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: 2017-03-08:

Schwannoma (100 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Dermatofibroma (53 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Epidermal Cyst (53 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Leiomyosarcoma (47 %)
Chondroid Syringoma (47 %) ( Mixed Tumor,)
Mixed Tumor (47 %) ( Chondroid Syringoma,)
Von Recklinghausens Disease (44 %) ( Neurofibromatosis Type1,)
Langerhans Cell Histiocytosis (44 %) ( HistiocytosisX,)
Pyogenic Granuloma (44 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
HistiocytosisX (44 %) ( Langerhans Cell Histiocytosis,)
Neurofibromatosis Type1 (44 %) ( Von Recklinghausens Disease,)
Dermoid Cyst (42 %)
Traumatic Neuroma (41 %) ( Amputation Neuroma,)
Lymphangioma (41 %) ( Lymphangiectasis,)
Amputation Neuroma (41 %) ( Traumatic Neuroma,)
Lymphangiectasis (41 %) ( Lymphangioma,)
Granulocytic Sarcoma (39 %) ( Chloroma, Myeloid Sarcoma,)
Glomus Tumor (39 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Liposarcoma (39 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Malignant Chondroid Syringoma (38 %) ( Malignant Mixed Tumor,)
Angiocentric Lymphoma (38 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Malignant Mixed Tumor (38 %) ( Malignant Chondroid Syringoma,)
Acrospiroma (38 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Lipoma (38 %)
Ehlers danlos Syndrome (38 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Complex Regional Pain Syndrome (36 %) ( Reflex Sympathetic Dystrophy,)
Reflex Sympathetic Dystrophy (36 %) ( Complex Regional Pain Syndrome,)
Malignant Peripheral Nerve Sheath Tumor (36 %) ( Malignant Schwannoma, Neurofibrosarcoma, Neurosarcoma,)
Fissured Tongue (36 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Hamartoma (36 %)
Clubbing (36 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Pilomatricoma (36 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Teratoma (35 %)
Branchial Cyst (35 %) ( Branchial Cleft Cyst,)
Mucous Cyst Of The Oral Mucosa (35 %) ( Mucocele,)
Nevoid Basal Cell Carcinoma Syndrome (35 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Ehlers-danlos Syndrome (35 %)
Malignant Acrospiroma (35 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Yaws (35 %) ( Bouba, Framb sie, Parangi, Pian,)
Giant Cell Tumor Of The Tendon Sheath (35 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Hidrocystoma (35 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Myxoid Cyst (35 %) ( Digital Mucous Cyst, Mucous Cyst,)
Mucocele (35 %) ( Mucous Cyst Of The Oral Mucosa,)
Cutaneous Small-vessel Vasculitis (35 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Malignant Fibrous Histiocytoma (35 %)
Branchial Cleft Cyst (35 %) ( Branchial Cyst,)
Nevus Of Ota (33 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Intravascular LargeB-cell Lymphoma (33 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Dermatofibrosarcoma Protuberans (33 %)
Paraneoplastic Syndrome (33 %)
Nodular Fasciitis (33 %) ( Nodular Pseudosarcomatous Fasciits, Pseudosarcomatous Fasciitis, Subcutaneous Pseudosarcomatous Fibromatosis,)
