Differentials: Malignant Mixed Tumor

Differential diagnosis for Malignant Mixed Tumor

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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 Malignant Mixed Tumor.

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Date Added: 2017-09-16:

Malignant Chondroid Syringoma (100 %) ( Malignant Mixed Tumor,)
Dermatofibroma (78 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Mixed Tumor (73 %) ( Chondroid Syringoma,)
Chondroid Syringoma (73 %) ( Mixed Tumor,)
Acrospiroma (71 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Cutaneous Small-vessel Vasculitis (68 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Malignant Pilomatricoma (63 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Malignant Acrospiroma (63 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Pilomatricoma (61 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Schwannoma (61 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Epidermal Cyst (61 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Dermal Eccrine Cylindroma (59 %) ( Cylindroma,)
Cylindroma (59 %) ( Dermal Eccrine Cylindroma,)
Amputation Neuroma (54 %) ( Traumatic Neuroma,)
Hidrocystoma (54 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Metastatic Carcinoma (54 %)
Traumatic Neuroma (54 %) ( Amputation Neuroma,)
Connective Tissue Nevus (54 %) ( Collagenoma, Elastoma, Shagreen Patch,)
HistiocytosisX (54 %) ( Langerhans Cell Histiocytosis,)
Langerhans Cell Histiocytosis (54 %) ( HistiocytosisX,)
Glomus Tumor (54 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Spiradenoma (51 %)
Proliferating Trichilemmal Cyst (51 %) ( Pilar Tumor, Proliferating Follicular Cystic Neoplasm, Proliferating Pilar Tumor, Proliferating Trichilemmal Tumor,)
Hamartoma (51 %)
Merkel Cell Carcinoma (51 %) ( Cutaneous Apudoma, Primary Neuroendocrine Carcinoma Of The Skin, Primary Small Cell Carcinoma Of The Skin, Trabecular Carcinoma Of The Skin,)
Hidradenoma (51 %)
Syringoma (49 %)
Liposarcoma (49 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Giant Pigmented Nevus (49 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Hypoparathyroidism (49 %)
Intravascular LargeB-cell Lymphoma (49 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Nevoid Basal Cell Carcinoma Syndrome (49 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Epithelioma Cuniculatum (49 %) ( Ackerman Tumor, Carcinoma Cuniculatum,)
Lymphangiectasis (49 %) ( Lymphangioma,)
Lymphangioma (49 %) ( Lymphangiectasis,)
Aggressive Digital Papillary Adenocarcinoma (49 %) ( Digital Papillary Adenocarcinoma, Papillary Adenoma,)
Soft-tissue Melanoma (46 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Congenital Melanocytic Nevus (46 %)
Reticulohistiocytoma (46 %)
Carcinoid (46 %)
Carney Complex (46 %) ( Lamb Syndrome, Name Syndrome,)
Giant Cell Tumor Of The Tendon Sheath (46 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Cutaneous Lymphoid Hyperplasia (46 %) ( 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,)
Hidradenocarcinoma (46 %)
North American Blastomycosis (46 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Nodular Fasciitis (46 %) ( Nodular Pseudosarcomatous Fasciits, Pseudosarcomatous Fasciitis, Subcutaneous Pseudosarcomatous Fibromatosis,)
Granulocytic Sarcoma (46 %) ( Chloroma, Myeloid Sarcoma,)
Miliary Tuberculosis (44 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Lentiginous Melanoma On Sun-damaged Skin (44 %) ( Lentigo Maligna,)
Dermoid Cyst (44 %)
Lentigo Maligna (44 %) ( Lentiginous Melanoma On Sun-damaged Skin,)
