Differentials: epithelioidhemangioendothelioma

Differential diagnosis for epithelioidhemangioendothelioma

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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 epithelioidhemangioendothelioma.

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Date Added: 2017-06-03:

Epithelioid Hemangioendothelioma (100 %)
Chondroid Syringoma (92 %) ( Mixed Tumor,)
Mixed Tumor (92 %) ( Chondroid Syringoma,)
Dermatofibroma (85 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Metastatic Carcinoma (85 %)
Sinus Histiocytosis With Massive Lymphadenopathy (77 %) ( Rosai dorfman Disease,)
Nevoid Basal Cell Carcinoma Syndrome (77 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Rosai dorfman Disease (77 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Schwannoma (77 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
HistiocytosisX (77 %) ( Langerhans Cell Histiocytosis,)
Langerhans Cell Histiocytosis (77 %) ( HistiocytosisX,)
Congenital Melanocytic Nevus (77 %)
Acrospiroma (77 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Reticulohistiocytoma (77 %)
Malignant Acrospiroma (77 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Cutaneous Lymphoid Hyperplasia (69 %) ( 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,)
Erythema Induratum (69 %) ( Bazin Disease, Nodular Vasculitis,)
Multiple Endocrine Neoplasia Type3 (69 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
Liposarcoma (69 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Intravascular LargeB-cell Lymphoma (69 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Miliary Tuberculosis (69 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Nodular Fasciitis (69 %) ( Nodular Pseudosarcomatous Fasciits, Pseudosarcomatous Fasciitis, Subcutaneous Pseudosarcomatous Fibromatosis,)
Pilomatricoma (69 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Malignant Pilomatricoma (69 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Histiocytic Medullary Reticulosis (69 %) ( Malignant Histiocytosis,)
Scrofuloderma (69 %) ( Tuberculosis Cutis Colliquativa,)
Malignant Histiocytosis (69 %) ( Histiocytic Medullary Reticulosis,)
Tuberculosis Cutis Colliquativa (69 %) ( Scrofuloderma,)
Malignant Mixed Tumor (69 %) ( Malignant Chondroid Syringoma,)
Malignant Chondroid Syringoma (69 %) ( Malignant Mixed Tumor,)
Generalized Eruptive Histiocytoma (69 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Hypoparathyroidism (69 %)
North American Blastomycosis (69 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Angiolymphoid Hyperplasia With Eosinophilia (62 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Hidrocystoma (62 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Infantile Myofibromatosis (62 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Leiomyosarcoma (62 %)
Lipoma (62 %)
Soft-tissue Melanoma (62 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Multiple Familial Trichoepithelioma (62 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Juvenile Hyaline Fibromatosis (62 %) ( Fibromatosis Hyalinica Multiplex Juvenilis, Murray puretic drescher Syndrome,)
Polyarteritis Nodosa (62 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Juvenile Xanthogranuloma (62 %)
Blueberry Muffin Baby (62 %)
Cutaneous Small-vessel Vasculitis (62 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Crest Syndrome (62 %) ( Calcinosis raynaud Phenomenon esophageal Dysmotility sclerodactyly telangiectasia Syndrome,)
Calcinosis raynaud Phenomenon esophageal Dysmotility sclerodactyly telangiectasia Syndrome (62 %) ( Crest Syndrome,)

Differentials from Google.

Date Added: 2017-08-06

Angiosarcoma
Epithelioid Hemangioendothelioma
Epithelioid Sarcoma

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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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