Pneumo Stagiu Sarcoidoza

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    SARCOIDOZADEFINIIE:

    - Granulomatoz multisistemic

    - Cauz necunoscut

    - Aduli tineri- Limfadenopatie hilar, infiltrat pulmonar i leziuni

    cutanate i oculare

    - Histologic - granulomul epitelioid necazeificat

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    EPIDEMIOLOGIE

    Prevalena 1 - 40 / 100.000 locuitoriAfecteaz n special vrsta 20-40 aniHeterogenitate epidemiologic prevalen i severitateMai frecventa n nordul Europei i la negrii americani

    (1,15 % la suedezi i 2,4% la negrii americani)Afecteaz aproximatic egal ambele sexe

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    ETIOLOGIE

    Susceptibilitate genetic a gazdei(genotipul sarcoidozei)

    Expunere la diferiiageni din mediu

    SarcoidozFenotip clinic

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    Etiologiefactori de mediu

    Ageni infecioiVirui (herpes, Epstein-Barr, retrovirus,coxsackie B, cytomegalovirus)Borrelia burgdorferiPropionibacterium acnesM. tuberculosisMycoplasmaRickettsia

    Substane anorganiceAluminiu

    ZirconiuTalc

    Substane organicePolen de pinRini

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    Etiologiefactori genetici

    Risc geneticpoligenicpredispoziie, clinic, evoluie,prognostic

    Evoluie favorabil sindrom Lofgren

    CW7DR3HLA-B8

    Evoluie cronicHLAB13

    Risc familial

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    Celule T, Macrofage

    Factori de cretereFactori chemoatractani

    Proliferare celularGranulom

    Fibroz

    FIZIOPATOLOGIE

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    MORFOPATOLOGIE

    Alveolita - infiltraia peretelui alveolar predominant macrofage i limfocite T

    Secundar neutrofile, eozinofile, bazofile, mastocite etc.

    Granulom epitelioid necazeificat

    Aglomerare de celule epitelioide pe fondul unei reele dereticulin care la periferie prezint o coroan de limfocite.

    Prezena de celule gigante care conin incluziuni citoplasmatice(corpi Schauman):

    Corpi asteroiziCorpi conchoizi

    Corpi birefringenti

    Granulomul nespecifictuberculoz, lepr, sifilis,bruceloz

    Fibroza

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    Sarcoid Granuloma

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    Sarcoidosis Lung Gross

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    LANGHANS' GIANT CELL

    Langhans' giant cell in center of granuloma is

    surrounded by epithelioid cells .

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    ADVANCED COLLAGENOUS FIBROSIS

    Elongated fibroblasts (FB) with extensive

    collagenous tissue (C). Giant cells (arrows)

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    CYTOPLASMIC INCLUSION BODY

    Schaumann body (arrow) is common in

    sarcoidosis but is nonspecific.

    CASEOUS NECROSIS

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    CASEOUS NECROSIS

    Cellular destruction in TB granuloma appears

    as clumped debris (arrows). This necrosis

    does not occur in sarcoidosis.

    M t b l i BACILLI

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    M. tuberculos isBACILLI

    Caseous necrosis is most common in TB, but

    Gram negative, acid fast bacilli must be

    identified to make the diagnosis.

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    SUBPLEURAL GRANULOMA IN LUNG

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    MECANISM IMUNOLOGIC

    Deprimarea imunitii de tip celular

    IDR la PPD

    Exacerbarea imunitii de tip umoral Hipergammaglobulinemie, complexe imune circulante

    Limfopenie absolut

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    MANIFESTRI CLINICE

    Simptomatologie de debut

    50% asimptomatic

    Simptomatologie general nespecific Simptomatologie dependent de organ

    (polimorfism simptomatic)

    30% debut acut

    - Sindrom Lofgren

    - Sindrom Heerfordt

    - Sindrom Miculicz-Sjogren

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    FORME CLINICE PARTICULARE

    Sindrom Lofgren:

    - adenopatie hilara bilaterala

    - febra

    - poliartralgii

    - eritem nodos

    Sindrom Heerfordt:

    - febr- uveita (iridociclita)

    - parotidit

    - paralizie nerv facial

    - Sindrom Miculicz-Sjogren:

    - keratoconjunctivita uscat

    - hiposecreie salivar, gastric, pancreatic- poliartrit cronic- eczeme.

