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Management of Barrett's esophagus and early esophageal cancer: update on endoscopic treatment strategies.
[esophageal adenocarcinoma]
Barrett
's
esophagus
represents
the
strongest
known
risk
factor
for
developing
esophageal
adenocarcinoma
.
The
traditional
management
strategy
for
identifying
and
managing
Barrett
's
esophagus
involves
screening
and
endoscopic
surveillance
to
identify
early
stage
,
curable
carcinoma
.
Recently
,
endoscopic
eradication
therapy
has
emerged
to
achieve
the
complete
eradication
of
Barrett
's
esophagus
and
intramucosal
cancer
to
prevent
the
development
of
invasive
cancer
with
lymphatic
spread
.
Randomized
trials
have
demonstrated
the
efficacy
of
these
approaches
to
reduce
the
progression
to
cancer
,
and
endoscopic
eradication
therapy
has
become
the
preferred
treatment
approach
for
patients
with
high
--grade
dysplasia
,
and
may
be
utilized
for
management
of
low
--grade
dysplasia
as
well
.
Owing
to
excellent
eradication
rates
and
favorable
side
effect
profile
,
radio
frequency
ablation
has
emerged
as
the
ablative
strategy
of
choice
for
patients
undergoing
endoscopic
eradication
therapy
.
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