Burdenko s Journal of Neurosurgery,
Journal Year:
2024,
Volume and Issue:
88(6), P. 77 - 77
Published: Jan. 1, 2024
Giant
non-traumatic
and
non-iatrogenic
cranial
vault
defects
are
poorly
studied
due
to
their
rarity.
Therefore,
diagnosis
analysis
of
causes
difficult.
In
available
literature,
we
found
only
4
cases
giant
pericranial
sinus
accompanied
by
extensive
defects.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
12(2)
Published: Nov. 18, 2024
Abstract
The
high
heterogeneity
and
severe
side
effects
of
chemotherapy
are
major
factors
contributing
to
the
failure
osteosarcoma
treatment.
Herein,
a
comprehensive
genomic
analysis
is
conducted,
identified
two
prominent
characteristics
osteosarcoma:
significant
cyclin‐dependent
kinases
4
(CDK4)
amplification
homologous
recombination
repair
deficiency.
Based
on
these
findings,
co‐delivery
system
loaded
with
CDK4/6
inhibitors
poly
ADP‐ribose
polymerase
(PARP)
designed.
By
employing
metal–organic
frameworks
(MOFs)
as
carriers,
issue
drug
insolubility
effectively
addressed,
while
also
enabling
controlled
release
in
response
tumor
microenvironment.
To
enhance
targeting
capability
biocompatibility,
MOFs
further
coated
bio‐membrane
B7H3.
This
targeted
biomimetic
possesses
several
key
features:
1)
it
can
precisely
target
B7H3
expression;
2)
combination
PARP
exhibits
synergistic
effects,
significantly
impairing
tumor's
DNA
capacity;
3)
has
potential
for
photodynamic
therapy,
amplifying
defects
maximize
cell
eradication.
Furthermore,
observed
that
this
activate
immune
microenvironment,
increasing
CD8
+
T
infiltration
converting
from
an
immune‐cold
immune‐hot
tumor.
In
summary,
effective
therapeutic
strategy
holds
promise
novel
approach
Diagnostics,
Journal Year:
2025,
Volume and Issue:
15(3), P. 266 - 266
Published: Jan. 23, 2025
Introduction:
Osteosarcoma
(OS)
is
the
most
common
type
of
primary
malignant
bone
and
cartilage
tumour.
Because
remarkable
developments
in
technology,
progress
has
been
made
medical
field
regarding
diagnosis
management
OS
patients.
The
aim
study
to
describe
clinical
pathological
profile
paediatric
patients
with
osteosarcoma
identify
potential
prognostic
factors
for
an
unfavourable
outcome
our
country.
Methods:
We
conducted
a
retrospective
all
children
adolescents
musculoskeletal
tumours
diagnosed
treated
at
tertiary
Orthopaedic
Department
period
10
years.
Results:
A
group
65
who
benefited
from
diagnosis,
neoadjuvant,
adjuvant
surgical
treatment
Emergency
Clinical
Hospital
Children
“Sfânta
Maria”
Iasi,
România,
was
analysed.
average
age
time
12.9
analysis
revealed
higher
frequency
male
case
femur
tibia
locations
significantly
scapula
clavicle
female
patients,
while
humerus
found
only
(χ2
=
19.46,
p
0.0149).
frequent
histopathological
subtype
osteoblastic
osteosarcoma,
but
there
no
significant
correlation
gender
or
0.73,
0.863
χ2
0.843,
0.839).
results
indicated
instead
(p
0.0185)
lower
values
undifferentiated
osteosarcomas,
being
9.4
years
±
2.1
SD.
After
performing
multivariate
logistic
regression
risk
death
based
on
parameters,
we
that
high
tumoural
grading
increases
2.8
times,
pleomorphic
histological
3.5
stage
IV
TNM
this
5.9
times.
Conclusions:
For
north-eastern
geographical
part
Romania,
epidemiological
child
13-year-old
boy
femoral
tumour
12-year-old
girl
femoral,
tibia,
tumour,
both
coming
rural
area.
around
12
cm
diameter
differentiated
osteosarcoma.
survival
rate
63%.
Tumour
grading,
staging
influence
probability
could
be
important
parameters
International Journal of Scientific Reports,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 6, 2025
Radiation
therapy
is
a
recognized
etiological
factor
for
osteomyelitis,
osteoradionecrosis
and
multiple
sarcomas
such
as
chondrosarcoma
osteosarcoma.
Here
we
present
case
of
mandibular
chondroblastic
type
osteosarcoma
induced
by
radiotherapy
which
was
primarily
misdiagnosed
chondrosarcoma.