Angiolymphoid Hyperplasia With Eosinophilia (33 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Cutis Laxa (33 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Callus (33 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Tuberous Sclerosis (33 %) ( Bourneville Disease, Epiloia,)
Acrochordon (33 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Malignant Pilomatricoma (33 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Amniotic Band Syndrome (33 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Metastatic Carcinoma (33 %)
Encephalocele (32 %)
Capillary Hemangioma (32 %) ( Infantile Hemangioma, Nevus Maternus, Strawberry Hemangioma Strawberry Nevus,)
Klippel trenaunay Syndrome (32 %) ( Angioosteohypertrophy Syndrome, Hemangiectatic Hypertrophy,)
Kimura Disease (32 %)
Nasal Glioma (32 %) ( Brain-like Heterotopia, Cephalic Brain-like Heterotopia, Glial Hamartoma, Heterotopic Neuroglial Tissue, Nasal Cerebral Heterotopia, Nasal Heterotopic Brain Tissue,)
Atypical Fibroxanthoma (32 %)
Carcinoid (32 %)
Soft-tissue Melanoma (32 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Actinic Keratosis (32 %) ( Senile Keratosis, Solar Keratosis,)
Epithelioma Cuniculatum (32 %) ( Ackerman Tumor, Carcinoma Cuniculatum,)
Hyperparathyroidism (32 %)
Polyarteritis Nodosa (30 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Neurothekeoma (30 %) ( Bizarre Cutaneous Neurofibroma, Cutaneous Lobular Neuromyxoma, Myxoma Of The Nerve Sheath, Myxomatous Perineurioma, Nerve Sheath Myxoma,)
Carney Complex (30 %) ( Lamb Syndrome, Name Syndrome,)
Wart (30 %) ( Verruca Vulgaris,)
Dermal Eccrine Cylindroma (30 %) ( Cylindroma,)
Verruca Vulgaris (30 %) ( Wart,)
Cylindroma (30 %) ( Dermal Eccrine Cylindroma,)
Multiple Endocrine Neoplasia Type2 (30 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Meningocele (30 %)
Congenital Melanocytic Nevus (30 %)
Chordoma (30 %)
Pilonidal Sinus (30 %) ( Barbers Interdigital Pilonidal Sinus, Pilonidal Cyst, Pilonidal Disease,)
Leiomyoma (30 %)
Angioleiomyoma (30 %) ( Vascular Leiomyoma,)
Granular Cell Tumor (30 %) ( Abrikossoffs Tumor, Abrikossovs Tumor, Granular Cell Myoblastoma, Granular Cell Nerve Sheath Tumor, Granular Cell Schwannoma,)
Vascular Leiomyoma (30 %) ( Angioleiomyoma,)
Juvenile Xanthogranuloma (29 %)
Solitary Neurofibroma (29 %) ( Plexiform Neurofibroma, Solitary Nerve Sheath Tumor, Sporadic Neurofibroma,)
Sebaceous Carcinoma (29 %)
Thyroglossal Duct Cyst (29 %)
Proliferating Trichilemmal Cyst (29 %) ( Pilar Tumor, Proliferating Follicular Cystic Neoplasm, Proliferating Pilar Tumor, Proliferating Trichilemmal Tumor,)
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,)
Spiradenoma (29 %)
Plasmacytoma (29 %)
Mccune albright Syndrome (29 %)
Hyperhidrosis (29 %)
Tic Douloureux (29 %) ( Trigeminal Neuralgia,)
Infectious Mononucleosis (29 %) ( Glandular Fever,)
Glandular Fever (29 %) ( Infectious Mononucleosis,)
Connective Tissue Nevus (29 %) ( Collagenoma, Elastoma, Shagreen Patch,)
Zoster (29 %) ( Herpes Zoster, Shingles,)
Aggressive Digital Papillary Adenocarcinoma (29 %) ( Digital Papillary Adenocarcinoma, Papillary Adenoma,)
Trigeminal Neuralgia (29 %) ( Tic Douloureux,)
