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Primary pleomorphic liposarcoma of liver: a case report and review of the literature.
[pleomorphic liposarcoma]
Primary
liver
liposarcoma
is
a
rare
disease
.
The
knowledge
of
the
clinical
course
,
management
,
and
prognosis
of
primary
liver
liposarcoma
are
all
limited
because
of
its
rarity
.
Twelve
cases
of
primary
liposarcoma
of
the
liver
have
been
previously
reported
.
We
present
the
thirteenth
case
,
which
occurred
in
an
adult
male
patient
.
A
42
-
year
-old
male
patient
came
to
our
outpatient
department
with
complaints
of
pain
abdomen
,
mass
per
abdomen
,
and
weight
loss
.
Ultrasonography
showed
a
mass
arising
from
the
the
left
lobe
of
liver
.
CT
abdomen
showed
a
heterogenous
enhancing
mass
from
left
lobe
of
liver
with
multiple
cystic
and
necrotic
areas
compressing
the
stomach
and
spleen
with
no
evidence
of
metastasis
.
Differential
diagnosis
included
adenoma
and
primary
malignancy
.
Exploratory
laparotomy
and
resection
were
done
.
HPE
was
found
to
be
pleomorphic
liposarcoma
of
liver
.
Diseases
Validation
Diseases presenting
"year-old male patient"
symptom
adrenal incidentaloma
adrenomyeloneuropathy
alexander disease
allergic bronchopulmonary aspergillosis
benign recurrent intrahepatic cholestasis
cadasil
coats disease
cohen syndrome
cystinuria
dentinogenesis imperfecta
erdheim-chester disease
erythropoietic protoporphyria
esophageal carcinoma
fabry disease
heparin-induced thrombocytopenia
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
liposarcoma
malignant atrophic papulosis
monosomy 21
oligodontia
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
triple a syndrome
waldenström macroglobulinemia
well-differentiated liposarcoma
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