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    Simptomatologie

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    Afectare organic

    Organ %

    Adenopatii mediastinale 95-98%

    Plmni >90%

    Ficat 50-80%Splin 40-80%

    Ochi 20-80%

    Adenopatii periferice 30%Cutanate 25%

    Sistem nervos 10%

    Cardiovascular 5%

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    Simptomatologie

    Pulmonar

    90%

    dispnea, tuse seac, dureri toracice difuze

    Renal Nefrit interstiial,insuficien renal,

    nefrocalcinozMetabolism

    fosfocalcic

    Hipercalcemie, hipercalciurie

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    Neurologic

    10%

    Paralizii de nervi cranieni, convulsii, meningitgranulomatoas, leziuni hipotalamus sau hipofiz,hidrocefalie, polineuropatie periferic i afectare

    psihiatricOcular

    20%

    Uveit, chorioretinit, keratoconjunctivit,glaucom, cataract, orbire

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    Cardiac

    5%

    Palpitaii, sincop, durere toracic, aritmii, moartesubit cardiac

    Endocrine Hipo/hipertiroidism, insuficien adrenalExocrin Tumefacia glandelor parotide, keratoconjunctivita

    sicca

    Hepatic Hepatalgii, hepatomegalie

    Limfatic Limfadenopatii, splenomegalie

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    Cutanate

    25%

    Eritem nodos, eritem polimorf sau vasculitic,

    lupus pernio, noduli subcutanai,erupiemaculopapular, alopecie, hiper/hipopigmentare

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    EN Lupus Pernio

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    LUPUS PERNIO

    Facial lesions are most common, but the

    extremities and buttocks can be involved.

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    LUPUS PERNIO

    Indurated and violaceous range from a few

    small lesions to large lesions

    SMALL NODULES

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    SMALL NODULES

    Papules and nodular lesions, can be found

    anywhere on the body. Papules are often

    multiple while nodules are often solitary.

    RAISED PLAQUES

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    RAISED PLAQUES

    These raised plaques are the result of

    coalescence of nodules.

    PSORIASIS LIKE LESIONS

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    PSORIASIS LIKE LESIONS

    These small white lesions closely

    resemble psoriasis.

    EARLY COLLAGEN FORMATION

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    EARLY COLLAGEN FORMATION

    Extracellular collagen (C) is being produced

    by fibroblasts

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    Adenopatii

    Localizri adenopatii centrale:

    Mediastinal 100 %

    Hilar bilateral 75 %Adenopatii periferice: laterocervical i supraclavicular,epitrohleari, axilari, inghinali

    Ganglionii sunt mobili, nedureroi, cu diametru variabil,

    nu ulcereaz, nu fistulizeazSplenomegaliarar, poate cauza hiperslenism

    E l d bil t l hil i ht t h l

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    Enlarged bilateral hilar, right paratracheal

    (arrow), and aortopulmonary window

    (arrowhead) nodes.

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    PARACARDIAC LYMPH NODE

    ABDOMINAL LYMPHADENOPATHY

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    ABDOMINAL LYMPHADENOPATHY

    Multiple enlarged paraaortic, paracaval, and

    porta hepatis lymph nodes (arrows).

    GASTRIC SARCOID

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    GASTRIC SARCOID

    Granuloma involves the gastric antrum leading

    to irregular nonspecific narrowing.

    COLONIC SARCOID

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    Irregular narrowing of the rectosigmoid has the

    appearance of inflammatory disease or

    malignancy.

    PUNCHED OUT LYTIC LESIONS

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    PUNCHED OUT LYTIC LESIONS

    Focal osteolytic lesions in the fingers are most

    common abnormality.

