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Recurrent retroperitoneal liposarcoma in a patient with neurofibromatosis type I.
[dedifferentiated liposarcoma]
Liposarcoma
complicating
neurofibromatosis
is
very
rare
.
Only
a
few
cases
have
been
described
until
now
.
We
present
a
case
of
recurrent
dedifferentiated
retroperitoneal
liposarcoma
in
a
patient
with
neurofibromatosis
type
I
(
NF-
1
)
.
A
47
-
year
-old
Caucasian
woman
with
NF-
1
presented
to
the
hospital
initially
complaining
of
left
lumbar
pain
irradiating
to
the
anterior
thigh
and
knee
.
Physical
examination
showed
atrophy
of
the
lower
extremities
bilaterally
and
decreased
motor
strength
on
the
left
lower
extremity
.
Radiological
studies
demonstrated
an
enhancing
lesion
in
the
left
paraspinal
region
,
suggesting
malignancy
.
The
patient
underwent
local
resection
of
tumour
with
safety
margins
.
Pathological
examination
was
consistent
with
dedifferentiated
liposarcoma
(
DDLS
)
with
positivity
for
MDM
2
and
CDK
4
markers
.
No
evidence
of
metastasis
was
noted
on
the
radiological
studies
.
The
final
diagnosis
was
DDLS
,
high
-grade
(
G
3
)
,
pT
2
bN
0
M
0
,
stage
III
.
After
6
weeks
post-tumour
resection
,
the
patient
experienced
recurrence
of
malignancy
.
Chemotherapy
with
cisplatin
and
doxorubicin
was
initiated
in
the
patient
.
Liposarcoma
in
the
context
of
neurofibromatosis
is
very
rare
.
To
the
best
of
our
knowledge
,
only
six
cases
have
been
reported
until
now
in
the
literature
.
We
are
presenting
this
case
to
underline
the
possibility
of
recurrence
in
the
case
of
retroperitoneal
DDLSs
despite
local
tumour
resection
.
Also
,
although
the
role
of
chemotherapy
is
controversial
we
decided
to
start
treatment
with
cisplatin
and
doxorubicin
given
the
success
of
chemotherapy
in
similar
case
presentations
.
Diseases
Validation
Diseases presenting
"pain"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
aniridia
aromatase deficiency
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital diaphragmatic hernia
congenital toxoplasmosis
cushing syndrome
cutaneous mastocytosis
cystinuria
dedifferentiated liposarcoma
dentin dysplasia
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
focal myositis
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
junctional epidermolysis bullosa
kabuki syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
neuralgic amyotrophy
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
phenylketonuria
pleomorphic liposarcoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
scrub typhus
sneddon syndrome
systemic capillary leak syndrome
thoracic outlet syndrome
trochlear dysplasia
typhoid
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
wolf-hirschhorn syndrome
This symptom has already been validated