papulo-erytroskuamosa kuliah sm vii edit.ppt
TRANSCRIPT
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dr. Luh Made Mas Rusyati, Sp.KK
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Difinition: recurrent, kronik, skin inflammatory ds with variations in clinical presentations
Belongs to dermatosis erythroskuamous lesionsmarked by increase in vascularization (erythema) and scales production in the epidermis
Universal, variations in incidence 0,1-11,8%
Highest incidence in Europe (Denmark 2,9%), no case has been reported from India
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Psoriasis may began at any ages Uncommon under the age of 10 years It most to appear between ages of 15
and 30 Christophers Divided into Type I
and II Type I before 40 yr and HLA
associated, type II after 40 yr, lacking HLA associated
No evidence that type I and type II respond differently to different therapies.
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Psoriasis Classification and Psoriasis Classification and Clinical Patterns of Skin Clinical Patterns of Skin
PresentationPresentation Psoriasis Vulgaris Eruptive (guttate) psoriasis Psoriasis eritrodermi Generalized pustular psoriasis (von
Zumbusch) Annular pustular psoriasis Localized pustular psoriasis
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4 Characteristics findings in psoriatic lesions:
1.Well-demarcated lesions2.Silvery, layered, rough scales at the
surface of the lesions 3.The skin are erythema and coiled
beneath the scales 4.Positive Auspitz sign
Koebner phenomenon presents in 20% cases
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LESION ON THE NAILS LESION ON THE KNEES
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Physical trauma Infections Stress Drugs
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DIAGNOSIS Anamnesis Clinical findings Histopathological
examinations
DD Seborrheic
dermatitis Pityriasis rosea Syphilis PRP
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Laboratory FindingsLaboratory Findings
Laboratory examinationsunspecific Histopathologic findings epidermal
and upper dermal changes Initial changes: oedeme of str
papillare of the dermis with mononuclear cells infiltrates and spongiosis
Late changes: neutrofil migration to the str korneum Munro’s microabcess
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PASI PASI ((Psoriasis Area and Severity Psoriasis Area and Severity
IndexIndex)) Badan dibagi 4 kuadran dgn bobot : Kepala (K=0.1), Badan (B=0.3), Ekstrimitas Atas (EA=0.2), Ekstrimitas Bawah (EB=0.4)
Area (A) yang terlibat diberi bobot : tidak ada=0, < 10%=1, 10-30%=2, 30-50%=3, 50-70%=4, 70-90%=5, 90-100%=6
Keparahan (S) diberi gradasi 0-4 Gejala klinis : Eritema (E), Infiltrat (I),
Deskuamasi (D) PASI = 0.1(EK+IK+DK)AK +
0.3(EB+IB+DB)AB + 0.2(EEA+IEA+DEA)AEA + 0.4 (EEB+IEB+DEB)AEB
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TreatmentTreatment
Treatment based on the extent and location of lesions, health problem.- lesions < 5% of the body topical drugs- lesions 5-10% of the body topical drugs + phototherapy/systemic drugs- lesions > 10% of the body phototherapy or systemic drugs
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TreatmentTreatment
Topical drugs :- Antralin (dithranol)- Vit D3 and analogues- Tazarotene- Tar- Topical corticosteroids- Emolient
Ultraviolet light- PUVA (Psoralen Ultra Violet A)- UVB
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TreatmentTreatment Systemic therapysevere cases with
extensive lesions or pustular or active psoriasis- Metotrexate (MTX)- Cyclosphorine- Retinoid- Esther Fumarat Acid- Glucocorticoids systemic- Macrolactam (Calcineurin Inhibitor)- Excimer Laser
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IntroductionIntroduction
Definition chronic dermatosis papulosquamous disease, associated with increase in sebum production (seborea)
Insidence 2 peaks, the first 3 month of life and 4th and 7th decade of adulthood with male preponderence
Clinical lesions on the scalp,, face, body parts with plenty of sebaceous follicle, varies in severity
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Seborrheic DermatitisSeborrheic Dermatitisin Infantsin Infants