Sinus Histiocytosis With Massive Lymphadenopathy (29 %) ( Rosai dorfman Disease,)
External Otitis (29 %) ( Otitis Externa, Swimmers Ear,)
North American Blastomycosis (29 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Nevus Flammeus (29 %) ( Capillary Malformation, Port-wine Stain,)
Spindle Cell Squamous Cell Carcinoma (29 %) ( Spindle Cell Carcinoma,)
Spindle Cell Carcinoma (29 %) ( Spindle Cell Squamous Cell Carcinoma,)
Rosai dorfman Disease (29 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Ganglion Cyst (29 %)
Merkel Cell Carcinoma (29 %) ( Cutaneous Apudoma, Primary Neuroendocrine Carcinoma Of The Skin, Primary Small Cell Carcinoma Of The Skin, Trabecular Carcinoma Of The Skin,)
Sarcoidosis (29 %)
Blue Nevus (29 %) ( Blue Neuronevus, Dermal Melanocytoma, Nevus Bleu,)
Mucosa-associated Lymphoid Tissue Lymphoma (29 %)
Coccidioidomycosis (29 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Takayasu Arteritis (29 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Systemic Sarcoidosis (27 %)
Multiple Familial Trichoepithelioma (27 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Solitary Keratoacanthoma (27 %) ( Subungual Keratoacanthoma,)
Mycetoma (27 %) ( Madura Foot, Maduromycosis,)
Apert Syndrome (27 %) ( Acrocephalosyndactyly,)
Melanocytic Nevi (27 %)
Histoplasmosis (27 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Spitz Nevus (27 %) ( Benign Juvenile Melanoma, Epithelioid And Spindle Cell Nevus, Spitzs Juvenile Melanoma,)
Letterer siwe Disease (27 %)
Hypohidrosis (27 %) ( Anhidrosis,)
Anhidrosis (27 %) ( Hypohidrosis,)
Disseminated Coccidioidomycosis (27 %) ( Coccidioidal Granuloma,)
Neurofibromatosis Type2 (27 %)
Acrocephalosyndactyly (27 %) ( Apert Syndrome,)
Pachydermoperiostosis (27 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Intravascular Papillary Endothelial Hyperplasia (27 %) ( Massons Hemangio-endotheliome Vegetant Intravasculaire, Massons Lesion, Massons Pseudoangiosarcoma, Massons Tumor, Papillary Endothelial Hyperplasia,)
Marfan Syndrome (27 %)
Coccidioidal Granuloma (27 %) ( Disseminated Coccidioidomycosis,)
Polyneuropathy organomegaly endocrinopathy monoclonal Gammopathy skin Changes Syndrome (27 %) ( Crow fukase Syndrome, Poems Syndrome,)
Subungual Keratoacanthoma (27 %) ( Solitary Keratoacanthoma,)
Acne Rosacea (27 %) ( Rosacea,)
Lupus Erythematosus Panniculitis (27 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Epithelioid Sarcoma (27 %)
Infantile Myofibromatosis (27 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Rosacea (27 %) ( Acne Rosacea,)
Panhypopituitarism (27 %)
Eosinophilic Granuloma (27 %)
Recurrent Aphthous Stomatitis (27 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Giant Pigmented Nevus (26 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Bronchogenic Cyst (26 %)
Echinococcosis (26 %) ( Hydatid Disease,)
Segmental Neurofibromatosis (26 %)
Juvenile Rheumatoid Arthritis (26 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Nail patella Syndrome (26 %) ( Fong Syndrome, Hereditary Osteoonychodysplasia, Hood Syndrome,)
Foreign Body Reaction (26 %)
Multiple Endocrine Neoplasia Type3 (26 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
