cpc final kurban nov 2009
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CPCCPC
KURBANKURBAN
MUHAMMAD KHAWAR NAZIRMUHAMMAD KHAWAR NAZIR
1111--0909--0909
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CASE1
CASE1
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FoamyFoamy histiocyteshistiocytes laden with intracellular fatdeposits primarily withinladen with intracellular fatdeposits primarily withinthe upper reticular dermisthe upper reticular dermis
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XANTHOMA CELLSXANTHOMA CELLS
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Foamcells in dermis ( positive for lipid withFoamcells in dermis ( positive for lipid with
special stains such asspecial stains such as OILOIL REDRED--O STAINO STAIN
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XANTHELASMAXANTHELASMA
derived from the Greekderived from the Greek xanthosxanthos(yellow) and(yellow) and elasmaelasma (beaten metal(beaten metalplate).plate).
Yellow plaquesthatoccur mostcommonlynear the inner canthusofYellow plaquesthatoccur mostcommonlynear the inner canthusofthe eyelid,more oftenon the upper lid than the lower lidthe eyelid,more oftenon the upper lid than the lower lid
Xanthelasma palpebrarum is the mostcommoncutaneousXanthelasma palpebrarum is the mostcommoncutaneousxanthoma.xanthoma.
canbe soft,semisolid,or calcareouscanbe soft,semisolid,or calcareous One halfof these lesionsare associated with elevated plasma lipidOne halfof these lesionsare associated with elevated plasma lipid
levelslevels Occurs in individuals> 50yrsOccurs in individuals> 50yrs
Inchildrenor young adults, associated with familialInchildrenor young adults, associated with familialhypercholestrolemiaor familial dysbetalipidemiahypercholestrolemiaor familial dysbetalipidemia
Management: Laser, excision, Electrodesiccation, topical applicationManagement: Laser, excision, Electrodesiccation, topical applicationof trichloroacetic acidof trichloroacetic acid
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CASE2
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VariableVariable epidermalepidermal spongiosisspongiosis or necrosis, Intense papillarydermalor necrosis, Intense papillarydermaledema, superficial anddeepedema, superficial anddeep perivascularperivascular lymphocytic infiltrate,lymphocytic infiltrate,
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FluffyFluffy edema"of vessel walls. Lymphocyticedema"of vessel walls. Lymphocytic vasculitisvasculitis may be presentmay be present
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PERNIOPERNIO
Inflammatory skin condition presentingafter exposure tocoldasInflammatory skin condition presentingafter exposure tocoldaspruriticpruritic and/or painfuland/or painful erythematouserythematous toto violaceousviolaceous acralacral lesionslesions
idiopathicor secondary toan underlyingdisease, likeidiopathicor secondary toan underlyingdisease, like ChronicChronicmyelomonocyticmyelomonocytic leukemia, Anorexia nervosa,leukemia, Anorexia nervosa, DysproteinemiasDysproteinemias,, MacroglobulinemiaMacroglobulinemia,,CryoglobulinemiaCryoglobulinemia,,cryofibrinogenemiacryofibrinogenemia,coldagglutinins,,coldagglutinins, AntiphospholipidAntiphospholipid antibodyantibody
syndrome,Raynaudsyndrome,Raynaud diseasedisease
due toan abnormal vascular response tocold exposure and is mostdue toan abnormal vascular response tocold exposure and is mostfrequent when damp or humidconditions coincidefrequent when damp or humidconditions coincide
Prophylactic warmingofProphylactic warmingofacralacral areas,achieved by heatandareas,achieved by heatandappropriate clothing,appropriate clothing, preventsprevents perniopernio
TTopicalopical and systemic steroids, vasodilators, IVcalcium followed byand systemic steroids, vasodilators, IVcalcium followed by
IM vitamin K,and ultraviolet B radiationIM vitamin K,and ultraviolet B radiation Calcium channel blockersCalcium channel blockers Peripheral arterial vasodilatorsPeripheral arterial vasodilators
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DIFFERENTIAL DIAGNOSISDIFFERENTIAL DIAGNOSIS
ErythemaErythema MultiformeMultiforme
HypersensitivityHypersensitivityVasculitisVasculitis((LeukocytoclasticLeukocytoclastic VasculitisVasculitis))
SarcoidosisSarcoidosis
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CASE3
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AAllll show a similarshow a similar histologichistologic appearanceappearance ,,perivascularperivascular infiltrate of lymphocytesinfiltrate of lymphocytes
