nocardia& actinomycosis

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    Nocardia&

    Actinomycosis

    Nattaya Mangkalapiwat

    28 April 2008

    Infect topic

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    Nocardia:History

    Edmond Nocard,

    1888

    Aerobic actinomycete

    from cattle with

    bovine farcy

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    Nocardia

    Genus: aerobic actinomycetes

    G+ branching filamentous bacteria

    Subgroup: aerobic nocardiform actinomycetes-Mycobacterium

    -Corynebacterium

    -Nocardia

    -Rhodococcus-Gordona-Tsukamurella

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    Nocardia

    At least 13 species : cause human infection 7most important

    1. Nocardia asteroidescomplex:80% of noncutaneous dz.

    :most systemic & CNS nocardiosis ***2. Nocardia farcin ica:less common,more virulent

    :more antibiotic-resistant member

    3.Nocardia nova

    4.Nocardia brasiliensis:skin,cutaneous,lymphocutaneous

    5.Nocardia pseudobrasiliensis:systemic infections, CNS

    6.Nocardia otitidiscaviarum

    7.Nocardia transvalensis

    .

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    Nocardia:ECOLOGY& EPIDEMIOLOGY

    Ubiquitous environmental saphrophyte Soil, organic matter,water

    Tropical and subtropical regions

    :Mexico, Central and South America,Africa and India

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    Nocardia:ECOLOGY& EPIDEMIOLOGY

    Nearly all cases :sporadic

    Human-to-human

    Animal-to-human not documented

    Outbreaks: Contamination of the

    hospital environment, solutions,druginjection equipment.

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    Nocardia:ECOLOGY& EPIDEMIOLOGY

    The risk of pulmonary ordisseminated disease

    *deficient cell-mediated*-Alcoholism

    -Diabetes

    -Lymphoma

    -Transplantation

    -Glucocorticoid therapy-AIDS CD4+ < 250

    Transmission

    Inhalation Skin

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    Nocardia: PATHOLOGY

    Acute pyogenic inflammatory reaction.Branching, beaded, filamentous bacteria

    G/S from a nocardial lung abscess G/S from nocardial pneumonia

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    Nocardia:PATHOGENESIS

    Neutralization of oxidants

    Prevention of phagosome-lysosome fusion

    Prevention of phagosome acidification.

    Mycolic acid polymers:ass.with virulence

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    CLINICAL MANIFESTATIONS

    : 4 main form

    Lymphocutaneous syndrome

    Pulmonary :Pneumonia

    CNS : Brain abscess

    Disseminated disease

    CNS

    Eyes (particularly the retinaKeratitis),

    Skin& subcutaneousKidneys,

    Joints, boneHeart

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    Lymphocutaneous syndrome

    Ubiquitous in soil

    inoculation injuries, Insect and animal bitescontaminated abrasions

    N. brasiliensis: most common

    N. asteroides: self-limited

    Because initial response Rx as staphylococcus

    underdiagnosed Mycetoma

    Days to months ,typical:distal limb

    -Cellulitis-Lymphocutaneous syndrome-Actinomycetoma

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    Nocardial actinomycetomaswelling, multiple sinus tracts,

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    Pulmonary disease

    PneumoniaSubacute(more acute in immunosuppressed)

    Cough**

    Small amounts of thick, purulent sputum

    Fever, anorexia, weight loss, malaise Endobronchial inflammatory mass

    Lung abscess

    Cavitary disease Inadequate therapyProgressive fibrotic disease

    Cerebral imaging,should be performed in allcases of pulmonary and disseminated

    nocardiosis

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    Nocardial pneumonia.Discrete nodular in midlung on both sides

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    CT scan (A),CXR (B)from : multiple abscesses : Nocardia farcinica

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    CNS : Brain abscess

    Insidious presentations : mistaken for neoplasia!!!

    Granulomatous , abscesses

    Cerebral cortex, basal ganglia and midbrain*** Less commonly: spinal cord or meninges.

    Brain tissue diagnosis in pulmonary nocardiosis

    : not necessary

    However,cerebral biopsy:considered early in immunocompromised

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    brain abscess ; Nocardia farcinic a Nocardial abscess:rt. occipital lobe

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    LABORATORY DIAGNOSIS

    Gram-positive, beaded, branching filaments

    usually weak acid fast+ve .

