Karl
Wernecke,
MD
Thymic CT and
#{149} Pierre
Vassallo,
Involvement Sonographic
To evaluate the morphologic characteristics and frequency of thymic en-
largement in Hodgkin disease, the initial and follow-up computed tomographic (CT) scans of 43 patients with newly diagnosed Hodgkin lymphoma were retrospectively analyzed. Sonograms of the thymic region in 21 patients were also available the CT
and scans.
showed
were Initial
thymic
with
compared CT scans
enlargement
in 17 of
the 43 patients, no evidence of thymic enlargement in 15 patients, and equivocal findings in 11 patients.
Analysis of follow-up CT scans mdicated that seven of the 11 patients with initially equivocal findings had had
thymic
enlargement.
patients, mor
the anterior
with
shrank
adopted mic
In all
thymic
of the
CT scans showed that sonography could not help differentiate the northymus tissue. All
fatty
from thymic
in Hodgkin Findings’
T
involvement
HYMIC
surrounding glands that
were considered diseased because of enlargement at CT were sonographically visible due to an abnormal, hypoechoic structure. The results of the study show that thymic enlargement presumed to be due to involvement
is a well-rec-
months
were
available
Since
September
vanced
the study both preparasternal
with
bulky
mediastinal
lesions, the differentiation between thymic and/or lymph node tumors is extremely difficult. Whether followup CT scans obtained after therapy can help to elucidate the identity of such mediastinal tumors is as yet unclear.
additional
information
mdi-
cating thymic enlargement was present. An attempt was also made to establish sonographic criteria to identify thymic glands that were considered diseased because they were enlarged at CT and to assess the diagnostic value of combined mediastinal CT and
sonography
for
this
purpose.
Patient
AND
of 104 consecutive diagnosed Hodgkin
ported.
available
were
67.3421
#{149} Me-
CT, 67.1211 #{149} Mediastinum, neo#{149} Mediastinum, US studies, 67.1298 #{149} Thymus, CT, 676.1211 #{149} Thymus, neoplasms, 676.342 diastinum, plasms,
67.342
Radiology
1991;
181:375-383
newly
treated
live
cluded
at our
study.
The
because
hospital
between
selected other
for
this
61 patients
CT scans
before
disease
developed
only
had
(n
Hodgkin
disease
within
0.5-36
months).
parasternal technique
the
latter
was
half
follow-up
and after
therapy
25 women
and
were
65)
=
of
21 patients had CT scans and Eighteen of the 21
undergone
during
There
of
of therapy
all patients
with this
period, only and posttherapy sonograms.
raphy
sonog-
(range, 18 men
in
our study; ages ranged from 17 to 65 years (mean, 33.4 years). Hodgkin disease was diagnosed by means of peripheral lymph node biopsy (n = 35), isolated mediastinal
lymphomas (n = 4), and
through mediastinoscopy percutaneous biopsy
Twenty-seven
patients
Hodgkin
disease,
had
eight
(n
stage
4).
=
II
had stage
III dis-
ease, six had stage IV disease, and two had stage I disease. Eighteen patients were treated with radiation therapy alone, two with
chemotherapy
combined
CT
alone,
and
23 with
obtained
with
a Tomo-
(Philips,
Shelton,
therapy.
Examination scans
Technique were
scan 350 imager
been
January
bolus
administration
material
previously
Image
retrospecwere
1986,
diagnosed examined Because
patients
a period
in 25 of our 43 patients.
Conn)
of 100-200
(Ultravist
Mediastinal sonograms with 3.5- and 5.0-MHz 7000; Picker International, technique of mediastinal
patients
January 1989 were reviewed. patients in whom CT scans before and after therapy were
disease,
newly
over
completion
mL
300; Scher-
ing-AG, Berlin) in a rapid sequence (scan time, 4.8 sec; section thickness, 0.9 cm).
METHODS
Selection
The records
after
have been sonography.
after
1984 and Forty-three obtained
Hodgkin
with
of contrast
MATERIALS
MD
obtained
3-30
cases
Potter,
examinations)
with
terms:
#{149} Richard
ognized feature of Hodgkin disease; however, its exact prevalence is unknown (1-3). To date, studies evaluating computed tomographic (CT) criteria of thymic involvement in Hodgkin disease are few (4-7). In ad-
by Hodgkin disease seems to occur more frequently than previously re-
Index
MD
Disease:
whether
enlargement,
the thymus remained enlarged after therapy and full clinical remission. The comparison of sonograms and
mal-size
E. Peters,
24
tu-
and
In nine
with
#{149} Peter
thy-
seven
tongue-shaped
configuration.
Rutsch
In this study, we have analyzed thoracic CT scans obtained in 43 patients with newly diagnosed Hodgkin disease to evaluate the frequency of thymic enlargement at initial examination. The follow-up CT examinations were then evaluated to assess
mediastinal
therapy
a typical
patients
#{149} Frank
MD
ex-
therapy
were obtained at other institutions and were not available for retrospective evaluation. Follow-up CT scans (one to three
were obtained transducers (LSC Munich). The sonography has
described
(8,9).
