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Malignant perivascular epithelioid cell tumor of the gallbladder: a case report and review of literature.
[lymphangioleiomyomatosis]
Perivascular
epithelioid
cell
tumors
are
rare
mesenchymal
neoplasms
composed
of
histologically
and
immunohistochemically
distinctive
perivascular
epithelioid
cells
.
The
perivascular
epithelioid
cell
tumor
family
includes
angiomyolipoma
,
clear
cell
sugar
tumor
of
the
lung
,
lymphangioleiomyomatosis
,
clear
cell
myomelanocytic
tumor
of
the
falciform
ligament
/
ligamentum
teres
,
and
rare
clear
cell
tumors
of
other
anatomic
sites
.
Perivascular
epithelioid
cell
tumors
have
been
reported
previously
in
various
sites
,
but
to
our
knowledge
not
in
the
gallbladder
.
We
report
here
,
for
the
first
time
,
a
malignant
perivascular
epithelioid
cell
tumor
arising
in
the
gallbladder
.
Diseases
Validation
Diseases presenting
"first time"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
classical phenylketonuria
congenital adrenal hyperplasia
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
dentinogenesis imperfecta
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
gm1 gangliosidosis
harlequin ichthyosis
heparin-induced thrombocytopenia
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
hydrocephalus with stenosis of the aqueduct of sylvius
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
megacystis-microcolon-intestinal hypoperistalsis syndrome
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
phenylketonuria
primary effusion lymphoma
primary hyperoxaluria type 1
severe combined immunodeficiency
sneddon syndrome
triple a syndrome
trochlear dysplasia
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
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