Nevus Spilus (44 %) ( Speckled Lentiginous Nevus, Zosteriform Lentiginous Nevus,)
Apocrine Hidrocystoma (44 %)
Mycosis Fungoides (44 %)
Lipoma (44 %)
Teratoma (44 %)
Angiolymphoid Hyperplasia With Eosinophilia (44 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Spitz Nevus (44 %) ( Benign Juvenile Melanoma, Epithelioid And Spindle Cell Nevus, Spitzs Juvenile Melanoma,)
Blue Nevus (44 %) ( Blue Neuronevus, Dermal Melanocytoma, Nevus Bleu,)
Myxoid Cyst (41 %) ( Digital Mucous Cyst, Mucous Cyst,)
Neurothekeoma (41 %) ( Bizarre Cutaneous Neurofibroma, Cutaneous Lobular Neuromyxoma, Myxoma Of The Nerve Sheath, Myxomatous Perineurioma, Nerve Sheath Myxoma,)
Multiple Familial Trichoepithelioma (41 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Wart (41 %) ( Verruca Vulgaris,)
Yaws (41 %) ( Bouba, Framb sie, Parangi, Pian,)
Actinic Keratosis (41 %) ( Senile Keratosis, Solar Keratosis,)
Verruca Vulgaris (41 %) ( Wart,)
Spindle Cell Carcinoma (41 %) ( Spindle Cell Squamous Cell Carcinoma,)
Cutaneous Focal Mucinosis (41 %)
Verrucous Carcinoma (41 %)
Acrochordon (41 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Spindle Cell Squamous Cell Carcinoma (41 %) ( Spindle Cell Carcinoma,)
Pyogenic Granuloma (41 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Branchial Cyst (41 %) ( Branchial Cleft Cyst,)
Tuberous Sclerosis (41 %) ( Bourneville Disease, Epiloia,)
Pachydermoperiostosis (41 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Sinus Histiocytosis With Massive Lymphadenopathy (41 %) ( Rosai dorfman Disease,)
Branchial Cleft Cyst (41 %) ( Branchial Cyst,)
Rosai dorfman Disease (41 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Hyperparathyroidism (41 %)
Leiomyosarcoma (41 %)
Dermatofibrosarcoma Protuberans (39 %)
Sclerosing Sweat Duct Carcinoma (39 %) ( Microcystic Adnexal Carcinoma,)
Plexiform Fibrohistiocytic Tumor (39 %)
Thyroglossal Duct Cyst (39 %)
Systemic Sarcoidosis (39 %)
Subcutaneous Granuloma Annulare (39 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Panniculitis-likeT-cell Lymphoma (39 %) ( SubcutaneousT-cell Lymphoma,)
Infantile Myofibromatosis (39 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Acral Lentiginous Melanoma (39 %)
Keratocyst (39 %)
Malignant Fibrous Histiocytoma (39 %)
Nevus Of Ota (39 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Atypical Fibroxanthoma (39 %)
Isthmicoma (39 %) ( Infundibuloma, Tumor Of The Follicular Infundibulum,)
Sebaceous Carcinoma (39 %)
Angiocentric Lymphoma (39 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Papillary Eccrine Adenoma (39 %) ( Tubular Apocrine Adenoma,)
Microcystic Adnexal Carcinoma (39 %) ( Sclerosing Sweat Duct Carcinoma,)
Callus (39 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
SubcutaneousT-cell Lymphoma (39 %) ( Panniculitis-likeT-cell Lymphoma,)
Cutis Laxa (39 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Mucinous Carcinoma (39 %)
Tubular Apocrine Adenoma (39 %) ( Papillary Eccrine Adenoma,)
Nevus Sebaceous (39 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Seborrheic Keratosis (39 %) ( Seborrheic Verruca, Senile Wart,)
Neuroblastoma (39 %) ( Infantile Neuroblastoma, Neuroepithelioma,)
Malakoplakia (37 %) ( Malacoplakia,)
Kimura Disease (37 %)
Mucosa-associated Lymphoid Tissue Lymphoma (37 %)
Angioimmunoblastic Lymphadenopathy With Dysproteinemia (37 %) ( AngioimmunoblasticT-cell Lymphoma,)
Desmoplastic Melanoma (37 %) ( Neurotropic Melanoma, Spindled Melanoma,)
Multiple Endocrine Neoplasia Type3 (37 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
