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Endometrial cancer in a 14-year-old girl with Cowden syndrome: a case report.
[cowden syndrome]
The
appearance
of
endometrial
cancer
in
adolescence
is
uncommon
and
warrants
investigation
for
an
hereditary
cancer
syndrome
.
Cowden
syndrome
is
an
autosomal
dominant
cancer
syndrome
associated
with
a
germline
PTEN
mutation
and
increased
risk
of
breast
,
thyroid
,
endometrial
and
colon
cancer
.
In
this
report
we
present
a
case
of
a
14
-
year
-old
nulligravid
female
diagnosed
with
grade
1
endometrial
adenocarcinoma
.
She
subsequently
developed
fibrocystic
breast
disease
and
colon
polyps
and
was
diagnosed
with
Cowden
syndrome
at
age
20
.
We
therefore
recommend
formal
evaluation
for
Cowden
syndrome
to
be
considered
when
endometrial
cancer
is
diagnosed
in
adolescence
.
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