Deep Venous Thrombosis (26 %)
Triangular Alopecia (26 %) ( Temporal Alopecia, Temporal Triangular Alopecia,)
Reticulohistiocytoma (26 %)
Leukonychia (26 %) ( White Nails,)
Keratocyst (26 %)
Angiosarcoma (26 %)
Syringoma (26 %)
Hidradenocarcinoma (26 %)
Mucinous Carcinoma (26 %)
Verrucous Carcinoma (26 %)
Hydatid Disease (26 %) ( Echinococcosis,)
Postoperative Hematoma (26 %)
Cutaneous Leishmaniasis (26 %) ( Aleppo Boil, Baghdad Boil, Bay Sore, Biskra Button, Chiclero Ulcer, Delhi Boil, Kandahar Sore, Lahore Sore, Leishmaniasis Tropica, Oriental Sore, Pian Bois, Uta,)
Toxoplasmosis (26 %)
Marginal ZoneB-cell Lymphoma (26 %)
Desmoplastic Melanoma (26 %) ( Neurotropic Melanoma, Spindled Melanoma,)
Sj grens Syndrome (26 %) ( Mikulicz Disease, Sicca Syndrome,)
White Nails (26 %) ( Leukonychia,)
Hypoparathyroidism (26 %)
Peutz jeghers Syndrome (24 %)
Ledderhoses Disease (24 %) ( Plantar Fibromatosis,)
Hand sch ller christian Disease (24 %)
Extramammary Paget Disease (24 %)
Varicella (24 %) ( Chickenpox,)
Dermatitis Herpetiformis (24 %) ( Duhring Disease,)
Subcutaneous Emphysema (24 %)
Herpes Simplex (24 %)
Sparganosis (24 %)
Chondrodermatitis Nodularis Helicis (24 %) ( Chondrodermatitis Nodularis Chronica Helicis,)
Chondrodermatitis Nodularis Chronica Helicis (24 %) ( Chondrodermatitis Nodularis Helicis,)
Benign Melanocytic Nevus (24 %) ( Banal Nevus, Common Acquired Melanocytic Nevus, Mole, Nevocellular Nevus, Nevocytic Nevus,)
Formaldehyde-induced (24 %)
Neuroblastoma (24 %) ( Infantile Neuroblastoma, Neuroepithelioma,)
Duhring Disease (24 %) ( Dermatitis Herpetiformis,)
Chickenpox (24 %) ( Varicella,)
Basaloid Squamous Cell Carcinoma (24 %)
Acute Febrile Neutrophilic Dermatosis (24 %) ( Sweets Syndrome,)
Tufted Angioma (24 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Focal Dermal Hypoplasia (24 %) ( Goltz Syndrome,)
Plantar Fibromatosis (24 %) ( Ledderhoses Disease,)
Hidradenoma (24 %)
VitaminK Deficiency (24 %)
Hemangiopericytoma (24 %)
Hemangiosarcoma (24 %)
Actinomycosis (24 %)
Basal Cell Carcinoma (24 %)
Ganglioneuroma (24 %)
Relapsing Polychondritis (24 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Cutaneous Melanoma (24 %)
Goltz Syndrome (24 %) ( Focal Dermal Hypoplasia,)
Microcystic Adnexal Carcinoma (23 %) ( Sclerosing Sweat Duct Carcinoma,)
Wermer Syndrome (23 %) ( Multiple Endocrine Neoplasia Type1,)
Lichen Sclerosus (23 %) ( Lichen Sclerosus Et Atrophicus,)
Epidermal Nevus Syndrome (23 %) ( Feuerstein And Mims Syndrome, Solomons Syndrome,)
Cat Scratch Disease (23 %) ( Cat Scratch Fever, English wear Infection, Inoculation Lymphoreticulosis, Subacute Regional Lymphadenitis,)
Juvenile Myelomonocytic Leukemia (23 %)
Mucosal Melanoma (23 %)
Sinus Pericranii (23 %)
Leukoplakia (23 %)
Lichen Sclerosus Et Atrophicus (23 %) ( Lichen Sclerosus,)
Diffuse LargeB-cell Lymphoma (23 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (23 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
Actinic Elastosis (23 %) ( Solar Elastosis,)
Sclerosing Sweat Duct Carcinoma (23 %) ( Microcystic Adnexal Carcinoma,)
Uveal Melanoma (23 %)
Klippel feil Syndrome (23 %)
Telangiectasia (23 %)
