Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Atypical lipomatous tumor with structural rearrangements involving chromosomes 3 and 8.
[well-differentiated liposarcoma]
Atypical
lipomatous
tumor
(
ALT
)
is
an
intermediate
(
locally
aggressive
)
mesenchymal
neoplasm
with
the
potential
to
dedifferentiate
to
higher
grades
over
time
.
It
is
cytogenetically
characterized
by
the
presence
of
one
or
more
supernumerary
ring
and
giant
marker
chromosomes
.
These
abnormal
chromosomes
invariably
contain
amplified
sequences
derived
from
the
12
q
14
-
15
region
.
We
describe
a
unique
cytogenetic
finding
of
ALT
arising
in
the
right
lower
back
of
a
42
-
year
-old
man
.
Magnetic
resonance
imaging
demonstrated
a
predominantly
fatty
mass
with
irregularly
thickened
,
linear
,
swirled
,
and
nodular
septa
.
Contrast-enhanced
fat-suppressed
T
1
-
weighted
images
showed
significant
enhancement
of
the
non-adipose
areas
.
A
sub-extensive
resection
was
performed
.
Histologically
,
the
tumor
consisted
predominantly
of
mature
fat
cells
with
atypical
stromal
cells
and
multivacuolated
lipoblasts
.
Immunohistochemically
,
the
tumor
cells
were
positive
for
p
16
(
diffuse
and
strong
signal
)
and
cyclin-dependent
kinase-
4
(
focal
and
weak
signal
)
but
negative
for
murine
double
-
minute
2
.
Cytogenetic
analysis
displayed
a
t
(
3
;
8
)
(
q
28
;
q
13
)
translocation
as
the
sole
anomaly
or
concomitant
with
a
few
other
numerical
and
structural
alterations
.
There
has
been
no
evidence
of
local
recurrence
two
months
after
surgery
.
To
the
best
of
our
knowledge
,
this
is
the
first
case
of
ALT
with
structural
aberrations
involving
chromosomes
3
and
8
,
associated
with
an
absence
of
12
q
rearrangements
.
Diseases
Validation
Diseases presenting
"tumor cells"
symptom
alpha-thalassemia
carcinoma of the gallbladder
cholangiocarcinoma
cushing syndrome
dedifferentiated liposarcoma
dentin dysplasia
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
hodgkin lymphoma, classical
junctional epidermolysis bullosa
kindler syndrome
liposarcoma
lymphangioleiomyomatosis
pleomorphic liposarcoma
primary effusion lymphoma
severe combined immunodeficiency
triple a syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
You can validate or delete this automatically detected symptom
Validate the Symptom
Delete the Symptom