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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
"fatigue"
symptom
benign recurrent intrahepatic cholestasis
cholangiocarcinoma
congenital adrenal hyperplasia
cowden syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dracunculiasis
erdheim-chester disease
esophageal carcinoma
fabry disease
familial hypocalciuric hypercalcemia
familial mediterranean fever
hydrocephalus with stenosis of the aqueduct of sylvius
inclusion body myositis
kabuki syndrome
lymphangioleiomyomatosis
neuralgic amyotrophy
pleomorphic liposarcoma
systemic capillary leak syndrome
triple a syndrome
typhoid
von hippel-lindau disease
waldenström macroglobulinemia
x-linked adrenoleukodystrophy
This symptom has already been validated