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: 2017-08-10:

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

Differentials from Google.

Date Added: 2017-08-28


Kimura
Mikulicz

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