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[Cerebral hemorrhage in Sneddon syndrome].
[sneddon syndrome]
Sneddon
syndrome
is
the
association
of
livedo
retricularis
and
cerebrovascular
lesions
.
It
is
a
vasculopathy
of
vessels
of
small
and
medium
calibre
which
affects
young
people
and
is
of
unknown
origin
.
It
is
often
associated
with
arterial
hypertension
and
repeated
ischemic
cerebrovascular
accidents
which
lead
to
intellectual
deterioration
.
We
describe
a
49
year
old
man
who
,
from
the
age
of
23
,
had
had
repeated
transient
or
established
episodes
compatible
with
ischemic
cerebrovascular
accidents
.
These
were
followed
by
various
neurological
sequelae
and
by
intellectual
deterioration
.
Finally
he
died
of
a
cerebral
hemorrhage
whilst
on
anticoagulant
treatment
with
Synthron
.
We
show
the
neuroimaging
findings
(
CT
,
MR
and
angiography
)
and
the
neuropathological
studies
(
cerebral
hemorrhage
,
fibrosis
of
the
intima
of
the
vessels
of
the
circle
of
Willis
,
absence
of
inflammation
,
bilateral
unsymmetrical
leukoencephalopathy
of
the
cerebral
hemispheres
and
multiple
cortical
infarcts
)
.
We
wish
to
draw
attention
to
the
occurrence
of
this
complication
,
its
possible
relationship
to
the
vasculopathy
mentioned
,
bursting
of
one
of
the
arteries
of
the
revascularization
complex
,
arterial
hypertension
or
anticoagulant
treatment
,
and
also
to
add
one
more
case
to
the
few
described
as
having
hemorrhage
and
neuropathology
in
Sneddon
syndrome
.
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