    Standard blood culture:48 hrs to several wks, but

    typical = 3 to 5 days

    Colonization of sputum

    :underlying pulmonary dz+not receiving steroid therapyno specific therapy

    Susceptibility testing

    -Deep-seated /disseminated dz. fail initial therapy

    -Relapse after therapy-Alternatives to sulfonamides are being considered

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    MANAGEMENT

    :Medication

    Sulfonamides : the mainstay of therapy

    treatment of choice :N. brasiliensis

    N. asteroidescomplexN. transvalensis.

    severely ill patients, CNS /disseminated/immunosuppressed patients=/> 2 drugs

    Amikacin and Carbapenem or3rdgeneration cephalosporin.

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    MANAGEMENT

    :Medication

    TMP-SMX:currently preferred:drugs in serum:CSF = 1:20

    :high MICs good therapeutic responses

    -General:5-10 mg/kgTMP & 25-50 mg/kgSMX divide2- 4times

    -Cerebral abscesses,severe,disseminated,AIDS

    :15 mg/kg TMP and 75 mg/kg SMX)

    -Cutaneous infection: 5 mg/kg/day (TMP) + DB

    Hypersensitivity reactions :Desensitization

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    MANAGEMENT

    Medication:alternative therapeutic drugs Failed sulfonamide Rx: N. otitidiscaviarum Intolerant : hypersensitivity,GI toxicity, myelotoxicity)

    Parenteral : Imipenem & amikacin: Meropenem

    : 3rd-gen cephalosporins Ceftriaxone, cefotaxime

    Oral:Amoxicillin clavulanate

    :Minocycline(100200 mg twice daily)

    :Linezolid :new oxazolidinone ;effective orally

    (bioavailability~100%), good CSF penetration

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    MANAGEMENT

    Surgical drainage: depend on site Extraneuralaspirate,drainage, excision

    Brain abscesses

    1) Accessible and relatively large AND

    2.1) Lesions progress within 2 wks or

    2.2) No reduction in abscess size within a month.

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    Durat ion o f Therapy

    HIV-negative

    immunosuppressed

    :12 mo or longer if thereare intercurrent

    increases in

    immunosuppression

    AIDS

    : at least 12 mo. +

    low-dose maintenance

    (long life)

    Clinical improvement: most 7 -10 days

    Parenteral 3 to 6 wks oral regimen

    Primary cutaneous infection :1-3 mo.

    Nonimmunosuppressed-Pulmonary /systemic nocardiosis: at least 6 mo-CNS involvement : for 12 months

    Immunocompromised

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    Outcome of therapy

    Cure rates

    -skin or soft tissue : almost 100%

    -pleuropulmonary disease : 90%

    -disseminated infection : 63%

    -brain abscess : 50%

    Mortality

    -brain abscesses :31%-multiple abscesses :41%-immunocompromised patients :55%

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    Actinomycosis

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    Genus : Act inomyces

    Slowly progressive infection

    Colonize : mouth, colon, vagina

    Infection : mucosal disruption

    In vivo : Grains / Sulfur granules The most misdiagnosed disease

    3 clinical presentations1.chronicity, progress across tissue boundaries,masslike

    2. develop sinus tract, resolve and recur3. refractory/relapsing after a short course therapy

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    Etiologic Agents

    A. israelii***

    A. naeslundii/v iscosus

    A. odontolyticus

    A. viscosus

    A. meyeri

    A. gerencseriae

    pelvic disease ass. IUCDs & lumpy jaw16S rRNA gene sequencing led to identification of anever-expanding list ofActinomycesspp

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    Concomitant bacteria

    Staphylococcus / Streptococcus

    Enterobacteriaceae

    Ac t inobac i llus com i tans

    Eikenel la co rrodens HACEK

    Fusobacter ium

    Bacteroides Capnocytophaga (Dog bite)

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    Epidemiology

    Members of oral, GI, and genital flora

    Never been cultured from nature

    No document of person-to-person transmission

    The peak incidence : mid-decades Male > Female

    (poorer dental hygiene & oral trauma)

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    Pathogenesis & Pathology

    Disruption of the mucosal barrier.

    Spreads : slow progressive manner, ignoring tissue planes.

    Hallmark: chronic, indolent phase (single /multiple indurations)

    Woodenfibrotic wallAs mature lesion : soft , fluctuant and suppurates centrally.

    The fibrous walls :wooden

    absence of suppuration: neoplasm???

    Sinus tracts : spontaneously close and re-form

    skin adjacent organs(bone)

    Pathology :Central necrosis consisting of neutrophils + sulfur granules.

