
Actinic Keratosis (33 %) ( Senile Keratosis, Solar Keratosis,)
Dermoid Cyst (33 %)
Amputation Neuroma (33 %) ( Traumatic Neuroma,)
Myxoid Cyst (33 %) ( Digital Mucous Cyst, Mucous Cyst,)
Fissured Tongue (33 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Follicular Mucinosis (33 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Nevus Of Ota (31 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Glomus Tumor (31 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Malignant Mixed Tumor (31 %) ( Malignant Chondroid Syringoma,)
Malignant Chondroid Syringoma (31 %) ( Malignant Mixed Tumor,)
Callus (31 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Angiolymphoid Hyperplasia With Eosinophilia (31 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Malignant Pilomatricoma (30 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Lymphangioma (30 %) ( Lymphangiectasis,)
Angiocentric Lymphoma (30 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Steatocystoma Multiplex (30 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Malignant Acrospiroma (30 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Cutis Laxa (30 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Verrucous Carcinoma (30 %)
Erythema Induratum (30 %) ( Bazin Disease, Nodular Vasculitis,)
Lymphangiectasis (30 %) ( Lymphangioma,)
Cicatricial Pemphigoid (30 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Tufted Angioma (30 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Spiradenoma (29 %)
Basal Cell Carcinoma (29 %)
Hidrocystoma (29 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Nevus Sebaceous (29 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Mycosis Fungoides (29 %)
Isthmicoma (29 %) ( Infundibuloma, Tumor Of The Follicular Infundibulum,)
Solar Elastosis (29 %) ( Actinic Elastosis,)
Pachydermoperiostosis (29 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Acute Febrile Neutrophilic Dermatosis (29 %) ( Sweets Syndrome,)
Sweets Syndrome (29 %) ( Acute Febrile Neutrophilic Dermatosis,)
Cutaneous Lymphoid Hyperplasia (29 %) ( 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,)
Actinic Elastosis (29 %) ( Solar Elastosis,)
Nasal Glioma (29 %) ( Brain-like Heterotopia, Cephalic Brain-like Heterotopia, Glial Hamartoma, Heterotopic Neuroglial Tissue, Nasal Cerebral Heterotopia, Nasal Heterotopic Brain Tissue,)
Clubbing (29 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Mucocele (29 %) ( Mucous Cyst Of The Oral Mucosa,)
Ehlers danlos Syndrome (29 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Mucous Cyst Of The Oral Mucosa (29 %) ( Mucocele,)
Proliferating Trichilemmal Cyst (29 %) ( Pilar Tumor, Proliferating Follicular Cystic Neoplasm, Proliferating Pilar Tumor, Proliferating Trichilemmal Tumor,)
Congenital Melanocytic Nevus (29 %)
Mucosa-associated Lymphoid Tissue Lymphoma (28 %)
Lichen Sclerosus Et Atrophicus (28 %) ( Lichen Sclerosus,)
Eosinophilic Granuloma (28 %)
Lichen Sclerosus (28 %) ( Lichen Sclerosus Et Atrophicus,)
Pilonidal Sinus (28 %) ( Barbers Interdigital Pilonidal Sinus, Pilonidal Cyst, Pilonidal Disease,)
Acne Rosacea (28 %) ( Rosacea,)
Langerhans Cell Histiocytosis (28 %) ( HistiocytosisX,)
Leiomyosarcoma (28 %)
HistiocytosisX (28 %) ( Langerhans Cell Histiocytosis,)
Lymphomatoid Papulosis (28 %)
Rosacea (28 %) ( Acne Rosacea,)
Branchial Cyst (26 %) ( Branchial Cleft Cyst,)
Tuberous Sclerosis (26 %) ( Bourneville Disease, Epiloia,)
Hypohidrosis (26 %) ( Anhidrosis,)
Syringoma (26 %)
Subungual Keratoacanthoma (26 %) ( Solitary Keratoacanthoma,)
Anhidrosis (26 %) ( Hypohidrosis,)
Plasmacytoma (26 %)
Lipoma (26 %)
Solitary Keratoacanthoma (26 %) ( Subungual Keratoacanthoma,)
Amniotic Band Syndrome (26 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Connective Tissue Nevus (26 %) ( Collagenoma, Elastoma, Shagreen Patch,)