Analysis
CT-Retrospective analysis CT scans included assessment ration, size, and internal texture
of the initial of configu-
thymus
lymph
and adjacent
nodes. The thymus mal if one or more
enlarged
of the
was considered of the following
abnorwas
found: (a) a triangular or bibbed thymus that was markedly enlarged (thickness of I From the Institute of Clinical Radiology, University of Muenster, D-4400 Muenster, Germany. Received December 6, 1990; revision sion received March 13; accepted May 16. Address reprint requests ©
RSNA,
1991
Albert-Schweitzer-Str requested February to K.W.
33, 5, 1991; reviAbbreviation:
SD = standard
deviation.
375
left thymic lobe over 2 standard deviations [SDs] greater than the normal age-related range) (4,7), (b) an obvious convex displacement
of the
visceral
the presence
(c)
diastinal
pleura
of cysts
tumor
(3,11)
(Fig
Anterior mediastinal globular configuration cysts
were
(6,10),
or
in an anterior
me-
Ia).
masses with a and no evidence
classified
as equivocal
of
lesions
because a definite differentiation from lymph node tumors was not possible with morphologic criteria alone. If follow-up CT showed a regression in size with the
adoption of a typical triangular shape in a previously equivocal anterior mediastinal mass, the mass was then reclassified as an
abnormal thymus (Fig I). In thymic glands with a globular uration, response accordance Francis
than
with et al (6),
criteria a sagittal
2 SDs from
range
was
suggested diameter
the normal
considered
assessed
findings.
age-related
knowledge
experience
have performed in more than
mediastinal 2,000 adults),
adult
cannot
thymus
b.
findings
without
In our
a.
by more
abnormal.
Sonography.-Sonographic
were
config-
changes in the sagittal diameter in to therapy were monitored. In
of CT
(to date,
we
sonography the normal
be delineated
from
surrounding tissue at sonography because of an inadequate difference in echogenicity.
If connective
and
anterior
mediastinum
neously normal.
hyperechoic, Any lesion
eated
from
fatty
tissue
were
that
of the
homoge-
this was recorded could be delin-
surrounding
tissue
of the
as ante-
nor mediastinum was recorded as abnormal and its configuration, size, and echo texture were assessed. Anterior
mediastinal
lesions
detected
(which
is best
nal sagittal there were id).
demonstrated
on
paraster-
sonograms [Fig Ic, ld]) or if cysts within the lesion (Fig ic,
All raphy
nodular lesions that showed
were
considered
detected no evidence
equivocal,
differentiation
between
and lymph
node
on the basis
with sonogof cysts
since
a reliable
enlarged
tumors
thymus
figuration
on follow-up
reclassified Finally, compared
as thymic tumors. the sonographic findings were with CT findings to establish
glands CT
that
were
sonograms
to identify considered
were
thymic diseased
with
CT Findings Therapy
before
evidence
and
376
of thymic
1; Table
#{149} Radiology
regression
therapy
extensive
of an enlarged
in a 25-year-old
globular
tumor
in the
patient anterior
thymic
gland
at CT and
sonography
before
with
Hodgkin
disease.
(a) Initial
CT scan
mediastinum
(sagittal
diameter,
5 cm),
unequivocally identified as the thymus. Only the presence of small cysts suggests that the tumor might be of thymic origin. (b) CT scan obtained after reduction in tumor size and the adoption of a typical thymic configuration left
thymic lobe, 1.2 cm). (c) Initial sonogram (left parasternal sagittal tumor (arrowheads) with a roughly triangular shape and a central (z) lying anterior to the right pulmonary artery (p). (d) Sonogram obtained after therapy shows that the tumor has regressed to an echogenic prevascular lesion (TH, arrowheads) a typical thymic tongue-shaped configuration. P = right pulmonary artery.
the CT findings were equivocal in regard to the nature of the anterior mediastinal tumor (Fig 2; Table 1). Follow-up CT enlargement
seven
scans had
of the
showed that been present
11 patients
findings.
who
In all seven
(sagittal
view) cyst
with
after
enlargement
1). In 11 patients,
after
thymic in
had pa-
therapy
(Fig
2, Table
four with
patients (Table a prevascular
measuring shrinkage
residual prevascular this patient.
1).
In spite of further follow-up with CT, the nature of prevascular lesions detected with CT remained unclear 1). In one
patient
nodular lesion 3.0 cm in sagittal diameter, was observed after therapy
diameter,
1.8 cm)
but
the
nodular configuration persisted (Fig 3). According to Francis et al (6), residual thymic tissue, particularly in patients older than age 50 years, may have a globular configuration. Thus, we were unable to differentiate between residual thymic tissue and a
tients, a previously nodular mass showed clear shrinkage and the adoption of a typical triangular shape
CT scans obtained before therapy showed no evidence of thymic enlargement in 15 of the 43 patients and in 17 (Fig
an
which cannot be within the lesion therapy shows a (thickness of the shows a hypoechoic
equivocal
criteria.
