Giant cell tumour
Enzo Redolfi Mema
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Radiopaedia.org,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 2, 2025
Intramuscular Soft Tissue Giant Cell Tumor of the Forearm: A Case Report
Clinical Case Reports,
Journal Year:
2025,
Volume and Issue:
13(4)
Published: March 28, 2025
We
report
the
case
of
a
33-year-old
female
who
presented
with
painful,
rapidly
growing
mass
on
her
left
dorsal
forearm.
Physical
examination
revealed
2
cm
firm,
well-demarcated,
non-erythematous
nodule
beneath
skin,
an
initial
diagnosis
lipoma.
Upon
removal,
was
found
to
be
intramuscular
antebrachial
fascia.
The
histopathology
confirmed
benign
giant
cell
tumor
soft
tissue
(GCT-ST).
patient
informed
potential
risk
recurrence,
and
regular
follow-up
recommended.
At
last
follow-up,
no
clinical
evidence
recurrence
noted.
This
highlights
rare
GCT
at
exceptional
location,
Language: Английский
Diagnostic Challenge of Localized Tenosynovial Giant Cell Tumor in Children
Diagnostics,
Journal Year:
2025,
Volume and Issue:
15(3), P. 281 - 281
Published: Jan. 24, 2025
This
report
describes
a
rare
case
of
pediatric
tenosynovial
giant
cell
tumor
(TSGCT)
with
delayed
diagnosis.
A
9-year-old
boy
presented
3-month
history
knee
pain
and
swelling,
initially
attributed
to
femoral
non-ossifying
fibroma
arthritis
based
on
computed
tomography
findings
slightly
elevated
C-reactive
protein
levels.
The
symptoms
persisted
despite
medical
treatment.
Magnetic
resonance
imaging
(MRI)
revealed
in
the
posterior
compartment.
He
underwent
surgery,
pathology
confirmed
diagnosis
localized
TSGCT.
Six
months
postoperatively,
patient
remained
asymptomatic.
Pediatric
is
complex
symptom
associated
inflammatory
conditions
benign
malignant
tumors.
Benign
tumors,
as
this
case,
can
be
misdiagnosed
arthritis,
delaying
MRI
recommended
cases
involving
persistence.
However,
histopathological,
immunohistochemical,
morphological
examinations
are
crucial
for
definitive
diagnosis,
particularly
when
inconclusive.
Language: Английский
Arthroscopic Management of Pigmented Villonodular Synovitis of the Hip: A Systematic Review
Journal of Clinical Medicine,
Journal Year:
2024,
Volume and Issue:
13(21), P. 6446 - 6446
Published: Oct. 28, 2024
Background/Objectives:
Pigmented
villonodular
synovitis
(PVNS)
is
a
benign
proliferation
of
synovial
tissue
that
can
cause
joint
damage.
The
hip,
although
less
commonly
affected
than
the
knee,
presents
challenging
diagnosis
and
treatment,
with
magnetic
resonance
imaging
(MRI)
as
gold
standard
for
detection.
Surgical
excision,
arthroscopic
or
open,
main
treatment
approach,
but
there
no
consensus
on
best
strategy
hip.
aim
this
systematic
review
to
evaluate
clinical
outcomes,
complications,
revision
rates
associated
hip
surgery
PVNS.
Methods:
A
was
performed
following
PRISMA
guidelines.
Relevant
studies
were
identified
by
searching
four
databases:
PubMed,
Scopus,
Embase,
Medline.
Selected
articles
evaluated
according
criteria
levels
evidence
(LoE).
For
retrospective
studies,
Coleman
Methodology
Score
(mCMS)
used.
This
registered
International
Prospective
Register
Systematic
Reviews.
Results:
Six
satisfied
criteria;
these
involved
77
patients
(48%
male,
52%
female)
mean
age
26.4
years
follow-up
54.3
months.
MRI
biopsy
confirmed
diagnoses,
synovectomy
primary
treatment.
Success
ranged
from
80%
100%,
recurrence
rate
7.8%,
1.3%
requiring
surgery,
eight
(10.4%)
in
three
reporting
conversion
THA.
Complications
included
mild
effusions
residual
synovitis.
All
who
underwent
subsequent
total
arthroplasty
advanced
osteoarthritis.
Conclusions:
Our
reveals
use
arthroscopy
diagnosing
treating
PVNS
has
shown
satisfactory
results
without
increasing
risk
complications
return
their
former
activity
levels,
provided
preoperative
osteochondral
status
good
early
management
joint.
Language: Английский
Giant cell tumor of the tendon sheath: A critical review of current diagnostic and therapeutic approaches with treatment recommendations for hand and foot lesions
Journal of Musculoskeletal Surgery and Research,
Journal Year:
2024,
Volume and Issue:
9, P. 28 - 41
Published: Dec. 2, 2024
Giant
cell
tumor
of
the
tendon
sheath
(GCTTS)
is
a
common
affecting
hand
and
foot,
often
presenting
diagnostic
therapeutic
challenges
due
to
its
variable
clinical
presentations
biological
behaviors.
Recent
evidence
supports
neoplastic
origin
for
this
tumor,
previously
known
by
various
names.
GCTTS
can
be
categorized
as
localized
or
diffuse,
with
distinct
predilections
specific
anatomical
locations.
While
typically
benign
more
in
wrist,
diffuse
form
aggressive,
also
foot
ankle.
This
critical
analysis
review
aims
provide
comprehensive
overview
encompassing
clinical,
radiological,
histological,
genomic
features.
In
addition,
we
summarize
current
management
practices,
discuss
differential
diagnoses,
analyze
recurrence
rates
following
surgical
excision,
offer
evidence-based
treatment
recommendations
diverse
group
tumors.
Language: Английский