    LACY TRABECULAR PATTERN

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    LACY TRABECULAR PATTERN

    Osteolysis has left a lacy trabecular pattern in

    this phalanx (arrow)

    DEFORMING LESIONS

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    Advanced sarcoidosis with osteolytic lesions

    of the distal forearm, wrist, and bones of the

    hand

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    SCLEROTIC LESION

    Rare and often in the axial skeleton.

    SCLEROTIC LESIONS,

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    NONSPECIFIC

    Focal sclerosis (arrows) of distal phalanges is

    unusual

    NASAL BONE LESION

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    NASAL BONE LESION

    Nasal sarcoidosis can lead to osteolysis of the

    nasal bone (arrows).

    T2-W MR IMAGE

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    T2-W MR IMAGE

    High signal intensity edema surrounding

    biopsy proven sarcoid lesion.

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    I Adenopatie hilar bilateral iparatraheal

    55-90%

    remisie

    II Adenopatie mediastinal culeziuni ale parenchimului

    pulmonar

    40-70%

    III Modificri parenchimul pulmonarfr adenopatii

    10-20%

    IV Fibroz pulmonar 0-5%

    ASPECTE RADIOLOGICE

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    Stadiile 14

    Limfadenopatii +Infiltrate

    infiltrate Fibroz

    Stages

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    Stages

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    Stadiu I Stadiu II

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    Tip 1

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    Tip 1

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    Tip 2

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    Tip 2

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    Stadiu III Stadiu IV

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    Tip 3

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    Atipice: - nodular-infiltrative

    - pseudotumorale

    - atelectazii

    - caverne

    ASPECTE RADIOLOGICE

    STAGE IV

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    STAGE IV

    Broad bands of fibrosis in the upper lobes.

    MILIARY SARCOIDOSIS

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    CT shows well defined lung nodules less than

    5mm in diameter. This pattern is rare.

    ALVEOLAR SARCOIDOSIS

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    Multiple lung masses are an unusual form of

    sarcoidosis, resembles lung metastases.

    ALVEOLAR SARCOIDOSIS

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    Computed tomography shows a mass which

    has air containing bronchi (arrows) within it.

    CAVITARY SARCOIDOSIS

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    Rare pattern of multiple cavitary sarcoid lung

    lesions. Note lymphadenopathy.

    RETICULONODULAR PATTERN

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    Common appearance of sarcoidosis involving

    the lung parenchyma.

    RETICULONODULAR PATTERN CLOSEUP

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    Well defined linear and nodular densities

    characteristic of lung interstitial disease.

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    NODULAR PATTERN

    Small 5mm nodules are subpleural along fissures and

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    Small 5mm nodules are subpleural, along fissures and

    bronchovascular bundles. Give the vessels (arrow) and

    fissures a beaded appearance.

    SUBPLEURAL NODULES

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    Cluster of small nodules looks like a tumor on

    a radiograph.

    MOST COMMON PATTERN

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    Bilateral symmetric hilar and right paratracheal

    mediastinal adenopathy.

    LYMPHADENOPATHY ON CTPara-aortic and retrocaval lymphadenopathy

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    Para-aortic and retrocaval lymphadenopathy.

    CT shows enlarged lymph nodes not visible on

    radiographs.

    POSTERIOR MEDIASTINAL LYMPH NODE

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    next to the aorta (A). Bilateral hilar adenopathy

    was also shown.

    STAGE IV

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    STAGE IV

    Permanent lung fibrosis. (20%)

    ADENOPATHY AT TIME OF DIAGNOSIS

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    Marked enlarged hilar and mediastinal lymph

    nodes.

    ADENOPATHY DECREASED 2 YRS LATER

    L h d ll d th i

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    Lymph nodes are smaller and there is

    parenchymal lung disease.

