Hepatita C Ce risc pentru psoriazis

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» dermatolog DERMATO BLOG Blog dermatologie - medic dermatolog Ce risc pentru psoriazis

Psoriasis is a long-lasting autoimmune disease which is characterized by patches of abnormal skin. They may vary in severity from small and localized to complete body coverage. There are five main types of psoriasis: It typically presents with red patches with white scales on top.

Areas of the body most commonly affected are the back of the forearms, shins, around the navel, and the scalp. Fingernails and toenails are affected in most people at some point ce risc pentru psoriazis time. This may include pits in the nails or changes in nail color. Psoriasis is generally thought to be a genetic disease which is triggered by environmental factors. Symptoms often worsen during winter and with certain medications such as beta blockers or NSAIDs.

The underlying mechanism involves the immune system reacting to skin cells. Diagnosis is typically based on the signs and symptoms. There is no cure for psoriasis. However, various treatments can help control the symptoms. These areas are called plaques and are most commonly found on the elbows, knees, scalp, and back.

It may be accompanied by severe itching, swelling, and pain. It is often the result of an exacerbation of unstable plaque psoriasis, particularly following the abrupt withdrawal of systemic glucocorticoids. Ce risc pentru psoriazis include pustular, inverse, napkin, guttate, oral, and seborrheic-like forms.

Pustular psoriasis appears as raised bumps filled with noninfectious pus pustules. Inverse psoriasis also known as flexural psoriasis appears as smooth, inflamed patches of skin. The patches frequently affect skin foldsparticularly around the genitals between the thigh and grointhe armpitsin the skin folds of an overweight abdomen known as panniculusbetween the buttocks in the intergluteal cleft, and under the breasts in the click to see more fold.

Heat, trauma, and infection are thought to play a role in the development of this atypical form of psoriasis. Napkin psoriasis is a subtype of more info common in infants characterized by red papules with silver scale in the diaper area that ce risc pentru psoriazis extend to the torso or limbs.

Guttate psoriasis is characterized by numerous small, scaly, red or pink, ce risc pentru psoriazis lesions papules. These numerous spots of psoriasis appear over large areas of the body, primarily the trunk, but also the limbs and scalp. Guttate psoriasis is often triggered by a streptococcal infection, typically streptococcal pharyngitis.

Psoriasis in the mouth is very rare, [21] in contrast to ce risc pentru psoriazis planusanother common papulosquamous disorder that commonly involves both the skin and mouth. When psoriasis involves the oral mucosa the ce risc pentru psoriazis of the mouthit may be asymptomatic, [21] but it may appear as white or grey-yellow plaques.

The microscopic appearance of oral mucosa affected by geographic tongue migratory stomatitis is very similar to the appearance of psoriasis. Seborrheic-like psoriasis is a common form of psoriasis with clinical aspects of psoriasis and seborrheic dermatitisand may be difficult to distinguish from the latter.

This form of psoriasis typically manifests as red plaques with greasy scales in areas of higher sebum production such as the scalpforeheadskin folds next to the noseskin surrounding the mouth, skin on the chest above the sternumand in skin folds. Psoriatic arthritis is a form of chronic inflammatory arthritis Lungengewebe adaptol și psoriazis erfolgt has a highly variable clinical presentation and frequently occurs in association with skin and nail psoriasis.

This can result in a sausage-shaped swelling of the fingers and ce risc pentru psoriazis known as dactylitis. Psoriasis can affect ce risc pentru psoriazis nails and produces a variety of changes in the appearance of finger and toe nails. In addition to the appearance and distribution of the rash, specific medical signs may be used by medical practitioners to assist with diagnosis. These may include Auspitz's sign pinpoint bleeding when scale is ce risc pentru psoriazisKoebner phenomenon psoriatic skin lesions induced by trauma to the ce risc pentru psoriazis[19] and itching and pain localized to papules and plaques.

Around one-third of people with psoriasis report a family history of ce risc pentru psoriazis disease, and researchers have identified genetic loci associated with the condition.

These findings suggest both a genetic susceptibility and an environmental response in developing psoriasis. Psoriasis has a strong hereditary component, and many genes are associated with it, but it is unclear how those genes work together. Most of the identified genes relate to the immune system, particularly the major histocompatibility complex MHC and Ce risc pentru psoriazis cells.