Thick, oily crust on hairy scalp, crease area for examples on the retroauricular fold, ear peak, mid face, neck, chest
Sometimes accompanied by fissures (crusta lactea, milk crust, cradle cap)
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Desquamative Erythroderma Desquamative Erythroderma ((Leiner’s DiseasesLeiner’s Diseases))
Skin lesions quickly coalescence into wide lesions all over the body, erythematous, covered with scales erythroderma
Look severly ill, with anemia, diarrhea, and vomitting
Frequently followed by secondary infections
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Seborrheic Dermatitis Seborrheic Dermatitis in Adultin Adult
Seborrhoeic eczematid Pityriasis sicca Erythema paranasale Patchy dermatitis seborrhoeic Pityriasiform type seborrheic
dermatitis Folliculare type seborrheic dermatitis Chronic Otitis Media Blefaritis
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Triggering FactorTriggering Factor
Seborrhea Microbial impact Drugs Neurologic/neurotransmitter
dysfunction Physical factors Nutritional imbalance
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Diagnosis and Differential Diagnosis and Differential DiagnosisDiagnosis
Diagnosisanamnesis + clinical findings
DD/ in infant : atophic dermatitis, psoriasis, scabies, Langerhans Cells Histiocytosis
DD/ in adult depends on location : psoriasis, atophic dermatitis, impetigo, contact dermatitis, allergic reactions, pityriasis versikolor, pityriasis rosea, demodocosis/demodicidosis, candidiasis
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TreatmentTreatment
Aim: releasing the scales, inhibiting yeast colonization, preventing secondary infections, reducing pruritus and oedeme
Treatment depends on the location of the lesion
Some therapeutic modalitiesantifungal, topical
Steroid topikal
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PrognosisPrognosis
Infantgood prognosis, mostly mild and healed spontaneously
Adultchronic disease, treatments for reducing symptoms and not for healingpatients education
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IntroductionIntroduction
The term first used by Gilbert in 1860 Definition: common, acute, self-limited
skin eruption that typically begins as a single thin oval scaly plaque on the trunkherald patch
Followed by numerous similar-appearing smaller lessions along the lines of cleavage of the trunkchristmas tree pattern
Usually asymptomatic, sometimes associated with pruritus and mild flu-like symptoms
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EpidemiologyEpidemiology
Reported in all races, irrespective of the climates
Average annual incidence: 0,16% Occurs most commonly in teenagers
and young adultbetween 10-35 years old
Slight female preponderance 1.5:1 Recurrences are raresuggests
lasting immunity after initial episode
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Etiology and Pathogenesis Etiology and Pathogenesis
Historically pityriasis rosea has been considered to be caused by an infectious agent
Scientific evident theory that pityriasis rosea represents a viral exanthem associated with reactivation of human herpesvirus (HHV-7) and (HHV-6)
The mech of reactivation is unknown The characteristic distribution of the
lesions are unexplained
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Clinical FindingsClinical Findings
Historysingle truncal lesion followed by numerous smaller lession in several days to weeks later, asymptomatic-pruritic, flu like symptoms
Cutaneous lesions: - herald patch well demarcated, Ø 2-4 cm, oval/round, salmon coloured, with fine scales- secondary lesions small plaque resembling primary plaque with christmas tree pattern or small, red, non-scaly papules spread peripherally
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Differential DiagnosisDifferential Diagnosis
Secondary syphilis Tinea corporis Nummular dermatitis Guttate psoriasis Pityriasis lichenoides chronica Pityriasis rosea – like drug eruption
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TreatmentTreatment
Self-limited Education dan reassurance Pruritic lesion topikal
corticosteroids medium potency Flu-like symptoms and extensive
lesions acyclovir oral 5 x 800 mg for a week
Special considerationphototherapy