Geographic Tongue (26 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Cylindroma (26 %) ( Dermal Eccrine Cylindroma,)
Dermal Eccrine Cylindroma (26 %) ( Cylindroma,)
Neurothekeoma (26 %) ( Bizarre Cutaneous Neurofibroma, Cutaneous Lobular Neuromyxoma, Myxoma Of The Nerve Sheath, Myxomatous Perineurioma, Nerve Sheath Myxoma,)
Giant Cell Tumor Of The Tendon Sheath (26 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Branchial Cleft Cyst (26 %) ( Branchial Cyst,)
Granulocytic Sarcoma (26 %) ( Chloroma, Myeloid Sarcoma,)
Liposarcoma (26 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Nodular Fasciitis (26 %) ( Nodular Pseudosarcomatous Fasciits, Pseudosarcomatous Fasciitis, Subcutaneous Pseudosarcomatous Fibromatosis,)
Squamous Cell Carcinoma In Situ (25 %) ( Bowens Disease,)
SubcutaneousT-cell Lymphoma (25 %) ( Panniculitis-likeT-cell Lymphoma,)
Leukoplakia (25 %)
Recurrent Aphthous Stomatitis (25 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Bowens Disease (25 %) ( Squamous Cell Carcinoma In Situ,)
Hidradenitis Suppurativa (25 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Panniculitis-likeT-cell Lymphoma (25 %) ( SubcutaneousT-cell Lymphoma,)
Microcystic Adnexal Carcinoma (25 %) ( Sclerosing Sweat Duct Carcinoma,)
Tic Douloureux (25 %) ( Trigeminal Neuralgia,)
Sclerosing Sweat Duct Carcinoma (25 %) ( Microcystic Adnexal Carcinoma,)
Trigeminal Neuralgia (25 %) ( Tic Douloureux,)
Keloidal Scar (25 %) ( Keloid,)
Meningocele (25 %)
White Nails (25 %) ( Leukonychia,)
Folliculitis (25 %)
Malignant Peripheral Nerve Sheath Tumor (25 %) ( Malignant Schwannoma, Neurofibrosarcoma, Neurosarcoma,)
Leukonychia (25 %) ( White Nails,)
Keloid (25 %) ( Keloidal Scar,)
Pinkus Tumor (24 %) ( Premalignant Fibroepithelial Tumor,)
Localized Cicatricial Pemphigoid (24 %) ( Brunsting perry Cicatricial Pemphigoid,)
Premalignant Fibroepithelial Tumor (24 %) ( Pinkus Tumor,)
Cutaneous Sinus Of Dental Origin (24 %) ( Dental Sinus,)
Madarosis (24 %)
Pemphigus Vulgaris (24 %)
North American Blastomycosis (24 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Atypical Fibroxanthoma (24 %)
Keratocyst (24 %)
Triangular Alopecia (24 %) ( Temporal Alopecia, Temporal Triangular Alopecia,)
Klippel trenaunay Syndrome (24 %) ( Angioosteohypertrophy Syndrome, Hemangiectatic Hypertrophy,)
Multiple Familial Trichoepithelioma (24 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Apocrine Hidrocystoma (24 %)
Leukemia Cutis (24 %)
Neurofibromatosis Type1 (24 %) ( Von Recklinghausens Disease,)
Brunsting perry Cicatricial Pemphigoid (24 %) ( Localized Cicatricial Pemphigoid,)
Von Recklinghausens Disease (24 %) ( Neurofibromatosis Type1,)
Encephalocele (24 %)
Nevus Flammeus (24 %) ( Capillary Malformation, Port-wine Stain,)
Duhring Disease (24 %) ( Dermatitis Herpetiformis,)
Dermatitis Herpetiformis (24 %) ( Duhring Disease,)
Sebaceous Carcinoma (24 %)
Nevus Spilus (24 %) ( Speckled Lentiginous Nevus, Zosteriform Lentiginous Nevus,)
Keratoacanthoma (24 %)
Kimura Disease (24 %)
Chromoblastomycosis (24 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Desmoplastic Melanoma (24 %) ( Neurotropic Melanoma, Spindled Melanoma,)
Acute Necrotizing Ulcerative Gingivitis (24 %) ( 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,)
Yaws (24 %) ( Bouba, Framb sie, Parangi, Pian,)
Dermatofibrosarcoma Protuberans (24 %)
Linear Verrucous Epidermal Nevus (24 %) ( Linear Epidermal Nevus, Verrucous Epidermal Nevus,)
Foreign Body Reaction (24 %)
Nevoid Basal Cell Carcinoma Syndrome (24 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Scleroderma (24 %)
