Differentials: Mikulicz Disease

Differential diagnosis for Mikulicz Disease

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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 Mikulicz Disease.

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Date Added: 2017-11-11:

Sj grens Syndrome (100 %) ( Mikulicz Disease, Sicca Syndrome,)
Lupus Erythematosus Panniculitis (57 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Cutaneous Small-vessel Vasculitis (54 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Recurrent Aphthous Stomatitis (54 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Takayasu Arteritis (52 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Polyarteritis Nodosa (52 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Dermatofibroma (50 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Zoster (48 %) ( Herpes Zoster, Shingles,)
Relapsing Polychondritis (48 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Systemic Sarcoidosis (48 %)
Churg strauss Syndrome (48 %) ( Allergic Granulomatosis,)
Allergic Granulomatosis (48 %) ( Churg strauss Syndrome,)
Scleroderma (46 %)
Fissured Tongue (46 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Juvenile Rheumatoid Arthritis (46 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Cicatricial Pemphigoid (43 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Langerhans Cell Histiocytosis (43 %) ( HistiocytosisX,)
Sarcoidosis (43 %)
Rheumatoid Arthritis (43 %)
HistiocytosisX (43 %) ( Langerhans Cell Histiocytosis,)
Cutaneous Lymphoid Hyperplasia (41 %) ( 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,)
Amputation Neuroma (41 %) ( Traumatic Neuroma,)
Erythema Nodosum (41 %)
Pyogenic Granuloma (41 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Traumatic Neuroma (41 %) ( Amputation Neuroma,)
Granulocytic Sarcoma (41 %) ( Chloroma, Myeloid Sarcoma,)
Wegener Granulomatosis (41 %)
Fabry Disease (41 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Clubbing (41 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Hyperparathyroidism (39 %)
Acute Febrile Neutrophilic Dermatosis (39 %) ( Sweets Syndrome,)
Angiolymphoid Hyperplasia With Eosinophilia (39 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Carcinoid (39 %)
Echinococcosis (39 %) ( Hydatid Disease,)
Erythema Induratum (39 %) ( Bazin Disease, Nodular Vasculitis,)
Mucosa-associated Lymphoid Tissue Lymphoma (39 %)
North American Blastomycosis (39 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Hydatid Disease (39 %) ( Echinococcosis,)
Nevus Of Ota (39 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Acne Rosacea (37 %) ( Rosacea,)
Glomus Tumor (37 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Sweets Syndrome (37 %) ( Acute Febrile Neutrophilic Dermatosis,)
Chilblains (37 %) ( Pernio, Perniosis,)
Schwannoma (37 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Rosacea (37 %) ( Acne Rosacea,)
Sparganosis (37 %)
Geographic Tongue (37 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Histoplasmosis (37 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Hypereosinophilic Syndrome (37 %)
Dermoid Cyst (37 %)
Miliary Tuberculosis (37 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Systemic Lupus Erythematosus (37 %)
Glossodynia (35 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Hamartoma (35 %)
Lymphomatoid Papulosis (35 %)
Pemphigus Vulgaris (35 %)
Lymphangiectasis (35 %) ( Lymphangioma,)
Liposarcoma (35 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Herpes Simplex (35 %)
Angiokeratoma (35 %)
