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: 2017-12-06:

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

Differentials from Google.

From Cache (Web service failed):

Lupus Erythematosus
Sicca Syndrome
Systemic Lupus Erythematosus

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