Differentials: Progressive Cardiomyopathic Lentiginosis

Differential diagnosis for Progressive Cardiomyopathic Lentiginosis

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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 Progressive Cardiomyopathic Lentiginosis.

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Date Added: 2017-11-27:

Multiple Lentigines Syndrome (100 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Carney Complex (51 %) ( Lamb Syndrome, Name Syndrome,)
Nevus Flammeus (44 %) ( Capillary Malformation, Port-wine Stain,)
Clubbing (44 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Glomus Tumor (42 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Palmoplantar Keratoderma (40 %)
Tuberous Sclerosis (40 %) ( Bourneville Disease, Epiloia,)
Giant Pigmented Nevus (40 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Fabry Disease (38 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Cutaneous Small-vessel Vasculitis (38 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Telangiectasia (38 %)
Pachydermoperiostosis (38 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Angiolymphoid Hyperplasia With Eosinophilia (38 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Nevus Of Ota (38 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Gingival Hypertrophy (38 %)
Systemic Sarcoidosis (38 %)
Dermatofibroma (38 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Hypohidrotic Ectodermal Dysplasia (36 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Zoster (36 %) ( Herpes Zoster, Shingles,)
Lymphomatoid Papulosis (36 %)
Body Dysmorphic Disorder (36 %) ( Dysmorphic Syndrome, Dysmorphophobia,)
Connective Tissue Nevus (36 %) ( Collagenoma, Elastoma, Shagreen Patch,)
Cardiofaciocutaneous Syndrome (36 %) ( Cardio-facio-cutaneous Syndrome,)
Costello Syndrome (36 %)
Cardio-facio-cutaneous Syndrome (36 %) ( Cardiofaciocutaneous Syndrome,)
Aplasia Cutis Congenita (36 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Multiple Endocrine Neoplasia Type3 (33 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
Eosinophilic Cellulitis (33 %) ( Wells Syndrome,)
HistiocytosisX (33 %) ( Langerhans Cell Histiocytosis,)
Benign Melanocytic Nevus (33 %) ( Banal Nevus, Common Acquired Melanocytic Nevus, Mole, Nevocellular Nevus, Nevocytic Nevus,)
Cylindroma (33 %) ( Dermal Eccrine Cylindroma,)
Nevus Spilus (33 %) ( Speckled Lentiginous Nevus, Zosteriform Lentiginous Nevus,)
Recurrent Aphthous Stomatitis (33 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Blue Nevus (33 %) ( Blue Neuronevus, Dermal Melanocytoma, Nevus Bleu,)
Waardenburg Syndrome (33 %)
Cutis Laxa (33 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Wells Syndrome (33 %) ( Eosinophilic Cellulitis,)
Sj grens Syndrome (33 %) ( Mikulicz Disease, Sicca Syndrome,)
Tufted Angioma (33 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Leukoderma (33 %)
Fissured Tongue (33 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Multiple Familial Trichoepithelioma (33 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Juvenile Hyaline Fibromatosis (33 %) ( Fibromatosis Hyalinica Multiplex Juvenilis, Murray puretic drescher Syndrome,)
Langerhans Cell Histiocytosis (33 %) ( HistiocytosisX,)
Epidermal Cyst (33 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Dermal Eccrine Cylindroma (33 %) ( Cylindroma,)
Freckles (31 %) ( Ephelides,)
Oculodentodigital Dysplasia (31 %)
Spiradenoma (31 %)
Blue Nevi (31 %)
Sinus Histiocytosis With Massive Lymphadenopathy (31 %) ( Rosai dorfman Disease,)
Rosai dorfman Disease (31 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Dermatofibrosis Lenticularis Disseminata (31 %) ( Buschke ollendorff Syndrome,)
Pilomatricoma (31 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Verruca Vulgaris (31 %) ( Wart,)