Acute Necrotizing Ulcerative Gingivitis (35 %) ( Acute Membranous Gingivitis, Acute Necrotizing Ulcerative Gingivostomatitis, Fusospirillary Gingivitis, Fusospirillosis, Fusospirochetal Gingivitis, Necrotizing Gingivitis, Phagedenic Gingivitis, Trench Mouth, Ulcerative Gingivitis, Vincent Gingivitis, Vincent Infection, Vincent Stomatitis, Vincents Disease,)
Leukoplakia (35 %)
Common Variable Immunodeficiency (35 %) ( Acquired Hypogammaglobulinemia,)
Livedoid Vasculopathy (35 %) ( Atrophie Blanche, Livedo Reticularis With Summer Ulceration, Livedoid Vasculitis, Purple Syndrome, Segmental Hyalinizing Vasculitis,)
Acquired Hypogammaglobulinemia (35 %) ( Common Variable Immunodeficiency,)
Henoch Schonlein Purpura (35 %)
Urticarial Vasculitis (35 %) ( Chronic Urticaria AsA Manifestation Of Venulitis, Hypocomplementemic Urticarial Vasculitis Syndrome, Hypocomplementemic Vasculitis, Unusual Lupus-like Syndrome,)
Duhring Disease (35 %) ( Dermatitis Herpetiformis,)
Lipodermatosclerosis (35 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
Mixed Connective Tissue Disease (35 %) ( Sharps Syndrome, Undifferentiated Connective Tissue Disease,)
Acrochordon (35 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Lymphangioma (35 %) ( Lymphangiectasis,)
Marginal ZoneB-cell Lymphoma (35 %)
Dermatitis Herpetiformis (35 %) ( Duhring Disease,)
Callus (35 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Telangiectasia (33 %)
Kimura Disease (33 %)
Hyperhidrosis (33 %)
Oral Lichen Planus (33 %)
Immune Reconstitution Inflammatory Syndrome (33 %) ( Immune Recovery Syndrome,)
Intravascular LargeB-cell Lymphoma (33 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Paroxysmal Nocturnal Hemoglobinuria (33 %)
Relapsing Febrile Non-suppurative Panniculitis (33 %) ( Weber christian Disease,)
Progressive Systemic Sclerosis (33 %)
Immune Recovery Syndrome (33 %) ( Immune Reconstitution Inflammatory Syndrome,)
Panhypopituitarism (33 %)
Multiple Lentigines Syndrome (33 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Microscopic Polyangiitis (33 %) ( Microscopic Polyarteritis, Microscopic Polyarteritis Nodosa,)
Epidermal Cyst (33 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Mycetoma (33 %) ( Madura Foot, Maduromycosis,)
Lipoma (33 %)
Weber christian Disease (33 %) ( Relapsing Febrile Non-suppurative Panniculitis,)
Cutis Laxa (33 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Angiocentric Lymphoma (33 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Diffuse LargeB-cell Lymphoma (30 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Varicella (30 %) ( Chickenpox,)
Tuberous Sclerosis (30 %) ( Bourneville Disease, Epiloia,)
Chickenpox (30 %) ( Varicella,)
Gout (30 %) ( Podagra, Urate Crystal Arthropathy, Urate Deposition Disease,)
Thrombophlebitis (30 %)
Wells Syndrome (30 %) ( Eosinophilic Cellulitis,)
Familial Mediterranean Fever (30 %)
Polyneuropathy organomegaly endocrinopathy monoclonal Gammopathy skin Changes Syndrome (30 %) ( Crow fukase Syndrome, Poems Syndrome,)
Oral Candidiasis (30 %) ( Thrush,)
Multiple Endocrine Neoplasia Type2 (30 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Anhidrosis (30 %) ( Hypohidrosis,)
Hidradenitis Suppurativa (30 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Wart (30 %) ( Verruca Vulgaris,)
Eosinophilic Vasculitis (30 %)
Hypohidrosis (30 %) ( Anhidrosis,)
Coccidioidomycosis (30 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Verruca Vulgaris (30 %) ( Wart,)
Kaposi Sarcoma (30 %)
Primary Cutaneous LargeB-cell Lymphoma (30 %) ( Diffuse LargeB-cell Lymphoma,)
