Jul 1, 1996 - 16.364. #{149}Neurocytoma. 16.364 ... neurocytoma occurs most .... Central neurocytoma: a synopsis of clinical and histological features. Brain.
Cases General Jonas
Case
H. Goldstein,
of the
of the
MD
#{149} Richard
Day1 A. Haas,
MD
#{149} Glenn
.
U HISTORY A 24-yeanld nificant
right-handed medical
history
and
decreased
headache logic
examination
pillary
response
tremity
woman had
revealed to light
weakness.
no sighistory
acuity.
mild
left
right upper
A.
terms:
Brain
pucx-
1mm 02903. accepted
. RSNA.
July
1996
the
neoplasms.
16:9’
1995
RSNA
t)epartmcnt
Front
the
I)ecenther
of
2’.
diagnosis.
16.364
revealed
Proton-density-weighted
material-enhanced
(CT) and magnetic were performed.
1996;
CT
reso-
Neurocytoma.
#{149}
a 6-cm-diameter
enhancing mass in the anterior right triele (Fig 1). No caleifleations were unenhanced CT seams (not shown), effect resulted in hydrocephalus.
of
showed
FIgure 1. Contrast-enhanced CT scan shows a hetenogeneously enhancing mass in the right lateral ventricle. Several small, nonenhancing foci are seen in the periphery of the niass.
RadioGraphics
MD
FINDINGS
MR
a predominantly
tricular
mass
septum
peblucidum
ventricular
Index
Tung,
Contrast-enhanced
Neuno-
a decreased and
Contrast
computed tomography nance (MR) imaging
with
a 6-week
visual
Day
with
lateral yenseen on and mass
imaging
hyperintense
a broad (Fig
dilatation
was
attachment 2).
intraven-
to the
Asymmetric
lateral
noted.
Figure 2. Transaxial proton-density-weighted image (repetition time msec/echo time msec 30) shows a heterogeneous hut predominantly intense mass with a broad base of attachment displaced septum pellucidum (arrowheads).
MR 2,50()/ hyperto the
=
16.364
1 -9’3
I)iagnostic
scientific
Address
intaging. assembly.
reprint
Brown tniversity School of Medicine, Rhode island Received September 26. 1995: revision requested
requests
hospital. October
593 Eddy St. Providence. 1 I and received I)ecemher
RI 2:
toJ.II.G.
1996
GoldsteIn
et al
U
RadioGraphics
U
971
(;ntrast-enlianced imaging mass
into
at the l)tIt
coronal
demonstrated the
third
fonamina
T 1-weighted
caudal ventricle
(Fig
of Monno
nesulted
dilatation
of the
asymmetric
MR
extension
of the
3).
Mass
effect
in bilateral lateral
yen-
tnicles.
DIAGNOSIS:
Intraventricuban
neunocytoma.
U DISCUSSION tumors are uncommon, ac1 0% of all intracranial neoplasms
Intraventriculan counting
for
( I ). Intraventnicular
neurocytoma
commonly
in Iatments
constitutes
nearly
tumors
However,
the
has
before
atice
(2,3).
tnicular
The
seizure.
septum
lateral
duces
fornix,
and
this
advantage
They
also
in which
CT concluded
MR
differential with
many
advantages
masses.
CT
extent
is an
planning
(5).
in detecting streak tic
MR
lesions,
from
of masses and
of calcification. were few cases altered MR
imaging hone,
vascular
mass iniaging
has
is also and
origin
MR
neunosungical more
hemorrhage
allows
malformations
of
attachment
suggests
the
charactercontent,
cys(4).
diagnosis
edema, associated
U
Special
Exhibit
differential hetenoge-
in the
and
age, can
location,
tumor
he valuable alternative
with involves
in 20%
and
imaging
in differentiating (5).
froni Peritumoral
of astnocytomas,
neunocytoma.
the
ch()-
oligodendroglioma
diagnoses
neurocytoma
trigone,
on
menin-
ependymoma,
papilloma,
present
lateral
astrocytonia,
subependyrnoma,
of these
in a young pellucidum
the
mass
includes
intraventricular
972
tumor
(3).
intravemtriculan
several
neo-
of a well-
septum
to neunocytoma,
plexus
are
of this
combination
to the
diagnosis
ventricle
(6). Patient appearance
quently
edema
of a well-circumscribed,
neous
noid
vasogenic
intraventnicular
and
is mild
lntnatu-
appearance the
(69X on vascu-
( 1 ). There
enhancement. the
pre-
of cases),
of cases) and
circumscribed adult
neurobut
calcifications
(85%
is nonspecific,
gioma,
sensitive is free
lipomatous
(62%
( 1 ). Although
third
with
contrast
rare plasm
niass spaces
In addition
completely,
enhancement, with
the
intraventriculan for
voids
moral
intraventriculan
more
solid
Ian flow
intnaventricular
as a heterogeneous
cystic
to moderate
pri-
intraventricular
tool
contrast
artifact
ization
lesion
the
intraventricular
However,
invaluable
appears
of cases). tumors.
