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Lnfections : M Ycobacterium Tuberculosis, M Kansasii, M Intracellularis
Lnfections : M Ycobacterium Tuberculosis, M Kansasii, M Intracellularis
Roentgenographic
Pulmonry
M ycobacterium
Edward
E. Christensen,
Ho
Ahn,
Geral
M.D.;
M.D.,
F.C.C.P.;
Robert
C. Murry,
Ph.D.;
George
A. Hurst,
M.D.,
W.
John
James
of
Tuberculosis,
Dietz,
M.D.;
S. Chapman,
Anderson,
lnfections*
and M Intracellularis
Kansasii,
Chal
Manifestations
M.D.;
M.D.;
and
F.C.C.P.
The Initial
radiographic
features
of 188 patients
with
pulmonary
infections
due to Mycobacterium
tuberculosis were compared
to 184 patients
with
M
kansasii
and 100 patients with M intraceilularis
infections
The
patients
were all from the University
of Texas
Health
Center at Tyler, all had at least two positive
sputum
cultures and no other potential
pathogen,
and none had a
past medical
history
of any type of tuberculosis.
The
comparison
showed
that
all three
organisms
have
a
strong
tendency
to produce
cavitary
infiltrates
in the
posterior
portions
of the upper lobes. No distinctive
or
pathognomonic
feature
could
be found.
The atypical
organisms
were more likely to produce
thin-wailed
cavities and far advanced
unilateral
disease,
but both
of these
patterns
also occurred
with M
tuberculosis.
Endobronchial
spread and volume
loss
were common
in all
three diseases.
The only definite
difference
seems
to be
the absence
of a primary
or juvenile
form of atypical
tuberculosis
and
a much greater
incidence
of empyema
and postprimary
pleural effusions
with M tuberculosis.
In an individual
case, the roentgenographic
manifestations of the three
diseases
are
indistinguishable.
included
he
incidence
of
pulmonary
infection
from
in the study.
Patients
with a past medical
history
of
of tuberculosis,
a second
potential
pathogen
within
six months,
normal
or equivocal
chest
x-ray films,
or more
than 30 days of antituberculosis
therapy
were
excluded.
A
group of 184 cases of M kansa.sii
and
100 cases of M intracellularis
met these
criteria,
and
they
were
compared
to a
randomly
selected
group
of 188 cases of M tuberculosis
seen
over approximately
the same
time,
and fulfilling
the same
criteria.
the
any
atypical
mycobacteria
has been
gradually
increasing
since
the
1950s.12
The
organisms
most
responsible
for
the
increase
are
Mycobacterium
and
kansasii
years,
losis
much
more
been
described
in
atypical
great
Several
detail
is a retrospective
study
The
tuberculosis
M
in
have
but
the
RESULTS
numerous
reported
the
M kansasii3
of
authors
same
tubercuis still
varieties.
of
three
forms
of tuberculosis,8-7
number
of patients
from
SUBJECrS
This
the
texts.
We recently
manifestations
intracellularis.4
these
large
than
these
from
M
tuberculosis
manifestations
articles
and
genographic
M
Over
of infection
but
typical
common
roentgenographic
have
intracellularis.
the incidence
has declined,
roentand
Age,
Lung
a
of Radiology
at the
University
of Texas
Health
University
of Texas
Health
Science
Reprint
requests:
Dr.
Christensen,
ology,
University
of Texas
Health
75235
132
and
roentof pul-
initial
Internal
Tyler,
Dallas.
Department
Science
age,
and
race,
of disease
of patients
with
almost
identical,
the
Center,
Center,
The
types
genographic
features
of the three
most common
forms
monary
tuberculosis:
M tuberculosis,
M kansasii,
and M introcellularis.
The
cases are all from
the University
of Texas
Health
Center
at Tyler
(formerly
the East Texas
Chest Hospital).
Patients
with
two
positive
sputum
cultures
for
M kansasii
or M intracellularis
between
1957 and 1977 are
#{176}Fromthe Departments
Race,
Sex
Disease
Associated
Obstructive
compared
never
with
same
hospital.