Ehlers danlos Syndrome (30 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
HepatitisC (30 %)
Tic Douloureux (30 %) ( Trigeminal Neuralgia,)
Malignant Mixed Tumor (30 %) ( Malignant Chondroid Syringoma,)
Gingival Hypertrophy (30 %)
South American Blastomycosis (30 %) ( Brazilian Blastomycosis, Paracoccidioidal Granuloma, Paracoccidioidomycosis,)
Trigeminal Neuralgia (30 %) ( Tic Douloureux,)
Sapho Syndrome (30 %) ( Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome,)
Palmoplantar Pustulosis (30 %) ( Persistent Palmoplantar Pustulosis, Pustular Psoriasis Of The Barber Type, Pustular Psoriasis Of The Extremities, Pustulosis Of Palms And Soles, Pustulosis Palmaris Et Plantaris,)
Malignant Chondroid Syringoma (30 %) ( Malignant Mixed Tumor,)
Blau Syndrome (30 %)
Vascular Leiomyoma (30 %) ( Angioleiomyoma,)
Toxoplasmosis (30 %)
Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome (30 %) ( Sapho Syndrome,)
Angioleiomyoma (30 %) ( Vascular Leiomyoma,)
Thrombotic Thrombocytopenic Purpura (30 %) ( Moschcowitz Syndrome,)
Raynaud Phenomenon (30 %)
Eosinophilic Cellulitis (30 %) ( Wells Syndrome,)
Lichen Planus (30 %)
Giant-cell Arteritis (30 %)
Waldenstr m Macroglobulinemia (30 %)
Moschcowitz Syndrome (30 %) ( Thrombotic Thrombocytopenic Purpura,)
Paraneoplastic Pemphigus (30 %)
Hyper-ige Syndrome (30 %) ( Buckley Syndrome, Job Syndrome,)
Thrush (30 %) ( Oral Candidiasis,)
Smooth Tongue (30 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Dermatomyositis (30 %)
Bowens Disease (28 %) ( Squamous Cell Carcinoma In Situ,)
Reflex Sympathetic Dystrophy (28 %) ( Complex Regional Pain Syndrome,)
Tnf Receptor Associated Periodic Syndrome (28 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Squamous Cell Carcinoma In Situ (28 %) ( Bowens Disease,)
Chondrodermatitis Nodularis Helicis (28 %) ( Chondrodermatitis Nodularis Chronica Helicis,)
Complex Regional Pain Syndrome (28 %) ( Reflex Sympathetic Dystrophy,)
Chondrodermatitis Nodularis Chronica Helicis (28 %) ( Chondrodermatitis Nodularis Helicis,)
Acrodermatitis Chronica Atrophicans (28 %) ( Herxheimer Disease, Primary Diffuse Atrophy,)
Hypersensitivity Vasculitis (28 %)
Hypoparathyroidism (28 %)
Hemangiosarcoma (28 %)
Basal Cell Carcinoma (28 %)
Stasis Dermatitis (28 %) ( Congestion Eczema, Gravitational Dermatitis, Gravitational Eczema, Stasis Eczema, Varicose Eczema,)
Connective Tissue Nevus (28 %) ( Collagenoma, Elastoma, Shagreen Patch,)
Muckle wells Syndrome (28 %)
Actinomycosis (28 %)
Marfan Syndrome (28 %)
Lepromatous Leprosy (28 %)
Carney Complex (28 %) ( Lamb Syndrome, Name Syndrome,)
X-linked Agammaglobulinemia (28 %) ( Bruton Syndrome, Sex-linked Agammaglobulinemia,)
Zoster-associated Pain (28 %) ( Postherpetic Neuralgia,)
Bronze Diabetes (28 %) ( Hemochromatosis,)
Lymphomatoid Granulomatosis (28 %)
Erythroplakia (28 %) ( Erythroplasia,)
Herpes Zoster Oticus (28 %) ( Ramsay hunt Syndrome,)
Erythroplasia (28 %) ( Erythroplakia,)
Deep Venous Thrombosis (28 %)
Hemochromatosis (28 %) ( Bronze Diabetes,)
Ramsay hunt Syndrome (28 %) ( Herpes Zoster Oticus,)
Actinic Keratosis (28 %) ( Senile Keratosis, Solar Keratosis,)
Systemic Sclerosis (28 %)
Disseminated Coccidioidomycosis (28 %) ( Coccidioidal Granuloma,)
Eosinophilic Granuloma (28 %)
Coccidioidal Granuloma (28 %) ( Disseminated Coccidioidomycosis,)
Acroosteolysis (28 %)
Postherpetic Neuralgia (28 %) ( Zoster-associated Pain,)

Differentials from Google.

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Kimura
Mikulicz

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