Differentials: Neurilemmoma

Differential diagnosis for Neurilemmoma

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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 Neurilemmoma.

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Date Added: 2018-03-07:

Schwannoma (100 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Dermatofibroma (54 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Epidermal Cyst (54 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Leiomyosarcoma (48 %)
Mixed Tumor (46 %) ( Chondroid Syringoma,)
Chondroid Syringoma (46 %) ( Mixed Tumor,)
HistiocytosisX (45 %) ( Langerhans Cell Histiocytosis,)
Neurofibromatosis Type1 (45 %) ( Von Recklinghausens Disease,)
Langerhans Cell Histiocytosis (45 %) ( HistiocytosisX,)
Von Recklinghausens Disease (45 %) ( Neurofibromatosis Type1,)
Pyogenic Granuloma (43 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Dermoid Cyst (43 %)
Lymphangiectasis (42 %) ( Lymphangioma,)
Amputation Neuroma (42 %) ( Traumatic Neuroma,)
Lymphangioma (42 %) ( Lymphangiectasis,)
Traumatic Neuroma (42 %) ( Amputation Neuroma,)
Glomus Tumor (40 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Granulocytic Sarcoma (40 %) ( Chloroma, Myeloid Sarcoma,)
Ehlers danlos Syndrome (39 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Liposarcoma (39 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Lipoma (39 %)
Angiocentric Lymphoma (39 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Hamartoma (37 %)
Malignant Chondroid Syringoma (37 %) ( Malignant Mixed Tumor,)
Fissured Tongue (37 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Malignant Peripheral Nerve Sheath Tumor (37 %) ( Malignant Schwannoma, Neurofibrosarcoma, Neurosarcoma,)
Reflex Sympathetic Dystrophy (37 %) ( Complex Regional Pain Syndrome,)
Malignant Mixed Tumor (37 %) ( Malignant Chondroid Syringoma,)
Complex Regional Pain Syndrome (37 %) ( Reflex Sympathetic Dystrophy,)
Acrospiroma (37 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Clubbing (37 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Pilomatricoma (36 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Myxoid Cyst (36 %) ( Digital Mucous Cyst, Mucous Cyst,)
Yaws (36 %) ( Bouba, Framb sie, Parangi, Pian,)
Malignant Fibrous Histiocytoma (36 %)
Giant Cell Tumor Of The Tendon Sheath (36 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Ehlers-danlos Syndrome (36 %)
Paraneoplastic Syndrome (34 %)
Mucous Cyst Of The Oral Mucosa (34 %) ( Mucocele,)
Branchial Cyst (34 %) ( Branchial Cleft Cyst,)
Cutaneous Small-vessel Vasculitis (34 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Mucocele (34 %) ( Mucous Cyst Of The Oral Mucosa,)
Angiolymphoid Hyperplasia With Eosinophilia (34 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Metastatic Carcinoma (34 %)
Teratoma (34 %)
Branchial Cleft Cyst (34 %) ( Branchial Cyst,)
Nevus Of Ota (34 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Callus (34 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Acrochordon (34 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Hidrocystoma (34 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Nevoid Basal Cell Carcinoma Syndrome (34 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Amniotic Band Syndrome (34 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Malignant Acrospiroma (34 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Carcinoid (33 %)
