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Paratesticular sarcomas: two cases with different evolutions.
[liposarcoma]
Paratesticular
sarcomas
are
rare
and
account
for
less
than
1
%
of
all
adult
sarcomas
.
Intrascrotal
tumours
can
be
testicular
or
paratesticular
,
paratesticular
tumours
being
rarer
(
7
-
10
%
)
.
Only
30
%
of
paratesticular
tumours
are
malignant
and
90
%
of
these
are
sarcomas
.
Histological
subtypes
include
leiomyosarcoma
,
rhabdomyosarcoma
,
liposarcoma
and
undifferentiated
high
-grade
pleomorphic
sarcoma
.
Recurrence
is
frequent
in
this
type
of
tumour
and
can
occur
years
from
initial
diagnosis
.
These
reports
show
two
cases
of
paratesticular
sarcoma
with
very
distinct
evolutions
.
The
first
case
concerns
a
patient
who
presented
with
low
-grade
leiomyosarcoma
with
two
local
recurrences
treated
with
surgery
,
and
distance
recurrence
with
cutaneous
,
subcutaneous
,
pulmonary
and
hepatic
metastasis
30
years
after
surgery
of
the
primary
tumour
.
The
second
case
reports
of
a
patient
who
presented
with
high
-grade
myxoid
liposarcoma
with
local
and
distance
recurrence
3
years
after
surgery
of
the
primary
tumour
,
which
progressed
after
chemotherapy
;
the
patient
died
7
months
after
diagnosis
of
recurrence
.
Diseases
Validation
Diseases presenting
"first case"
symptom
achondroplasia
adrenal incidentaloma
allergic bronchopulmonary aspergillosis
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
carcinoma of the gallbladder
child syndrome
cholangiocarcinoma
classical phenylketonuria
coats disease
cohen syndrome
congenital toxoplasmosis
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
esophageal adenocarcinoma
esophageal carcinoma
fabry disease
familial mediterranean fever
focal myositis
gm1 gangliosidosis
harlequin ichthyosis
hodgkin lymphoma, classical
homocystinuria without methylmalonic aciduria
junctional epidermolysis bullosa
kabuki syndrome
krabbe disease
lamellar ichthyosis
legionellosis
liposarcoma
locked-in syndrome
malignant atrophic papulosis
monosomy 21
neonatal adrenoleukodystrophy
oculocutaneous albinism
omenn syndrome
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
systemic capillary leak syndrome
thoracic outlet syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
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