AngioimmunoblasticT-cell Lymphoma (37 %) ( Angioimmunoblastic Lymphadenopathy With Dysproteinemia,)
Basal Cell Carcinoma (37 %)
Marginal ZoneB-cell Lymphoma (37 %)
Juvenile Xanthogranuloma (37 %)
Coccidioidomycosis (37 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Malacoplakia (37 %) ( Malakoplakia,)
Goltz Syndrome (37 %) ( Focal Dermal Hypoplasia,)
Lentigo Maligna Melanoma (37 %)
Primary Cutaneous Adenoid Cystic Carcinoma (37 %)
Desmoplastic Fibroblastoma (37 %) ( Collagenous Fibroma,)
Lentigo (37 %)
Epithelioid Sarcoma (37 %)
Generalized Eruptive Histiocytoma (37 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Extramammary Paget Disease (37 %)
Acute Febrile Neutrophilic Dermatosis (37 %) ( Sweets Syndrome,)
Collagenous Fibroma (37 %) ( Desmoplastic Fibroblastoma,)
Nodular Melanoma (37 %)
Mucous Cyst Of The Oral Mucosa (37 %) ( Mucocele,)
Pagetoid Reticulosis (37 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Focal Dermal Hypoplasia (37 %) ( Goltz Syndrome,)
Clubbing (37 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Sweets Syndrome (37 %) ( Acute Febrile Neutrophilic Dermatosis,)
Lupus Erythematosus Panniculitis (37 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Mucocele (37 %) ( Mucous Cyst Of The Oral Mucosa,)
Lupus Pernio (37 %)
Mccune albright Syndrome (34 %)
Erythema Induratum (34 %) ( Bazin Disease, Nodular Vasculitis,)
Mycetoma (34 %) ( Madura Foot, Maduromycosis,)
Chromoblastomycosis (34 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Diffuse LargeB-cell Lymphoma (34 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Histiocytic Medullary Reticulosis (34 %) ( Malignant Histiocytosis,)
Mucosal Squamous Cell Carcinoma (34 %)
Peutz jeghers Syndrome (34 %)
Melanocytic Nevi (34 %)
Leiomyoma (34 %)
Birt-hogg-dube Syndrome (34 %)
Hyperhidrosis (34 %)
Rheumatoid Arthritis (34 %)
Polyarteritis Nodosa (34 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Bowens Disease (34 %) ( Squamous Cell Carcinoma In Situ,)
Squamous Cell Carcinoma In Situ (34 %) ( Bowens Disease,)
Hemangiosarcoma (34 %)
Hemangiopericytoma (34 %)
Foreign Body Reaction (34 %)
Kaposi Sarcoma (34 %)
Waldenstr m Macroglobulinemia (34 %)
Hydatid Disease (34 %) ( Echinococcosis,)
Lichenoid Keratosis (34 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Mucosal Melanoma (34 %)
Freckle (34 %) ( Ephelis,)
PleomorphicT-cell Lymphoma (34 %) ( Non-mycosis Fungoides Cd30- Pleomorphic Small/medium Sized CutaneousT-cell Lymphoma,)
Lymphomatoid Papulosis (34 %)
Malignant Histiocytosis (34 %) ( Histiocytic Medullary Reticulosis,)
Congenital Self-healing Reticulohistiocytosis (34 %) ( Hashimoto pritzker Disease, Hashimoto pritzker Syndrome,)
Benign Melanocytic Nevus (34 %) ( Banal Nevus, Common Acquired Melanocytic Nevus, Mole, Nevocellular Nevus, Nevocytic Nevus,)
Non-mycosis Fungoides Cd30- Pleomorphic Small/medium Sized CutaneousT-cell Lymphoma (34 %) ( PleomorphicT-cell Lymphoma,)
Echinococcosis (34 %) ( Hydatid Disease,)
Nail patella Syndrome (34 %) ( Fong Syndrome, Hereditary Osteoonychodysplasia, Hood Syndrome,)
Trichofolliculoma (34 %)
Ephelis (34 %) ( Freckle,)
Subungual Keratoacanthoma (34 %) ( Solitary Keratoacanthoma,)
Primary Cutaneous LargeB-cell Lymphoma (34 %) ( Diffuse LargeB-cell Lymphoma,)
Leukemia Cutis (34 %)
Birt hogg dub Syndrome (34 %)
Eosinophilic Granuloma (34 %)
Sebaceoma (34 %) ( Sebaceous Epithelioma,)
Sebaceous Epithelioma (34 %) ( Sebaceoma,)
Gingival Hypertrophy (34 %)
Encephalocele (34 %)
