Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Retroperitoneal Pleomorphic Liposarcoma Mimicking Adrenal Cancer in F-18 FDG PET/CT.
[pleomorphic liposarcoma]
Liposarcoma
is
the
second
most
common
type
of
soft
tissue
sarcoma
,
but
pleomorphic
liposarcoma
is
the
least
common
subtype
.
We
present
the
case
of
a
42
-
year
-old
man
who
had
experienced
intermittent
left
flank
pain
for
a
month
.
A
large
soft
-tissue
mass
was
detected
by
ultrasonography
in
a
local
clinic
,
and
he
was
referred
for
further
evaluation
.
Positron
emission
tomography
/
computed
tomography
(
PET
/
CT
)
with
F-
18
fluoro-
2
-
deoxy-
D-
glucose
(
F-
18
FDG
)
showed
intense
uptake
in
the
retroperitoneal
mass
,
which
mimicked
an
adrenal
cancer
.
The
patient
underwent
left
radical
nephroadrenalectomy
,
and
the
tumor
was
revealed
to
be
a
pleomorphic
liposarcoma
upon
pathological
examination
.
When
there
is
a
large
retroperitoneal
mass
with
intense
F-
18
FDG
activity
,
the
possibility
of
a
pleomorphic
liposarcoma
should
be
considered
.
Diseases
Validation
Diseases presenting
"cancer"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
benign recurrent intrahepatic cholestasis
cadasil
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
hirschsprung disease
hodgkin lymphoma, classical
inclusion body myositis
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
This symptom has already been validated