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: 2018-02-26:

Multiple Lentigines Syndrome (100 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Carney Complex (50 %) ( Lamb Syndrome, Name Syndrome,)
Nevus Flammeus (46 %) ( Capillary Malformation, Port-wine Stain,)
Clubbing (46 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Glomus Tumor (43 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Giant Pigmented Nevus (41 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Angiolymphoid Hyperplasia With Eosinophilia (39 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Tuberous Sclerosis (39 %) ( Bourneville Disease, Epiloia,)
Pachydermoperiostosis (39 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Cutaneous Small-vessel Vasculitis (39 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Palmoplantar Keratoderma (39 %)
Dermatofibroma (39 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Gingival Hypertrophy (37 %)
Systemic Sarcoidosis (37 %)
Telangiectasia (37 %)
Aplasia Cutis Congenita (37 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Lymphomatoid Papulosis (37 %)
Fabry Disease (37 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Nevus Of Ota (37 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Cardio-facio-cutaneous Syndrome (35 %) ( Cardiofaciocutaneous Syndrome,)
Hypohidrotic Ectodermal Dysplasia (35 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Body Dysmorphic Disorder (35 %) ( Dysmorphic Syndrome, Dysmorphophobia,)
Connective Tissue Nevus (35 %) ( Collagenoma, Elastoma, Shagreen Patch,)
Eosinophilic Cellulitis (35 %) ( Wells Syndrome,)
Zoster (35 %) ( Herpes Zoster, Shingles,)
Cardiofaciocutaneous Syndrome (35 %) ( Cardio-facio-cutaneous Syndrome,)
Costello Syndrome (35 %)
Epidermal Cyst (35 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Wells Syndrome (35 %) ( Eosinophilic Cellulitis,)
Tufted Angioma (35 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Benign Melanocytic Nevus (33 %) ( Banal Nevus, Common Acquired Melanocytic Nevus, Mole, Nevocellular Nevus, Nevocytic Nevus,)
Cylindroma (33 %) ( Dermal Eccrine Cylindroma,)
Leukoderma (33 %)
Multiple Familial Trichoepithelioma (33 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Waardenburg Syndrome (33 %)
Multiple Endocrine Neoplasia Type3 (33 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
Juvenile Hyaline Fibromatosis (33 %) ( Fibromatosis Hyalinica Multiplex Juvenilis, Murray puretic drescher Syndrome,)
Cutis Laxa (33 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Langerhans Cell Histiocytosis (33 %) ( HistiocytosisX,)
Dermal Eccrine Cylindroma (33 %) ( Cylindroma,)
Fissured Tongue (33 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
HistiocytosisX (33 %) ( Langerhans Cell Histiocytosis,)
Blue Nevus (33 %) ( Blue Neuronevus, Dermal Melanocytoma, Nevus Bleu,)
Recurrent Aphthous Stomatitis (33 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Dyschromatosis Symmetrica Hereditaria (33 %) ( Reticulate Acropigmentation Of Dohi, Symmetrical Dyschromatosis Of The Extremities,)
Pilomatricoma (33 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Nevus Spilus (33 %) ( Speckled Lentiginous Nevus, Zosteriform Lentiginous Nevus,)
Sj grens Syndrome (33 %) ( Mikulicz Disease, Sicca Syndrome,)
Acrochordon (30 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Ehlers danlos Syndrome (30 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Freckles (30 %) ( Ephelides,)
Buschke ollendorff Syndrome (30 %) ( Dermatofibrosis Lenticularis Disseminata,)
Wart (30 %) ( Verruca Vulgaris,)
Barraquer simons Syndrome (30 %) ( Acquired Partial Lipodystrophy, Cephalothoracic Lipodystrophy, Progressive Lipodystrophy,)
Dyschromatosis Universalis Hereditaria (30 %)
Dysplastic Nevus Syndrome (30 %) ( B-k Mole Syndrome, Familial Atypical Multiple Mole melanoma Syndrome, Familial Melanoma Syndrome,)
Spiradenoma (30 %)
Juvenile Systemic Hyalinosis (30 %) ( Infantile Systemic Hyalinosis,)