RESULTS
clear
shows
show
characteristics
alone. Initially, globular anterior mediastinal lesions that had a tongue-shaped con-
criteria
Figure 1. Images and after radiation
was not possible
of sonographic
sonographic
d.
C.
with sonography were considered to represent thymic tissue if they had a typical thymic tongue-shaped configuration
in
lymph
node
in
In two patients with multiple enlarged anterior mediastinal nodes, complete regression was observed in one patient after therapy; a multinodular lesion persisted in the second patient (Fig 4). The differential diagnosis proposed in both these cases was of nodular involvement of the November
1991
Table
1
CT Findings
at Initial
and Follow-up
Examination
in 43 Patients
with
Hodgkin
Disease
Findings Examination
No Thymic
Initial
Thymus
Enlargement
of normal
size
Equivocal
(n = 12)
Large
Thymic
prevascular
tissue
(n = 3)
Follow-up
Thymic
size unchanged
Regression
=
Complete
disappearance
of the thymus
4)
(n
No thymic
tissue
identified
(n
Enlarged
8)
=
(n = 3)
Initially multiple cm in diameter) sion (n = 1)
prevascular
Initially
prevascular
show
multiple
cm in diameter)
nodules
complete
show
displacement
(2.0
nodules
(2.0
to mul-
dence
residual nodules of 1.0 cm in diameter (n = 1) Thymus of marginal size shows regression to normal size (n = 1) Patients
with
equivocal
thymic
involvement
thymus by Hodgkin disease or multiple enlarged prevascular lymph nodes, with complete regression in the first case and residual lesions in the second. In
one
patient
with
a thymic
size
CT enabled us to diagnose enlargement in 24 (56%) of 43
short,
thymic patients
and
ment
in
15
exclude
CT findings
Thymic
Internal
enlarge-
In four (9%) pawere equivocal.
(35%).
tients,
thymic
Size
In
six
(25%)
of
24
mic enlargement, tially homogeneous.
patients
the
the 24 patients, the had an inhomogeneous nal structure at CT
with
thy-
available
in
enlarged
12
patients
tial thymic enlargement; the showed no evidence of new mation within the thymus.
Volume
181
#{149} Number
2
with
mi-
scans cyst for-
Sonographic after Therapy
enlarged lobe over
Patients
2
and
tently There
thymic the
size
size,
enlarged
both
glands,
of a persis-
after therapy. in decrease
of normal
relating
ences in type of therapy therapy alone, n = 18; apy and chemotherapy,
and
and
to differ-
n
=
involvement
23).
the
histologic
in all 24 patients are shown
than
years, Only years
with in Ta-
without enlargement years ± 16.9) (x2 test; P < .05). patients between 17 and 40 72.4% had thymic enlargement. 35.7% of patients more than 40 of age showed thymic enlarge-
ment. quency
men ever,
those
Women
showed
of thymic
(women, the
according
significant.
enlargement
64%;
differences to
a higher
sex
men, in
were
frethan
44%).
How-
distribution
not
tients,
initial
statistically
had In
tongue-shaped
multiple, the anterior with
nodules
the prevascular origin in only
within lar
mass.
n
The
an
mass
patients
1, 3). In the sonography
hypoechoic mediastinum.
CT scans were
nodules
indicated
located
thymus (Fig 7). indicated that
of thymic
enlargement
thymic tongue-shaped and cysts, n = 2; cysts
an anterior
mass,
pa-
lesion was of thymic four of the 15 patients
evidence
at CT (typical configuration
15
showed in two
within an enlarged Initial sonography
with
follow-up
all
sonography
mediastinal
these
at
of thymic at CT. Twelve
and nodular in 10 (Figs three remaining patients,
that
and
enlargement
also
available.
Comparison
lymph
ble 3. A statistically significant difference in age was observed between patients with and without thymic enlargement. Patients with thymic enlargement were younger (29.6 years ± (38.6
shows
before
evidence was seen
15 patients
showed within
Data
and
subclassification thymic enlargement
Among
2)
obtained before available in 15 patients
clear
sonograms
was
ther-
of concurrent
of the
anterior
(radiation
radiation
Pathologic
frequency
before
frequency
enlarged thymus was no difference
in thymic
8.6)
=
displacement
with thymic
in whom enlargement
between
therapy
node
(n
Findings
lation
The
thymus nodular inter(Fig 2). In five (21%) patients, CT showed cysts measuring 1.0-3.0 cm in diameter within the enlarged thymus (one patient had one cyst, two had two cysts, and two had multiple small cysts) (Fig 1). In all five patients, the cysts showed a reduction in size with therapy and completely disappeared at completion of therapy (Fig 1). Follow-up CT scans obtained 3-30 months after therapy were
Therapy
CT.-Sonograms therapy were
at CT
thymus was miIn 13 (54%) of
of pleural
SDs) in nine of 24 patients after therapy (Figs 2, 6). Table 2 shows a corre-
Clinical Texture
during
The thymus remained (thickness of left thymic at
of the pleura
examination.