Soft-tissue Melanoma (24 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Plaque-type Porokeratosis (24 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Dental Sinus (24 %) ( Cutaneous Sinus Of Dental Origin,)
Carney Complex (24 %) ( Lamb Syndrome, Name Syndrome,)
Lipodermatosclerosis (23 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
Lentigo Maligna (23 %) ( Lentiginous Melanoma On Sun-damaged Skin,)
Hidradenoma (23 %)
Multiple Endocrine Neoplasia Type1 (23 %) ( Wermer Syndrome,)
Teratoma (23 %)
Chondrodermatitis Nodularis Helicis (23 %) ( Chondrodermatitis Nodularis Chronica Helicis,)
Chondrodermatitis Nodularis Chronica Helicis (23 %) ( Chondrodermatitis Nodularis Helicis,)
Benign Melanocytic Nevus (23 %) ( Banal Nevus, Common Acquired Melanocytic Nevus, Mole, Nevocellular Nevus, Nevocytic Nevus,)
Lentiginous Melanoma On Sun-damaged Skin (23 %) ( Lentigo Maligna,)
Zoster (23 %) ( Herpes Zoster, Shingles,)
Wermer Syndrome (23 %) ( Multiple Endocrine Neoplasia Type1,)
Favre racouchot Syndrome (23 %) ( Favre racouchot Disease, Nodular Cutaneous Elastosis With Cysts And Comedones,)
Marginal ZoneB-cell Lymphoma (23 %)
Verruciform Xanthoma (23 %)
Actinomycosis (23 %)
Oral Lichen Planus (23 %)
Eosinophilic Pustular Folliculitis (23 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Alopecia Neoplastica (23 %)
Blue Nevus (23 %) ( Blue Neuronevus, Dermal Melanocytoma, Nevus Bleu,)
Coccidioidomycosis (23 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Seborrheic Keratosis (23 %) ( Seborrheic Verruca, Senile Wart,)
Syringadenoma Papilliferum (23 %) ( Syringocystadenoma Papilliferum,)
Metastatic Carcinoma (23 %)
Mycetoma (23 %) ( Madura Foot, Maduromycosis,)
Syringocystadenoma Papilliferum (23 %) ( Syringadenoma Papilliferum,)
Granular Cell Tumor (23 %) ( Abrikossoffs Tumor, Abrikossovs Tumor, Granular Cell Myoblastoma, Granular Cell Nerve Sheath Tumor, Granular Cell Schwannoma,)
Carcinoid (23 %)
Rhinophyma (23 %)
Verruca Plana (23 %) ( Flat Warts,)
Congenital Self-healing Reticulohistiocytosis (23 %) ( Hashimoto pritzker Disease, Hashimoto pritzker Syndrome,)
Hidradenocarcinoma (23 %)
Flat Warts (23 %) ( Verruca Plana,)
Frontal Linear Scleroderma (23 %) ( En Coup De Sabre, Morphea En Coup De Sabre,)
Panhypopituitarism (21 %)
Paraneoplastic Syndrome (21 %)
Longitudinal Melanonychia (21 %)
Chordoma (21 %)
Juvenile Xanthogranuloma (21 %)
Histoplasmosis (21 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Hypoparathyroidism (21 %)
Eccrine Carcinoma (21 %) ( Syringoid Carcinoma,)
Aplasia Cutis Congenita (21 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Factitious Dermatitis (21 %) ( Dermatitis Artefacta, Factitial Dermatitis,)
Postoperative Hematoma (21 %)
Juvenile Hyaline Fibromatosis (21 %) ( Fibromatosis Hyalinica Multiplex Juvenilis, Murray puretic drescher Syndrome,)
Scarring Alopecia (21 %)
Morphea (21 %)
Complex Regional Pain Syndrome (21 %) ( Reflex Sympathetic Dystrophy,)
Tinea Capitis (21 %) ( Herpes Tonsurans, Ringworm Of The Hair, Ringworm Of The Scalp, Scalp Ringworm, Tinea Tonsurans,)
Malignant Fibrous Histiocytoma (21 %)
Linear Scleroderma (21 %)
Reflex Sympathetic Dystrophy (21 %) ( Complex Regional Pain Syndrome,)
Stasis Dermatitis (21 %) ( Congestion Eczema, Gravitational Dermatitis, Gravitational Eczema, Stasis Eczema, Varicose Eczema,)
Leukocytoclastic Vasculitis (21 %)
Erythema Nodosum (21 %)
Calcinosis Cutis (21 %)
External Otitis (21 %) ( Otitis Externa, Swimmers Ear,)
Chronic Paronychia (21 %)
Syringoid Carcinoma (21 %) ( Eccrine Carcinoma,)
Cutaneous Focal Mucinosis (21 %)
Ganglion Cyst (21 %)
Inverted Follicular Keratosis (21 %)
Comedo Nevus (21 %) ( Nevus Comedonicus,)
Nevus Comedonicus (21 %) ( Comedo Nevus,)
Thyroglossal Duct Cyst (21 %)