Genetic studies are valuable due to their ability to identify molecular mechanisms and pathways for further study and potential drug targets. Classic genome-wide linkage analysis has identified nine loci on different chromosomes associated with psoriasis. They are called psoriasis susceptibility 1 through 9 Ce risc pentru psoriazis through PSORS9. Within those loci are genes on pathways that lead to ce risc pentru psoriazis. Certain variations mutations of those genes are commonly found in psoriasis.

Some of these genes express inflammatory signal proteins, which affect cells in the immune system that are also involved in psoriasis. Some of these genes are also involved in other autoimmune diseases. PSORS1 is located on chromosome 6 in the major histocompatibility complex MHCwhich controls important immune functions.

Three genes in the PSORS1 locus have a strong association with psoriasis vulgaris: HLA-C variant HLA-Cw6[31] which ce risc pentru psoriazis a MHC class I protein; CCHCR1variant WWC, which encodes a coiled protein that is overexpressed in psoriatic epidermis; and CDSNvariant allele 5, which encodes corneodesmosina protein which is expressed in the granular and cornified layers of the epidermis and upregulated in psoriasis.

Two major immune system genes under investigation are interleukin subunit beta IL12B on chromosome 5qwhich expresses interleukinB; and IL23R on chromosome 1p, which expresses the interleukin receptor, and is involved in T cell differentiation.

Interleukin receptor and IL12B have both been strongly linked with psoriasis. A rare mutation in the gene encoding for the CARD14 protein plus an environmental trigger was enough to cause plaque psoriasis the most common form of psoriasis.

Conditions reported as worsening the disease ce risc pentru psoriazis chronic infections, stress, and changes in season and climate. The rate of psoriasis in HIV-positive individuals is comparable to that of HIV-negative individuals, however, psoriasis tends to be more severe in people infected with HIV.

Psoriasis has been described as occurring after strep throatand may be worsened by skin or gut colonization with Staphylococcus aureusMalasseziaand Candida albicans. Drug-induced ce risc pentru psoriazis may occur with beta blockers[10] lithium[10] antimalarial medications ce risc pentru psoriazis, [10] non-steroidal anti-inflammatory drugs[10] terbinafinecalcium channel blockerscaptoprilglyburidegranulocyte colony-stimulating factor[10] interleukinsinterferons[10] lipid-lowering drugs[15]: Psoriasis is characterized by an abnormally excessive and rapid growth of the epidermal layer of the skin.

Gene mutations of proteins involved in the skin's ability to function as a barrier have been identified as markers of susceptibility for the development of psoriasis. DNA released from dying cells acts as an inflammatory stimulus in psoriasis [49] and stimulates the receptors on certain dendritic cells, which in turn produce the cytokine interferon-α.

Dendritic cells bridge the innate immune system and adaptive immune system. They are increased in psoriatic lesions [44] and induce the proliferation of T cells and type 1 helper T cells Th1. A diagnosis of psoriasis apei pentru psoriazis ce risc pentru psoriazis based on the appearance of the skin. Skin characteristics typical for psoriasis are scaly, erythematous plaques, papules, or patches of skin that may be painful and itch.

If the clinical diagnosis is uncertain, a skin biopsy or scraping may be performed to rule out other disorders and to confirm the diagnosis. Skin from a biopsy will show clubbed epidermal projections that interdigitate with http://switchonswitchoff.org/vaselin-medical-de-psoriazis.php on microscopy. Epidermal thickening is another characteristic histologic finding of psoriasis lesions.

Unlike their mature counterparts, these superficial cells keep their nucleus. Psoriasis is classified as a papulosquamous disorder and is most commonly subdivided into different categories based on histological characteristics. Each form has a dedicated ICD code. Another classification scheme considers genetic ce risc pentru psoriazis demographic factors.

Type 1 has a positive family history, starts before the age ce risc pentru psoriazis 40, and is associated with the human leukocyte antigenHLA-Cw6. Conversely, type 2 does not show a family history, presents after age 40, and is not associated with HLA-Cw6. Ce risc pentru psoriazis classification of psoriasis as an autoimmune disease has sparked considerable debate.

Researchers have proposed differing descriptions of psoriasis and psoriatic arthritis; some authors have classified them as autoimmune diseases [17] [31] [57] while others have classified them as distinct from autoimmune diseases and referred to ce risc pentru psoriazis as immune-mediated inflammatory diseases.

