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Disseminated cerebellar hemangioblastoma in two patients without von Hippel-Lindau disease.
[von hippel-lindau disease]
Two
patients
who
had
received
a
total
resection
of
cerebellar
hemangioblastoma
developed
cerebrospinal
fluid
dissemination
during
a
long
-term
follow-up
period
.
We
present
this
rare
disease
with
discussion
based
on
the
literature
.
The
patients
were
two
women
aged
45
and
57
years
.
In
the
cerebellar
hemisphere
,
one
patient
had
cystic
hemangioblastoma
of
mural
nodule
type
and
the
other
had
solid
type
.
Both
the
patients
successfully
underwent
total
resection
by
craniotomy
.
They
presented
no
mutations
in
the
von
Hippel-
Lindau
disease
(
VHL
)
gene
or
lesions
in
the
other
organs
.
One
patient
developed
local
recurrence
38
months
after
the
initial
surgery
,
and
received
stereotactic
radiosurgery
.
Three
spinal
cord
tumors
developed
91
months
later
,
and
the
tumors
were
disseminated
to
the
entire
cerebrospinal
cavity
107
months
later
.
The
other
patient
developed
hydrocephalus
53
months
after
the
initial
surgery
with
tumor
tissues
disseminated
in
the
intracranial
subarachnoid
space
.
The
conditions
of
the
two
patients
gradually
aggravated
despite
treatment
with
ventriculo-peritoneal
shunt
and
irradiation
to
the
whole
brain
and
whole
spinal
cord
.
Cerebrospinal
fluid
dissemination
of
cerebellar
hemangioblastoma
was
found
dominantly
in
non-
VHL
patients
.
The
diagnosis
was
made
10
years
after
the
initial
surgery
.
Irradiation
therapy
was
performed
,
but
the
patients
died
about
2
years
after
the
diagnosis
was
given
.
Molecular
targeted
therapies
including
vascular
proliferation
suppression
have
been
attempted
lately
,
but
no
effective
therapy
has
been
established
.
Early
diagnosis
of
dissemination
as
well
as
combination
of
aggressive
excision
and
stereotactic
radiosurgery
are
considered
to
be
appropriate
for
current
interventions
.
Diseases
Validation
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"early diagnosis"
symptom
achondroplasia
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adrenal incidentaloma
adrenomyeloneuropathy
alexander disease
allergic bronchopulmonary aspergillosis
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cutaneous mastocytosis
cystinuria
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gm1 gangliosidosis
hirschsprung disease
holt-oram syndrome
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
inclusion body myositis
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monosomy 21
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oculocutaneous albinism
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proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
scrub typhus
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
thoracic outlet syndrome
triple a syndrome
typhoid
von hippel-lindau disease
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
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