Comprehensive characteristics of pulmonary antineutrophil cytoplasmic antibody-associated vasculitis and the development of a predictive nomogram for mortality
International Immunopharmacology,
Journal Year:
2025,
Volume and Issue:
147, P. 113986 - 113986
Published: Jan. 5, 2025
Language: Английский
Late-onset Systemic Lupus Erythematosus
Rheumatology International,
Journal Year:
2025,
Volume and Issue:
45(1)
Published: Jan. 15, 2025
Language: Английский
Update on Takayasu arteritis: Year in review 2024
International Journal of Rheumatic Diseases,
Journal Year:
2024,
Volume and Issue:
27(9)
Published: Sept. 1, 2024
Takayasu
arteritis
is
an
uncommon
systemic
inflammatory
large
vessel
vasculitis
affecting
women
in
their
third
and
fourth
decades
frequently.
The
disease
poses
considerable
morbidity
mortality
owing
to
the
involvement
of
aorta
its
major
branches.
Treatment
comprises
medical
vascular
interventions,
tailored
each
patient.
We
review
high-impact
publications
year
2023
up
April
2024,
which
provide
great
insight
into
clinical,
biomarker,
imaging,
pathogenetic,
therapeutic
updates.
Language: Английский
Systemic vasculitis in Kazakhstan: a complex research approach
Central Asian Journal of Medical Hypotheses and Ethics,
Journal Year:
2024,
Volume and Issue:
5(2), P. 87 - 92
Published: June 30, 2024
Rare
diseases
known
as
systemic
vasculitides
involve
the
inflammatory
destruction
of
blood
vessels,
leading
to
complex
disorders
that
can
affect
a
single
organ
or
multiple
organs
and
systems.
The
challenges
in
diagnosis,
coupled
with
lack
awareness
among
healthcare
providers,
particularly
primary
care
physicians,
delayed
treatment,
often
result
disability
worsen
prognosis
vasculitis
patients.
We
have
conducted
comprehensive
research
approach
understand
features
vasculitis,
considering
demographic,
clinical,
laboratory
data
Kazakhstan
(Shymkent
city
Turkestan
region).
This
approach,
which
encompasses
retrospective
method,
an
analytical
one-stage
cross-examination
(online
survey),
is
essential
our
quest
improve
understanding
management
Kazakhstan.
Language: Английский
Polymyalgia Rheumatica Presenting as Nocturnal Pyrexia of Unknown Origin: A Case Report
Nauman Ismat Butt,
No information about this author
Muhammad Sohail Ajmal Ghoauri,
No information about this author
Muhammad Waseem Riaz
No information about this author
et al.
Galician Medical Journal,
Journal Year:
2024,
Volume and Issue:
31(3)
Published: June 24, 2024
Background.
Polymyalgia
rheumatica
(PMR)
is
a
rheumatic
disorder
characterized
by
musculoskeletal
stiffness
and
pain,
primarily
affecting
the
shoulder,
neck,
hip
areas.
It
more
common
in
females,
with
peak
incidence
usually
after
age
of
70.
Case
Report.
A
74-year-old
man
presented
two-month
history
low-grade
nocturnal
fever
up
to
100oF
(37.7oC)
which
did
not
respond
multiple
courses
antibiotics.
There
was
unintentional
weight
loss
5
kg
mild
shoulder
stiffness.
The
patient
had
Type
2
diabetes
mellitus
treated
34
units
insulin
(Humulin
70/30)
daily
active
smoking
40
pack-years.
On
examination,
tenderness
both
girdle
muscles
discomfort
on
external
rotation
were
noted.
initial
blood
work-up
revealed
raised
erythrocyte
sedimentation
rate
(ESR)
C-reactive
protein
(CRP)
levels.
Serologies
for
syphilis,
human
immunodeficiency
virus
(HIV),
hepatitis
B
(HBV),
C
(HCV)
negative.
Given
negative
results
infective
malignancy
screening,
along
inflammatory
markers
stiffness,
diagnosis
PMR
made
trial
prednisolone
initiated,
resulting
resolution
symptoms.
Conclusions.
present
case
report
highlights
importance
thoroughly
investigating
all
differential
diagnoses
pyrexia
unknown
origin,
regardless
patient’s
ethnic
facilitate
timely
diagnosis.
Language: Английский