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Our Team
Combined chemotherapy and surgery in primary small cell carcinoma of the esophagus.
[esophageal carcinoma]
The
study
was
to
retrospectively
analyze
survival
outcomes
of
surgery
combined
with
chemotherapy
in
primary
small
cell
carcinoma
of
esophagus
.
From
January
2000
to
December
2009
,
all
patients
with
esophageal
carcinoma
and
underwent
esophagectomy
were
selected
from
the
Department
of
Thoracic
Surgery
,
Henan
Cancer
Hospital
,
China
.
They
were
performed
trans--left
thoracic
incision
esophagectomy
.
For
tumor
located
in
the
upper
third
thoracic
esophagus
,
trans--
right
thoracic
incision
and
abdomen
incision
esophagectomy
was
selected
.
We
chose
EP
regimen
for
chemotherapy
.
Results
:
The
percentage
of
pure
esophagus
small
cell
carcinoma
(
57
cases
)
in
all
patients
underwent
esophagectomy
was
1
.
1
%
.
The
median
survival
time
was
45
months
.
In
stage
I
,
II
,
III
,
the
survival
rate
was
25
%
,
5
.
9
%
,
4
.
3
%
respectively
.
In
the
subgroup
analysis
,
overall
median
survival
time
of
surgery
was
23
.
2
months
while
the
time
of
combined
surgery
and
chemotherapy
was
60
.
7
months
(
P
<
0
.
01
)
.
For
stage
I
patients
,
combined
therapy
was
associated
with
a
significant
longer
median
survival
time
(
81
.
9
months
)
than
surgery
alone
(
22
.
3
months
)
.
(
P
<
0
.
01
)
.
Systemic
chemotherapy
of
cisplatin--based
regimens
should
be
considered
as
important
treatment
options
to
improve
survival
outcome
,
even
early
small
cell
esophageal
cancer
.
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