Balanitis Plasmacellularis (20 %) ( Balanoposthitis Chronica Circumscripta Plasmacellularis, Balanitis Circumscripta Plasmacellularis, Plasma Cell Balanitis, Plasma Cell Vulvitis, Vulvitis Circumscripta Plasmacellularis, Zoons Balanitis, Zoons Erythroplasia, Zoons Vulvitis,)
Hemangiopericytoma (20 %)
Koilonychia (20 %) ( Spoon Nails,)
Pagetoid Reticulosis (20 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Malakoplakia (20 %) ( Malacoplakia,)
Aggressive Digital Papillary Adenocarcinoma (20 %) ( Digital Papillary Adenocarcinoma, Papillary Adenoma,)
Pseudoglandular Squamous Cell Carcinoma (20 %) ( Adenoid Squamous Cell Carcinoma,)
Mccune albright Syndrome (20 %)
Takayasu Arteritis (20 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Juvenile Rheumatoid Arthritis (20 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Warty Dyskeratoma (20 %) ( Isolated Dyskeratosis Follicularis,)
Hyper-ige Syndrome (20 %) ( Buckley Syndrome, Job Syndrome,)
Infectious Mononucleosis (20 %) ( Glandular Fever,)
Infantile Myofibromatosis (20 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Acute Febrile Ulcerative Acne (20 %) ( Acne Fulminans,)
Spindle Cell Squamous Cell Carcinoma (20 %) ( Spindle Cell Carcinoma,)
Extramammary Paget Disease (20 %)
Eccrine Nevus (20 %)
Pressure Alopecia (20 %) ( Postoperative Alopecia, Pressure-induced Alopecia,)
Rhinosporidiosis (20 %)
Trichoblastoma (20 %)
Glossodynia (20 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Lentigo (20 %)
Adenoid Squamous Cell Carcinoma (20 %) ( Pseudoglandular Squamous Cell Carcinoma,)
Vitiligo (20 %)
Angiosarcoma (20 %)
Glandular Fever (20 %) ( Infectious Mononucleosis,)
Epithelioid Sarcoma (20 %)
Eosinophilic Cellulitis (20 %) ( Wells Syndrome,)
Spoon Nails (20 %) ( Koilonychia,)
Hypohidrotic Ectodermal Dysplasia (20 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Smooth Tongue (20 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Wells Syndrome (20 %) ( Eosinophilic Cellulitis,)
Onychocryptosis (20 %) ( Ingrown Nail, Unguis Incarnatus,)
Acne Fulminans (20 %) ( Acute Febrile Ulcerative Acne,)
Superficial Lymphatic Malformation (20 %) ( Lymphangioma Circumscriptum,)
Formaldehyde-induced (20 %)
Multiple Endocrine Neoplasia Type2 (20 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Seborrheic Dermatitis (20 %) ( Seborrheic Eczema,)
Seborrheic Eczema (20 %) ( Seborrheic Dermatitis,)
Alopecia Areata (20 %)
Malacoplakia (20 %) ( Malakoplakia,)
Blau Syndrome (20 %)
Lymphangioma Circumscriptum (20 %) ( Superficial Lymphatic Malformation,)
Isolated Dyskeratosis Follicularis (20 %) ( Warty Dyskeratoma,)
Systemic Sarcoidosis (20 %)
Acne Keloidalis Nuchae (20 %) ( Acne Keloidalis, Dermatitis Papillaris Capillitii, Folliculitis Keloidalis, Folliculitis Keloidis Nuchae, Nuchal Keloid Acne,)
Spindle Cell Carcinoma (20 %) ( Spindle Cell Squamous Cell Carcinoma,)
Sinus Pericranii (20 %)
Spitz Nevus (20 %) ( Benign Juvenile Melanoma, Epithelioid And Spindle Cell Nevus, Spitzs Juvenile Melanoma,)
Trichofolliculoma (20 %)
Subungual Exostosis (20 %)
Rheumatoid Arthritis (20 %)
Longitudinal Erythronychia (19 %)
Coccidioidal Granuloma (19 %) ( Disseminated Coccidioidomycosis,)
Trichoadenoma Of Nikolowski (19 %) ( Trichoadenoma,)
Androgenic Alopecia (19 %) ( Androgenetic Alopecia,)
Cutaneous Melanoma (19 %)
Diabetic Dermopathy (19 %) ( Shin Spots,)
Recurrent Palmoplantar Hidradenitis (19 %) ( Idiopathic Palmoplantar Hidradenitis, Idiopathic Plantar Hidradenitis, Painful Plantar Erythema, Palmoplantar Eccrine Hidradenitis, Plantar Panniculitis,)
Olmsted Syndrome (19 %) ( Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Mutilating Palmoplantar Keratoderma With Periorificial Plaques, Polykeratosis Of Touraine,)
Bullous Pemphigoid (19 %)
Polyarteritis Nodosa (19 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Linear Iga Bullous Dermatosis (19 %) ( Linear Iga Dermatosis,)
