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Pheochromocytoma: an uncommon presentation of an asymptomatic and biochemically silent adrenal incidentaloma.
[adrenal incidentaloma]
Pheochromocytomas
are
rare
tumours
originating
from
the
chromaffin
tissue
.
The
clinical
manifestations
are
variable
and
are
not
specific
;
as
a
result
,
pheochromocytomas
often
imitate
other
diseases
.
The
diagnosis
is
usually
established
by
biochemical
studies
,
i
.
e
.
,
the
measurement
of
catecholamines
or
their
metabolites
in
urine
or
plasma
,
followed
by
radiographic
and
scintigraphic
studies
for
localisation
.
Surgical
removal
of
the
tumour
is
the
preferred
treatment
.
We
report
a
30
-
year
-old
woman
presenting
with
an
adrenal
incidentaloma
that
was
7
.
6
×
5
.
3
×
4
.
8
cm
in
size
on
an
abdominal
computed
tomography
scan
.
Investigations
for
adrenal
hormones
,
including
a
low
-dose
dexamethasone
suppression
test
,
plasma
aldosterone
level
,
24
-
hour
urinary
metanephrine
and
vanillylmandelic
acid
levels
,
and
plasma
metanephrine
level
were
all
within
the
normal
ranges
.
During
the
surgical
resection
,
the
patient
had
a
hypertensive
spell
.
Surgery
was
postponed
,
and
the
blood
pressure
was
adequately
controlled
with
α
blockers
,
followed
by
β
blockers
.
After
2
weeks
,
the
surgery
was
followed
by
a
pathological
biopsy
that
confirmed
the
pheochromocytoma
diagnosis
.
Diseases
Validation
Diseases presenting
"blood pressure"
symptom
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
cadasil
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cushing syndrome
fabry disease
familial mediterranean fever
lymphangioleiomyomatosis
pendred syndrome
proteus syndrome
scrub typhus
systemic capillary leak syndrome
thoracic outlet syndrome
typhoid
von hippel-lindau disease
werner syndrome
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