There is no consensus about how to classify the severity of psoriasis. The DLQI ce risc pentru psoriazis ranges from 0 minimal impairment to 30 maximal impairment and click at this page calculated with each answer being assigned 0—3 points with higher ce risc pentru psoriazis indicating greater social or occupational impairment. The psoriasis area severity index PASI is the most widely used measurement tool for psoriasis.

PASI assesses the severity of lesions and the area affected and combines these two factors into Kemerovo psoriazis single score from 0 no disease to 72 maximal disease.

While no cure is available for psoriasis, [43] many treatment options exist. Topical agents are typically used for mild disease, phototherapy for moderate disease, and systemic agents for severe disease. Topical corticosteroid preparations are the most effective agents when used continuously for 8 weeks; retinoids read more coal tar were found to be of limited benefit and may be no better than placebo.

Vitamin D analogues such as paricalcitol were found to be significantly superior to placebo. Combination therapy with vitamin D and a corticosteroid was superior to either treatment alone and vitamin D was found to be superior to coal tar for chronic plaque psoriasis.

Moisturizers and emollients such as mineral oilpetroleum jellycalcipotriol ce risc pentru psoriazis, and decubal an oil-in-water emollient were found to increase the clearance of psoriatic plaques. Emollients have been shown to be even more effective at clearing psoriatic plaques when combined with phototherapy. The emollient salicylic acid is structurally similar to para-aminobenzoic acid PABAcommonly found in ce risc pentru psoriazis, and is known to interfere with phototherapy in psoriasis.

Coconut oilwhen used as an emollient in psoriasis, has been found to decrease plaque clearance with phototherapy. Ointment and creams containing coal tardithranolcorticosteroids i. The use of the finger tip unit may be helpful in guiding how much topical treatment to use. Vitamin D analogues may be useful with steroids; however, alone have a higher rate of side effects.

Another topical therapy used to treat psoriasis is a form of balneotherapywhich involves daily baths in the Dead Sea. This is usually done for four weeks with the benefit attributed to sun exposure and specifically UVB light.

This is cost-effective and it has been propagated as an effective way to treat psoriasis without medication. Phototherapy in the form of sunlight has long been used for psoriasis. The UVB lamps should have a timer that ce risc pentru psoriazis turn off the lamp when the time ends. The amount of light used is ce risc pentru psoriazis by a person's skin ce risc pentru psoriazis. One of the problems with clinical phototherapy is the difficulty ce risc pentru psoriazis patients have gaining access to a facility.

Indoor tanning resources are almost ubiquitous today and could be considered as a means for patients to get UV exposure when dermatologist provided phototherapy is not available. However, a concern with the use of commercial tanning is that tanning beds that primarily emit UVA might not effectively treat psoriasis. One study found that plaque psoriasis is responsive to erythemogenic doses of either UVA or UVB, as exposure to either can cause dissipation of psoriatic plaques.

It does require more energy to reach erythemogenic dosing with UVA. UV light therapies all have risks; tanning beds are no exception, particularly in the link between UV light and the increased chance of skin cancer.

There are increased ce risc pentru psoriazis of melanoma, squamous cell and basal cell carcinomas; ce risc pentru psoriazis psoriasis patients, particularly those under age 35, are at increased risk from melanoma from UV light treatment.

The World Health Organization WHO listed tanning ce risc pentru psoriazis as carcinogens. A review of studies recommends that people who are susceptible to skin cancers exercise caution when using UV light therapy as a treatment.

A major mechanism of NBUVB is the induction of DNA damage in the form of pyrimidine dimers. This type of ce risc pentru psoriazis is useful in the treatment of psoriasis because the formation of these dimers interferes with the cell cycle and stops it.

The interruption of the cell cycle induced by NBUVB opposes the characteristic rapid division of skin cells seen in psoriasis. The most common short-term ce risc pentru psoriazis effect of check this out form of ce risc pentru psoriazis is redness of the skin; less common side effects of NBUVB phototherapy are itching and blistering of the treated skin, irritation of the eyes in the form of conjunctival inflammation or inflammation of the corneaor cold sores due to reactivation of the herpes simplex virus in the skin surrounding the lips.

Eye protection is usually given during phototherapy treatments. Psoralen and ultraviolet A phototherapy PUVA combines the oral or topical administration of psoralen with exposure to ultraviolet Ce risc pentru psoriazis UVA light. The mechanism of action of PUVA is unknown, but probably involves activation of psoralen by UVA light, which inhibits the abnormally rapid production of the cells in psoriatic skin. There are multiple mechanisms of action associated with PUVA, including effects on the skin's immune system.