Thymic
the upper limit of the normal range, shrinkage was observed after therapy, and we could not differentiate between a regressing thymic lymphoma and normal thymic involution (Fig 5). In
CT
at initial
lobe,
regression (n = 2) Initially globular tumor shows regression in size with the adoption of a typical triangular shape (n = 7*)
tiple
*
ofleft
triangular(a = 10)
Initially enlarged thymus shows shrinkage to normal size and typical triangularshaped configuration (n = 10) Initially globular tumor with cysts shows shrinkage and adoption of typical thymic triangular shape. Cysts disappeared completely (n = 5) Thymus of initially marginal size with evi-
regres-
shrinkage
(thickness
cm) with typical
shaped configuration Large prevascular globular tumor (4.5-12.0 cm in sagittal diameter) with cysts (n = 5) Thymic size at the upper limit, but convex
of multiple nodules meacm in diameter (ii = 2)
0.5-2.0
Enlargement
thymus
2.0-3.5
Thymic size at the upper limit of the normal range (n = 1) Initially globular tumor (3.0 cm in diameter) shows shrinkage to a residual nodule of 1.8 cm in diameter (n = 1)
(n = 2) size (n = 6)
of thymic
measur-
cm in diameter
Conglomeration
suring
Thymic
globularlesion
ing 3.0-11.0 No thymic
Involvement
=
mediastinal
globu-
2).
In the 12 patients low-up sonograms
in whom folwere available,
clear shrinkage of all prevascular masses was evident after therapy (Figs 1, 3). In all eight patients with globular anterior mediastinal mass
a
a on
initial sonograms, a further shrinkage in lesion size was observed after completion of therapy, along with the adoption of a typical tongue-shaped configuration
best
demonstrated Radiology
with
#{149} 377
the
parasternal
3). The
sagittal
prevascular
therefore,
view
(Figs
masses
1,
could,
be retrospectively
classified
as thymic tumors in all these cases. One anterior mediastinal mass with typical tongue-shaped thymic config-
uration
at initial
a
showed three with multiple, hypoechoic nodules, shrinkage to a single residual tongue-shaped mass was observed in one patient, and shrinkage to multiple small nodular lesions was observed in two patients. It is worth noting that an abnormal shrinkage patients
echogenicity
long
sonography
after
of the
after
In the
therapy.
thymus
full clinical
persisted
remission
(up
to
a.
b.
months after therapy) in all 12 patients with follow-up sonograms and thymic enlargement at CT. This obser17
vation was true for patients with residual thymic enlargement at CT after therapy, as well as for patients whose thymus
had
size.
Thus,
eated
from
long the
to its normal
thymus
clinical
1, 2). In eight increased follow-up
the
of the
12 patients,
thymus
during period.
the
remained
sonoIn four
structure
pa-
of the
unchanged.
In five patients, initial sonographic after
tissue
occurred
of the
hypoechoic
appeared
be delin-
fatty
remission
echogenicity
slowly graphic tients, thymus
could
surrounding
after
(Figs
returned
the
thymic cysts examinations therapy.
seen at dis-
In only
one
patient, showed
follow-up sonography the development of a thymic
cyst
cm
(0.8
detected Patients
In the
in diameter)
with with
that
was
not
CT. normal
thymus
at CT.-
three
patients with a normal at initial CT, sonography not enable delineation of the from surrounding fatty tissue.
thymus
could gland
Patients with equivocal ment at CT-Follow-up
thymic
nodular
diameter
sisted unchanged 3). In another
CT findings, tiple nodules
for patient
of 1.8
maintained this lesion
configuration;
its per-
ules 378
persistence (Fig
a conglomeration (resembling
of multiple
4). In one
#{149} Radiology
the CT findings. larged residual
of mula bunch of
patient
small with
Because of its triangular thymic gland. TP = main
mic
size
at the
noda thy-
upper
at CT, sonograms hypoechoic ules, which, scans, were
within
the
gressed preaortic
limit
configuration, pulmonary
of normal
showed
multiple
anterior mediastinal nodwhen compared with CT determined to be located
thymus.
These
with therapy; node persisted
12 months (Fig with equivocal
grapes) was seen in the anterior mediastinum at CT and sonography (Fig 4). At completion of therapy, the antenor mediastinum was sonographically normal, whereas CT indicated
the
2. CT scans and sonograms in a 22-year-old patient with a prevascular tumor of unclear origin (thymus or lymph node) at initial CT. (a) Initial CT scan shows a large tumor (sagittal diameter, 6 cm) with an inhomogeneous nodular internal structure in the anterior mediastinum. A differentiation between lymph node tumor and an enlarged thymus was not possible from this image. (b) CT scan obtained after therapy shows the triangular-shaped configuration of the lesion, indicating that the lesion was the thymus. The thymic size (thickness of the left lobe, 2.5 cm) is above the limits of the normal age-related range. The lesion also shows a persistent nodular internal structure. (c) Initial sonogram (left parasternal transverse section) shows a prevascular echogenic tumor (T, arrowheads) with a nodular internal structure. TP = main pulmonary artery, A = ascending aorta. (d) Follow-up sonogram obtained after therapy shows an echogenic residual tumor (T, arrowheads), which correlates well with Figure
the lesion was identified A = ascending aorta.
as an en-
artery,
enlarge-
sonograms were available in three of the four patients with equivocal thymic enlargement at CT. In one patient with an equivocal nodular anterior mediastinal lesion at CT, sonography also demonstrated an identical lesion of hypoechoic structure, which shrank to a maximal sagittal cm after therapy but
d.