Ectodermal Dysplasia (19 %)
Primary Cutaneous Follicular Lymphoma (19 %) ( Follicular Center Cell Lymphoma, Follicular Center Lymphoma,)
Linear Iga Dermatosis (19 %) ( Linear Iga Bullous Dermatosis,)
Allergic Granulomatosis (19 %) ( Churg strauss Syndrome,)
Churg strauss Syndrome (19 %) ( Allergic Granulomatosis,)
Xanthoma Planum (19 %) ( Plane Xanthoma,)
Leukoderma (19 %)
Discoid Lupus Erythematosus (19 %)
Freckle (19 %) ( Ephelis,)
Plane Xanthoma (19 %) ( Xanthoma Planum,)
Solar Purpura (19 %) ( Actinic Purpura, Senile Purpura,)
Trichoadenoma (19 %) ( Trichoadenoma Of Nikolowski,)
Pseudopelade Of Brocq (19 %) ( Alopecia Cicatrisata,)
Relapsing Polychondritis (19 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Necrobiotic Xanthogranuloma With Paraproteinemia (19 %) ( Necrobiotic Xanthogranuloma,)
Xanthelasma (19 %) ( Xanthelasma Palpebrarum,)
Desmoplastic Fibroblastoma (19 %) ( Collagenous Fibroma,)
Blastomycosis-like Pyoderma (19 %) ( Pyoderma Vegetans,)
Sj grens Syndrome (19 %) ( Mikulicz Disease, Sicca Syndrome,)
Linear Lichen Planus (19 %)
Androgenetic Alopecia (19 %) ( Androgenic Alopecia,)
Collagenous Fibroma (19 %) ( Desmoplastic Fibroblastoma,)
Lichenoid Keratosis (19 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Alopecia Cicatrisata (19 %) ( Pseudopelade Of Brocq,)
Necrobiotic Xanthogranuloma (19 %) ( Necrobiotic Xanthogranuloma With Paraproteinemia,)
Melanocytic Nevi (19 %)
Pyoderma Vegetans (19 %) ( Blastomycosis-like Pyoderma,)
Palmoplantar Keratoderma (19 %)
Livedoid Vasculopathy (19 %) ( Atrophie Blanche, Livedo Reticularis With Summer Ulceration, Livedoid Vasculitis, Purple Syndrome, Segmental Hyalinizing Vasculitis,)
Pityriasis Rosea (19 %) ( Pityriasis Rosea Gibert,)
Halo Nevus (19 %) ( Leukoderma Acquisitum Centrifugum, Perinevoid Vitiligo, Sutton Nevus,)
Maffucci Syndrome (19 %)
Intravascular Papillary Endothelial Hyperplasia (19 %) ( Massons Hemangio-endotheliome Vegetant Intravasculaire, Massons Lesion, Massons Pseudoangiosarcoma, Massons Tumor, Papillary Endothelial Hyperplasia,)
Lupus Vulgaris (19 %) ( Tuberculosis Luposa,)
Parry romberg Syndrome (19 %) ( Progressive Hemifacial Atrophy,)
Progressive Hemifacial Atrophy (19 %) ( Parry romberg Syndrome,)
Mucosal Squamous Cell Carcinoma (19 %)
Melanotic Neuroectodermal Tumor Of Infancy (19 %)
Flesh-eating Bacteria Syndrome (19 %) ( Necrotizing Fasciitis,)
Necrotizing Fasciitis (19 %) ( Flesh-eating Bacteria Syndrome,)
Segmental Neurofibromatosis (19 %)
Malignant Atrophic Papulosis (19 %) ( Degos Disease,)
Cystic Papilloma (19 %) ( Verrucous Cyst,)
Verrucous Cyst (19 %) ( Cystic Papilloma,)
Phaeohyphomycosis (19 %)
Xanthelasma Palpebrarum (19 %) ( Xanthelasma,)
Merkel Cell Carcinoma (19 %) ( Cutaneous Apudoma, Primary Neuroendocrine Carcinoma Of The Skin, Primary Small Cell Carcinoma Of The Skin, Trabecular Carcinoma Of The Skin,)
Tuberculosis Luposa (19 %) ( Lupus Vulgaris,)
Degos Disease (19 %) ( Malignant Atrophic Papulosis,)
Perforating Folliculitis (19 %)
Grovers Disease (19 %) ( Benign Papular Acantholytic Dermatosis, Persistent Acantholytic Dermatosis, Transient Acantholytic Dermatosis,)
Multiple Lentigines Syndrome (19 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Basaloid Squamous Cell Carcinoma (19 %)
Ainhum (19 %) ( Bankokerend, Dactylolysis Spontanea, Sukhapakla,)
Disseminated Coccidioidomycosis (19 %) ( Coccidioidal Granuloma,)
Bronchogenic Cyst (19 %)
Tnf Receptor Associated Periodic Syndrome (19 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Kaposi Sarcoma (19 %)
Acne Necrotica (19 %)
Shin Spots (19 %) ( Diabetic Dermopathy,)
Ephelis (19 %) ( Freckle,)
Sparganosis (19 %)
Pityriasis Rosea Gibert (19 %) ( Pityriasis Rosea,)
Limbal Dermoid (19 %)
