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Extracorporal albumin dialysis (MARS) improves cholestasis and normalizes low apo A-I levels in a patient with benign recurrent intrahepatic cholestasis (BRIC).
[benign recurrent intrahepatic cholestasis]
The
familial
cholestatic
diseases
Benign
Recurrent
Intrahepatic
Cholestasis
(
BRIC
)
and
Progessive
Familial
Intrahepatic
Cholestasis
type
1
(
PFIC
1
)
are
characterized
by
intermittent
or
permanently
elevated
plasma
bile
salt
levels
,
therapy-resistant
extreme
pruritus
and
peculiar
biochemical
abnormalities
including
low
apolipoprotein
apo
A-
I
.
Previously
,
symptomatic
improvement
has
been
demonstrated
in
BRIC
patients
after
extracorporal
albumin
dialysis
(
MARS
)
.
We
hypothesized
that
MARS
improves
cholestasis
,
induces
changes
in
the
bile
salt
profile
and
normalizes
apo
A-
I
serum
levels
in
BRIC
.
A
17
-
year
-old-
female
patient
with
BRIC
experienced
an
episode
of
cholestasis
lasting
for
more
than
6
months
with
extreme
pruritus
and
diarrhoea
not
responding
to
standard
therapy
.
During
a
period
of
five
days
the
patient
was
treated
3
x
8
h
with
MARS
.
The
procedures
were
well
tolerated
and
resulted
in
reduction
of
plasma
bile
salts
by
58
%
.
The
plasma
bile
salt
profile
changed
into
a
more
hydrophilic
composition
after
MARS
.
Diarrhoea
discontinued
and
the
pruritus
improved
significantly
from
9
to
4
on
a
subjective
scale
.
These
effects
lasted
4
months
until
a
relapse
occurred
.
Low
plasma
apo
A-
I
levels
(
0
.
52
g
/
l
)
normalized
after
MARS
(
0
.
98
g
/
l
)
.
The
procedures
were
well
tolerated
.
Fatigue
was
noted
as
the
only
transient
side-effect
.
In
conclusion
,
MARS
may
induce
a
long
-term
symptomatic
improvement
and
decrease
of
cholestatic
markers
in
BRIC
.
Further
studies
evaluating
efficacy
and
mechanism
of
MARS
in
patients
with
BRIC
are
needed
.
Diseases
Validation
Diseases presenting
"pruritus"
symptom
benign recurrent intrahepatic cholestasis
cholangiocarcinoma
cutaneous mastocytosis
dystrophic epidermolysis bullosa
erdheim-chester disease
lamellar ichthyosis
pleomorphic liposarcoma
pyomyositis
zellweger syndrome
This symptom has already been validated