METHODS
comparing
form
Medicine
and
of
Center,
CHRISTENSEN ET Al.
the
RadiDallas
patients
at
least
and
are
sex
shown
distribution
of
in Table
1. The
M tuberculosis
and
but
M intracetlularis
a decade
M kansasii
occurred
older.
Female
acquired
M kansasii
infections
at
than
male
subjects
by approximately
three
diseases
were
more
common
especially
women
subjects
mycobacterioses
10 percent
were
black
where
kansasii,
by
were
the
mean
men
three
age
was
in
subjects
a younger
ten years.
in men,
age
All
but
outnumbered
ratio
of 4:1.
The
atypical
less common
in blacks.
Only
of the patients
with
M intracellularis
as opposed
to 40 percent
with
M tuber-
culosis.
Roentgenographically-evident
chronic
obstruc-
Table
1-Age,
Race,
Sex
and
Table
COPD
2-Distribution
of Disease
(Percentage
a/Patients)
M
M
kansasii
tuberculosis
No.
of patients
188
M
intracetlulare
184
48
50
63
Males
50
52
63
Bilateral
Females
45
41
61
Unilateral
Age
(mean),
yr
disease
disease
Right
Race
(percent)
60
Black
39
Latin
Sex
lung
Left
White
80
1
lung
18
Lobar
the
distribution
initial
Right
Male
71
81
65
29
19
35
Left
Right
COPD
(percent)
Bullous
disease
(percent)
pulmonary
emphysema
1)
than
years
with
Fxcunz
bullous
either
Left
18
39
24
Right
and!
intracellularis
The
64
41
36
59
35
22
40
24
14
19
11
78
63
73
72
49
48
65
of
site(s)
of
and
the
fact
more
significant
were
by
an
*Far
or M tuthe inci-
kansasii
intra-
average
lower
lower
lobe
lobe
middle
lobe
0.5
15
unilateral
disease*
kansasii
in
upper lobe
upper
lobe
Extensive
bullous
difference
M
kansasii
or
with
between
is made
with
advanced
in these
similar
three
with
diseas
e in
at
least
two
forms
of tuberculosis
only
one important
lobes.
was remarkably
exception
(Table
that
of
ten
younger.
Characteristics
The
52
common
1).
of COPD
cellularis
61
(COPD)
more
(Table
patients
44
disease
was
berculosis
dence
intracellukiris,
Percent
infection
Female
(Fig
kansa8ii,
Percent
92
(percent)
tive
tuberculosis,
Percent
100
of the
distribution
Pulmonary
and
1. Severe
chronic
emphysema
in
extent
obstructive
Disease
of pulmonary
pulmonary
disease
disease
and
a 44-year-old
white
woman
with
from M kansasii.
Disease
is primari-
Ficuax
2. Extensive
unilateral
M kansasil
in a 52-year-old
white
man. There
are multiple
cavities
in right
upper
lobe
with extensive
surrounding
lung disease
and endobronchial
spread to right middle and lower lobes. Left lung was normal.
133
2).The
is that
exception
prone
to
(Fig
produce
2).
All
dilection
far
three
for
the
unilateral.
This
was somewhat
terioses
per
organisms
had
when
Atypical
always
had
Cavitary
disease
M
with
and
96
is one
berculosis,
and
identical
with
of
patients
of
the
significant
and
the
sizes
of
with
little
ease
(Fig
with
4),
three
organisms.