Tuberous Sclerosis (33 %) ( Bourneville Disease, Epiloia,)
Actinic Keratosis (33 %) ( Senile Keratosis, Solar Keratosis,)
Intravascular LargeB-cell Lymphoma (33 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Hyperparathyroidism (33 %)
Capillary Hemangioma (33 %) ( Infantile Hemangioma, Nevus Maternus, Strawberry Hemangioma Strawberry Nevus,)
Dermatofibrosarcoma Protuberans (33 %)
Malignant Pilomatricoma (33 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Nodular Fasciitis (33 %) ( Nodular Pseudosarcomatous Fasciits, Pseudosarcomatous Fasciitis, Subcutaneous Pseudosarcomatous Fibromatosis,)
Klippel trenaunay Syndrome (33 %) ( Angioosteohypertrophy Syndrome, Hemangiectatic Hypertrophy,)
Cutis Laxa (33 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Soft-tissue Melanoma (31 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Meningocele (31 %)
Zoster (31 %) ( Herpes Zoster, Shingles,)
Atypical Fibroxanthoma (31 %)
Granular Cell Tumor (31 %) ( Abrikossoffs Tumor, Abrikossovs Tumor, Granular Cell Myoblastoma, Granular Cell Nerve Sheath Tumor, Granular Cell Schwannoma,)
Polyarteritis Nodosa (31 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Carney Complex (31 %) ( Lamb Syndrome, Name Syndrome,)
Epithelioma Cuniculatum (31 %) ( Ackerman Tumor, Carcinoma Cuniculatum,)
Angioleiomyoma (31 %) ( Vascular Leiomyoma,)
Leiomyoma (31 %)
Chordoma (31 %)
Kimura Disease (31 %)
Nasal Glioma (31 %) ( Brain-like Heterotopia, Cephalic Brain-like Heterotopia, Glial Hamartoma, Heterotopic Neuroglial Tissue, Nasal Cerebral Heterotopia, Nasal Heterotopic Brain Tissue,)
Pilonidal Sinus (31 %) ( Barbers Interdigital Pilonidal Sinus, Pilonidal Cyst, Pilonidal Disease,)
Vascular Leiomyoma (31 %) ( Angioleiomyoma,)
Encephalocele (31 %)
Dermal Eccrine Cylindroma (30 %) ( Cylindroma,)
Glandular Fever (30 %) ( Infectious Mononucleosis,)
Hyperhidrosis (30 %)
Infectious Mononucleosis (30 %) ( Glandular Fever,)
Takayasu Arteritis (30 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Mccune albright Syndrome (30 %)
Spiradenoma (30 %)
Cylindroma (30 %) ( Dermal Eccrine Cylindroma,)
Sarcoidosis (30 %)
Plasmacytoma (30 %)
Tic Douloureux (30 %) ( Trigeminal Neuralgia,)
Trigeminal Neuralgia (30 %) ( Tic Douloureux,)
Congenital Melanocytic Nevus (30 %)
External Otitis (30 %) ( Otitis Externa, Swimmers Ear,)
North American Blastomycosis (30 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Multiple Endocrine Neoplasia Type2 (30 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Verruca Vulgaris (30 %) ( Wart,)
Wart (30 %) ( Verruca Vulgaris,)
Ganglion Cyst (30 %)
Nevus Flammeus (30 %) ( Capillary Malformation, Port-wine Stain,)
Neurothekeoma (30 %) ( Bizarre Cutaneous Neurofibroma, Cutaneous Lobular Neuromyxoma, Myxoma Of The Nerve Sheath, Myxomatous Perineurioma, Nerve Sheath Myxoma,)
Blue Nevus (28 %) ( Blue Neuronevus, Dermal Melanocytoma, Nevus Bleu,)
Eosinophilic Granuloma (28 %)
Panhypopituitarism (28 %)
Thyroglossal Duct Cyst (28 %)
Rosai dorfman Disease (28 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Cutaneous Lymphoid Hyperplasia (28 %) ( 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,)
Merkel Cell Carcinoma (28 %) ( Cutaneous Apudoma, Primary Neuroendocrine Carcinoma Of The Skin, Primary Small Cell Carcinoma Of The Skin, Trabecular Carcinoma Of The Skin,)