Oral Candidiasis (23 %) ( Thrush,)
Primary Cutaneous LargeB-cell Lymphoma (23 %) ( Diffuse LargeB-cell Lymphoma,)
Waldenstr m Macroglobulinemia (23 %)
Solar Elastosis (23 %) ( Actinic Elastosis,)
Turner Syndrome (23 %)
Angiokeratoma (23 %)
Hyperthyroidism (23 %)
Erythema Induratum (23 %) ( Bazin Disease, Nodular Vasculitis,)
Malacoplakia (23 %) ( Malakoplakia,)
Familial Dysautonomia (23 %) ( Riley day Syndrome,)
Malakoplakia (23 %) ( Malacoplakia,)
Costello Syndrome (23 %)
Thrush (23 %) ( Oral Candidiasis,)
Pancreatic Panniculitis (23 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Angioedema (23 %)
Klippel-trenaunay-weber Syndrome (23 %)
Cicatricial Pemphigoid (23 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Wiskott aldrich Syndrome (23 %)
Multiple Endocrine Neoplasia Type1 (23 %) ( Wermer Syndrome,)
Smooth Tongue (23 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Rhinophyma (23 %)
Morvans Disease (23 %) ( Syringomyelia,)
Primary Cutaneous Adenoid Cystic Carcinoma (23 %)
Riley day Syndrome (23 %) ( Familial Dysautonomia,)
Syringomyelia (23 %) ( Morvans Disease,)
Madarosis (23 %)
Spoon Nails (21 %) ( Koilonychia,)
Koilonychia (21 %) ( Spoon Nails,)
Lentigo Maligna (21 %) ( Lentiginous Melanoma On Sun-damaged Skin,)
Glossodynia (21 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Sweets Syndrome (21 %) ( Acute Febrile Neutrophilic Dermatosis,)
Familial Mediterranean Fever (21 %)
Jacobi Ulcer (21 %) ( Rodent Ulcer,)
Fabry Disease (21 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Thrombotic Thrombocytopenic Purpura (21 %) ( Moschcowitz Syndrome,)
Desmoid Tumor (21 %)
Maffucci Syndrome (21 %)
Stewart treves Syndrome (21 %) ( Postmastectomy Lymphangiosarcoma,)
Panniculitis-likeT-cell Lymphoma (21 %) ( SubcutaneousT-cell Lymphoma,)
SubcutaneousT-cell Lymphoma (21 %) ( Panniculitis-likeT-cell Lymphoma,)
Limbal Dermoid (21 %)
Lentiginous Melanoma On Sun-damaged Skin (21 %) ( Lentigo Maligna,)
Lymphangioma Circumscriptum (21 %) ( Superficial Lymphatic Malformation,)
Histiocytic Medullary Reticulosis (21 %) ( Malignant Histiocytosis,)
Palmoplantar Keratoderma (21 %)
Lymphangiectasia (21 %)
Postmastectomy Lymphangiosarcoma (21 %) ( Stewart treves Syndrome,)
Moschcowitz Syndrome (21 %) ( Thrombotic Thrombocytopenic Purpura,)
Apocrine Hidrocystoma (21 %)
Multicentric Reticulohistiocytosis (21 %)
Tumor Lysis Syndrome (21 %)
Hyper-ige Syndrome (21 %) ( Buckley Syndrome, Job Syndrome,)
Eosinophilic Cellulitis (21 %) ( Wells Syndrome,)
Immune Recovery Syndrome (21 %) ( Immune Reconstitution Inflammatory Syndrome,)
Wells Syndrome (21 %) ( Eosinophilic Cellulitis,)
Melanotic Neuroectodermal Tumor Of Infancy (21 %)
Proteus Syndrome (21 %)
Fibrinolysis Syndrome (21 %) ( Defibrinating Syndrome, Hypofibrinogenemia,)
Superficial Lymphatic Malformation (21 %) ( Lymphangioma Circumscriptum,)
Nevus Sebaceous (21 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Churg strauss Syndrome (21 %) ( Allergic Granulomatosis,)
Rodent Ulcer (21 %) ( Jacobi Ulcer,)
Acanthosis Nigricans (21 %)
Nevus Spilus (21 %) ( Speckled Lentiginous Nevus, Zosteriform Lentiginous Nevus,)
Allergic Granulomatosis (21 %) ( Churg strauss Syndrome,)