Pityriasis Lichenoides Et Varioliformis Acuta (19 %) ( Acute Guttate Parapsoriasis, Acute Parapsoriasis, Acute Pityriasis Lichenoides, Mucha habermann Disease, Parapsoriasis Acuta, Parapsoriasis Lichenoides Et Varioliformis Acuta, Parapsoriasis Varioliformis,)
Giant Condyloma Acuminatum (19 %) ( Buschke l wenstein Tumor, Giant Condyloma Of Buschke l wenstein Tumor,)
Multiple Endocrine Neoplasia Type3 (19 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
Sinus Histiocytosis With Massive Lymphadenopathy (19 %) ( Rosai dorfman Disease,)
Dysplastic Nevus (19 %) ( Atypical Mole, Atypical Nevus, B-k Mole, Clarks Nevus, Dysplastic Melanocytic Nevus, Nevus With Architectural Disorder,)
Rosai dorfman Disease (19 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Tripe Palms (19 %)
Superficial Multicentric Basal Cell Carcinoma (18 %) ( Superficial Basal Cell Carcinoma,)
Postinflammatory Hyperpigmentation (18 %) ( Postinflammatory Hypermelanosis,)
Popsicle Panniculitis (18 %) ( Cold Panniculitis,)
Nevus Sebaceus (18 %)
Trigeminal Trophic Lesion (18 %) ( Trigeminal Trophic Syndrome,)
Nevus Comedonicus Syndrome (18 %)
Malignant Histiocytosis (18 %) ( Histiocytic Medullary Reticulosis,)
Trigeminal Trophic Syndrome (18 %) ( Trigeminal Trophic Lesion,)
Subcutaneous Granuloma Annulare (18 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Onycholysis (18 %)
Pustular (18 %)
Cold Panniculitis (18 %) ( Popsicle Panniculitis,)
Pili Torti (18 %) ( Twisted Hairs,)
Cronkhite canada Syndrome (18 %)
Traumatic Alopecia (18 %)
Twisted Hairs (18 %) ( Pili Torti,)
Sneddon wilkinson Disease (18 %) ( Subcorneal Pustular Dermatosis,)
Erythema Annulare Centrifugum (18 %) ( Deep Gyrate Erythema, Erythema Perstans, Palpable Migrating Erythema, Superficial Gyrate Erythema,)
Peutz jeghers Syndrome (18 %)
Subcorneal Pustular Dermatosis (18 %) ( Sneddon wilkinson Disease,)
Lupus Pernio (18 %)
Kerion (18 %)
Linea Alba (18 %)
Porokeratosis (18 %)
Subcutaneous Emphysema (18 %)
Erosive Lichen Planus (18 %)
Hypertrophic Lichen Planus (18 %) ( Lichen Planus Verrucosus,)
Acral Lentiginous Melanoma (18 %)
Sebaceous Hyperplasia (18 %)
Lichen Planus Verrucosus (18 %) ( Hypertrophic Lichen Planus,)
Histiocytic Medullary Reticulosis (18 %) ( Malignant Histiocytosis,)
Microcystic Lymphatic Malformation (18 %)
Sarcoidosis (18 %)
Trichorrhexis Nodosa (18 %)
Lichen Planus Pigmentosus (18 %)
Kindler Syndrome (18 %) ( 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,)
Superficial Basal Cell Carcinoma (18 %) ( Superficial Multicentric Basal Cell Carcinoma,)
Lichen Striatus (18 %) ( Blaschko Linear Acquired Inflammatory Skin Eruption, Linear Lichenoid Dermatosis,)
Hyperparathyroidism (18 %)
Lentigo Maligna Melanoma (18 %)
Postinflammatory Hypermelanosis (18 %) ( Postinflammatory Hyperpigmentation,)
Angiokeratoma (18 %)
Plasma Cell Cheilitis (18 %) ( Plasma Cell Gingivitis, Plasma Cell Orificial Mucositi,)
Erythroplasia (18 %) ( Erythroplakia,)
Erythroplakia (18 %) ( Erythroplasia,)
Acroangiodermatitis (18 %) ( Acroangiodermatitis Of Mali, Mali Acroangiodermatitis, Pseudo-kaposis Sarcoma, Pseudo-kaposi Sarcoma,)
Angiolipoma (18 %)
Postherpetic Neuralgia (18 %) ( Zoster-associated Pain,)
Zoster-associated Pain (18 %) ( Postherpetic Neuralgia,)
Intravascular LargeB-cell Lymphoma (18 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Diffuse LargeB-cell Lymphoma (18 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Dermatomyositis (18 %)
Phycomycosis (18 %) ( Zygomycosis,)
Acquired Ichthyosis (18 %) ( Ichthyosis Acquisita,)
Ichthyosis Acquisita (18 %) ( Acquired Ichthyosis,)
Cryoglobulinemic Vasculitis (18 %)
Perifolliculitis Capitis Abscedens Et Suffodiens (18 %) ( Dissecting Cellulitis Of The Scalp, Dissecting Folliculitis, Perifolliculitis Capitis Abscedens Et Suffodiens Of Hoffman,)