PUVA is associated with nauseaheadachefatigueburning, and itching. Long-term treatment is associated with squamous cell carcinoma but not with melanoma. Psoriasis resistant to topical treatment and phototherapy may be treated with systemic therapies including medications by mouth or injectable treatments.

The majority of people experience a recurrence of psoriasis after systemic treatment is discontinued. Non-biologic systemic treatments frequently used for psoriasis psoriazis pe imaginea capului și tratamentul methotrexateciclosporinhydroxycarbamidefumarates such as dimethyl fumarateand retinoids.

These agents are also regarded as first-line treatments for psoriatic erythroderma. Biologics are manufactured proteins that interrupt the immune process involved in psoriasis. Unlike generalised immunosuppressive drug therapies such as methotrexate, biologics target specific aspects of the immune system contributing to psoriasis. Guidelines regard biologics as third-line treatment for plaque psoriasis following inadequate response to topical treatment, phototherapy, and non-biologic systemic treatments.

European guidelines recommend avoiding biologics if a pregnancy is planned; anti-TNF therapies such Psoriazisul primele semne infliximab are not recommended for use in chronic carriers of the hepatitis B virus or individuals infected with HIV.

Several monoclonal antibodies target cytokines, the molecules that cells use to send inflammatory ce risc pentru psoriazis to each other. TNF-α is one of the main executor inflammatory cytokines. Four monoclonal antibodies MAbs infliximabadalimumabgolimumab ce risc pentru psoriazis, and certolizumab pegol and one recombinant TNF-α decoy receptoretanercepthave been developed to inhibit TNF-α signaling.

Additional monoclonal antibodies, such as ixekizumab[81] have been developed against pro-inflammatory cytokines [82] and inhibit the inflammatory pathway at a different point than the anti-TNF-α antibodies.

Two drugs that target T cells are efalizumab and alefacept. Efalizumab is a monoclonal antibody that specifically targets the CD11a subunit of LFA Efalizumab was voluntarily withdrawn from the European market in February and from the US market in June by the manufacturer due to the medication's association with cases of progressive multifocal leukoencephalopathy.

Individuals with psoriasis may develop neutralizing antibodies against monoclonal antibodies. Neutralization occurs when an antidrug antibody prevents a monoclonal antibody such as infliximab from binding antigen in a laboratory test. Specifically, neutralization occurs when the antidrug antibody binds to infliximab's antigen binding site instead of TNF-α. When infliximab no longer binds tumor necrosis factor alphait ce risc pentru psoriazis longer decreases inflammation, and psoriasis may worsen.

Neutralizing antibodies have not been reported against etanercept, a biologic drug that is a fusion protein composed ce risc pentru psoriazis two TNF-α receptors.

The lack of neutralizing antibodies against etanercept is probably secondary to the innate presence of the TNF-α receptor, and the development of immune tolerance. Limited evidence suggests removal of the tonsils may benefit people with chronic plaque psoriasis, guttate see more, and palmoplantar pustulosis.

Uncontrolled studies have suggested that individuals with psoriasis or ce risc pentru psoriazis arthritis may benefit from a diet supplemented with fish oil rich in eicosapentaenoic acid EPA and docosahexaenoic acid DHA. The effect of consumption of caffeine including coffee, black tea, mate, and dark chocolate remains to be determined. There is a higher rate of celiac disease among people with psoriasis. Most ce risc pentru psoriazis with psoriasis experience nothing more than mild skin lesions that can be treated effectively with topical therapies.

Psoriasis is known to have a negative impact on the quality of life of both the affected person and the individual's family members. Itching and pain can interfere with basic functions, such as self-care and sleep. Individuals with psoriasis may feel self-conscious about their appearance and have a poor self-image that stems from fear of public rejection and psychosexual concerns. Psoriasis has been associated with low self-esteem and depression is more common among those with the condition.

Clinical research has indicated individuals often experience a diminished quality of life. Several conditions are associated with psoriasis. These occur more frequently in older people. Nearly half of individuals with psoriasis over the age of 65 ce risc pentru psoriazis at least three comorbidities, and two-thirds have at least two comorbidities. Psoriasis has been associated with obesity [3] and several other cardiovascular ulei esential de evaluări psoriazis metabolic disturbances.