VitaminB1 Deficiency (21 %) ( Beriberi, Thiamine Deficiency,)
Miliary Tuberculosis (21 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Malignant Histiocytosis (21 %) ( Histiocytic Medullary Reticulosis,)
Giant Condyloma Acuminatum (21 %) ( Buschke l wenstein Tumor, Giant Condyloma Of Buschke l wenstein Tumor,)
Necrotizing Fasciitis (21 %) ( Flesh-eating Bacteria Syndrome,)
Flesh-eating Bacteria Syndrome (21 %) ( Necrotizing Fasciitis,)
Rhinosporidiosis (21 %)
Immune Reconstitution Inflammatory Syndrome (21 %) ( Immune Recovery Syndrome,)
Henoch Schonlein Purpura (21 %)
Dysplastic Nevus Syndrome (21 %) ( B-k Mole Syndrome, Familial Atypical Multiple Mole melanoma Syndrome, Familial Melanoma Syndrome,)
Scleroderma (21 %)
HypovitaminosisA (20 %) ( Phrynoderma,)
Traumatic Alopecia (20 %)
Dermatitis Repens (20 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Polyostotic Fibrous Dysplasia (20 %) ( Albrights Disease,)
Alopecia Neoplastica (20 %)
Zinsser cole engman Syndrome (20 %) ( Dyskeratosis Congenita,)
Hidradenitis Suppurativa (20 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Pemphigus Vulgaris (20 %)
Infantile Hemangiopericytoma (20 %) ( Congenital Hemangiopericytoma,)
Bowens Disease (20 %) ( Squamous Cell Carcinoma In Situ,)
Congenital Hemangiopericytoma (20 %) ( Infantile Hemangiopericytoma,)
Parry romberg Syndrome (20 %) ( Progressive Hemifacial Atrophy,)
Dyskeratosis Congenita (20 %) ( Zinsser cole engman Syndrome,)
Temporal Arteritis (20 %) ( Cranial Arteritis, Hortons Disease,)
Superficial Thrombophlebitis (20 %)
Subcutaneous Granuloma Annulare (20 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Delusional Parasitosis (20 %) ( Delusions Of Parasitosis, Ekbom Syndrome, Monosymptomatic Hypochondriacal Psychosis,)
Cutaneous Sinus Of Dental Origin (20 %) ( Dental Sinus,)
Phrynoderma (20 %) ( HypovitaminosisA,)
Kikuchis Disease (20 %) ( Histiocytic Necrotizing Lymphadenitis,)
Blau Syndrome (20 %)
Bronze Diabetes (20 %) ( Hemochromatosis,)
Rheumatoid Arthritis (20 %)
Muir-torre Syndrome (20 %)
Hemochromatosis (20 %) ( Bronze Diabetes,)
Orofaciodigital Syndrome (20 %)
Familial Cold Autoinflammatory Syndrome (20 %) ( Familial Cold Urticaria,)
Radiation Dermatitis (20 %) ( Radiodermatitis,)
Thrombophlebitis (20 %)
Angiolipoma (20 %)
Dental Sinus (20 %) ( Cutaneous Sinus Of Dental Origin,)
Familial Cold Urticaria (20 %) ( Familial Cold Autoinflammatory Syndrome,)
Histiocytic Necrotizing Lymphadenitis (20 %) ( Kikuchis Disease,)
Diffuse Sclerosis (20 %)
Herpes Zoster Oticus (20 %) ( Ramsay hunt Syndrome,)
Radiodermatitis (20 %) ( Radiation Dermatitis,)
Progressive Hemifacial Atrophy (20 %) ( Parry romberg Syndrome,)
Mucosal Squamous Cell Carcinoma (20 %)
Lentigo Maligna Melanoma (20 %)
Ramsay hunt Syndrome (20 %) ( Herpes Zoster Oticus,)
Generalized Pustular Psoriasis (20 %) ( Pustular Psoriasis Of Von Zumbusch,)
Angiofibroma (20 %)
Subungual Exostosis (20 %)
Glanders (20 %) ( Equinia, Farcy, Malleus,)
Spindle Cell Lipoma (20 %)
Leukemia Cutis (20 %)
Mckusick Type Metaphyseal Chondrodysplasia (20 %) ( Cartilage hair Hypoplasia,)
Cardiofaciocutaneous Syndrome (20 %) ( Cardio-facio-cutaneous Syndrome,)