VitaminK Deficiency (18 %)
Primary Cutaneous LargeB-cell Lymphoma (18 %) ( Diffuse LargeB-cell Lymphoma,)
Rodent Ulcer (18 %) ( Jacobi Ulcer,)
Dyshidrosis (18 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Zygomycosis (18 %) ( Phycomycosis,)
Sebaceous Epithelioma (18 %) ( Sebaceoma,)
Sebaceoma (18 %) ( Sebaceous Epithelioma,)
Lupus Erythematosus lichen Planus Overlap Syndrome (18 %) ( Lichen Planus lupus Erythematosus Overlap Syndrome,)
Calciphylaxis (18 %)
Gas Gangrene (18 %) ( Clostridial Myonecrosis, Myonecrosis,)
Capillary Hemangioma (18 %) ( Infantile Hemangioma, Nevus Maternus, Strawberry Hemangioma Strawberry Nevus,)
Primary Cutaneous Adenoid Cystic Carcinoma (18 %)
Reticulohistiocytoma (18 %)
Jacobi Ulcer (18 %) ( Rodent Ulcer,)
Lichen Planus lupus Erythematosus Overlap Syndrome (18 %) ( Lupus Erythematosus lichen Planus Overlap Syndrome,)
Phrynoderma (18 %) ( HypovitaminosisA,)
Epulis (18 %)
HypovitaminosisA (18 %) ( Phrynoderma,)
Dermatitis Repens (18 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Lymphangiomatosis (18 %)
Lipoid Proteinosis (18 %) ( Hyalinosis Cutis Et Mucosae, Urbach wiethe Disease,)
Pleomorphic Fibroma (18 %)
Bowenoid Papulosis (18 %)
Superficial Granulomatous Pyoderma (18 %)
Acanthosis Nigricans (18 %)
Wegener Granulomatosis (18 %)
Palmoplantar Pustulosis (18 %) ( Persistent Palmoplantar Pustulosis, Pustular Psoriasis Of The Barber Type, Pustular Psoriasis Of The Extremities, Pustulosis Of Palms And Soles, Pustulosis Palmaris Et Plantaris,)
Sclerotic Fibroma (18 %)
Pilar Leiomyoma (16 %) ( Multiple Cutaneous Leiomyoma,)
Basaloid Follicular Hamartoma (16 %)
Folliculosebaceous Cystic Hamartoma (16 %)
Thymoma With Immunodeficiency (16 %) ( Good Syndrome,)
Hay wells Syndrome (16 %) ( Aec Syndrome, Ankyloblepharon Filiforme Adnatum ectodermal Dysplasia cleft Palate Syndrome, Ankyloblepharon ectodermal Defects cleft Lip And Palate Syndrome, Ankyloblepharon ectodermal Dysplasia clefting Syndrome,)
Glucagonoma Syndrome (16 %) ( Necrolytic Migratory Erythema,)
Proteus Syndrome (16 %)
Primary Cutaneous Anaplastic Large Cell Lymphoma (16 %) ( Cd30+ CutaneousT-cell Lymphoma,)
Chilblains (16 %) ( Pernio, Perniosis,)
Multiple Cutaneous Leiomyoma (16 %) ( Pilar Leiomyoma,)
Pemphigus Herpetiformis (16 %) ( Acantholytic Herpetiform Dermatitis, Herpetiform Pemphigus, Mixed Bullous Disease, Pemphigus Controlled By Sulfapyridine,)
Autoimmune Polyendocrinopathy candidiasis ectodermal Dystrophy Syndrome (16 %) ( Apeced Syndrome,)
Acne Vulgaris (16 %)
Apeced Syndrome (16 %) ( Autoimmune Polyendocrinopathy candidiasis ectodermal Dystrophy Syndrome,)
Aponeurotic Fibroma (16 %) ( Calcifying Aponeurotic Fibroma, Juvenile Aponeurotic Fibroma,)
Ephelides (16 %) ( Freckles,)
Necrobiosis Lipoidica (16 %) ( Necrobiosis Lipoidica Diabeticorum,)
Necrobiosis Lipoidica Diabeticorum (16 %) ( Necrobiosis Lipoidica,)
Sebaceous Adenoma (16 %)
Noncicatricial Alopecia (16 %)
Scrofuloderma (16 %) ( Tuberculosis Cutis Colliquativa,)
Solitary Neurofibroma (16 %) ( Plexiform Neurofibroma, Solitary Nerve Sheath Tumor, Sporadic Neurofibroma,)
Dystrophic Epidermolysis Bullosa (16 %)
Pseudocyst Of The Auricle (16 %) ( Auricular Endochondrial Pseudocyst, Cystic Chondromalacia, Endochondral Pseudocyst, Intracartilaginous Cyst,)
Induratio Penis Plastica (16 %) ( Peyronies Disease,)
Peyronies Disease (16 %) ( Induratio Penis Plastica,)
Trichostasis Spinulosa (16 %)
Progeria (16 %) ( Hutchinson gilford Progeria Syndrome, Hutchinson gilford Syndrome, Progeria Syndrome,)
Neuropathic Ulcer (16 %) ( Mal Perforans,)
Mal Perforans (16 %) ( Neuropathic Ulcer,)
Aphthous Stomatitis (16 %)
Papillary Hidradenoma (16 %) ( Hidradenoma Papilliferum,)
