Differentials: Sicca Syndrome

Differential diagnosis for Sicca Syndrome

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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 Sicca Syndrome.

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Date Added: 2017-06-07:

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

Differentials from Google.

Date Added: 2017-08-13


Lupus Erythematosus
Sicca Syndrome
Systemic Lupus Erythematosus

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