Internal Medicine,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
A
79-year-old
man
with
smoldering
multiple
myeloma
(MM)
developed
sudden
severe
thrombocytopenia
and
active
bleeding.
Since
anti-GPIIb/IIIa
autoantibodies
were
detected
on
the
platelet
surface,
due
to
an
autoimmune
etiology
was
diagnosed.
Although
neither
steroids
nor
intravenous
immunoglobulins
provided
improvement,
bortezomib
rapid
normalization
of
counts
disappearance
anti-GPIIb/IIIb
autoantibodies.
MM
is
rarely
associated
immune
thrombocytopenic
purpura
(ITP).
underlying
pathogenesis
ITP
remains
elusive,
anti-myeloma
drugs
might
be
beneficial.
Journal of Neurology Neurosurgery & Psychiatry,
Journal Year:
2024,
Volume and Issue:
unknown, P. jnnp - 334165
Published: Oct. 2, 2024
Chronic
inflammatory
demyelinating
polyradiculoneuropathy
(CIDP)
is
a
heterogeneous
but
clinically
well-described
disease
within
circumscribed
parameters.
It
immunologically
mediated
through
several
poorly
understood
mechanisms.
First-line
therapies
with
steroids,
intravenous
immunoglobulin
(IVIG)
or
plasma
exchange
are
each
effective
in
about
two-thirds
of
patients.
These
treatments
seldom
associated
complete
resolution
cure,
and
often
pose
considerable
practical,
financial
medical
implications.
Our
understanding
many
the
key
pathological
processes
autoimmune
diseases
expanding,
novel
targeted
therapeutics
being
developed
promise
neurological
disorders.
This
narrative
review
looks
first
at
detailing
pathogenic
mechanisms
CIDP,
followed
by
an
in-depth
description
potential
current
evidence
their
application
clinical
practice.
Internal Medicine,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
A
79-year-old
man
with
smoldering
multiple
myeloma
(MM)
developed
sudden
severe
thrombocytopenia
and
active
bleeding.
Since
anti-GPIIb/IIIa
autoantibodies
were
detected
on
the
platelet
surface,
due
to
an
autoimmune
etiology
was
diagnosed.
Although
neither
steroids
nor
intravenous
immunoglobulins
provided
improvement,
bortezomib
rapid
normalization
of
counts
disappearance
anti-GPIIb/IIIb
autoantibodies.
MM
is
rarely
associated
immune
thrombocytopenic
purpura
(ITP).
underlying
pathogenesis
ITP
remains
elusive,
anti-myeloma
drugs
might
be
beneficial.