A
female
presented
with
main
complaint
pain
at
the
extraction
site
following
teeth
sequestrectomy
on
right
lower
jaw.
Medical
history
revealed
stage
IV
squamous
cell
carcinoma
base
tongue
treated
surgical
excision,
chemotherapy
ten
years
ago.
Four
recurring
sequestrectomies
were
performed,
but
only
histological
material
from
fourth
grade
2
This
followed
resection
tumour
floor
mouth,
mandibular,
lip
facial
skin
reconstruction
operation
through
histology
again
confirmed
to
be
chondrosarcomas.
In
year’s
time,
pathological
nodule
in
thyroid
gland
found
CT,
surgery
performed.
Operation
now
high
additional
prescribed.
illustrated
rare
malignant
incidence,
diagnostical
difficulties
treatment.
Differential
diagnosis
should
considered
if
no
positive
changes
are
observed
after
designated
well
importance
immuno
evaluation.
One
malignancy
does
not
exclude
development
another
unrelated
malignancy.
Cancers,
Journal Year:
2025,
Volume and Issue:
17(4), P. 599 - 599
Published: Feb. 10, 2025
Osteosarcoma
is
a
primary
malignant
bone
tumor
characterized
by
the
production
of
an
osteoid
matrix.
Although
histology
remains
definitive
diagnostic
standard,
imaging
plays
crucial
role
in
diagnosis,
therapeutic
planning,
and
follow-up.
Conventional
radiography
serves
as
initial
checkpoint
for
detecting
this
pathology,
which
often
presents
challenges
due
to
vague
nonspecific
symptoms,
especially
its
early
stages.
Today,
integration
different
techniques
enables
increasingly
personalized
diagnosis
management,
with
each
contributing
unique
complementary
information.
typically
initiates
assessment,
Bone
Reporting
Data
System
(Bone-RADS)
Society
Skeletal
Radiology
(SSR)
valuable
tool
stratifying
risk
suspicious
lesions.
CT
preferred
modality
evaluating
matrix,
while
scans
PET/CT
are
effective
distant
metastases.
MRI
reveals
extent
lesion
adjacent
soft
tissues,
medullary
canal,
joints,
well
relationship
neurovascular
structures
presence
skip
Advanced
such
dynamic
contrast-enhanced
magnetic
resonance
(DCE-MRI),
diffusion-weighted
(DWI),
perfusion
help
characterize
environment
assess
treatment
response.
comprises
range
subtypes
differing
clinical
characteristics,
some
particularly
distinctive,
case
telangiectatic
osteosarcoma.
Knowledge
these
variants
can
guide
radiologists
differential
includes
both
central
surface
forms,
ranging
from
highly
aggressive
more
indolent
types.
In
review,
we
present
wide
representative
cases
our
hospital
series
illustrate
typical
atypical
presentations.
Finally,
discuss
recent
advancements
applying
artificial
intelligence
approaches
Romanian Journal of Morphology and Embryology,
Journal Year:
2025,
Volume and Issue:
65(4), P. 723 - 736
Published: Feb. 13, 2025
Osteosarcoma
(OS)
is
the
most
prevalent
primary
bone
malignancy,
predominantly
affecting
adolescents
and
young
adults,
presents
significant
clinical
challenges
due
to
its
aggressive
nature
high
potential
for
metastasis.
This
retrospective
study
analyzed
34
cases
of
OS,
aged
10
65
years,
identify
clinicopathological
correlations
that
could
inform
future
research
treatment
strategies.
The
findings
aim
guide
larger
cohort
studies,
essential
validating
these
developing
tailored
approaches
enhance
patient
outcomes.
analysis
focused
on
demographic
factors,
sex,
tumor
grade,
stage,
size,
histological
subtype,
utilizing
criteria
established
by
American
Joint
Committee
Cancer
(AJCC)
World
Health
Organization
(WHO).
results
revealed
a
predominance
disease
in
males
under
25
years
age,
with
femur
being
common
site
occurrence.
Conventional
osteoblastic
OS
emerged
as
frequent
accounting
50%
cases,
presenting
high-grade
(G3)
tumors.
Over
70%
tumors
were
T1
extension
(≤8
cm)
classified
stage
IIA,
indicating
locally
advanced
state.
Correlations
observed
between
type,
underscoring
importance
detailed
histopathological
(HP)
assessments
determining
prognosis
guiding
treatment.
highlight
reaffirming
critical
role
HP
planning.
While
limited
sample
size
necessitates
cautious
interpretation,
this
provides
valuable
regional
age-specific
insights
decision-making.
Future
should
prioritize
multi-center
studies
delve
into
genetic
molecular
underpinnings
subtypes
understanding
develop
targeted
therapies.