C.
only
lesions
re-
a single, (Fig 5).
DISCUSSION
The that
results the
of this
frequency
study of thymic
suggest enlarge-
ment in Hodgkin disease (56%)-either isolated (14%) or combined with mediastinal (42%)-seems
reported (7). The enlargement
lymph node involvement to be greater than that
in previous CT studies (30%) higher frequency of thymic in our
series
could
prob-
ably be attributed to the availability of follow-up CT scans in all patients. The thymic origin of an anterior mediastinal mass in Hodgkin disease can frequently be diagnosed only with follow-up CT scans. Analysis of CT scans obtained before therapy showed clear morphologic indications of enlarged thymus in only 17 of the 43 patients with Hodgkin disease. The two morphologic criteria suggesting the presence of an enlarged thymus were a triangular-shaped configuration of the mass or the presence of cysts (Fig
1). CT findings
in regard
to thymic
enlargement were initially equivocal in 11 patients. In most of these cases, problems were encounted in classifying large globular lesions as an enlarged thymus or a lymph node tuNovember
1991
for our patients was the availability of CT scans obtained before and after therapy. Sixty-one of 104 consecutive patients seen during the study period were excluded because initial CT scans
obtained
at other
institutions
were not available for retrospective analysis. Our study population included patients with (79%) and without (21 %) mediastinal manifestation of Hodgkin disease. This constitutes a representative
with ease. cluded
only
thoracic scans; with
a.
sample
patients
no
Hodgkin diset al (7) inwith
Hodgkin
disease
evidence
of
on initial
CT
16 of 66 consecutive evidence of thoracic
and a thymus were excluded. been included,
b.
of patients
newly diagnosed In contrast, Heron
frequency
patients disease
of normal size at CT in If these patients had as in our study, the
of thymic
enlargement
would have been even lower (23%) than we observed. An important factor that could induce an overestimation of thymic involvement is the frequency of advanced stages of disease. Although in at least half of the patients Hodgkin disease localized to the mediastinum appears to originate in mediastinal lymph nodes, involvement of the thymus will secondarily occur when the disease advances (3). Twenty-nine (67%)
of our
patients
had
stage
I or II
disease and 14 (33%) had stage III or IV disease. Unfortunately, data about the stages of disease in the study by Heron et al (7) are not available; thus, it is not possible to compare the distribution of early and advanced cases in both d.
C.
Figure
3. CT scans and sonograms in a 49-year-old patient with a prevascular lesion of unclear origin. (a) Initial CT scan shows a globular prevascular tumor (sagittal diameter, 3.0 cm). (b) After therapy, CT scan shows a globular residual lesion (sagittal diameter, 1.8 cm), which remained unchanged on follow-up CT scans obtained 1 year later. (c) Initial sonogram (right parasternal sagittal view) shows a globular hypoechoic tumor (LK) anterior to the ascending aorta (AA). (d) Sonogram obtained after therapy, 1 year later, shows an oval hypoechoic residual lesion (L, arrowheads). With the sonographic criteria mentioned in the Discussion (persistence of hypoechoic structure), this lesion may be classified as residual thymic tissue. AA = ascending
mor
ocal
1, 2, 5). Follow-up thymic
of the
CT scans
enlargement
11 patients findings.
with
in seven
initially
In all seven
patients,
equivthe
anterior mediastinal tumor showed reduction in size and adopted a typical triangular thymic configuration after therapy (Figs 1, 2, 5; Table 1). The anterior mediastinal lesions in four patients could not be classified with morphologic criteria, even on further follow-up CT scans. In the study by Heron et al (7), only Volume
181
study
by
Keller
who examined of mediastinal obtained mic
#{149} Number
2
10 of 50 patients with newly diagnosed Hodgkin disease had both preand posttherapy CT scans available. If a larger number of these patients had undergone follow-up CT, more cases of thymic enlargement might have been identified. Other factors that could account for differences in the number of patients with thymic enlargement might be patient selection criteria and the proportion of patients with advanced disease.
The
only
selection
criterion
and
involvement
and
Castleman
histologic Hodgkin
at the
sis. Keller tients. They the increasing
aorta.
(Figs
showed
studies.
The higher frequency of thymic enlargement in our patient sample supported by the histopathologic
time
(3),
specimens lymphoma
of initial
Castleman
diagno-
found
in 21 (48%)
concluded
is
that,
thy-
of 44 pa-
due
to
fibrous reactions around lymphomatous infiltrates in at least half of the cases, Hodgkin disease located in the mediastinum appears to arise in the thymus. Keller and Castleman (3) have mdicated that cyst formation is a frequent and typical morphologic finding in lymphomatous involvement of the thymus. However, the presence of
cysts
in lymphomatous-involved
thy-
mic glands has rarely been described with previous cross-sectional imaging techniques (5,7). In our series, thymic cysts were found in five (21%) of 24 patients with an enlarged thymus.