Connective Tissue Nevus (28 %) ( Collagenoma, Elastoma, Shagreen Patch,)
Aggressive Digital Papillary Adenocarcinoma (28 %) ( Digital Papillary Adenocarcinoma, Papillary Adenoma,)
Solitary Keratoacanthoma (28 %) ( Subungual Keratoacanthoma,)
Sebaceous Carcinoma (28 %)
Pachydermoperiostosis (28 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Recurrent Aphthous Stomatitis (28 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Proliferating Trichilemmal Cyst (28 %) ( Pilar Tumor, Proliferating Follicular Cystic Neoplasm, Proliferating Pilar Tumor, Proliferating Trichilemmal Tumor,)
Mucosa-associated Lymphoid Tissue Lymphoma (28 %)
Subungual Keratoacanthoma (28 %) ( Solitary Keratoacanthoma,)
Sinus Histiocytosis With Massive Lymphadenopathy (28 %) ( Rosai dorfman Disease,)
Marfan Syndrome (28 %)
Histoplasmosis (28 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Anhidrosis (28 %) ( Hypohidrosis,)
Hypohidrosis (28 %) ( Anhidrosis,)
Acne Rosacea (28 %) ( Rosacea,)
Mycetoma (28 %) ( Madura Foot, Maduromycosis,)
Rosacea (28 %) ( Acne Rosacea,)
Solitary Neurofibroma (28 %) ( Plexiform Neurofibroma, Solitary Nerve Sheath Tumor, Sporadic Neurofibroma,)
Juvenile Xanthogranuloma (28 %)
Coccidioidomycosis (28 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Spindle Cell Carcinoma (28 %) ( Spindle Cell Squamous Cell Carcinoma,)
Intravascular Papillary Endothelial Hyperplasia (28 %) ( Massons Hemangio-endotheliome Vegetant Intravasculaire, Massons Lesion, Massons Pseudoangiosarcoma, Massons Tumor, Papillary Endothelial Hyperplasia,)
Spindle Cell Squamous Cell Carcinoma (28 %) ( Spindle Cell Carcinoma,)
Lupus Erythematosus Panniculitis (28 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Cutaneous Leishmaniasis (27 %) ( Aleppo Boil, Baghdad Boil, Bay Sore, Biskra Button, Chiclero Ulcer, Delhi Boil, Kandahar Sore, Lahore Sore, Leishmaniasis Tropica, Oriental Sore, Pian Bois, Uta,)
Hydatid Disease (27 %) ( Echinococcosis,)
Coccidioidal Granuloma (27 %) ( Disseminated Coccidioidomycosis,)
Echinococcosis (27 %) ( Hydatid Disease,)
Multiple Familial Trichoepithelioma (27 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Letterer siwe Disease (27 %)
Hypoparathyroidism (27 %)
Disseminated Coccidioidomycosis (27 %) ( Coccidioidal Granuloma,)
Leukonychia (27 %) ( White Nails,)
Postoperative Hematoma (27 %)
Melanocytic Nevi (27 %)
Foreign Body Reaction (27 %)
Deep Venous Thrombosis (27 %)
Apert Syndrome (27 %) ( Acrocephalosyndactyly,)
Bronchogenic Cyst (27 %)
Spitz Nevus (27 %) ( Benign Juvenile Melanoma, Epithelioid And Spindle Cell Nevus, Spitzs Juvenile Melanoma,)
Epithelioid Sarcoma (27 %)
Neurofibromatosis Type2 (27 %)
Systemic Sarcoidosis (27 %)
White Nails (27 %) ( Leukonychia,)
Acrocephalosyndactyly (27 %) ( Apert Syndrome,)
Polyneuropathy organomegaly endocrinopathy monoclonal Gammopathy skin Changes Syndrome (27 %) ( Crow fukase Syndrome, Poems Syndrome,)
Infantile Myofibromatosis (27 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Juvenile Rheumatoid Arthritis (27 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Sj grens Syndrome (27 %) ( Mikulicz Disease, Sicca Syndrome,)
Marginal ZoneB-cell Lymphoma (25 %)
Segmental Neurofibromatosis (25 %)
Subcutaneous Emphysema (25 %)
Reticulohistiocytoma (25 %)
Chondrodermatitis Nodularis Helicis (25 %) ( Chondrodermatitis Nodularis Chronica Helicis,)