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    Aspecte funcionale

    Corelaie imperfect cu aspectul clinico-radiologic Anomalii predominant de tip restrictiv

    Tulburri ale transferului gazos Sindromul obstructiv distal 30-40 % din stadiile I si II Anomalii diverse la 74 % din pacieni n stadiul I

    MODIFICARI BRONHOSCOPICE

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    MODIFICARI BRONHOSCOPICE

    ASPECTE

    PATOLOGICE:

    capilaritate crescut

    proliferri de mucoas

    stenoze bronice

    granulaii sidefii-glbui

    compresii extrinseci

    TEHNICISUPLIMENTARE

    Prelevri bioptice demucoasPuncia-biopsie

    transbronicLavajul bronho-alveolar

    ASPECT NORMAL LA 50 % DIN CAZURI !!

    (Discordan ntre modificrile bronhoscopice i aspectul radiologic)

    L j b h l l

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    Lavaj bronhoalveolar

    Alveolit limfocitarlimfocitoz 80-90% din cazuri,nespecific pentru sarcoidoz

    Severitatea limfocitozei

    > 28% - debut acut - evoluie favorabil< 28% debut insidiosevoluie cronic

    PMN>3% i eozinofile >1% markeri ai progresieiraport LTh/ LTS (CD4/CD8) > 3,5

    Alveolita neutrofilicsingurul element care indicnecesitatea tratamentului

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    Transbronchial Needle Aspiration (TBNA) Cytology in

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    Transbronchial Needle Aspiration (TBNA) Cytology in

    Sarcoidosis

    Smojver-Jezek S, et al. Cytopathology 2007; 18: 3

    Multinucleated giant cell

    of Langhans type

    Scattered epithelioid cells

    and lymphocytes

    Linear Real-time Endobronchial Ultrasound-guidedTransbronchial Needle Aspiration Scope

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    Transbronchial Needle Aspiration Scope

    Herth FJF. Eur Respir J

    (BF-UC160F-OL8; Olympus Medical Systems, Tokyo,

    Japan)

    Endobronchial Ultrasound

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    in Sarcoidosis

    Wong M et al. Eur Respir J 2007; 29: 1182

    Right paratracheal

    LN

    Vena cava

    superior

    Endobronchial Ultrasound

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    in Sarcoidosis

    Wong M et al. Eur Respir J 2007; 29: 1182

    Needle

    BIOCHIMIE

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    BIOCHIMIE

    Cresc

    .-VSH, PCR, globuline- Calcemia

    - Calciuria

    - Proteinemia

    - Lizozim

    - Angiotensin convertaza

    seric

    Scad

    - Limfocite. CD4

    COMPUTER TOMOGRAFIE

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    COMPUTER TOMOGRAFIE

    Tomografia computerizat evaluare extindere leziuni iprognostic:

    - Micronoduli bronhovasculari i subpleuralireversibilitate crescut

    - Imagini n fagure de miere sau reticularefibroz-ireversibil

    - Sticl matcu evoluie variabil

    Confirm prezen adenopatii

    Nu este necesar de rutin, doar n cazuri atipiceradiologic sau clinic.

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    Scintigrafia cu galiu

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    Scintigrafia cu galiu

    Extinderea i distribuia leziunilor inflamatorii

    Captare n celulele mononucleare

    Dou aspecte distincte:

    - captare n lambdagg limfatici intratoracici

    - captare n pandagl parotide i lacrimale

    Examenul histologic

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    Examenul histologic

    Test Kveimcel mai specific test pentru sarcoidoz

    Biopsii

    Ganglionar prin mediastinoscopie

    Pulmonar

    Bronic

    Ganglionii periferici

    Leziuni cutanate

    Leziuni hepatice Sediul leziunii

    Investigaii specifice afectrii de organ

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    Investigaii specifice afectrii de organ

    RMNafectare cerebral, muscular, osoasAngiografia cu fluorescen - vascular retinian

    Scintigrafia cu Thaliu, monitorizare Holter,

    angiografie coronarian afectare cardiac

    Biopsie miocardic

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    Biopsie miocardic

    Diagnostic

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    Diagnostic

    Diagnostic de excludereadenopatie hilarbilateral

    IDR negativ

    ACS crescut

    Observaie ndelungat Ansamblu concordant de semne

    Scopuri: - confirmare histologic, evaluare

    extindere i severitate, progresie i necesitatetratamentPrezena granulomului epitelioid necazeificat