Conradi h nermann Syndrome (31 %) ( Conradi h nermann happle Syndrome, Happle Syndrome, X-linked Dominant Chondrodysplasia Punctata,)
Buschke ollendorff Syndrome (31 %) ( Dermatofibrosis Lenticularis Disseminata,)
Wart (31 %) ( Verruca Vulgaris,)
Hidrocystoma (31 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Infantile Systemic Hyalinosis (31 %) ( Juvenile Systemic Hyalinosis,)
Multiple Endocrine Neoplasia Type2 (31 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Pseudomelanoma (31 %) ( Recurrent Melanocytic Nevus, Recurrent Nevus,)
Ehlers danlos Syndrome (31 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Dyschromatosis Symmetrica Hereditaria (31 %) ( Reticulate Acropigmentation Of Dohi, Symmetrical Dyschromatosis Of The Extremities,)
Generalized Eruptive Histiocytoma (31 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Ephelides (31 %) ( Freckles,)
Macular Amyloidosis (31 %)
Dyschromatosis Universalis Hereditaria (31 %)
Juvenile Systemic Hyalinosis (31 %) ( Infantile Systemic Hyalinosis,)
Infantile Myofibromatosis (29 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Birt hogg dub Syndrome (29 %)
Keratitis ichthyosis deafness Syndrome (29 %) ( Erythrokeratodermia Progressiva Burns, Ichthyosiform Erythroderma With Corneal Involvement And Deafness, Kid Syndrome,)
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,)
Marfan Syndrome (29 %)
Steatocystoma Multiplex (29 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Oculocutaneous Albinism (29 %)
Generalized Pustular Psoriasis (29 %) ( Pustular Psoriasis Of Von Zumbusch,)
Barraquer simons Syndrome (29 %) ( Acquired Partial Lipodystrophy, Cephalothoracic Lipodystrophy, Progressive Lipodystrophy,)
Rosacea (29 %) ( Acne Rosacea,)
Hereditary Hemorrhagic Telangiectasia (29 %) ( Oslers Disease, Osler weber rendu Disease,)
Keratosis Pilaris Atrophicans Faciei (29 %) ( Folliculitis Rubra, Keratosis Pilaris Rubra Atrophicans Faciei, Lichen Pilare, Lichen Pilaire Ou Xerodermie Pilaire Symmetrique De La Face, Ulerythema Ophryogenes, Xerodermi Pilaire Symmetrique De La Face,)
Acrochordon (29 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Malignant Chondroid Syringoma (29 %) ( Malignant Mixed Tumor,)
Dysplastic Nevus Syndrome (29 %) ( B-k Mole Syndrome, Familial Atypical Multiple Mole melanoma Syndrome, Familial Melanoma Syndrome,)
Noonan Syndrome (29 %)
Malignant Mixed Tumor (29 %) ( Malignant Chondroid Syringoma,)
Goltz Syndrome (29 %) ( Focal Dermal Hypoplasia,)
Freckle (29 %) ( Ephelis,)
Halo Nevus (29 %) ( Leukoderma Acquisitum Centrifugum, Perinevoid Vitiligo, Sutton Nevus,)
Spitz Nevus (29 %) ( Benign Juvenile Melanoma, Epithelioid And Spindle Cell Nevus, Spitzs Juvenile Melanoma,)
Lentiginous Melanoma On Sun-damaged Skin (29 %) ( Lentigo Maligna,)
Ephelis (29 %) ( Freckle,)
Digeorge Syndrome (29 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Takayasu Arteritis (29 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Lentigo Maligna (29 %) ( Lentiginous Melanoma On Sun-damaged Skin,)
Acne Rosacea (29 %) ( Rosacea,)
Hidradenitis Suppurativa (29 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Amniotic Band Syndrome (29 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Birt-hogg-dube Syndrome (29 %)
Incontinentia Pigmenti (29 %) ( Bloch siemens Syndrome, Bloch sulzberger Disease, Bloch sulzberger Syndrome,)
Nevus Sebaceous (29 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Focal Dermal Hypoplasia (29 %) ( Goltz Syndrome,)
Hyper-ige Syndrome (29 %) ( Buckley Syndrome, Job Syndrome,)
Lentigo (29 %)

Differentials from Google.

Date Added: 2018-01-19

Allergic
Blue Nevi
Cardiocutaneous Syndrome
Cutaneous Myxoma

Lentigo
Leopard Syndrome
Multiple Lentigines Syndrome
Progressive Cardiomyopathic Lentiginosis

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