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Prognosis andPrognosis andClinical CourseClinical Course
All patients have spontaneous resolutions
Disease durations 4-10 weeks No residual effects secondary to
occurance of pityriasis rosea Reccurency is possible, but rare
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IntroductionIntroduction
Exfoliativa dermatitis, exfoliativa erythroderma, Red Man syndrome
Definitioninflammatory skin ds with erythematous and scales formation all over the body either idiopathic or caused by extention of other skin ds (psoriasis, atophic dermatitis, drug eruption, cutaneus T-cell lymphoma)
almost 50% associated with underlying ds
25% idiophatic
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EpidemiologyEpidemiology
Rare case male : female = 2:1 to 4:1 Average age of onset are 40-60 years
old, but can also affecting neonates and infants
In the adulthood mostly related to psoriasis, atophic dermatitis, drug eruption, idiophatic
In neonates and infants mostly caused by atophic dermatitis, seborrheic dermatitis, drug eruption, psoriasis, infections (for example Staphylococcal Scalded Skin Syndrome)
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EtiopathogenesisEtiopathogenesis
Pathogenesisunclear Increase in germinativum cells mitosis
and shortening of functional epidermal keratinization
Increase in scales degradation rate Increase in vascular endothelial growth
factor/vascular permeability factorincrease in permeability and vascularization
Increase in adhession molecules expressionaffecting production and proliferation of inflammatory mediators
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EtiopathogenesisEtiopathogenesis Drug eruption eritroderma: alopurinol,
ampisillin/amoxcysilin, dapson, carbamazepine, fenbarbital, sulfonamide, Ca-channel blockers, simetidine, gold, obat tradisional
Eritroderma ec systemic disease : malignancy (solid tumor and haematologic), infection (syphillis, HIV)
Psoriatic erythroderma : effect of the disease, corticosteroid, methotrexate, phototherapy, lithium, pregnancy, infection
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Clinical ManifestationClinical Manifestation Eritema generalisata, 90% with scales
formation, without affecting the mucousa Acute: erithemawhite/yellowish fine
scales starting in flexures areaforming platelike leson on the palmsgrey, dry scales, with light red skin lesions
Secondary infections: wet lesions, tightly adherent scales, bad odour caused by colonization of bacteria
Chronic: thick skin and nails, induration, oedeme and lichenifications, hair fall, subungual hyperkeratosis, onykilosis, beau lines of the nails
Drug eruption: shoreline feature in the nails
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Clinical ManifestationClinical Manifestation Primary type(idiopathic)erythem starts
in the trunk, spreading with scales production mostly in old man, chronic, relaps, severe pruritus, limfadenopati, dermatopati, extensive keratoderma palmoplantarRed Man Syndrome
Secondary typewith associated underlying ds- topical drug eruption: initial lesion as dermatitis- systemic drug eruption: initial lesion morbiliformis/skarlatiniformis-2/3 histopathologic findings are consistent with underlying ds- exacerbation occurs in lesion with sunlight exposure
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Systemic Findings in Systemic Findings in ErythrodermaErythroderma
62% cases present with axillaris and inguinalis limfadenopati, >37% hepatomegaly, 23% splenomegaly
Poikilothermia Decrease in systemic blood flowheart
failure 80% cases presents with fever and
tachycardia Dehidration Increase in blood ureum level Protein loss dan nitrogen, potassium,
folate imbalancehipoalbuminemia, oedeme, reduce in muscle mass
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Commonly find erythroderma
Psoriasis Athopic
dermatitis Drug eruption Idiophatic
Rare form of erythroderma
Cutaneus T-Cell Lymphoma (CTCL)
Pitiriasis Rubra Pilaris (PRP)
Dermatosis Bulosa- Pemfigus foliaseus- Pemfigoid bulosa- Pemfigus paraneoplastik
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Laboratory FindingsLaboratory Findings