Hidradenocarcinoma (25 %)
Relapsing Polychondritis (25 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Multiple Endocrine Neoplasia Type3 (25 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
Ledderhoses Disease (25 %) ( Plantar Fibromatosis,)
Verrucous Carcinoma (25 %)
Duhring Disease (25 %) ( Dermatitis Herpetiformis,)
Nail patella Syndrome (25 %) ( Fong Syndrome, Hereditary Osteoonychodysplasia, Hood Syndrome,)
Giant Pigmented Nevus (25 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Chondrodermatitis Nodularis Chronica Helicis (25 %) ( Chondrodermatitis Nodularis Helicis,)
Syringoma (25 %)
Herpes Simplex (25 %)
Chickenpox (25 %) ( Varicella,)
Angiosarcoma (25 %)
Plantar Fibromatosis (25 %) ( Ledderhoses Disease,)
Ganglioneuroma (25 %)
Sparganosis (25 %)
Dermatitis Herpetiformis (25 %) ( Duhring Disease,)
Desmoplastic Melanoma (25 %) ( Neurotropic Melanoma, Spindled Melanoma,)
Triangular Alopecia (25 %) ( Temporal Alopecia, Temporal Triangular Alopecia,)
Keratocyst (25 %)
Acute Febrile Neutrophilic Dermatosis (25 %) ( Sweets Syndrome,)
Mucinous Carcinoma (25 %)
Actinomycosis (25 %)
Formaldehyde-induced (25 %)
Toxoplasmosis (25 %)
Varicella (25 %) ( Chickenpox,)
Angiokeratoma (24 %)
Lichen Sclerosus Et Atrophicus (24 %) ( Lichen Sclerosus,)
VitaminK Deficiency (24 %)
Cat Scratch Disease (24 %) ( Cat Scratch Fever, English wear Infection, Inoculation Lymphoreticulosis, Subacute Regional Lymphadenitis,)
Cicatricial Pemphigoid (24 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Benign Melanocytic Nevus (24 %) ( Banal Nevus, Common Acquired Melanocytic Nevus, Mole, Nevocellular Nevus, Nevocytic Nevus,)
Lichen Sclerosus (24 %) ( Lichen Sclerosus Et Atrophicus,)
Erythema Induratum (24 %) ( Bazin Disease, Nodular Vasculitis,)
Cutaneous Melanoma (24 %)
Tufted Angioma (24 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Hemangiopericytoma (24 %)
Morvans Disease (24 %) ( Syringomyelia,)
Hemangiosarcoma (24 %)
Familial Dysautonomia (24 %) ( Riley day Syndrome,)
Basal Cell Carcinoma (24 %)
Angioedema (24 %)
Focal Dermal Hypoplasia (24 %) ( Goltz Syndrome,)
Turner Syndrome (24 %)
Klippel feil Syndrome (24 %)
Syringomyelia (24 %) ( Morvans Disease,)
Pancreatic Panniculitis (24 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Hand sch ller christian Disease (24 %)
Goltz Syndrome (24 %) ( Focal Dermal Hypoplasia,)
Neuroblastoma (24 %) ( Infantile Neuroblastoma, Neuroepithelioma,)
Riley day Syndrome (24 %) ( Familial Dysautonomia,)
Hidradenoma (24 %)
Peutz jeghers Syndrome (24 %)
Basaloid Squamous Cell Carcinoma (24 %)
Extramammary Paget Disease (24 %)
Wiskott aldrich Syndrome (22 %)
Telangiectasia (22 %)
Palmoplantar Keratoderma (22 %)
Solar Elastosis (22 %) ( Actinic Elastosis,)
Hyper-ige Syndrome (22 %) ( Buckley Syndrome, Job Syndrome,)
Rhinophyma (22 %)
Uveal Melanoma (22 %)
VitaminB1 Deficiency (22 %) ( Beriberi, Thiamine Deficiency,)
Oral Candidiasis (22 %) ( Thrush,)
Spoon Nails (22 %) ( Koilonychia,)
Thrush (22 %) ( Oral Candidiasis,)
Madarosis (22 %)
Flesh-eating Bacteria Syndrome (22 %) ( Necrotizing Fasciitis,)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (22 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
Multiple Endocrine Neoplasia Type1 (22 %) ( Wermer Syndrome,)
Hyperthyroidism (22 %)
Malacoplakia (22 %) ( Malakoplakia,)
Necrotizing Fasciitis (22 %) ( Flesh-eating Bacteria Syndrome,)