Radiology
#{149} 379
Figure 4. CT scans and sonograms in a 23year-old patient with prevascular lesions of unclear origin (multiple lymph nodes or multifocal thymic involvement). scan shows a multinodular cm in diameter) prevascular scan obtained after therapy
tence
of multiple
(a) Initial CT (nodules up to 2.0 mass. (b) CT shows a persis-
nodular
prevascular
lesions
(up
to 1.0 cm in diameter). (c) Initial sonogram (right parasternal sagittal view) shows one of the several nodes (L) anterior to the ascending aorta (AA). (d) After therapy, this lesion and other lesions seen at CT are no longer evident on the sonogram. These sonographic and CT findings suggest that the lesions
seen
CT probably
at
residual
lymph
multinodular nary
nodes
represent
rather
residual P = right pulmo-
thymic tissue. LA = left atrium.
artery,
multiple
than
a. Moreover,
cysts,
our
when
results
morphologic
at the
that
are a reliable
indicator
of thymic tumor; ular prevascular correctly classified
glands
indicate
present,
b.
of the
presence
all five initially lesions, which as enlarged
initial
globwere thymic
examination
be-
cause of the presence of cysts, adopted a typical triangular thymic configuration after therapy (Table 1). The higher detection rate of thymic
cysts
in our
series
compared
with
those of previous studies might have several explanations. First, all of our patients received intravenous contrast medium. Contrast material enhancement of thymic tissue may assist in the identification of cysts. Second, the interpretation of a hypoattenuating area within a mass as a cyst or tumor necrosis is exceedingly difficult with morphologic criteria alone, particularly in the interpretation of small le-
sions.
Because
findings tleman of low
masses rather
of the
most than
likely
represented
necrosis.
This
is supported ings, which patients with our experience,
sistency
histopathologic
described by Keller and Cas(3), we assumed that the areas attenuation within prevascular
cysts
assumption
with sonographic findwere available in all five cystic the
of cystic
changes margin
lesions
at CT. In and con-
can
often
be
demonstrated more precisely with sonography than with CT-especially with use of 5.0-MHz transducers. Tumor necrosis often displays irregular margins and low-level internal echoes due to particulate necrotic debris. In contrast, the margins of cysts are generally sharper and internal echoes are fewer (Figs ic, 6b). However, the cystic nature of the lesions noted with CT and sonography has not been histologically proved in our study. Isolated thymic enlargement presumed to be Hodgkin disease was found in six (14%) of our 43 patients. 380
#{149} Radiology
d.
C.
Heron lated
et al (7) found thymic enlargement
tients
with
disease.
ancy
newly
In our
may
no
case of isoin 66 pa-
diagnosed opinion,
be due
Hodgkin
this
discrep-
to misinterpretation
of isolated thymic enlargement as antenor mediastinal lymph node involvement on initial CT scans. If a larger number of patients in the study by Heron et al had had both pre- and posttherapy scans, more cases of isolated thymic enlargement may have been identified as the thymus shrank and became triangular. The higher frequency of isolated thymic enlargement in our patients is again supported by the study of Keller and Castleman (3), who found isolated thymic involvement in 10 (23%) of 44 patients with newly diagnosed Hodgkin disHodgkin benign
ease. We ment
may with
postulated that thymic seen in 24 patients on
have been due to infiltration Hodgkin disease. Although
tologic
only
enlargeCT scans
confirmation
two
supported treatment mediastinal retically largement
of these
was
patients,
this
served in the spleen. logic study of Keller (3) does not support
his-
available
in
view
by the parallel response to with concurrently involved lymph nodes. It is theopossible that the thymic enobserved in patients with
lymphoma hyperplasia
is
To our knowledge, that show a purely
tic thymic pathologic
enlargement verification
is the result of as is often ob-
The histopathoand Castleman this hypothesis. no studies exist benign hyperplas-
with
histo-
at diagnosis
(3).
mic
Benign thymic enlargement rebound hyperplasia)
may
November
(thybe 1991
a.
b.
Figure lymph
5. Equivocal node (diameter,
being
at the upper
limit
of normal
size. (c) Initial sonogram mic region. Comparison
vena
cava
superior.
d.
C.
thymic involvement in a 28-year-old patient with Hodgkin 1.5 cm) and a marginally large thymic gland (thickness
range.
(right parasternal with CT scans
(d) Follow-up
of a single preaortic residual node ously described probably represented
a.
(b) Follow-up
CT scan obtained
transverse showed these
section) nodules
lymphomatous
after
radiation
6.
vascular
CT scans globular
(approximately
and
sonograms
mass
(sagittal
35 HU),
these
therapy
shows
involvement
diameter,
10 cm)
hypoattenuated
patient with
areas
with
several
could
a globular
small
a considerable
(arrows) enlarged
regression
prevascular
hypoattenuated
not unequivocally
as
in thymic
up to 1.0 cm in diameter thymus. AA = ascending
in the aorta,
thy-
C
=
with the persistence that the lesions previcava superior.
d.
