Rare Diseases Symptoms Automatic Extraction
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A random Abstract
Our Project
Our Team
Diagnosis and staging of superficial esophageal precursor based on pre-endoscopic resection system comparable to endoscopic resection.
[esophageal squamous cell carcinoma]
Endoscopic
treatments
for
early
esophageal
squamous
cell
carcinoma
and
the
esophageal
neoplasm
are
two
types
:
endoscopic
resection
(
ER
)
and
ablation
.
Resection
enables
evaluation
of
the
lesion
in
the
ER
specimens
,
while
ablation
can
not
.
We
sought
to
establish
a
pre-
ER
evaluated
system
with
a
diagnostic
and
staging
accuracy
similar
to
ER
for
the
development
of
ablation
therapy
.
In
our
study
,
we
collected
data
pertaining
to
early
esophageal
cancer
and
esophageal
neoplasm
treated
with
ER
,
analyzed
the
pre-
and
post-
ER
data
of
the
lesions
and
evaluated
the
diagnostic
accuracy
of
pre-
ER
system
compared
with
the
gold
standard
.
The
diagnostic
accuracy
rate
was
91
%
based
on
the
pre-
ER
system
compared
with
the
gold
standard
,
and
93
%
based
on
the
ER
diagnosis
.
The
AUC
of
the
pre-
ER
system
was
0
.
964
,
while
the
ER
examination
was
0
.
971
.
These
results
suggest
that
the
accuracy
of
pre-
ER
system
was
comparable
to
ER
.
The
pre-
ER
system
enables
prediction
of
histological
diagnosis
and
stage
of
the
lesions
,
and
the
choice
of
treatment
for
superficial
esophageal
neoplasm
.
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