Cicatricial
Hilar
mon
and
sasii,
0.5
percent.
athy
had
ipsilateral,
ease
which
losis.
as
younger
than
kansasii,
pyema.
in
all
all
three
70 percent
cavities
disease
No
had
with
in
patient
either
of
Thickening
with
common
modest
amount
72-year-old
of
white
man
surwith
to
cavities
common
Some
degree
losis,
in
37
the
occurred
more
present
with
M kansasii
a large
pleural
with
all
of contiguous
24
percent
percent
with
three
atypical
the
pleural
of patients
M
intracelor em-
immediately
pleura
with
or M
effusion
kansasii,
adjacent
diseases
but
mycobacterioses.
thickening
with
and
was
was
tubercu-
56
percent
of patients
were
of the
posterior,
these
incidence
tubercuksis,
and
patients
with
upper
lobe
cavitary
and
of re-activation
patients
other
uncom-
The
4 percent;
usually
general,
unusual
Multiple
lung
intracellularis.
pyema.
lularis
tuberculosis.
follows:
characteristic
In
patients
of
of tuberculosis.
All
was
rounding
dis-
and
were
intracellularis,
considered
percent
3.
FIGURE
the numbers
thin-walled
adenopathy
types
was
Most
there
and
Disease
mediastinal
adenopathy
of
10
and
Pleural
in all three
percent;
disease.
atelectasis
occurred
in 55 perM tuberculosis,
68 percent
of
patients
with M kansasii,
with M intracellularis.
and
tu-
parenchymal
were
lobar
with
Lung
3),
between
Solitary,
but
reactions
diseases.
Partial
cent of patients
Adenopathy
of
Mycobacterium
occurred
pa-
is virtually
(Fig
in
with
levels
pulmonary
intracellularis
percent
Fluid
kansasii.
of
cavities.
occurred
of
intracellularis,
surrounding
mycobacterioses
and
percent
with
difference
or
region).
varieties
alMost
apices
the
87
cavities
the
disease
cavitation
three
no
cavities,
in
and
trachea.
and
hallmarks
multiple
was
the
either
resulting
the
had
patients
in
occurred
the
in
infraclavicular
tuberculosis
percent
necrosis
location
lobe
to
disease
upThe
in 2 percent,
Upper
immediate
all three
unusual.
atypical
posterior
some
(the
tients
percent.
was
of the
were
M tuberculosis
pre-
right
lung
mycobac-
portions
an
in
2:1
disease
Typically,
posterior
began
subapices
the
infect
the
the atypical
for
began
more
disease
an almost
distributions
M intracellularis
patients
to
in the
percent
of patients,
M kansasii
in 0.5
most
side
is much
unilateral
M tuberculosis.
began
lobes.
kansasil
right
tendency
stronger
for
than
diseases
advanced,
in
kan-
adenoplung
of
were
patients
5
M
dis-
the type
tubercu-
considerably
their
respective
groups.
Pleural
effusions
percent
of
tracellularis,
were
man
in the
134
small
with
right
patients
and
were
lobe
and
in
M
6
in-
with
M kansasii.
All
for one, a 67-year-old
except
M tuberculosis,
occurring
tuberculosis
4 percent
effusions,
upper
unusual,
M
with
who
and
had
a large
cavitary
disease
ipsilateral
CHRISTENSEN El AL
em-
Ficuax
pleural
4. Solitary,
disease
from
thin-walled
M
kansa.csi
cavity
with
in a 63-year-old
contiguous
white
man.
with
ing,
intracellularis.
is, over
cellularis
(16
percent)
Extensive
2 cm,
was
more
percent)
pleural
common
than
with
with
or M tuberculosis
thicken-
were
all
first.
Post
intra-
kansasii
(3
Spread
Intrapulmonary
one
with
all
of
the
lung
forms
three
dissemination
with
least
common
M tuberculosis
general,
diminished
the
immediately
and
per
the
lobe
with
all
the
was
(42
was
types
and
percent).
The
(58
lung
percent).
was
In
disease
of origin;
is,
at greatest
at lowest
spread
risk
risk. Left
upto the lingula
of tuberculosis.
roentgenographic
monary
disease
so
protean
of
that
an
the
For
are
more
example,
rounding
lung
often
in both
cellularis
(10
percent).
frequent
than
than
the
a factor
larger
incidences
of thin-walled
than
by
in
little
than
and
incidence
of the
that
sur-
twice
as
M intra-
tuberculosis
(4
of M tuberculosis
atypical
mycobacterioses
the
cavities.
difference
Therefore,
in the
a thin-
cavity
is more
likely
to be from
M tubercuksis
than
from
either
M kansasti
or M intracellularis.
