Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
[Carcinoma of the gallbladder--current surgical treatment options].
[carcinoma of the gallbladder]
The
effect
of
radical
resection
in
gallbladder
cancer
is
still
area
of
debate
.
To
determine
the
criteria
of
surgery
in
primary
and
incidental
gallbladder
cancer
.
method
:
Eighty
-
four
patients
with
gallbladder
cancer
were
evaluated
between
1999
and
2008
.
Sixty
patients
(
72
.
4
%
)
were
symptomatic
.
Explorative
laparotomy
was
performed
in
40
(
66
.
7
%
)
,
palliative
procedure
in
5
(
8
.
3
%
)
patients
in
stage
pT
3
-
4
,
N
1
,
M
0
-
1
.
Cholecystectomy
only
or
completed
with
wedge
resection
of
the
gallbladder
bed
and
lymfadenectomy
as
radical
procedure
was
performed
only
in
7
(
1
.
7
%
)
patients
in
pT
1
-
2
,
N
0
-
1
,
M
0
.
Twenty
four
(
28
.
6
%
)
patients
had
incidental
gall
bladder
carcinoma
.
Radical
cholecystectomy
was
performed
in
4
(
16
.
7
%
)
-
pT
1
a
,
N
0
,
M
0
,
palliative
cholecystectomy
in
3
patients
(
12
.
5
%
)
-
pT
3
,
N
1
,
M
0
.
Radical
reoperation
was
performed
in
15
(
62
.
5
%
)
patients
in
stage
pT
1
b
-
2
,
N
0
-
1
,
M
0
.
Patients
survival
after
explorative
laparotomy
and
palliative
procedures
was
no
longer
than
7
months
.
Four
from
seven
patients
died
after
radical
operation
12
-
18
months
after
operation
.
Six
from
15
radically
re
-operated
patients
are
alive
in
interval
4
months
and
8
years
.
Nine
patients
died
in
interval
9
months
and
4
years
after
re
-operation
.
Radical
surgical
procedure
is
the
treatment
of
choice
for
patients
with
gall
bladder
carcinoma
especially
in
stage
pT
1
-
2
,
N
0
,
M
0
.
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