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    Actinomycosis

    G/S :Variable cellular morphology, ranging from diphtheroidalto coccoid filaments sulfur granule gram

    mAFB

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    Actinomycosis

    G/S :sulfur granuleSulfur granules

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    Risk Factors

    Foreign bodies : IUCDs

    Abnormal host defense : HIV

    Post transplantation

    Radio-Chemotherapy

    Ulcerative mucosal infection: HSV/CMV

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    Clinical Manifestations

    Oral-Cervicofacial Disease

    Thoracic Disease

    Abdominal Disease Pelvic Disease

    Central Nervous System Disease

    Musculoskeletal & Soft tissue infection Disseminated Disease

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    Oral-Cervicofacial Disease

    Most frequently site

    Soft tissue swelling / mass/ abscess : mistaken

    for a neoplasm Most common site : Angle of jaws

    Dx: mass lesion/relapsinginfection in head &neck

    Complication

    :-Otitis, sinusitis, and canaliculitis:-extend to cranium,c- spine, thorax

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    Most common site : Angle of jaws

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    Thoracic Disease

    Chest pain, fever, and weight loss ***.

    Cavitary disease / hilar adenopathy

    >50% pleural thickening / effusion / empyema

    pulmonary nodules or endobronchial lesions :Rare

    CT scan:central low attenuation + ringlike rimenhancement

    Complication:- Mediastinal infection***

    :uncommon, usually from thoracic extension

    - Breast disease

    - Primary Endocarditis

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    Band C:Chest x-ray + CTscan :pulmonary infiltrate, pleural effusion,

    pleural and chest wall extension (arrow).

    A:Chest

    wallmass

    D:Purulent

    pleural fluid

    (aspiration)

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    Abdominal Disease(1)

    Usually pass from inciting event Appendicitis

    Diverticulitis

    PUD

    Foreign bodies

    Bowel surgery ascension from IUCD-associated pelvic disease

    Abscess, mass, mixed lesion : mistakentumor???CT: heterogeneous enhance+ thick adjacent bowel.

    Sinus tracts abd. wall / perianal/ between bowel

    (Mimic inflammatory bowel disease)

    Clue : Recurrent dz /wound or fistula : fails to heal

    Imaging and percutaneous techniques:Therapeutic diagnosis

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    A.CTscan:multiple hepatic abscesses and small splenic lesion extend out side liver.Inset:Gram's stain of abscess

    B.Subsequent formation of a sinus tract.

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    Abdominal Disease(2)

    KUB Disease

    All levels: can be infected

    - pyelonephritis

    - renal and perinephric abscess

    Bladder involvement:usually due to pelvic disease

    urine : stains and cultures

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    Pelvic Disease

    Risk:IUD in place >1yr-months after removed

    S&S: Typically indolent

    fever, wt loss, abd pain,

    abnormal vaginal bleeding or discharge

    Endometritis masses/tuboovarian abscess

    delayed Rxfrozen pelvis

    Removed as early as possible:but not removalof the IUCD unless a suitable contraceptive

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    An IUCD encased by endometrial fibrosis (sol id arrowh ead)

    paraendometrial fibrosis (open arrow)

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    CNS Disease

    Rare

    Single/multiple abscess**

    Irregular nodular Rim-enhancing thick wall

    Meningitis / Epidural /Subdural space infection

    Cavernous sinus syndrome

    MS & Soft t issue

    Associated trauma:Fx

    Adjacent soft tissue Bone

    Periostitis / Osteomyelitis/

    Cutaneous sinus tracts** .

    Disseminated Disease:Lung* / Liver*

    :multiple nodules ~ CA metasbut, indolent

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    MS & Soft t issue: Cutaneous sinus tracts

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    Diagnosis

    Avoid unnecessary surgery

    Aspirations & Biopsy

    Material for C/S + microscopic identification

    Sulfur granules: In vivo matrix of bacterial + CaPO4 + host debris

    Grossly identified from sinus tract

    DDx : Mycetoma / Botryomycosis

    C/S isolated in 5-7 dbut 2-4 wk. if previous ATB

    16S rRNA gene amplification and sequencing: not routinely used

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    Can cure with medical Rx alone even in extensive dz

    Medical ManagementHigh doses and prolonged period

    1. serious infections and bulky disease

    Intravenous PGS 18-24 mU /day : 2-6 wk.then Oral Penicillin / Amoxycillin : 6-12 mo.

    2.Less extensive disease,e.g. oral-cervicofacial

    : cured with shorter course.

    Combined medical-surgical therapyinitial attempt cure with medical Rx alone, CT and MRI : monitor Critical organs : Reproductive /CNS e.g. epidural space Fails suitable medical therapy

    Treatment

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    Thank you for

    your attention

    Reference

    -Mandell, Douglas, and BennettsPrinciples and Practice of Infectious Diseases,6TH Edition

    -Harrison's PRINCIPLES OF INTERNAL MEDICINE,17th Edition-CLINICAL MICROBIOLOGY REVIEWS, Apr. 2006, p. 259282