that
in imaging
of the
imaging
cytoma doniinantly
detection that there
the
At CT or MR imaging,
pro-
to obstruction
significantly
By showing
in the
often
complementary
of an (4).
horn.
the
lateral
found
reported
imaging
diagnosis
imaged
and
is the
poral
include
neoplasni
of imaging
with
in-
pressure,
intraventriculan
et al (4)
masses
and
nostral
secondary
in characterizing
Figure 3. (ontrast-enhanced coronal T 1-weighted MR image (600/1 1 ) shows caudal extension of the mass into the third ventricle (at-now), deviation of the septum l)elltlCiduni (arrowheads), and asynimetnc dilatation of the lateral ventricles. * dilated tern-
of intraven-
of origin
of the fonamina of Monno. (;T and MR imaging have
mary
it was
appear-
it is coninionly
ventricle,
Mc(oncachie
1982,
microscopic
sites
hydrocephalus
roles
description in
intracranial
Comnion
( 1 ). Since
nostral
initial
increased
l)ellucidtlni,
ventricle
(1). is prob-
oligodendnoglioma,
light
headache,
and
group
symptoms and signs are nonspecific
neunocytoma
elude
with
a similar
and
tumor
neunocytoma
confused
which
age
of this
underestiniated;
most
years
of all supratentorial in this
prevalence
of intraventniculan frequently
occurs 20-40
one-half
intra’entriculan ably
aged
is rarely
frethe
Meningiorna
usually
spares
Volume
16
Number
4
frontal
horn,
and
of 30 years for
is more
(3,6).
The
subependymonia
fourth
(6).
in younger
more
cation
in the
crab
Intraventniculan droglioma can logically
and
distinction
radiographically; because
of these
Intraventricular of neural
origin
has
cur
incomplete
cause
gnee
reported, surgical
tion
therapy
with
may
resection
(7). be
neunologic
bosal
adjuvant
recommended
(8).
Our
resection
patient
and
neunobogic
high
4.
in patients tumor
underwent
at the
3.
de-
is not radia-
partial
a tnanscal-
demonstrated
deficits
neBe-
(2).
value
2.
as
may
therapy However,
after
appropriate
I
Al-
as long
and
of clinical
syniptoms
no
residual
I 2-month
5.
follow-up
visit.
In contrast, neural origin
oligodendroglioma is of nonand may have malignant compo-
nents;
therefore,
tion,
chemotherapy,
section and
(9).
it is often on both
Since
oligodendroglioma
electron
microscopy, between
of intr-aventriculan
ported
by the
reactivity found features
for
1996
(6).
be
The
of axons
7.
mi-
required
neunonal
at silver
im-
of inimuno-
(2).
protein
9.
Ultrastructural
include clear
8.
is sup-
a 38-kd
vesicles
granules,
ne-
bight
neurocytoma
synaptophysin,
microtubules,
synaptic
vesicles,
(6). intnaventriculan
neunocytonia that
and
junctions
In summary,
July
may
them
of meurocytoma
synapselike
a similar
by demonstration
in synaptic
dense-core
surgical neurocytoma
or both
presence
and
6.
radia-
immunohistochemistry,
nature pregnation
after
have
appearance,
distinguish
with
intraventricular
croscopic tO
treated
a benign
tumor
of young
included
in the
differential
adults
diagnosis
to be
evaluation
ealeffleation
pathologic
perform
stir-
tumor
rate
though
appears
overall
of is bet-
diagnosis
If intraventrieular the
neo-
resection
proliferation
of differentiation,
generally
for
a specific
suspected,
a specific
is
neurocytoma
pathologist
should
be
supplemental
is
alerted
to
analyses
to
diagnosis.
should
REFERENCES
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for
is the
19 years with
glioma,
lat-
treatment
may
neoplasm,
imaging
CT in the
such
the
tumors
neurocytoma
resection
though
1-
of the
however,
is important
plasm
and
horn
MR
than
ten evaluated with CT. Because of the difference in prognosis and treatment between intraventricular neurocytoma and oligodendno-
papilloma
is characterized
posterior
mass.
useful
this
neurocytoma and oligodenbe difficult to distinguish patho-
prognosis
gical
more
intraven-
enhancement
and
ventricular
(6).
ventricle
and
with plexus and
age
is the
choroid
contrast body
the
location
ependymoma
patients
intense
after
common
Compared
neurocytorna,
occurs by
and
ventricle
triculan
common
most
.
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al.
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is be
of an intra-
GoldsteIn
et al
U
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U
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