andmacrophages is centeredon the superficial small blood vessels of the skin,andmacrophages is centeredon the superficial small blood vessels of the skin,
endothelial cell swellingand narrowingofendothelial cell swellingand narrowingof luminalumina,,
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Extravasation of red bloodcells with marked hemosiderin deposition inExtravasation of red bloodcells with marked hemosiderin deposition inmacrophagesmacrophages
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SCHAMBERG,S DISEASESCHAMBERG,S DISEASE
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LICHEN AUREUSLICHEN AUREUS
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PIGMENTED PURPURIC DERMATOSISPIGMENTED PURPURIC DERMATOSIS
GroupGroup ofchronicdiseases ofmostly unknown etiology that have a veryofchronicdiseases ofmostly unknown etiology that have a verydistinctive clinical appearancedistinctive clinical appearance
CharacterizedCharacterized byby extravasationextravasation of erythrocytes in the skin with markedof erythrocytes in the skin with markedhemosiderinhemosiderin depositiondeposition
characteristicorangecharacteristicorange--brown, speckled,cayenne pepperbrown, speckled,cayenne pepperlike discolorationlike discoloration IIncludesncludes SchambergSchamberg disease (disease (ieie, progressive, progressive pigmentarypigmentary dermatosisdermatosis),),purpurapurpura annularisannularis telangiectodestelangiectodes ((MajocchiMajocchi disease), lichendisease), lichen aureusaureus, itching, itchingpurpurapurpura,, eczematidlikeeczematidlike purpurapurpura ofof DoucasDoucas andand KapetanakisKapetanakis,and the,and thepigmentedpigmented purpuricpurpuric lichenoidlichenoid dermatosisdermatosis ofof GougerotGougerotand Blumand Blum
LLlowerlower limbs are affected inlimbs are affected in SchambergSchamberg diseasedisease LLichenichen aureusaureus, the eruption is usuallya solitary lesion or a localizedgroup, the eruption is usuallya solitary lesion or a localizedgroup
of lesionsof lesions MajocchiMajocchi diseasedisease isis characterized by small annular plaques ofcharacterized by small annular plaques ofpurpurapurpura that contain prominentthat contain prominent telangiectasiatelangiectasia
PigmentedPigmented purpurapurpura withwith lichenoidlichenoid--typetype skin change is yet anotherskin change is yet anotherclinical variant, whichclinical variant, which GougerotGougerot and Blumand Blum first reported.first reported.
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CAYENNE PEPPERCAYENNE PEPPER
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DIFFERENTIALDIFFERENTIAL
ScurvyScurvy Other Problems to Be ConsideredOther Problems to Be Considered earlyearly cutaneous Tcutaneous T--cell lymphomacell lymphoma purpuricclothingdermatitispurpuricclothingdermatitis stasis pigmentation, scurvystasis pigmentation, scurvy leukocytoclastic vasculitisleukocytoclastic vasculitis purpuricgeneralized lichen nitiduspurpuricgeneralized lichen nitidus
drug hypersensitivity reactions (eg,allergy to rituximab,drug hypersensitivity reactions (eg,allergy to rituximab,carbamazepine,meprobamate,chlordiazepoxide,carbamazepine,meprobamate,chlordiazepoxide,furosemide, nitroglycerin,or vitamin Bfurosemide, nitroglycerin,or vitamin B--1).1,2,3,4,1).1,2,3,4,
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CASE4
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interface dermatitis,difficult todifferentiate from lupus erythematosus ,interface dermatitis,difficult todifferentiate from lupus erythematosus ,
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DERMATOMYOSITISDERMATOMYOSITIS
idiopathic inflammatoryidiopathic inflammatorymyopathymyopathy (IIM) with characteristic(IIM) with characteristiccutaneouscutaneous findingsfindings
systemicdisorder that frequentlyaffects the joints, the esophagus,systemicdisorder that frequentlyaffects the joints, the esophagus,the lungs,and, less commonly, the heartthe lungs,and, less commonly, the heart
pathognomonicpathognomonic features are the heliotrope rash andfeatures are the heliotrope rash and GottronGottronpapulespapules PoikilodermaPoikiloderma mayoccur on exposed skin, such as the extensormayoccur on exposed skin, such as the extensor
surfaces of the arm, the Vofsurfaces of the arm, the Vof the neck ,the neck ,or the upper partof theor the upper partof theback (Shawl sign).back (Shawl sign).
