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Survival Rate of Esophageal Carcinoma in Iran - A Systematic Review and Meta-analysis.
[esophageal carcinoma]
Esophageal
cancer
is
often
diagnosed
in
the
last
stages
where
the
chance
of
patient
's
survival
is
very
low
.
The
aim
of
this
systematic
review
was
presentation
of
valid
estimation
of
survival
in
patients
with
esophageal
cancer
in
different
regions
of
Iran
.
A
SYSTEMATIC
REVIEW
WAS
CARRIED
OUT
BASED
ON
THE
RELIABLE
DOMESTIC
MEDICAL
DATABASES
INCLUDING
:
SID
,
Magiran
,
Irandoc
and
Iranmedex
as
well
as
reliable
foreign
databases
like
PubMed
and
Scopus
using
"
Cancer
"
,
"
Esophagus
"
,
"
survival
"
"
Neoplasms
"
and
"
Longevity
"
as
keywords
.
Then
all
the
reviewed
articles
and
dissertations
which
met
the
entry
criteria
were
analyzed
.
The
data
were
analyzed
by
using
meta
-analysis
method
(
random
model
)
and
by
means
of
STATA
software
application
version
11
.
1
.
In
18
studies
the
total
numbers
of
2932
people
were
analyzed
.
The
one
year
survival
rate
in
Iran
is
estimated
at
47
percent
(
95
%
CI
:
34
-
61
)
and
the
five
year
survival
rate
is
estimated
at
12
%
(
95
%
CI
:
8
-
16
)
.
The
two
,
three
and
four
year
survival
rates
were
31
%
(
95
%
CI
:
18
-
44
)
,
22
%
(
95
%
CI
:
13
-
31
)
and
21
%
(
95
%
CI
:
4
-
38
)
,
respectively
.
According
to
the
findings
one
year
survival
rate
for
esophageal
cancer
in
Iran
is
almost
four
times
higher
than
its
five
year
survival
rate
.
Moreover
the
five
year
survival
rate
in
Iran
is
less
than
many
other
countries
.
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