C.
in a 22-year-old
shows an enlarged paratracheal size of the latter was classified
obvious regression of the prevascular nodules sonographic findings suggest, retrospectively, of the thymus. AA = ascending aorta, C = vena
b.
Figure
(a) Initial CT scan lobe, 1.1 cm). The
shows multiple hypoechoic nodules to be located within the marginally
sonogram obtained after therapy shows (L, arrowheads). The combined CT and focal
disease. of the left
mass zones
be identified
(up
at initial
CT. (a) Initial
CT scan
in diameter).
Because
of CT
(b) Corresponding
initial
sonogram
to 1.0 cm
as cysts.
shows
a large
pre-
numbers
(left
parasternal
transverse view) shows a large tumor (TH, arrowheads) with multiple disseminated cysts measuring 0.3-1.0 cm in diameter. C = heart. (c) CT scan obtained after radiation therapy shows a triangular residual thymic gland, the size of which is clearly larger than the age-related normal size (thickness of the left thymic lobe, 2.3 cm). (d) On the corresponding sonogram (left parasternal transverse view), the residual thymic gland (TH) has a hypoechoic internal texture. The cystic areas seen in b are no longer evident. AA = ascending aorta, TP = main
pulmonary
artery.
seen after chemotherapy for Hodgkin disease and other tumors (12). In all our patients with an initially normal thymus who underwent follow-up CT over a 20-month period (n = 7), no
sonography. This observation lates well with our experience that the normal adult thymus be delineated from surrounding
correso far cannot me-
diastinal
due
evidence of recurrent thymic plasia was seen. The comparison of sonograms CT scans showed the following
an inadequate nicity.
sults. In all patients thymus at CT (n gland from
Volume
could not surrounding 181
with
hyper-
a normal
the thymus be differentiated fatty tissue at =
#{149} Number
3),
2
and re-
tissue
at sonography difference
In all patients
with
to
in echoge-
thymic
enlarge-
ment diagnosed at CT (n = 15), sonography showed hypoechoic antenor mediastinal lesions that were clearly delineated from surrounding mediastinal
fatty
tissue.
Due
to the
predominantly globular configuration of these anterior mediastinal lesions, it was initially difficult to differentiate between an enlarged thymus and a lymph node tumor. The sonographic criteria at initial examination mdicated that the prevascular lesion was of thymic origin in only four of the 15 patients; a typical tongue-shaped configuration was seen on sagittal sonograms in two patients, and cysts within an anterior mediastinal globular mass were seen in two patients. Radiology
#{149} 381
a.
b.
Figure with
7. an
Focal involvement of the thymic inhomogeneous internal structure.
heads) within one hypoechoic ous
bulking
gland in a 19-year-old (b) Initial sonogram
the thymic bed (large arrowheads). TP = main pulmonary artery. (c) Initial node (L, small arrowheads) adjacent to normal hyperechoic thymic tissue of the thymic contours. A = ascending aorta, T = main pulmonary artery.
Follow-up sonography performed after therapy showed that all initially globular thymic tumors adopted a typical tongue-shaped configuration, indicating that the lesion initially detected node.
was not an enlarged lymph It is worth noting that all sono-
graphically detected thymic glands remained hypoechoic after completion of therapy and could be delineated from surrounding fatty tissue long after full remission (up to 17 months after therapy) (Figs 3, 6).
The drawn
following from our
normal
hypoechoic
conclusions findings:
may
be
(a) Normalsize thymic glands cannot be detected with sonography, and (b) thymic glands that are considered diseased because of size criteria at CT become sonographically visible due to an abechogenicity sonography
ence
of thymic
echo
(qualitative may indicate
disease
texture.
#{149} Radiology
The
criterion) the pres-
even
absence of thymic enlargement (quantitative criterion) at CT
382
C.
patient. (a) Initial CT scan shows (left parasternal sagittal view) shows
in the as illus-
at
sonogram (TH, large
trated in Figure 5. The results of this study also indicate that the changes in echogenicity observed in diseased thymic glands are identical to those seen in lymphomatous involved mediastinal lymph nodes with one exception: In contrast to mediastinal lymph node tumors, which disappear completely on full remission (13), an initially enlarged thymus remained identifiable at sonography because it had a different echo texture than the surrounding connective tissue. The significance of this finding in regard to the absence or presence of residual tumor within the thymus is uncertain. Why does the echo texture of the thymus persist? Although we evaluated all possible reasons, we did not
find an explanation tion. The persistence
for this of the
a roughly triangular two hypoechoic
observahypo-
echoic thymic texture is certainly not due to radiation therapy. Patients with lymphoma not originally involving the anterior mediastinum or patients with carcinoma of the lung who
(left parasternal arrowheads).