Keloidal Scar (20 %) ( Keloid,)
Trigeminal Trophic Lesion (20 %) ( Trigeminal Trophic Syndrome,)
Pressure Ulcer (20 %) ( Decubitus Ulcer,)
Dysplastic Nevus (20 %) ( Atypical Mole, Atypical Nevus, B-k Mole, Clarks Nevus, Dysplastic Melanocytic Nevus, Nevus With Architectural Disorder,)
Isthmicoma (20 %) ( Infundibuloma, Tumor Of The Follicular Infundibulum,)
Pseudomelanoma (20 %) ( Recurrent Melanocytic Nevus, Recurrent Nevus,)
Acral Lentiginous Melanoma (20 %)
Superficial Spreading Melanoma (20 %) ( Superficially Spreading Melanoma,)
Superficially Spreading Melanoma (20 %) ( Superficial Spreading Melanoma,)
Giant-cell Arteritis (20 %)
Albrights Disease (20 %) ( Polyostotic Fibrous Dysplasia,)
Linear Verrucous Epidermal Nevus (20 %) ( Linear Epidermal Nevus, Verrucous Epidermal Nevus,)
Plexiform Fibrohistiocytic Tumor (20 %)
Pleomorphic Lipoma (20 %)
Secondary Lymphedema (20 %)
Congenital Nevi (20 %)
Trigeminal Trophic Syndrome (20 %) ( Trigeminal Trophic Lesion,)
Freckles (20 %) ( Ephelides,)
Papillary Hidradenoma (20 %) ( Hidradenoma Papilliferum,)
Aplasia Cutis Congenita (20 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Hereditary Hemorrhagic Telangiectasia (20 %) ( Oslers Disease, Osler weber rendu Disease,)
Muir torre Syndrome (20 %)
Pseudoglandular Squamous Cell Carcinoma (20 %) ( Adenoid Squamous Cell Carcinoma,)
Ephelides (20 %) ( Freckles,)
Multiple Pterygium Syndrome (20 %)
Keratoacanthoma (20 %)
Mondor Disease (20 %)
Crouzon Syndrome (20 %)
Seborrheic Keratosis (20 %) ( Seborrheic Verruca, Senile Wart,)
Acquired Hypogammaglobulinemia (20 %) ( Common Variable Immunodeficiency,)
Common Variable Immunodeficiency (20 %) ( Acquired Hypogammaglobulinemia,)
Keloid (20 %) ( Keloidal Scar,)
Geographic Tongue (20 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Cartilage hair Hypoplasia (20 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Adenoid Squamous Cell Carcinoma (20 %) ( Pseudoglandular Squamous Cell Carcinoma,)
Adrenal Adenoma (20 %)
Lymphangiomatosis (20 %)
Cardio-facio-cutaneous Syndrome (20 %) ( Cardiofaciocutaneous Syndrome,)
Generalized Eruptive Histiocytoma (20 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Stasis Dermatitis (20 %) ( Congestion Eczema, Gravitational Dermatitis, Gravitational Eczema, Stasis Eczema, Varicose Eczema,)
Mycosis Fungoides (20 %)
Cutaneous Focal Mucinosis (20 %)
Decubitus Ulcer (20 %) ( Pressure Ulcer,)
Adiposis Dolorosa (20 %) ( Dercums Disease,)
Severe Combined Immunodeficiency (20 %) ( Alymphocytosis, Glanzmann riniker Syndrome, Severe Mixed Immunodeficiency Syndrome, Thymic Alymphoplasia,)
Dercums Disease (20 %) ( Adiposis Dolorosa,)
Squamous Cell Carcinoma In Situ (20 %) ( Bowens Disease,)
Hidradenoma Papilliferum (20 %) ( Papillary Hidradenoma,)
Lupus Pernio (20 %)
Digeorge Syndrome (20 %) ( Digeorge Anomaly, Thymic Hypoplasia,)

Differentials from Google.

Leiomyoma
Leiomyosarcoma
Neurilemmoma
Neurolemmoma
Palisaded Encapsulated Neuroma
Schwannoma
Traumatic Neuroma

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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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