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    ETAPE DIAGNOSTIC

    Anamnez i examen clinicRadiografie toracicCT

    Biopsie Diagnostic de certitudinebiopsie pulmonar transbronicExplorri funcionale respiratorii, gaze

    arterialeAlte teste specifice: ecg, examenoftalmologic, etc

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    Kveim Test

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    Kveim test, or Kveim-Siltzbach test is a skin test usedto detect sarcoidosis:

    Part of spleen of person with known sarcoidosis is

    injected in the skin of the patient being tested

    If granulomas are found, usually 4-6 weeks latertest is positive

    It is named for the Norwegian pathologist Morten Ansgar

    Kveim, who first reported the test in 1941 using lymphnode tissue from sarcoidosis patients

    Diagnostic diferenial

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    Pulmonare Adenopatii

    Tuberculoz Tuberculoz

    Pneumonii atipice Micobacterii atipice

    Criptococcoz Bruceloz

    Aspergiloz Toxoplasmoz

    Histoplasmoz

    Coccidioidomicoz tumorale

    Blastomiocoz

    Pneumocistic carini

    Micoplasma

    Pneumonii de hipersensibilitate

    Pneumoconioz: Limfom Non-Hodgkin

    berillium, titaniu, aluminiu

    Aspiraie de corp strin

    Granulomatoz Wegener

    Pneumonie interstiiale

    PROGNOSTIC

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    PROGNOSTIC

    Remisie 60% din cazuriDificil de prezis

    Boal cronic progresiv10-20%

    Mortalitate 1-5%

    Prognostic bun:

    Stadiu I 80% remisie spontan

    sindrom Lofgren

    Asimptomatic

    Europeni

    Prognostic nefavorabil:

    Multisistemic (>3)Ras neagr

    Infiltrate pulmonare

    Neurologic, cardiac, uveitcronic

    Vrst > 40 ani

    Lupus pernio

    Hipercalcemie

    AG OS C SA CO O

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    DIAGNOSTIC: SARCOIDOZ

    TRATM PACIENTUL?

    60%: rezoluie spontan!

    Tratament: motive s nu-l administrm!

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    Tratament: motive s nu l administrm!

    Cauza bolii necunoscutMoment optim de iniiere a terapiei greu destabilit

    Vindecare spontan frecventCorticosteroizii prezint efecte secundare multiple

    Recidivele dup vindecarea spontan sunt rare

    Tratamentul nceput trebuie s fie de lung durat

    TRATAMENT

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    TRATAMENT

    Corticosteroizi sistemicmanifestri cardiace, neurologice,afectare pulmonar progresiv sau n cazul hipercalcemieiPrednison = 20 - 40 mg/zi

    Indicaii absolute:afectarea organelor vitale

    tendina la fibrozDurata: aproximativ 1 an

    Monitorizare la 3 luniCorticosteroizi topici-afectare cutanat sau oftalmic

    TRATAMENT

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    TRATAMENT

    TRATAMENT

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    TRATAMENT

    TRATAMENT

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    TRATAMENT

    Monitorizare

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    Monitorizare

    ClinicRadiologic

    Adesea rezorbie lezional

    Uneori: imagine adenopatii inghetateFuncional

    Cretere ACS = puseu evolutiv

    Efecte adverse ale corticoterapiei

    Alternative terapeutice la corticoterapie

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    Medicament, dozaj Utilizare n sarcoidoz Efecte adverse

    Metotrexat 10-25 mg/sptmn, maxim 1-2 g/an

    Sarcoidoz sever, cronicMedicaie de linia II Greuri, neutropenie,

    toxicitate hepatic

    Azatioprin 50-200mg/zi

    Fibroz pulmonarSarcoidoz sever, cronic

    Medicaie de linia II

    Greuri, neutropenie

    Ciclofosfamid 50-150mg/zi sau 500-2000 mg

    la 2 sptmni IV

    Sarcoidoz refractar lacorticoterapie

    Greuri, neutropenie

    Hidroxiclorochin 200-400 mg/zi

    Manifestricutanate,hipercalcemie,

    fibroz pulmonar

    Retinopatie, depozite

    corneene.