Deep Venous Thrombosis (16 %)
Pyoderma Gangrenosum (16 %)
Epidermal Nevus Syndrome (16 %) ( Feuerstein And Mims Syndrome, Solomons Syndrome,)
Polyneuropathy organomegaly endocrinopathy monoclonal Gammopathy skin Changes Syndrome (16 %) ( Crow fukase Syndrome, Poems Syndrome,)
Generalized Pustular Psoriasis (16 %) ( Pustular Psoriasis Of Von Zumbusch,)
Mucosal Melanoma (16 %)
Angioleiomyoma (16 %) ( Vascular Leiomyoma,)
Vascular Leiomyoma (16 %) ( Angioleiomyoma,)
Thrush (16 %) ( Oral Candidiasis,)
Schimmelpenning Syndrome (16 %) ( Schimmelpenning feuerstein mims Syndrome,)
Mucinous Carcinoma (16 %)
Necrolytic Migratory Erythema (16 %) ( Glucagonoma Syndrome,)
Schimmelpenning feuerstein mims Syndrome (16 %) ( Schimmelpenning Syndrome,)
Syringomyelia (16 %) ( Morvans Disease,)
Morvans Disease (16 %) ( Syringomyelia,)
Blepharophyma (16 %)
Acid-induced (16 %)
Metophyma (16 %)
Chemical Burn (16 %)
Dysplastic Nevus Syndrome (16 %) ( B-k Mole Syndrome, Familial Atypical Multiple Mole melanoma Syndrome, Familial Melanoma Syndrome,)
Hidradenoma Papilliferum (16 %) ( Papillary Hidradenoma,)
Tubular Apocrine Adenoma (16 %) ( Papillary Eccrine Adenoma,)
Red Lunulae (16 %)
Tuberculosis Cutis Colliquativa (16 %) ( Scrofuloderma,)
Giant Cell Fibroblastoma (16 %)
Generalized Eruptive Histiocytoma (16 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Eumycetoma (16 %) ( Fungal Mycetoma,)
Good Syndrome (16 %) ( Thymoma With Immunodeficiency,)
Klippel-trenaunay-weber Syndrome (16 %)
Nodular Melanoma (16 %)
Acne Conglobata (16 %)
Freckles (16 %) ( Ephelides,)
Fabry Disease (16 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Fox fordyce Disease (16 %)
Sunburn (16 %)
Blue Nevi (16 %)
Waldenstr m Macroglobulinemia (16 %)
Erythroplasia Of Queyrat (16 %) ( Bowen Disease Of The Glans Penis,)
Acrocephalosyndactyly (16 %) ( Apert Syndrome,)
Plantar Fibromatosis (16 %) ( Ledderhoses Disease,)
Ledderhoses Disease (16 %) ( Plantar Fibromatosis,)
Microscopic Polyangiitis (16 %) ( Microscopic Polyarteritis, Microscopic Polyarteritis Nodosa,)
Pancreatic Panniculitis (16 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Otophyma (16 %)
Apert Syndrome (16 %) ( Acrocephalosyndactyly,)
Sclerosing Lipogranuloma (16 %) ( Paraffinoma,)
Papillary Eccrine Adenoma (16 %) ( Tubular Apocrine Adenoma,)
Erythema Dyschromicum Perstans (16 %) ( Ashy Dermatosis, Dermatosis Cinecienta,)
Bowen Disease Of The Glans Penis (16 %) ( Erythroplasia Of Queyrat,)
Cd30+ CutaneousT-cell Lymphoma (16 %) ( Primary Cutaneous Anaplastic Large Cell Lymphoma,)
Paraffinoma (16 %) ( Sclerosing Lipogranuloma,)
Onychomadesis (16 %)
Rams Horn Nails (16 %) ( Onychogryphosis,)
Solar Lentigo (16 %) ( Lentigo Senilis, Liver Spot, Old Age Spot, Senile Freckle,)
Onychogryphosis (16 %) ( Rams Horn Nails,)
Cheilitis Granulomatosa (16 %) ( Granulomatous Cheilitis, Orofacial Granulomatosis,)
Pressure Ulcer (16 %) ( Decubitus Ulcer,)
Molluscum Contagiosum (16 %)
Oral Candidiasis (16 %) ( Thrush,)
Fungal Mycetoma (16 %) ( Eumycetoma,)
Pseudomelanoma (16 %) ( Recurrent Melanocytic Nevus, Recurrent Nevus,)
Erythema Toxicum Neonatorum (16 %) ( Erythema Toxicum, Toxic Erythema Of The Newborn,)
Congenital Fascial Dystrophy (16 %) ( Stiff Skin Syndrome,)
Stiff Skin Syndrome (16 %) ( Congenital Fascial Dystrophy,)
Decubitus Ulcer (16 %) ( Pressure Ulcer,)

Differentials from Google.

Date Added: 2017-12-24

Basal Cell Carcinoma
Branchial Cleft Cyst
Corn
Dermatofibrosarcoma Protuberans
Dermoid Cyst

Epidermal Cyst
Epidermoid Cyst
Ganglion Cyst
Infundibular Cyst
Nodular Fasciitis
Syphilis
Trichilemmal Cyst
Trichoblastoma

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About Me

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.

Address

Bell Raj Eapen
Hamilton, ON
Canada