Rare Diseases Symptoms Automatic Extraction
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A random Abstract
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Minimally Invasive Esophagectomy for Dysplastic Barrett's Esophagus.
[esophageal adenocarcinoma]
A
substantial
portion
of
patients
diagnosed
preoperatively
with
high
grade
dysplasia
(
HGD
)
alone
will
have
occult
esophageal
adenocarcinoma
on
analysis
of
the
surgical
specimen
.
Therefore
,
because
of
an
increased
risk
of
disease
progression
and
malignancy
,
patients
with
HGD
should
be
referred
for
esophagectomy
promptly
when
endoscopic
therapy
has
failed
.
The
required
extent
of
lymphadenectomy
in
this
cohort
of
patients
is
unknown
because
of
the
variable
incidence
of
submucosal
cancer
observed
.
Improvements
in
perioperative
care
,
adoption
of
a
minimally
invasive
surgical
approach
,
and
centralization
of
esophageal
cancer
services
have
substantially
reduced
the
rates
of
mortality
and
morbidity
associated
with
esophagectomy
in
recent
years
.
Minimally
invasive
esophagectomy
should
be
considered
the
treatment
of
choice
in
patients
with
dysplastic
Barrett
's
esophagus
that
is
refractory
to
endoscopic
therapy
or
those
at
high
risk
of
invasive
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