The
same
sort of an analogy
can be made
extensive
tern.
The
curate
unilateral
disease
differences
that
the
was
by
early
any
other
pat-
too
small
to
allow
ac-
at
this
time.
It
must
be
differentiation
remembered
or
are
name
atypical
mycobacterium
cavitary
rior
diseases
portions
There
a few
mycobacterioses
nisms
do
frequently
M
that
bacilli,
tuberculosis
First,
not form
a primary
encountered
in
did
This
not
is
demonstrate
the
complex
younger
an
site,
not
type
with
difference
our
patients
to another.8
the
atypical
the
lungs
or
in
the
material
rior
and
lobes.
however,
the
case
the
distribution
of
the
intracellularis
they
fact
be
is
no
complex
in the
caused
ab-
be
resembles
that
of the
usual
disease.
with
The
typical
hi-
case,
pattern
from
the
the
site
anywhere
of
in the
evidence
produce
M kansasii
by
same
deposited
fashion
mycolung
sedimentation
from
circupoorly
identified
factors.
the
almost
may
of liquid
For
ex-
would
is,
granulomas
lesions
the
alterna-
mycobacterioses,
pulmonary
existing
intraceltularis
An
lobes
or supeof the lower
that
follow
also
are
is in
tubercuof these
of deposition
atypical
to be
other
the
apical-
of the atypical
an anaerobic
of lesions
of apical
berculosis
is held
lating
blood,
plus
that
of the
progressive
that
the
mycobacteria
tuberculosis,
pathogenesis
fact
to
of the upper
basilar
segments
portions
of re-activation
variety
of
site
posterior
In
halves
from
the aspiration
the pharynx.
from
frequent
axillaiy
lower
foci.10
is through
most
the
disseminates
atypical
fre-
of typical
of the lungs.
Secondary
subsequent
re-activation
ample,
if the pathogenesis
bacterioses
was like that
the
case
bloodstream,
which
semisolid
The distribusilica
dust or
in approximate-
in
disseminated
by
impli-
characteristically
lungs
more
disease
then
of
is not
important
begins
the
atypiroute
disease
In the
primary
via
route
reach
orga-
of the
patients
important
because
are
atypical
the
human
of
halves.
disease
posterior
portions
losis occurs
with
tive
with
of the
bacilli,
of the
patients
The
conceivably
atypical
that
the
upper
of
lungs.
there
the
common
The
but
have
tubercle
If
M tuberculosis,
in the
apical-poste-
between
study.
may
the
that
bacillus.
like
lobes.
differences
in our
tuberculosis.8
we
occur
upper
and
out
brought
that
of the
are
just
with
major
extrapulmo-
understood.
from one
distribution
than
of the
my-
M intra-
and
less
is unknown,
quently
are
body
of tubercle
lower
halves
The
mycobacteria,
pathogenesis
nuclei
the
emphasize
atypical
and
droplet
involves
differences
investigators
kansasii
in patients
Localized
much
the
with
Disseminated
cations
with
respect
to pathogenesis.
tion of inhaled
particles,
for example,
to
The
the
mycobacterioses
bacteriologic
and not roentgenographic
between
these
organisms
and the tubercle
chosen
rare.
also
considered
contagious
The
apical-posterior
scess,
walled
with
into
is not
hematogeneously
disease.
with
occur
more
(10 percent)
percent)
are
epidemiology
entry
follows
common
the atypical
organisms.
mycobacterioses
primary
from
Some
atypical
cavities
disease
M kansasii
However,
is greater
with
thin-walled
pul-
individual
case of M tuberculosis
cannot
be distinguished
#{149}one
of either
M kansas#{252} or M intracellularis.
patterns
atypical
both
usually
occurs
deficiencies.9
ly two-thirds
manifestations
are
infections
these
is also
with
and
nary
cal
DIscussioN
The
Empyema
is rare
The
most
percent)
of endobronchial
from
the site
more
distant
lung
disease
frequently
common
origin
(68
kansasii
adjacent
three
of
intermediate
incidence
centrifugally
from
was
Endobronchial
lobe
intracellularis
with
the
another
of tuberculosis.
beyond
common
disease
of
to
difference
pleural
effusions,
do not occur
with
M tuberculosis,
cellularis
immunologic
dissemination
portion
second
primary
cobacterioses.
