Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
A case of pure endophytic squamous cell carcinoma of the gallbladder: a rare entity with aggressive behaviour.
[carcinoma of the gallbladder]
Pure
squamous
cell
carcinoma
of
gallbladder
is
a
rare
tumor
accounting
for
only
3
%
of
the
malignancies
of
gallbladder
.
A
35
-
year
-old
female
presented
with
pain
and
lump
in
right
hypochondrium
.
Ultrasonography
and
computed
tomography
revealed
a
thickened
gallbladder
filled
with
stones
without
any
obvious
growth
and
a
large
hepatic
mass
.
Histologically
,
a
pure
type
of
well
differentiated
squamous
cell
carcinoma
of
gallbladder
was
diagnosed
after
excluding
all
possible
differential
diagnoses
owing
to
different
histogenesis
and
aggressive
biological
behaviour
.
Early
diagnosis
is
the
most
important
parameter
for
improving
the
survival
indices
among
the
patients
with
squamous
cell
carcinoma
of
the
gallbladder
.
Diseases
Validation
Diseases presenting
"early diagnosis"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
alexander disease
allergic bronchopulmonary aspergillosis
aromatase deficiency
carcinoma of the gallbladder
cholangiocarcinoma
classical phenylketonuria
coats disease
cohen syndrome
congenital adrenal hyperplasia
congenital diaphragmatic hernia
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
cystinuria
dentin dysplasia
dentinogenesis imperfecta
dracunculiasis
erdheim-chester disease
erythropoietic protoporphyria
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
hirschsprung disease
holt-oram syndrome
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
inclusion body myositis
kabuki syndrome
kallmann syndrome
kindler syndrome
krabbe disease
locked-in syndrome
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
oral submucous fibrosis
papillon-lefèvre syndrome
phenylketonuria
primary effusion lymphoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
scrub typhus
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
thoracic outlet syndrome
triple a syndrome
typhoid
von hippel-lindau disease
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
You can validate or delete this automatically detected symptom
Validate the Symptom
Delete the Symptom