Local recurrence of non‐lentigo maligna melanoma in situ and safety excision margins: A systematic review
JDDG Journal der Deutschen Dermatologischen Gesellschaft,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 15, 2025
Summary
The
strength
of
evidence
supporting
a
2‐step
wide
local
excision
(WLE)
with
5
mm
safety
margins
for
melanoma
in
situ
non‐lentigo
maligna
(non‐LM)
type,
compared
narrower
margins,
is
unclear.
This
review
aims
to
compare
the
frequency
recurrence
(LR)
different
after
complete
surgical
(R0)
non‐LM
MIS.
We
performed
systematic
literature
search
PubMed,
Scopus,
and
Cochrane
Library
up
March
17,
2024.
PRISMA
checklist
was
used.
Of
3,047
articles
retrieved,
seven
retrospective
studies
were
included,
enrolling
total
1,526
MIS
cases
excised
clear
WLE
(6
studies)
or
Mohs
surgery
(1
study).
Most
located
on
trunk/extremities
(68%–100%).
Narrower
used
four
studies,
ranging
from
no
4
mm,
there
only
one
LR.
Standard
wider
remaining
three
reporting
two
median
follow‐up
ranged
48
months
6.6
years.
overall
certainty
quality
very
low.
These
findings
our
highlight
that
current
guidelines
recommending
re‐excision
initial
lack
strong
support
this
practice.
Language: Английский
Recurrence Rate of Melanoma In Situ Excised With a 5-mm Excisional Margin
JAMA Dermatology,
Journal Year:
2024,
Volume and Issue:
160(8), P. 803 - 803
Published: Aug. 1, 2024
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Language: Английский
Impact of alternative diagnostic labels for melanoma in situ on management choices and psychological outcomes: protocol for an online randomised study
BMJ Open,
Journal Year:
2024,
Volume and Issue:
14(12), P. e089558 - e089558
Published: Dec. 1, 2024
A
diagnosis
of
melanoma
in
situ
presents
negligible
risk
to
a
person's
lifespan
or
physical
well-being,
but
existing
terminology
makes
it
difficult
for
patients
distinguish
these
from
higher
invasive
melanomas.
This
study
aims
explore
whether
using
an
alternative
label
may
influence
patients'
management
choices
and
anxiety
levels.
is
between-subjects
randomised
online
experiment,
hypothetical
scenarios.
Following
consent,
eligible
participants
will
be
1:1:1
three
labels:
'melanoma
situ'
(control),
'low-risk
melanocytic
neoplasm'
(intervention
1)
neoplasm,
2).
The
required
sample
size
1668
people.
co-primary
outcomes
are
(1)
choice
between
no
further
surgery
ensure
clear
histological
margins
greater
than
5
mm
(2)
patient-initiated
clinical
follow-up
when
needed
(patient-led
surveillance)
regular
routinely
scheduled
(clinician-led
surveillance).
Secondary
include
anxiety,
perceived
dying
(after
choice).
We
make
pairwise
comparisons
across
the
diagnostic
groups
regression
models
(univariable
multivariable).
has
been
registered
with
Australian
New
Zealand
Clinical
Trials
Registry
(ACTRN12624000740594).
Ethics
approval
received
University
Sydney
Human
Research
Committee
(2024/HE000019).
results
published
peer-reviewed
medical
journal,
plain
language
summary
findings
shared
on
Wiser
Healthcare
publication
page
(https://www.wiserhealthcare.org.au/category/publications/).
(ID
386943).
Language: Английский