Cardiovascular disease risk appeared to be correlated with the severity of psoriasis and its duration. There is no strong evidence to suggest that psoriasis is associated with an increased risk of death from cardiovascular events. Methotrexate may provide a degree of protection for the heart.

The ce risc pentru psoriazis of having hypertension are 1. A similar association was noted in people who have psoriatic arthritis—the odds of having hypertension were found to be 2. The link between psoriasis and hypertension is not currently understood. Mechanisms hypothesized to be involved in this relationship include the following: Statin use in those with psoriasis and hyperlipidemia was associated with decreased levels of high-sensitivity C-reactive protein and TNFα as well as decreased activity of the immune protein LFA The rates of Crohn's disease and ulcerative colitis are increased when compared with the general population, by a factor of 3.

Pensie de psoriazis one third of people with psoriasis report being diagnosed before age Psoriasis affects about 6.

People with inflammatory bowel disease such as Crohn's disease or ulcerative colitis are at an increased risk of developing psoriasis. Scholars believe psoriasis to have been included among the various skin conditions called tzaraath translated as leprosy in the Hebrew Biblea condition imposed as a punishment for slander. The patient was deemed "impure" see tumah and taharah during their afflicted phase and is ultimately treated by the kohen.

The Greeks used the term lepra λεπρα for scaly skin conditions. They used the term psora to describe itchy skin conditions. Leprosythey said, is distinguished by the regular, circular form of patches, while psoriasis is always irregular. Willan identified two categories: Psoriasis is thought to have first been described in Ancient Rome by Cornelius Celsus. The disease was first classified by English physician Thomas Willan. The British dermatologist Thomas Bateman described a possible link between psoriasis and arthritic symptoms in The history of psoriasis is littered with treatments of dubious effectiveness and high toxicity.

In the 18th and 19th centuries, Fowler's solutionwhich contains a poisonous and carcinogenic arsenic compound, was used by dermatologists as a treatment for psoriasis. The word psoriasis is from Greek ψωρίασις, meaning "itching condition" or "being itchy" [] from psora"itch" and -iasis"action, condition".

The International Federation of Psoriasis Associations IFPA see more the global umbrella organization for national and regional psoriasis patient associations and also gathers the leading experts in psoriasis and psoriatic arthritis research for scientific conferences every three years.

Non-profit organizations the National Psoriasis Foundation in the United States, the Psoriasis Association in the United Kingdom and Psoriasis Australia offer advocacy and education about psoriasis in their respective countries. Pharmacy costs ce risc pentru psoriazis the main source of direct expense, with biologic therapy the most prevalent.

These costs increase significantly when co-morbid conditions such as heart disease, ce risc pentru psoriazis, diabetes, lung disease and psychiatric disorders dacă este posibil de face permanent psoriazis factored in.

The role of insulin resistance in the pathogenesis of psoriasis is currently under investigation. Preliminary research has suggested that antioxidants such as polyphenols may have beneficial effects on the inflammation characteristic of psoriasis. List of human leukocyte antigen alleles associated with cutaneous ce risc pentru psoriazis. Cambridge University Press, ISBN     CS1 maint: Overview of psoriasis and guidelines of care for the treatment of psoriasis with biologics".

J Am Acad Dermatol. Retrieved 22 April National Institute of Arthritis and Musculoskeletal and Skin Diseases. Retrieved 1 July Identification and Management of Psoriasis and Associated ComorbidiTy IMPACT project team. Drug Des Devel Ther. Davidson's principles and practice of medicine.

Retrieved 16 March Andrews' Diseases of the Skin: Clinical Dermatology cauzele și tratamentul mâncărimi mâinile ed.

From the Medical Board of the National Psoriasis Foundation". Fitzpatrick's Dermatology in General Medicine 8th ed. Am J Clin Dermatol.

Greenberg, Michael Glick, Jonathan A. Burket's oral ce risc pentru psoriazis 11th ed. N Engl J Med. Retrieved 8 October The American Journal of Human Genetics. J Eur Acad Dermatol Venereol. J Int AIDS Soc. A Review of T-cell Subsets and Cytokine Profiles". J Cutan Med Surg. Expert Rev Gastroenterol Hepatol. Clinical dermatology 4th der psoriazis John Pagano und. Ce risc pentru psoriazis Growth Factor Ce risc pentru psoriazis. Br J Community Nurs.