PoikilodermaPoikiloderma mayoccur on exposed skinmayoccur on exposed skin cause ofcause ofdermatomyositisdermatomyositis is unknownis unknown genetic predisposition may existgenetic predisposition may exist Infectious agents, including viruses (particularlyInfectious agents, including viruses (particularlycoxsackieviruscoxsackievirus,,
echovirus, human Techovirus, human T--lymphotropiclymphotropic virus 1 [HTLVvirus 1 [HTLV--1],and human1],and humanimmunodeficiency virus [HIV]),immunodeficiency virus [HIV]), ToxoplasmaToxoplasma species,andspecies,and BorreliaBorrelia
species, have been suggestedas possible triggers of the disease.species, have been suggestedas possible triggers of the disease.
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DIFFERENTIALDIAGNOSISDIFFERENTIALDIAGNOSIS
CREST SyndromeCREST Syndrome ParapsoriasisParapsoriasis GraftVersus Host DiseaseGraftVersus Host Disease Pityriasis Rubra PilarisPityriasis Rubra Pilaris
Lichen MyxedematosusLichen Myxedematosus Polymorphous Light EruptionPolymorphous Light Eruption Lichen PlanusLichen Planus Psoriasis, PlaquePsoriasis, Plaque Lupus Erythematosus, AcuteLupus Erythematosus, Acute RosaceaRosacea
Lupus Erythematosus, DiscoidLupus Erythematosus, Discoid SarcoidosisSarcoidosis Lupus Erythematosus, Subacute CutaneousLupus Erythematosus, Subacute Cutaneous Tinea CorporisTinea Corporis MorpheaMorphea Urticaria, ChronicUrticaria, Chronic
Multicentric ReticulohistiocytosisMulticentric Reticulohistiocytosis
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CASE5
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ADIPOCYTESADIPOCYTES
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LIPOMASLIPOMAS
A benign neoplasmofadipocytes that forms in the subcutaneous fatA benign neoplasmofadipocytes that forms in the subcutaneous fat(as well as in other organs sometimes)(as well as in other organs sometimes)
manifests itselfclinicallyas either an elevated tumor or a tumor thatmanifests itselfclinicallyas either an elevated tumor or a tumor thatcannot be visualizedclinically, but thatcan be palpated,cannot be visualizedclinically, but thatcan be palpated,
the skin overlying it in both circumstances being normalthe skin overlying it in both circumstances being normal A lipoma,once it presents itself, remains there for the lifetime ofaA lipoma,once it presents itself, remains there for the lifetime ofaperson whocarries it.person whocarries it.
Itmay stay small or become larger, sometimes assuminggiganticItmay stay small or become larger, sometimes assuminggiganticdimensionsdimensions
benign neoplasmmade up ofadipocytes,benign neoplasmmade up ofadipocytes,
Surgical excision is curative ifa patient wants surgery for a notSurgical excision is curative ifa patient wants surgery for a not--tootoo--large tumor. For those lipomas thatare too large to be excised,large tumor. For those lipomas thatare too large to be excised,liposuction may be employedliposuction may be employed
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DIFFERENTIAL DIAGNOSISDIFFERENTIAL DIAGNOSIS
sebaceous cystsebaceous cyst abscessabscess
LiposarcomasLiposarcomas
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CASE6
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SYPHILITIC CHANCRESYPHILITIC CHANCRE
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PLASMA CELLSPLASMA CELLS
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SYPHILLISSYPHILLIS
Treponema pallidumTreponema pallidum is the microaerophilic spirochete thatcauses syphilis, ais the microaerophilic spirochete thatcauses syphilis, achronic systemic venerealdisease with multiple clinicalpresentationschronic systemic venerealdisease with multiple clinicalpresentations
Syphilis is characterized by episodes of active disease (primary, secondary,Syphilis is characterized by episodes of active disease (primary, secondary,tertiary stages) interrupted byperiods oflatency.tertiary stages) interrupted byperiods oflatency.