Wermer Syndrome (22 %) ( Multiple Endocrine Neoplasia Type1,)
Koilonychia (22 %) ( Spoon Nails,)
Familial Mediterranean Fever (22 %)
Mucosal Melanoma (22 %)
Henoch Schonlein Purpura (22 %)
Fabry Disease (22 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Sinus Pericranii (22 %)
Leukoplakia (22 %)
Maffucci Syndrome (22 %)
Waldenstr m Macroglobulinemia (22 %)
Giant Condyloma Acuminatum (22 %) ( Buschke l wenstein Tumor, Giant Condyloma Of Buschke l wenstein Tumor,)
Scleroderma (22 %)
Actinic Elastosis (22 %) ( Solar Elastosis,)
Smooth Tongue (22 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Churg strauss Syndrome (22 %) ( Allergic Granulomatosis,)
Costello Syndrome (22 %)
Allergic Granulomatosis (22 %) ( Churg strauss Syndrome,)
Malakoplakia (22 %) ( Malacoplakia,)
Klippel-trenaunay-weber Syndrome (22 %)
Multicentric Reticulohistiocytosis (22 %)
Epidermal Nevus Syndrome (22 %) ( Feuerstein And Mims Syndrome, Solomons Syndrome,)
Microcystic Adnexal Carcinoma (22 %) ( Sclerosing Sweat Duct Carcinoma,)
Juvenile Myelomonocytic Leukemia (22 %)
Glossodynia (22 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Sclerosing Sweat Duct Carcinoma (22 %) ( Microcystic Adnexal Carcinoma,)
Primary Cutaneous Adenoid Cystic Carcinoma (22 %)
Sweets Syndrome (22 %) ( Acute Febrile Neutrophilic Dermatosis,)
Diffuse LargeB-cell Lymphoma (22 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Primary Cutaneous LargeB-cell Lymphoma (22 %) ( Diffuse LargeB-cell Lymphoma,)
Nevus Sebaceous (21 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Dercums Disease (21 %) ( Adiposis Dolorosa,)
Multiple Pterygium Syndrome (21 %)
Diffuse Sclerosis (21 %)
Eosinophilic Cellulitis (21 %) ( Wells Syndrome,)
Geographic Tongue (21 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Jacobi Ulcer (21 %) ( Rodent Ulcer,)
Rhinosporidiosis (21 %)
Decubitus Ulcer (21 %) ( Pressure Ulcer,)
Postmastectomy Lymphangiosarcoma (21 %) ( Stewart treves Syndrome,)
Herpes Zoster Oticus (21 %) ( Ramsay hunt Syndrome,)
Radiodermatitis (21 %) ( Radiation Dermatitis,)
Delusional Parasitosis (21 %) ( Delusions Of Parasitosis, Ekbom Syndrome, Monosymptomatic Hypochondriacal Psychosis,)
Limbal Dermoid (21 %)
Malignant Histiocytosis (21 %) ( Histiocytic Medullary Reticulosis,)
Pressure Ulcer (21 %) ( Decubitus Ulcer,)
Lymphangioma Circumscriptum (21 %) ( Superficial Lymphatic Malformation,)
Keloid (21 %) ( Keloidal Scar,)
Dermatitis Repens (21 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
SubcutaneousT-cell Lymphoma (21 %) ( Panniculitis-likeT-cell Lymphoma,)
Wells Syndrome (21 %) ( Eosinophilic Cellulitis,)
Ramsay hunt Syndrome (21 %) ( Herpes Zoster Oticus,)
Moschcowitz Syndrome (21 %) ( Thrombotic Thrombocytopenic Purpura,)
Stasis Dermatitis (21 %) ( Congestion Eczema, Gravitational Dermatitis, Gravitational Eczema, Stasis Eczema, Varicose Eczema,)
Stewart treves Syndrome (21 %) ( Postmastectomy Lymphangiosarcoma,)
Rodent Ulcer (21 %) ( Jacobi Ulcer,)
Secondary Lymphedema (21 %)
Familial Cold Urticaria (21 %) ( Familial Cold Autoinflammatory Syndrome,)
Radiation Dermatitis (21 %) ( Radiodermatitis,)
Seborrheic Keratosis (21 %) ( Seborrheic Verruca, Senile Wart,)
Giant-cell Arteritis (21 %)
Keloidal Scar (21 %) ( Keloid,)
Familial Cold Autoinflammatory Syndrome (21 %) ( Familial Cold Urticaria,)
