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Mycobacteriosis

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Over 100 species, most of little, no or unknown virulence ... 1 77 y/o with new nodules on screening CT 5 years after remission of NSCLC ... – PowerPoint PPT presentation

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Title: Mycobacteriosis


1
Mycobacteriosis
Joseph Horvath, M.D. USC Division of Infectious
Diseases
  • Clinical correlations 7
  • Med Micro 2008

2
Mycobacteria
  • Tuberculosis
  • Leprosy (Hansen Disease)
  • BCG hypersensitivity and infection
  • MOTT
  • AIDS related disseminated MAC
  • Immune reconstitution disease

3
Mycobacteria
  • All species resist decloration, i.e. acid fast
  • All cause granulomatous inflammation
  • All are more common and/or more severe with cell
    mediated immune dysfunction
  • Can cause delayed diagnosis if not specifically
    sought
  • Only TB spread person to person

4
Dx of Mycobacteria
  • Smear- acid fast stains (Kinyoun, auromine)
    rare false positives
  • Culture all species other than M.tb and M.
    leprae must be correlated clinically
  • PCR currently only for interpretation
    respiratory secretion smear () and PCR ()
    means TB, smear () but PCR (-) means MOTT, smear
    (-) but PCR () means TB
  • Histology granulomatous inflammation narrows
    differential greatly even if stains (-) for AFB

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7
Mycobacterium leprae
  • Unique infection able to manifest full spectrum
    from nearly unopposed to intense granulomatous
    immune response
  • Temperate climates worldwide
  • La.,Ark.,Tx.,Miss.in USA
  • Not grown in vitro
  • Respiratory tract entry, seeks cooler areas
  • Infects schwan cells causing neuropathy

8
Histology of Leprosy
9
Acid-Fast Stain M. leprae
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MOTT
  • Over 100 species, most of little, no or unknown
    virulence
  • Similar to TB in histology and staining, trained
    technicians can distinguish
  • All can be normal flora except M.kansasii
  • None person to person
  • Diagnosis requires more than simply recovering
    from non-sterile specimen

13
MOTT Classification
  • Growth-rate /morphologic system obsolete
  • Clinically useful to classify by host, organ
    system (pulmonary vs. lymphatic, cutaneous,
    disseminated)
  • Treatment varies greatly with species

14
MOTT Risk Factors
  • Structural lung disease (MAC, kansasii,)
  • Trauma/surgical (M.marinum, rapid growers)
  • Cellular immune defect (rapid growers, MAC)
  • Gamma interferon/IL-12 defect
  • AIDS (MAC, rapid growers, genevensa, hemophilum)
  • Recurrent aspiration, achalasia (MAC, rapid
    growers)
  • Fish tank (M.marinum)
  • Reptiles ( M chelonei)
  • Children Scrofula (M. scrufula, MAC)
  • Hot-Tubs Hypersensitivity pneumonitis (MAC)

15
MAC
  • M. avium complex includes M. intracellulare,
    other clinically insignificant ones
  • By far main MOTT in AIDS
  • 4 types in relatively competent hosts
  • 1) fibrocavitary COPD, etc.
  • 2) fibronodular older women,
  • collagen
    defect
  • 3) cystic fibrosis
  • 4) hypersensitivity (hot tub)
    pneumonitis

Presumed by assoc. with mitral valve prolapse,
scoliosis,joint hypermobility,pectus excavatum
16
Fibronodular MAC with bronchiectasis
17
Rx of MOTT
  • Very little correlation or predictive data from
    susceptibilty testing except for
  • M.kansasii - rifampin
  • MAC clarithromycin
  • M.chelonei, fortuitum, abscessus
    formal
  • mics
  • None susceptible to PZA
  • Most susceptible to clarithro, amikacin imipenem,
    quinolones except M. abscessus
  • Duration varies usually at least 1- 11/2 year
    after sputum smears turn negative

18
Dx. Of M.tb
  • PPD very limited role in dx of active disease
    due to high rate of false (-) and true - but
    unrelated phenonenon
  • Can help in CNS disease, pericarditis
  • Definition of () PPD depends on circumstances
    (size, prior tests, host etc.)
  • Prior BCG must assume positive skin test could
    be due to subsequent TB infection
  • Interferon based assays M.tb specific immune
    response to TB proteins, identifies PPD reaction
    as TB rather than MOTT, more sensitive than PPD
    for screening, less for active disease

19
Rx. of TB
  • Standard regimen for all unless
  • -Suspected resistance ( foreign born,
    failed
  • prior Rx)
  • -Pregnancy, coexistent liver disease,
    drug
  • interaction concerns, intolerance
  • Direct observed Rx when possible
  • Some strains not treatable

20
Clinical Cases Mycobacteria
  • 1 77 y/o with new nodules on screening CT 5
    years after remission of NSCLC
  • 2 77 y/o with worsening lesions while on
    prednisone for recent ITP
  • 3 55 y/o with fever and cough for 3 weeks
  • 4 70 y/o with chronic dyspnea

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TB Miliary, Extra-Pulmonary Disease
  • Non specific symptoms may dominate miliary or
    disseminated TB
  • Psoas abscess, with or without vertebral
    osteomyelitis, CNS disease relatively common
  • May occur with or without active pulmonary disease

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TABLE 4 Characteristics of patients with
nontuberculous mycobacteria pulmonary
infections
MAC M.xenopi
M. kansasii RGM/non-CF
Subjects n
125 66
34 16 Underlying
conditions Pre-existing pulmonary disease
89 (71.2) 28 (42.4) 7 (20.6)
8 (50) Previous M. tuberculosis
35 (28) 17 (25.8)
9 (26.5) 3 (18.7)
Immunosupression/transplantation 34 (27.7)
17 (25.8) 5 (14.7) 1 (6.2)
None/anorexia
14 (11.2) 18 (27.3) 15
(44.1) 4 (25) Radiographic
abnormalities Infiltrates
46 (36.8) 1 (31.8)
12 (35.3) 8 (50) Nodules
28
(22.4) 21 (31.8) 10 (29.4)
3 (18.7) Cavitation
13 (10.4) 11 (16.7)
13 (38.2) 1 (6.2) Nonspecific
4 (35.2)
19 (28.8) 4 (11.7) 7
(43.7) No symptoms
35 (28) 22 (33.3) 10 (29.4)
0 (0) Data are presented as n,
mean (range) or n (), unless otherwise stated.
MAC Mycobacterium avium-intracellulare complex
M. xenopi Mycobacterium xenopi M. Adapted from
Dailloux et.al. Eur.Respir.J.,2006281211
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