Primary syphilis occurs within3 weeks ofcontact with aninfectedindividualPrimary syphilis occurs within3 weeks ofcontact with aninfectedindividual Secondary syphilis usuallypresents with acutaneous eruptionwithin2Secondary syphilis usuallypresents with acutaneous eruptionwithin2--1010
weeks after the primarychancre andis most florid 3weeks after the primarychancre andis most florid 3--4 months after4 months afterinfectioninfection
lesions of benigntertiary syphilis usually developwithin3lesions of benigntertiary syphilis usually developwithin3--10 years of10 years ofinfectioninfection
primarylesion(chancre) occurs onthe penis orscrotum of 70% of menprimarylesion(chancre) occurs onthe penis orscrotum of 70% of menwith syphilis and on the vulva,cervix, orperineum of more than50% ofwith syphilis and on the vulva,cervix, orperineum of more than50% ofwomenwith syphilis.womenwith syphilis.
single ulceratedlesionwith a surroundingred areola. The edge and base ofsingle ulceratedlesionwith a surroundingred areola. The edge and base ofthe ulcerhave acartilaginous (buttonlike) consistency onpalpation.the ulcerhave acartilaginous (buttonlike) consistency onpalpation.
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Differential DiagnosisDifferential Diagnosis
ChancroidChancroid Herpes SimplexHerpes Simplex
LymphogranulomaVenereumLymphogranulomaVenereum Erosive balanitisErosive balanitis Traumatic superinfected lesionsTraumatic superinfected lesions
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CASE7
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PerivascularPerivascular andand perijunctionalperijunctional infiltrate of lymphocytes, plasmacells,andinfiltrate of lymphocytes, plasmacells,andmacrophagesmacrophages
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DISCOID LUPUS ERYTHEMATOUSDISCOID LUPUS ERYTHEMATOUS
chronic, scarring,atrophy producing,chronic, scarring,atrophy producing,photosensitivephotosensitive dermatosisdermatosis..
primary lesion is anprimary lesion is an erythematouserythematous papule orpapule orplaque with slightplaque with slight--toto--moderate scalingmoderate scaling Resolution of the active lesion results in atrophyResolution of the active lesion results in atrophy
and scarring.and scarring.
Therapy with sunscreens, topical corticosteroids,Therapy with sunscreens, topical corticosteroids,andandantimalarialantimalarial agents is usually effective.agents is usually effective.
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DIFFERENTIALDIAGNOSISDIFFERENTIALDIAGNOSIS
ActinicActinic KeratosisKeratosis Psoriasis, PlaquePsoriasis, Plaque DermatomyositisDermatomyositis RosaceaRosacea
GranulomaGranulomaAnnulareAnnulare SarcoidosisSarcoidosis GranulomaGranuloma FacialeFaciale SquamousSquamous Cell CarcinomaCell Carcinoma KeratoacanthomaKeratoacanthoma
SyphilisSyphilis LichenLichen PlanusPlanus Warts,Warts, NongenitalNongenital LupusLupus ErythematosusErythematosus,, SubacuteSubacute CutaneousCutaneous
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CASE8
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POLYMORPHOUS LIGHT ERUPTIONPOLYMORPHOUS LIGHT ERUPTION
an acquireddisease and is the mostcommon of the idiopathican acquireddisease and is the mostcommon of the idiopathicphotodermatosesphotodermatoses
characterized by recurrent,abnormal,delayed reactions to sunlight,characterized by recurrent,abnormal,delayed reactions to sunlight,ranging from erythematous papules, papulovesicles,and plaques toranging from erythematous papules, papulovesicles,and plaques toerythemamultiformeerythemamultiformelike lesions on sunlightlike lesions on sunlight--exposed surfaces.exposed surfaces.
Within any 1 patient,only 1 clinical form is consistentlymanifestedWithin any 1 patient,only 1 clinical form is consistentlymanifested Papules (greatest incidence), plaques, papulovesicles,and erythemaPapules (greatest incidence), plaques, papulovesicles,and erythema
multiformemultiformelike lesions are the mostcommon morphologieslike lesions are the mostcommon morphologies Prophylactic phototherapyor photochemotherapyat the beginningProphylactic phototherapyor photochemotherapyat the beginning
of spring for several weeks may prevent flareof spring for several weeks may prevent flare--ups throughout theups throughout thesummersummer
Topical corticosteroidsTopical corticosteroids Antimalarials at low doses are sometimes helpfulAntimalarials at low doses are sometimes helpful Nicotinamide , AzathioprineNicotinamide , Azathioprine
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Differential DiagnosesDifferential Diagnoses
Contact Dermatitis, AllergicContact Dermatitis, Allergic
Lupus Erythematosus, SubacuteLupus Erythematosus, SubacuteCutaneousCutaneous
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THANK YOUTHANK YOU