Visit web page Disease, Immune Response and Cytokines. Clin Rev Allerg Immunol. The International League of Dermatological Societies. Archived from the original on Fitzpatrick's dermatology in general medicine 6th ed. J Am Board Fam Med. Clin Cosmet Investig Dermatol. Br J Clin Dermatol. Arthritis Care Res Hoboken. Cochrane Database Syst Rev. Guidelines of care for the management and treatment of psoriasis with topical therapies".

The Cochrane database of systematic reviews. International Journal of Dermatology. Indian J Dermatol Venereol Leprol. Psoriasis American Academy of Dermatology". A Review of Phase III Trials.

Ce risc pentru psoriazis Point of View of the Nutritionist. Int J Environ Res Public Health Review. Clin Cosmet Investig Dermatol Ce risc pentru psoriazis. Nat Rev Gastroenterol Hepatol Review.

Health Qual Life Outcomes. Clinical dermatology a color guide to diagnosis and therapy 5th ed. Am J Med Sci. Ir J Med Sci Psoriatic and Reactive Arthritis: A Companion to Rheumatology 1st ed. The American Journal of Managed Care. L40 ICD - 9-CM: Diseases of the skin and appendages by morphology. Ce risc pentru psoriazis lentigo melasma nevus melanoma. Aphthous stomatitis oral candidiasis lichen planus leukoplakia pemphigus vulgaris mucous membrane pemphigoid cicatricial pemphigoid herpesvirus coxsackievirus syphilis systemic histoplasmosis squamous-cell carcinoma.

Papulosquamous disorders L40—L45— Guttate psoriasis Psoriatic arthritis Psoriatic erythroderma Drug-induced psoriasis Inverse psoriasis Napkin psoriasis Seborrheic-like psoriasis. Pityriasis lichenoides Pityriasis lichenoides et varioliformis acutaPityriasis lichenoides chronica Lymphomatoid papulosis Small plaque parapsoriasis Digitate dermatosisXanthoerythrodermia perstans Large plaque parapsoriasis Retiform parapsoriasis. Pityriasis rosea Pityriasis rubra pilaris Pityriasis rotunda Pityriasis amiantacea.

Hepatitis-associated lichen planus Lichen planus pemphigoides. Lichen nitidus Lichen striatus Lichen ruber moniliformis Gianotti—Crosti syndrome Erythema dyschromicum perstans Idiopathic eruptive macular pigmentation Keratosis lichenoides chronica Kraurosis vulvae Lichen sclerosus Lichenoid dermatitis Lichenoid reaction of graft-versus-host disease.

Retrieved from " https: Autoimmune diseases Cutaneous conditions Psoriasis. Uses editors parameter CS1 maint: Uses authors parameter Good articles Articles with DMOZ links Wikipedia ce risc pentru psoriazis with LCCN identifiers RTT. The article ce risc pentru psoriazis a derivative under the Creative Commons Attribution-ShareAlike License. A link to the original article can be found here and attribution parties here. By using this site, you agree to the Terms of Use.

Navigation menu Namespaces Article News Images Video Audio Shopping Books Advertise. Navigation Main page Contents Featured content Current events. Reditchy, scaly patches of skin [3]. Genetic disease ce risc pentru psoriazis by environmental factors [3]. Based on symptoms [4]. Steroid creamsvitamin D3 cream, ultraviolet lightimmune system suppressing medications such as ce risc pentru psoriazis [6]. Pustulosis palmaris et plantaris.

Epidermal wart callus seborrheic keratosis acrochordon molluscum contagiosum actinic keratosis squamous-cell carcinoma basal-cell carcinoma Merkel-cell carcinoma nevus sebaceous trichoepithelioma. With epidermal involvement Eczematous contact dermatitis atopic dermatitis seborrheic dermatitis stasis dermatitis lichen simplex chronicus Darier's disease glucagonoma syndrome langerhans cell histiocytosis lichen sclerosus pemphigus foliaceus Ce risc pentru psoriazis syndrome Zinc deficiency.

Red Blanchable Erythema Generalized drug eruptions viral exanthems toxic erythema systemic lupus erythematosus. Lichen planus configuration Annular Linear morphology Hypertrophic Atrophic Bullous Ulcerative Actinic Pigmented site Mucosal Nails Peno-ginival Vulvovaginal overlap synromes with lichen sclerosus with lupus erythematosis other:


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