Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Pars plana vitrectomy for treatment of advanced Coats' disease--presentation of a modified surgical technique and long-term follow-up.
[coats disease]
To
present
a
modified
surgical
technique
in
the
treatment
of
retinal
detachment
secondary
to
advanced
Coats
'
disease
in
children
,
and
report
on
long
-term
anatomical
and
functional
outcome
.
We
analysed
an
interventional
case
series
of
13
patients
(
13
eyes
)
with
advanced
Coats
'
disease
characterised
by
retinal
detachment
in
addition
to
massive
subretinal
exudates
and
vascular
malformation
.
The
presented
patients
underwent
pars
plana
vitrectomy
(
PPV
)
,
including
a
modified
technique
of
exocryotherapy
applied
after
fluid-air
exchange
in
order
to
achieve
complete
treatment
of
the
vascular
changes
,
to
reduce
associated
side-effects
,
and
to
avoid
retinectomy
and
silicone
oil
tamponade
.
Within
a
median
follow-up
period
of
37
Â
months
(
range
:
18
-
66
Â
months
)
,
no
enucleation
was
necessary
.
Four
eyes
(
31
Â
%
)
did
not
need
any
further
therapy
,
and
in
nine
eyes
(
69
Â
%
)
additional
treatments
were
performed
.
Six
patients
(
46
Â
%
)
required
revisional
surgery
with
silicone
oil
tamponade
.
In
ten
eyes
(
77
Â
%
)
,
the
pathologic
vessels
and
exudates
finally
regressed
and
the
retina
reattached
.
Visual
acuity
(
VA
)
could
be
stabilized
in
the
majority
of
patients
:
in
three
eyes
(
27
Â
%
)
VA
improved
,
in
four
eyes
(
36
Â
%
)
VA
remained
stable
,
in
four
eyes
(
36
Â
%
)
visual
acuity
(
VA
)
deteriorated
,
and
in
two
eyes
VA
could
not
be
evaluated
.
The
presented
modified
technique
allows
for
sufficient
cryotherapy
of
vascular
malformations
,
even
in
the
presence
of
massive
exudation
,
in
a
subset
of
patients
with
advanced
Coats
'
disease
,
and
thus
may
reduce
surgery-related
complications
and
improve
the
rehabilitation
process
of
these
young
patients
.
Diseases
Validation
Diseases presenting
"visual acuity"
symptom
achondroplasia
acute rheumatic fever
aniridia
coats disease
cohen syndrome
congenital toxoplasmosis
homocystinuria without methylmalonic aciduria
lamellar ichthyosis
oculocutaneous albinism
typhoid
von hippel-lindau disease
zellweger syndrome
You can validate or delete this automatically detected symptom
Validate the Symptom
Delete the Symptom