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    Bilateral hilar lymphadenopathy :

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    A 30 - year - old man with

    bilateral lymph node

    enlargement and fine

    reticulations in both lung fields

    Judges wig appearance

    Deepak D and Shah A. Indian J Radiol Imag

    2001 ; 11 : 191 198

    Bilateral asymmetrical hilar nodes

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    A 50 - year - old man with

    bilateral asymmetrical hilar

    lymph nodes with lobulated

    border on the right side .

    Bilateral reticulonodular

    opacities are also visible

    Deepak D and Shah A. Indian J Radiol Imag2001 ; 11 : 191 198

    Asymmetrical mediastinal lymphadenopathy

    in a 32 - year - old man with sarcoidosis

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    Radiograph shows striking

    asymmetric enlargement of

    mediastinal lymph nodes

    potato nodes

    y

    HRCT of the same patient shows

    bilateral multiple mediastinal

    lymphadenopathy

    Deepak D and Shah A. Indian J Radiol Imag2001 ; 11 : 191 198

    1 - 2 - 3 sign orGarlands / pawnbrokers sign

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    p g

    Radiograph of 34 - year - old

    man shows bilateral hilar and

    right paratracheal lymph nodesenlargement ( 1 - 2 - 3 sign ).

    Also visible is bilateral

    parenchymal involvement with

    reduced lung volumes

    Deepak D and Shah A. Indian J Radiol Imag2001; 11 : 191 198

    Unilateral hilar adenopathy

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    Postero - anterior chest

    radiograph in a 42 - year - old

    man with sarcoidosis shows

    a left hilar lymph node and

    consolidation in right upper

    and mid zones mistaken for

    tuberculosis

    Deepak D and Shah A . Indian J Radiol Imag2001 ; 11 : 191 - 198

    Regression of lymphadenopathy and

    progression of pulmonary lesion

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    p g p y

    Deepak D and Shah A. Ind ian J Radiol Imag2001 ; 11 : 191 198

    2 years later

    Bilateral hilar lymph

    nodes with prominent

    reticulonodular shadows

    regression of the hilar lymph

    nodes with calcification ( arrow )

    and honeycombing

    Unilateral disease

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    Radiograph of 49 - year - old

    woman shows predominantly

    unilateral disease involving left

    side with cavities ( arrows )

    and features of parenchymal

    fibrosis in the left upper zone

    as evidenced by the pulled - up

    left hilum & tracheal deviation

    Deepak D and Shah A. Indian J Radiol Imag2001; 11 : 191 198

    Parenchymal nodules

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    CECT of a 52 - year - old

    woman through the level

    of left upper lobe

    bronchus shows bilateral

    nodular opacities

    Deepak D and Shah A. Ind ian J Radiol Imag2001; 11 : 191 198

    Reticulations

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    Chest radiograph in a

    40 - year - old man shows

    bilateral reticulations.

    Pleural thickening ( arrow )

    is also seen in the left

    upper zone

    Deepak D and Shah A. Indian J Radiol Imag2001; 11 : 191 198

    Pulmonary sarcoidosis : alveolar pattern

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    areas of consolidation with

    irregular borders preferentially

    involving central areas

    Deepak D and Shah A. Indian J Radiol Imag2001; 11 : 191 198

    HRCT showing bilateral

    consolidation with air

    bronchogram ( arrow )

    Alveolar pattern : 11 years post treatmentDeepak D and Shah A. Ind ian J Radiol Imag2001; 11 : 191 198

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    bilateral bullous areas

    pleural thickening

    clearing of consolidation

    HRCT :

    bronchiectasis and bullae

    Alveolar sarcoidosis with subpleural nodules

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    HRCT of a 30 year old man

    through the level of left lower

    lobe bronchus showing

    alveolar pattern of

    involvement on the left side.