Nasal Glioma (34 %) ( Brain-like Heterotopia, Cephalic Brain-like Heterotopia, Glial Hamartoma, Heterotopic Neuroglial Tissue, Nasal Cerebral Heterotopia, Nasal Heterotopic Brain Tissue,)
Acrodermatitis Chronica Atrophicans (34 %) ( Herxheimer Disease, Primary Diffuse Atrophy,)
Chondrodermatitis Nodularis Helicis (34 %) ( Chondrodermatitis Nodularis Chronica Helicis,)
Nevus Flammeus (34 %) ( Capillary Malformation, Port-wine Stain,)
Sj grens Syndrome (34 %) ( Mikulicz Disease, Sicca Syndrome,)
Fissured Tongue (34 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Chondrodermatitis Nodularis Chronica Helicis (34 %) ( Chondrodermatitis Nodularis Helicis,)
Solitary Keratoacanthoma (34 %) ( Subungual Keratoacanthoma,)
Infectious Mononucleosis (32 %) ( Glandular Fever,)
Syringoid Carcinoma (32 %) ( Eccrine Carcinoma,)
Juvenile Hyaline Fibromatosis (32 %) ( Fibromatosis Hyalinica Multiplex Juvenilis, Murray puretic drescher Syndrome,)
Disseminated Coccidioidomycosis (32 %) ( Coccidioidal Granuloma,)
Sarcoidosis (32 %)
Acroosteolysis (32 %)
Perforating Folliculitis (32 %)
Subungual Exostosis (32 %)
Chondroma Of Soft Parts (32 %) ( Extraskeletal Chondroma,)
Von Recklinghausens Disease (32 %) ( Neurofibromatosis Type1,)
Tufted Angioma (32 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Juvenile Systemic Hyalinosis (32 %) ( Infantile Systemic Hyalinosis,)
Ehlers danlos Syndrome (32 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Ganglion Cyst (32 %)
Eccrine Carcinoma (32 %) ( Syringoid Carcinoma,)
Costello Syndrome (32 %)
Sclerotic Fibroma (32 %)
Chordoma (32 %)
Adrenal Adenoma (32 %)
Infantile Systemic Hyalinosis (32 %) ( Juvenile Systemic Hyalinosis,)
Bronchogenic Cyst (32 %)
Superficially Spreading Melanoma (32 %) ( Superficial Spreading Melanoma,)
Angiokeratoma (32 %)
Plasmacytoma (32 %)
Superficial Spreading Melanoma (32 %) ( Superficially Spreading Melanoma,)
Solitary Neurofibroma (32 %) ( Plexiform Neurofibroma, Solitary Nerve Sheath Tumor, Sporadic Neurofibroma,)
Coccidioidal Granuloma (32 %) ( Disseminated Coccidioidomycosis,)
Favre racouchot Syndrome (32 %) ( Favre racouchot Disease, Nodular Cutaneous Elastosis With Cysts And Comedones,)
Rhinophyma (32 %)
Basaloid Squamous Cell Carcinoma (32 %)
Extraskeletal Chondroma (32 %) ( Chondroma Of Soft Parts,)
Pigmented Basal Cell Carcinoma (32 %)
Neurofibromatosis Type1 (32 %) ( Von Recklinghausens Disease,)
Intravascular Papillary Endothelial Hyperplasia (32 %) ( Massons Hemangio-endotheliome Vegetant Intravasculaire, Massons Lesion, Massons Pseudoangiosarcoma, Massons Tumor, Papillary Endothelial Hyperplasia,)
Multiple Lentigines Syndrome (32 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Leukoplakia (32 %)
Trichoepithelioma (32 %)
Malignant Peripheral Nerve Sheath Tumor (32 %) ( Malignant Schwannoma, Neurofibrosarcoma, Neurosarcoma,)
Syringocystadenoma Papilliferum (32 %) ( Syringadenoma Papilliferum,)
Hidradenitis Suppurativa (32 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Primary Cutaneous Follicular Lymphoma (32 %) ( Follicular Center Cell Lymphoma, Follicular Center Lymphoma,)
Syringadenoma Papilliferum (32 %) ( Syringocystadenoma Papilliferum,)
Paraneoplastic Syndrome (32 %)
Acral Fibrokeratoma (32 %) ( Acquired Digital Fibrokeratoma, Acquired Periungual Fibrokeratoma,)
Histoplasmosis (32 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Glandular Fever (32 %) ( Infectious Mononucleosis,)

Differentials from Google.

From Cache (Web service failed):
Chondroid Syringoma
Malignant Chondroid Syringoma
Malignant Mixed Tumor
Mixed Tumor
Syringoma

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