Steatocystoma Multiplex (30 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Conradi h nermann Syndrome (30 %) ( Conradi h nermann happle Syndrome, Happle Syndrome, X-linked Dominant Chondrodysplasia Punctata,)
Oculodentodigital Dysplasia (30 %)
Pseudomelanoma (30 %) ( Recurrent Melanocytic Nevus, Recurrent Nevus,)
Macular Amyloidosis (30 %)
Hidrocystoma (30 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Amniotic Band Syndrome (30 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Verruca Vulgaris (30 %) ( Wart,)
Ephelides (30 %) ( Freckles,)
Rosai dorfman Disease (30 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Infantile Systemic Hyalinosis (30 %) ( Juvenile Systemic Hyalinosis,)
Blue Nevi (30 %)
Dermatofibrosis Lenticularis Disseminata (30 %) ( Buschke ollendorff Syndrome,)
Sinus Histiocytosis With Massive Lymphadenopathy (30 %) ( Rosai dorfman Disease,)
Generalized Eruptive Histiocytoma (30 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Multiple Endocrine Neoplasia Type2 (30 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Takayasu Arteritis (30 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Hereditary Hemorrhagic Telangiectasia (28 %) ( Oslers Disease, Osler weber rendu Disease,)
Lentigo (28 %)
Mixed Tumor (28 %) ( Chondroid Syringoma,)
Infantile Myofibromatosis (28 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Hyper-ige Syndrome (28 %) ( Buckley Syndrome, Job Syndrome,)
Freckle (28 %) ( Ephelis,)
Malignant Mixed Tumor (28 %) ( Malignant Chondroid Syringoma,)
Dysplastic Nevus (28 %) ( Atypical Mole, Atypical Nevus, B-k Mole, Clarks Nevus, Dysplastic Melanocytic Nevus, Nevus With Architectural Disorder,)
Keratosis Pilaris Atrophicans Faciei (28 %) ( 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,)
Halo Nevus (28 %) ( Leukoderma Acquisitum Centrifugum, Perinevoid Vitiligo, Sutton Nevus,)
Focal Dermal Hypoplasia (28 %) ( Goltz Syndrome,)
Porokeratosis (28 %)
Liposarcoma (28 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Congenital Melanocytic Nevus (28 %)
Noonan Syndrome (28 %)
Ephelis (28 %) ( Freckle,)
Spitz Nevus (28 %) ( Benign Juvenile Melanoma, Epithelioid And Spindle Cell Nevus, Spitzs Juvenile Melanoma,)
Digeorge Syndrome (28 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Sclerotic Fibroma (28 %)
Marfan Syndrome (28 %)
Goltz Syndrome (28 %) ( Focal Dermal Hypoplasia,)
Rosacea (28 %) ( Acne Rosacea,)
Hypomelanosis Of Ito (28 %) ( Incontinentia Pigmenti Achromians,)
Malignant Chondroid Syringoma (28 %) ( Malignant Mixed Tumor,)
Generalized Pustular Psoriasis (28 %) ( Pustular Psoriasis Of Von Zumbusch,)
Keratitis ichthyosis deafness Syndrome (28 %) ( Erythrokeratodermia Progressiva Burns, Ichthyosiform Erythroderma With Corneal Involvement And Deafness, Kid Syndrome,)
Birt hogg dub Syndrome (28 %)
Chondroid Syringoma (28 %) ( Mixed Tumor,)
Nevus Sebaceous (28 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Hidradenitis Suppurativa (28 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Birt-hogg-dube Syndrome (28 %)
Acne Rosacea (28 %) ( Rosacea,)
Lentiginous Melanoma On Sun-damaged Skin (28 %) ( Lentigo Maligna,)
Acute Febrile Neutrophilic Dermatosis (28 %) ( Sweets Syndrome,)
Lentigo Maligna (28 %) ( Lentiginous Melanoma On Sun-damaged Skin,)
Incontinentia Pigmenti (28 %) ( Bloch siemens Syndrome, Bloch sulzberger Disease, Bloch sulzberger Syndrome,)
Incontinentia Pigmenti Achromians (28 %) ( Hypomelanosis Of Ito,)
N kams Disease (28 %) ( Keratosis Lichenoides Chronica,)
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,)
Oculocutaneous Albinism (28 %)
Keratosis Lichenoides Chronica (28 %) ( N kams Disease,)

Differentials from Google.

From Cache (Web service failed):
Allergic
Blue Nevi
Cardiocutaneous Syndrome
Cutaneous Myxoma

Lentigo
Leopard Syndrome
Multiple Lentigines Syndrome
Progressive Cardiomyopathic Lentiginosis

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