(0 percent).
disease
Endobronchial
adults.
a
of other
that
primary
and
suggests
circulation.
origin
could
body,
since
M kansa.s
i or
pulmonary
granulomatous
dis-
eases.
ACKNOWLEDGMENTS:
Glenda
Parkison
The
for manuscript
authors
preparation,
for photography,
John
Moore
and Curtis
assistance
in Dallas,
and Mary Bailey and
technical
assistance
would
like
to
thank
Nancy
Schreiber
Chaney
for technical
Reba
Hackney
for
in Tyler.
REFERENCES
1 Ahn
CH,
demographic
Lowell
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or
75:120-25.
2 Mares
J.
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ir.racellulareavium
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GA.
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1979;
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EE,
Dietz
GW,
Ahn
CH,
Chapman
JS,
Murry
RC,
Hurst
GA.
Radiographic
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of
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Mycobacterium
konsassi
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Am J Roentgenol
1978; 131:985-93.
4 Christensen
EE,
Diets
GW,
Ahu
CH,
Chapman
JS,
Murry
RC, Anderson
J, Hurst GA. Pulmonary
manifestations of Mycobacterium
intracellularis.
Am J Roentgenol
1979; 133:59-66.
American
5 Chapman
disease.
1960.
JS. The
Springfield,
Wiot
JF,
Spitz
anonymous
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IL:
Charles
C Thomas
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Atypical
in human
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tuberculosis.
Radiol
Clin North
Am 1973;
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7 Anderson
DH, Grech
P. Townshend
RH,
Pulmonary
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due
to opportunistic
Clin Radiol
1975; 26:461-69.
8 Chapman
JS.
cobacterioses.
9
The
New
Engstrom
PF,
Dewey
atypical
York:
CC,
mycobacteria
Plenum,
Barrett
and
1977:
0.
Jephcott
AE.
mycobacteria.
human
my-
60-62.
Disseminated
Myco-
kansasii
infection:
successful
treatment
of a
patient
with pancytopenia.
Am J Med
1972;
52:533-37.
10 Stead
NW.
Pathogenesis
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of chronic
pulmonary
tuberculosis
in man. Am Rev Respir
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95:729-45.
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Edward
Livingston
Trudeau
Fellowships
are awarded
to holders
of an M.D.
or
equivalent
degree
who
have
completed
graduate
training
in the field
of lung
disease
and
who
have
appointments
in schools
of medicine
or osteopathy.
The
Fellowships
are intended
to give
promising
instructors
an opportunity
to stay in academic
medicine
and
to
the
Trudeau
by
lowship
prove
themselves
school.
as
Awards
Fellowship
support
are
support.
allowable
teachers
up
and
to
$15,000.
If preceded
is four
years.
investigators.
Renewals
The
award
requires
are
possible
for
by a Training
Fellowship,
Limited
to U.S.
citizens
supplement
three
years
of
the maximum
Felin U.S.
or Canadian
citizens
in U.S. schools.
Completed
applications
must be received
by October
1, 1981. Payments
are
made
directly
to the Fellow
on a quarterly
basis. Fellowships
are granted
for one year and
may begin
on any date approved
by the Review
Committees.
The usual
beginning
date
is July 1. Fellowship
grants
will be given
only
to individuals
in institutions
identified
as Equal
Opportunity
Employers.
Further
information
and application
forms
may be
obtained
from:
American
Lung
Association,
Director
of Medical
Affairs,
1740
Broadway, New York, N.Y. 10019.
schools
136
and
to Canadian
CHRISTENSENEl AL