Parry romberg Syndrome (21 %) ( Progressive Hemifacial Atrophy,)
Trigeminal Trophic Lesion (21 %) ( Trigeminal Trophic Syndrome,)
Histiocytic Medullary Reticulosis (21 %) ( Malignant Histiocytosis,)
Progressive Hemifacial Atrophy (21 %) ( Parry romberg Syndrome,)
Acquired Hypogammaglobulinemia (21 %) ( Common Variable Immunodeficiency,)
Mondor Disease (21 %)
Immune Reconstitution Inflammatory Syndrome (21 %) ( Immune Recovery Syndrome,)
Thrombotic Thrombocytopenic Purpura (21 %) ( Moschcowitz Syndrome,)
Immune Recovery Syndrome (21 %) ( Immune Reconstitution Inflammatory Syndrome,)
Fibrinolysis Syndrome (21 %) ( Defibrinating Syndrome, Hypofibrinogenemia,)
Rheumatoid Arthritis (21 %)
Dysplastic Nevus Syndrome (21 %) ( B-k Mole Syndrome, Familial Atypical Multiple Mole melanoma Syndrome, Familial Melanoma Syndrome,)
Melanotic Neuroectodermal Tumor Of Infancy (21 %)
Miliary Tuberculosis (21 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Dental Sinus (21 %) ( Cutaneous Sinus Of Dental Origin,)
Cutaneous Sinus Of Dental Origin (21 %) ( Dental Sinus,)
Nevus Spilus (21 %) ( Speckled Lentiginous Nevus, Zosteriform Lentiginous Nevus,)
Lentigo Maligna (21 %) ( Lentiginous Melanoma On Sun-damaged Skin,)
Tumor Lysis Syndrome (21 %)
Superficial Lymphatic Malformation (21 %) ( Lymphangioma Circumscriptum,)
Desmoid Tumor (21 %)
Adiposis Dolorosa (21 %) ( Dercums Disease,)
Thrombophlebitis (21 %)
Superficial Thrombophlebitis (21 %)
Panniculitis-likeT-cell Lymphoma (21 %) ( SubcutaneousT-cell Lymphoma,)
Common Variable Immunodeficiency (21 %) ( Acquired Hypogammaglobulinemia,)
Trigeminal Trophic Syndrome (21 %) ( Trigeminal Trophic Lesion,)
Proteus Syndrome (21 %)
Lymphangiectasia (21 %)
Lentiginous Melanoma On Sun-damaged Skin (21 %) ( Lentigo Maligna,)
Acanthosis Nigricans (21 %)
Temporal Arteritis (21 %) ( Cranial Arteritis, Hortons Disease,)
Alopecia Neoplastica (21 %)
Hidradenitis Suppurativa (21 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Apocrine Hidrocystoma (21 %)
Subungual Exostosis (21 %)
Bronze Diabetes (19 %) ( Hemochromatosis,)
Erythema Nodosum (19 %)
Piloleiomyoma (19 %)
Aplasia Cutis Congenita (19 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Traumatic Alopecia (19 %)
Muir-torre Syndrome (19 %)
Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome (19 %) ( Sapho Syndrome,)
Orofaciodigital Syndrome (19 %)
HypovitaminosisA (19 %) ( Phrynoderma,)
Longitudinal Erythronychia (19 %)
Phrynoderma (19 %) ( HypovitaminosisA,)
Mucosal Squamous Cell Carcinoma (19 %)
Blau Syndrome (19 %)
Stevens johnson Syndrome (19 %)
Sapho Syndrome (19 %) ( Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome,)
Lobstein Syndrome (19 %) ( Osteogenesis Imperfecta,)
Lentigo Maligna Melanoma (19 %)
Infantile Hemangiopericytoma (19 %) ( Congenital Hemangiopericytoma,)
Zinsser cole engman Syndrome (19 %) ( Dyskeratosis Congenita,)
Squamous Cell Carcinoma In Situ (19 %) ( Bowens Disease,)
Adrenal Adenoma (19 %)
Bowens Disease (19 %) ( Squamous Cell Carcinoma In Situ,)
Generalized Eruptive Histiocytoma (19 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Dyskeratosis Congenita (19 %) ( Zinsser cole engman Syndrome,)
Angiolipoma (19 %)
Digeorge Syndrome (19 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Onychocryptosis (19 %) ( Ingrown Nail, Unguis Incarnatus,)
Septic Thrombophlebitis (19 %)
Pemphigus Vulgaris (19 %)
Phycomycosis (19 %) ( Zygomycosis,)
