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Congenital cerebellar malignant rhabdoid tumor in an infant with junctional epidermolysis bullosa.
[junctional epidermolysis bullosa]
Epidermolysis
bullosa
(
EB
)
,
a
hereditary
blistering
condition
of
the
skin
,
is
divided
into
simplex
,
hemidesmosomal
,
junctional
,
and
dystrophic
types
.
It
may
be
complicated
by
the
development
of
squamous
cell
carcinoma
of
the
skin
,
but
other
neoplasms
,
especially
those
separate
from
involved
skin
,
are
distinctly
rare
.
We
report
a
male
infant
with
junctional
EB
who
died
of
Pseudomonas
sepsis
and
was
found
at
autopsy
to
have
a
clinically
unrecognized
cerebellar
malignant
rhabdoid
tumor
(
MRT
)
.
This
is
the
first
reported
case
of
an
infant
with
EB
and
a
coincident
extracutaneous
neoplasm
.
It
is
also
the
first
known
case
of
EB
associated
with
a
pathologically
confirmed
malignant
brain
tumor
.
Cytogenetic
results
from
the
infant
and
his
tumor
and
both
of
his
parents
suggest
the
infant
's
EB
and
MRT
were
not
genetically
linked
.
Diseases
Validation
Diseases presenting
"known case of"
symptom
junctional epidermolysis bullosa
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