Anemia, limfositosis, eosinofilia, increase in ESR (erythrocyte sedimentation rate)
Decrease in serum protein Decrease in electrolytes and renal
function Increase in IgE serum Sezary Syndrome>20% sel Sezary Erythroderma idiophatic bone
marrow biopsy: eosinofilia (32%)
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Pathologic ExaminationsPathologic Examinations
Multiple consecutive biopsy needed
Erythroderma psoriatic histopathologic findings have >90% accuracy, but in erythroderma associated with CTCL histopathologic examinations are difficult
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TreatmentTreatment Adequate nutrition, fluid and electrolytes
balance, high protein diet, folic acid supplementation
Warm and moist environmet Hospitalizationsevere cases, observation
in fluid intake and renal function, possibility of cardiac failure
Supportive skin careemolient, weak to mid potency topical corticosteroids
Antibiotics for bacteria superinfections, antihistamin and behavioural therapy to decrease itch and scratch
Consider corticosteroids and immunosuppresant therapy in severe/refracter cases
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IntroductionIntroduction
Definition unique, common inflammatory disorders efecting skins, mucous membranes, nails, hairs
Lessions symmetric, grouped, erythematous-violaceous, flat-topped, polygonals papules
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EpidemiologyEpidemiology
Overall prevalence less than 1% worlwide
2/3 of the cases occur between 30-60 years old
No sexual predilection is evident Predilection in flexural aspects of
arms and legs Familial lichen planus have been
reported
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Etiology & PathogenesisEtiology & Pathogenesis
Lichen planus almost certainly immunological mediated
The most characteristic change in lichenoid reactionsapoptosis
Cell-mediated immunity plays major role
Humoral immunity as a secondary response
Both CD4+ and CD8+ T cells are found in the skin lesions
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Clinical FindingsClinical Findings
Cutaneous lessions:faintly erythematous –violaceous, flat-topped, polygonal papules
Thin, transparent, adherent scales at the top
Wickham striae Lessions are symmetrically and
bilaterally distributed over the extrimities
Asymptomatic-quite pruritic
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Histopathologic DiagnosisHistopathologic Diagnosis
Major pathologic findings basal epidermal keratinocyte damage
Epidermal changeshyperkeratosis, hypergranulosis, elongation of rete ridges
Multiple apoptotic bodies or colloid-hyaline (Civatte) bodies at dermal-epidermal junction
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Differential DiagnosisDifferential Diagnosis Classic: psoriasis, drug eruption, lichen
simplex chronicus Annulare: granuloma annulare, tinea Linear: nevus unius lateris, lichen
striatus, linear epidermal nevus Hypertrophic: lichen simplex
chronicus, prurigo nodularis, lichenoid cutaneous, amylidosis, kaposi sarcoma
Atrophic: lichen sclerosus Follicular: lichen nitidus, lichen
spinulosus Childhood: lichen nitidus, lichen
striatus, pityriasis lichenoides, papular acrodermatitis of childhood
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TreatmentTreatment Cutaneous Lichen planus
- first line: topical topical steroids, intralesional
steroids, tacrolimus, pimecrolimus
physical psoralen and UVAsystemic systemic steroids, etretinate,
acitretin, isotretinoin
- second line (systemic): cyclosporine, dapsone, hydroxychloroquine, azathioprine
- special forms (systemic): doxycycline, tetracycline, nicotinamide, interferon α-2b, metronidazole, cyclophosphamide, methotrexate
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TreatmentTreatment Oral Lichen Planus
- first line: topical topical steroids, intralesional steroids,
tacrolimus, pimecrolimus, lidocaine, tretinoin gel, isotretinoin gel
systemic anti candidal-systemic steroids, etretinate, acitretin, isotretinoin - second line :
topical cyclosporine mouthwashphysical extracorporeal photochemotherapy,
photodynamic therapy systemic cyclosporine, griseovulfin,
hydroxychloroquine, azathioprine, mycophenolate mofetil, thalidomide, cyclophosphamide