Spindle Cell Lipoma (19 %)
Albrights Disease (19 %) ( Polyostotic Fibrous Dysplasia,)
Psoriatic Arthritis (19 %)
Sciatic Nerve Injury (19 %)
Congenital Hemangiopericytoma (19 %) ( Infantile Hemangiopericytoma,)
Glanders (19 %) ( Equinia, Farcy, Malleus,)
Raynaud Phenomenon (19 %)
Pseudomelanoma (19 %) ( Recurrent Melanocytic Nevus, Recurrent Nevus,)
Acral Lentiginous Melanoma (19 %)
Subcutaneous Granuloma Annulare (19 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Isthmicoma (19 %) ( Infundibuloma, Tumor Of The Follicular Infundibulum,)
Dysplastic Nevus (19 %) ( Atypical Mole, Atypical Nevus, B-k Mole, Clarks Nevus, Dysplastic Melanocytic Nevus, Nevus With Architectural Disorder,)
Mycosis Fungoides (19 %)
Leukocytoclastic Vasculitis (19 %)
Ephelides (19 %) ( Freckles,)
Superficial Spreading Melanoma (19 %) ( Superficially Spreading Melanoma,)
Superficially Spreading Melanoma (19 %) ( Superficial Spreading Melanoma,)
Severe Combined Immunodeficiency (19 %) ( Alymphocytosis, Glanzmann riniker Syndrome, Severe Mixed Immunodeficiency Syndrome, Thymic Alymphoplasia,)
Postherpetic Neuralgia (19 %) ( Zoster-associated Pain,)
Generalized Pustular Psoriasis (19 %) ( Pustular Psoriasis Of Von Zumbusch,)
Pseudoglandular Squamous Cell Carcinoma (19 %) ( Adenoid Squamous Cell Carcinoma,)
Zoster-associated Pain (19 %) ( Postherpetic Neuralgia,)
Zoster Sine Herpete (19 %)
Lupus Pernio (19 %)
Cutaneous Focal Mucinosis (19 %)
Leukemia Cutis (19 %)
Cartilage hair Hypoplasia (19 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Pleomorphic Lipoma (19 %)
Pyomyositis (19 %)
Adenoid Squamous Cell Carcinoma (19 %) ( Pseudoglandular Squamous Cell Carcinoma,)
Cardio-facio-cutaneous Syndrome (19 %) ( Cardiofaciocutaneous Syndrome,)
Keratoacanthoma (19 %)
Muir torre Syndrome (19 %)
Congenital Nevi (19 %)
Papillary Hidradenoma (19 %) ( Hidradenoma Papilliferum,)
Mckusick Type Metaphyseal Chondrodysplasia (19 %) ( Cartilage hair Hypoplasia,)
Crouzon Syndrome (19 %)
VitaminC Deficiency (19 %) ( Scurvy,)
Acute Necrotizing Ulcerative Gingivitis (19 %) ( 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,)
Tnf Receptor Associated Periodic Syndrome (19 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Plexiform Fibrohistiocytic Tumor (19 %)
Scurvy (19 %) ( VitaminC Deficiency,)
Hereditary Hemorrhagic Telangiectasia (19 %) ( Oslers Disease, Osler weber rendu Disease,)
Cardiofaciocutaneous Syndrome (19 %) ( Cardio-facio-cutaneous Syndrome,)
Lymphangiomatosis (19 %)
Linear Verrucous Epidermal Nevus (19 %) ( Linear Epidermal Nevus, Verrucous Epidermal Nevus,)
Sunburn (19 %)
Freckles (19 %) ( Ephelides,)
Zygomycosis (19 %) ( Phycomycosis,)
Kikuchis Disease (19 %) ( Histiocytic Necrotizing Lymphadenitis,)
Tyrosinemia Type Ii (19 %) ( Oculocutaneous Tyrosinemia, Richner hanhart Syndrome,)
Histiocytic Necrotizing Lymphadenitis (19 %) ( Kikuchis Disease,)
Polyostotic Fibrous Dysplasia (19 %) ( Albrights Disease,)
Angiofibroma (19 %)
Hidradenoma Papilliferum (19 %) ( Papillary Hidradenoma,)
Hemochromatosis (19 %) ( Bronze Diabetes,)
Osteogenesis Imperfecta (19 %) ( Lobstein Syndrome,)

Differentials from Google.

Date Added: 2018-02-10


Neurilemmoma
Schwannoma

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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.

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