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Bilateral adrenal incidentaloma with subclinical hypercortisolemia: indications for surgery.
[adrenal incidentaloma]
According
to
some
authors
,
a
higher
incidence
of
subclinical
hypercortisolemia
is
found
among
patients
with
bilateral
benign
adrenal
tumors
than
in
those
with
unilateral
tumors
.
It
is
still
unknown
whether
all
patients
with
bilateral
adrenal
tumors
and
subclinical
hypercortisolemia
should
undergo
surgery
,
and
,
if
so
,
which
tumor
should
be
removed
first
.
The
aim
of
the
study
was
to
investigate
whether
unilateral
adrenalectomy
can
lead
to
resolution
of
hypercortisolemia
in
patients
with
bilateral
adrenal
tumors
and
to
improvement
of
their
clinical
status
.
The
study
group
consisted
of
25
patients
with
bilateral
benign
adrenal
tumors
and
subclinical
hypercortisolemia
.
In
24
patients
,
unilateral
adrenalectomy
was
performed
.
The
adrenal
gland
was
selected
for
removal
on
the
basis
of
scintigraphy
and
/
or
tumor
diameter
.
Cortisol
concentrations
were
measured
before
the
surgery
and
at
1
and
6
months
after
the
surgery
at
8
:
00
AM
,
10
:
00
PM
,
and
after
dexamethasone
suppression
.
The
morning
blood
levels
of
adrenocorticotropic
hormone
,
dehydroepiandrosterone
,
17
‑
hydroxyprogesterone
,
glycated
hemoglobin
,
and
lipid
profile
were
determined
.
In
all
surgical
patients
,
hypercortisolemia
resolved
after
the
surgery
.
However
,
only
in
14
patients
(
58
%
)
,
the
clinical
improvement
was
evident
(
improved
control
of
diabetes
and
hypertension
,
body
mass
loss
)
.
Although
subclinical
hypercortisolemia
resolved
after
surgery
in
all
patients
with
bilateral
adrenal
tumors
,
only
patients
with
poorly
controlled
diabetes
and
hypertension
and
a
rapid
increase
in
body
mass
benefited
from
the
surgery
.
Diseases
Validation
Diseases presenting
"hypertension"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
aniridia
aromatase deficiency
cadasil
child syndrome
cohen syndrome
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cushing syndrome
cystinuria
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
fabry disease
familial hypocalciuric hypercalcemia
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
holt-oram syndrome
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
inclusion body myositis
kallmann syndrome
kindler syndrome
lamellar ichthyosis
lymphangioleiomyomatosis
pendred syndrome
primary effusion lymphoma
scrub typhus
severe combined immunodeficiency
sneddon syndrome
typhoid
von hippel-lindau disease
well-differentiated liposarcoma
werner syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
This symptom has already been validated