    Also visible are bilateral

    sub - pleural nodules (arrows)

    Deepak D and Shah A. Ind ian J Radiol Imag2001; 11 : 191 198

    Stage IV sarcoidosis : 50 - year - old womanDeepak D and Shah A. Indian J Radiol Imag2001; 11 : 191 198

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    - beaded appearance of

    bronchovascular bundles with

    - perihilar concentration of

    fibrosis and lobular distortion

    Left side : cystic spaces & fibrosis

    Pulmonary sarcoidosis :simultaneous ground glass & honeycombing

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    HRCT through right lower lobe

    bronchus shows :

    - air bronchogram ( arrow )

    - ground glass opacities

    Deepak D and Shah A. Indian J Radiol Imag2001 ; 11 : 191 - 198

    HRCT through apical region :

    - honeycombing on right side

    Pleura : a 35 - year - old man with

    a non - resolving pleural effusion

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    a non resolving pleural effusion

    Panjabi C et al. Indian J Tuberc2004 ; 51 ; 37 - 41

    B / l mediastinal lymphadenopathy & thickening of both fissures

    Merci lessly received second l ine ant i tuberculou s therapy

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    Well circumscribed noncaseating granuloma consisting of

    epitheloid cells and multinucleated giant cells ( H & E 100 )Panjabi C et al. Indian J Tuberc2004 ; 51 : 37 - 41

    Spontaneous pneumothorax

    R 2 4 %

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    Chest radiograph in a

    45 - year - old woman with

    sarcoidosis shows

    pneumothorax ( arrows )

    along with b / l hilar

    prominence, reticular

    opacities in lower zones

    Deepak D and Shah A. Indian J Radiol Imag2001 ; 11 : 191 198

    Rare : 2 - 4 %

    Mihailovic - Vucinic V and Jovanovic D . Clin Chest Med2008 ; 29 : 459 - 473

    Sarcoidosis : miliary pattern in

    a 40 - year - old man

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    Deepak D and Shah A . Indian J Radiol Imag2001; 11 : 191 - 198

    a 40 year old man

    A 65 - year - old lady with cavitation9 months pr ior to referral

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    Bilateral diffuse

    non - homogeneous opacities

    Bilateral hilar enlargement

    Acinar pattern seen in the

    right mid and lower zones

    A well - defined cavitary lesion

    in the anterior segment of the

    right upper lobe

    Panjabi C et al. Brazi l ian J Pulmonol2009 ( in press )

    Aspergilloma formation in a sarcoid cavity

    1 - year after commencement o f therapy for sarcoidos is

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    C T in prone position

    showing positional change

    of the fungal ball

    C T in supine position

    showing fungal ball

    within the cavity

    Panjabi C et al. Brazi lian J Pulmono l2009 ( in press )

    Mediastinal lymphadenopathy in a

    35 - year - old lady

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    A 35 - year - old lady

    presented with a history

    of dry cough , fever and

    weight loss for one month

    Chest X - ray showed

    bilateral symmetrical

    hilar lymphadenopathy

    FOB done elsewhere :

    inconclusive

    35 year old lady

    On presentation :investigated for pulmonary sarcoidosis

    Spirometry : mixed obstruction with restriction

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    Spirometry : mixed obstruction with restriction ,

    diffusion per unit volume normal

    Serum ACE : 25.7 IU / ml ( 8 52 IU / ml )

    Mantoux test : 20 mm x 22 mm ( 1 TU )

    Bilateral extensive

    mediastinal lymphadenopathy

    Bilateral ground glass haze with

    right upper lobe consolidation and

    peri - bronchial cuffing

    Six weeks later

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    Patient went out of town and

    reported later with persistent

    fever and productive cough

    Chest X - ray revealed a cavity

    in the right middle zone

    All three consecutive samples for

    AFB were positive

    Sputum culture : positive

    Bronchial aspirate culture by

    BACTEC : positive

    cavity

    After six months of ATT

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    She complained of dyspnoeaChest X- ray :

    shrunken lung fields

    Bilateral multiple mediastinal

    lymphadenopathy

    Ground glass haze