prevascular nodes (L, small
transverse The
node
tumor arrow-
view) produces
shows an obvi-
have undergone radiation therapy (not included in this study) never developed an abnormal echo texture of the thymus at sonography. Likewise, this phenomenon apparently does not portend an increase in the recurrence rate, since patients with and without recurrences had persistent hypoechoic thymic glands. The only cause of persisting hypoechoic texture of thymic glands seems to be prior involvement by Hodgkin disease. The sonographic criteria mentioned above may help in further characterization of equivocal anterior mediastinal lesions as demonstrated in Figures 3-5. In Hodgkin disease, thymic infiltration is most frequently diffuse, and rarely, if at all, focal as in infiltration of liver or spleen. In patients with marked (n = 3) or marginal diffuse (n = 1) enlargement of the thymus seen at CT, sonography tiple, hypoechoic nodules nor mediastinum, which
showed mulin the antewere shown
November
1991
to lie within the thymic bed when correlation with CT scans was performed (Figs 5, 7). We assume that these findings suggest the presence focal thymic lymphomatous involvement. In patients with extensive lymphomatous involvement of the thy-
mus,
a residual
and
frequently
of
en-
larged thymic gland is often detected after therapy (Fig 2, Table 2). Except for one residual enlarged paratracheal lymph node, all residual mediastinal tumors persisting after therapy in our patient group were due to residual enlarged thymic glands. This observation supports the hypothesis by Katz et al (14), which states that residual mediastinal masses found after treatment of Hodgkin disease are the re-
sult
of thymic
our patients glands after frequency of The clinical involvement phoma-particularly immunologic
prognosis-is
enlargement.
None
of
with enlarged thymic therapy showed a higher subsequent relapse. significance of thymic in Hodgkin lymregarding its role and its influence on
as yet unclear.
consequences concerning whether an anterior mediastinal mass represents involved lymph nodes or involved thymus. This study was designed to provide new information, which, although perhaps currently without clinical or management importance, might provide data that could influence patient treatment. In our study, patients both with and without thymic involvement showed similar rates of recurrence: 25% for patients with
CT evidence and
for
ment
regimen
2.
3.
#{149} Number
2
during
the
11.
can sugbe examof patients, basis. U
thymus
gland.
Cancer
1974;
Pnndull
G, Beck
W, Rahlf
Hodgkin’s
disease
and
mor.
Pediatr
1983;
EurJ
G, Gadner
H.
a mediastinal
141:117-1
JE, Nicholas
tu-
19.
12.
Kissin CM, Husband
13.
smann W. Benign thymic enlargement in adults after chemotherapy: CT demonstration. Radiology 1987; 163:67-70. Wernecke K, Vassallo P, Hoffmann C, et al. Value of sonography to monitor the therapeutic response of mediastinal lymphoma: comparison with chest radiographs and
D, Ever-
CT. AJR 1991; 156:265-272. 14.
BI. Hodgkin’s disease, autoimmunity, and the thymus. Br Med J 1965; 1:1592-1596. Keller AR, Castleman B. Hodgkin’s disof the
145:249-254.
Heron CW, Husband JE, Williams MP. Hodgkin disease: CT of the thymus. Radiology 1988; 167:647-651. Wernecke K, Peters PE, Galanski M. Mediastinal tumors: evaluation with suprasternal sonography. Radiology 1986; 159:405-409. Wernecke K, Potter R, Peters PE, Koch P. Parasternal mediastinal sonography: sensitivity in the detection of anterior mediastinal and subcarinal tumors. AJR 1988; 150: 1021-1026. Moore AV, Korobkin M, Olanow W, et al. Age-related changes in the thymus gland: CT-pathologic correlation. AJR 1983; 141:
241-246.
first
we
Hoffbrand
Katz
M, Piekarski
JD, Bayle-Weisgerber
CH, et al. Masses mediastinales residuelles post-radiotherapiques au cours de la maladie 1977;
de Hodgkin.
Ann
Radiol
(Paris)
20:667-672.
33:
1615-1623.
4.
Baron mus.
181
used
Thomas F, Cosset JM, Cherel P, Renaudy N, Carde P, Piekarski JD. Thoracic CTscanning follow-up of residual mediastinal masses after treatment of Hodgkin’s disease. Radiother Oncol 1988; 11:119-122.
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9.
10.
References 1.
8.
follow-up,
part of the study period, gest only that our findings med with a larger number possibly on a multicenter
Lindfors KK, MeyerJE. Thymic cysts in mediastinal Hodgkin disease. Radiology 1985; 156:37-41. Francis IR, Glazer GM, Bookstein FL, Gross BH. The thymus: reexamination of age related changes in size and shape. AJR 1984;
7.
without
(clinical
RL, LeeJKT,
Computed
Volume
patients
6.
involvement
thymic 4-55 months; mean, 28 months). Because of the small number of patients studied and the nonstandardized treat-
involvement
With
current staging and management, the thymus is considered to be a “lymph node” and, therefore, its involvement does not change the stage to an or “IV” stage. Likewise, there are no radiation therapy or chemotherapy
20%
of thymic
5.
Sagel 55, Peterson
tomography Radiology 1982;
of the normal 142:121-125.
RR. thy-
Radiology
#{149} 383