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Histopathological Difficulties in an Adolescent Lymphoma Patient.
[hodgkin lymphoma, classical]
The
B-
cell
lymphoma
,
unclassifiable
,
showing
intermediate
features
typical
for
both
diffuse
large
B-
cell
lymphoma
(
DLBCL
)
and
classical
Hodgkin
lymphoma
(
HL
)
is
a
novel
category
of
diffuse
large
B-
cell
lymphomas
(
DLBCL
/
HL
)
,
which
has
been
described
by
the
WHO
classification
in
2008
.
This
rare
type
of
lymphomas
,
previously
called
as
gray
zone
lymphoma
presents
peculiar
clinical
,
morphological
and
immunophenotypical
patterns
.
In
December
2011
a
17
-
year
old
male
was
diagnosed
with
mixed
cellularity
subtype
of
classical
HL
.
His
clinical
stage
was
IV
/
BXS
(
abdominal
bulky
)
with
unfavourable
prognosis
.
Because
of
the
unusally
extended
disease
(
nodal-extranodal-bulky
)
a
histological
revision
was
performed
.
After
an
incomplete
course
of
ABVD
chemotherapy
the
patient
's
symptoms
disappeared
and
regression
was
detected
in
the
size
of
peripheral
lymph
nodes
.
The
diagnosis
changed
into
DLBCL
/
HL
,
so
the
treatment
was
modified
to
R-CHOP-
14
regimen
.
After
the
administration
of
3
Â
cycles
of
R-CHOP-
14
,
he
achieved
a
complete
metabolic
remission
(
CMR
)
,
which
was
confirmed
by
a
(
18
)
FDG-PET
/
CT
scan
.
Receiving
further
4
cycles
of
R-CHOP-
14
therapy
the
patient
was
still
in
CMR
,
but
a
PET
negative
large
mass
(
70
 
×
 
30
Â
mm
)
still
remained
visible
in
the
abdominal
region
.
Considering
this
residuum
and
the
agressive
subtype
of
lymphoma
he
was
referred
for
an
autologous
hemopoietic
stem
cell
transplantation
(
AHSCT
)
.
After
2
Â
cycles
of
R-DHAP
regimen
,
successful
CD
34
positive
stem
cell
collection
was
performed
in
August
2012
.
In
September
2012
,
he
underwent
a
R-BEAM
conditioning
followed
by
AHSCT
.
The
next
(
18
)
FDG-PET
/
CT
still
detected
CMR
100
Â
days
after
the
AHSCT
.
The
patient
was
in
excellent
clinical
condition
and
also
in
complete
remission
15
Â
months
after
the
AHSCT
.
Upon
this
case
,
it
should
be
underlined
that
the
diagnosis
may
need
revision
if
a
patient
represents
atypical
clinical
signs
and
behavior
,
and
the
importance
of
cooperation
between
clinicians
and
pathologists
is
also
strongly
emphasized
.
Diseases
Validation
Diseases presenting
"hodgkin lymphoma"
symptom
esophageal adenocarcinoma
hodgkin lymphoma, classical
monosomy 21
primary effusion lymphoma
severe combined immunodeficiency
systemic capillary leak syndrome
waldenström macroglobulinemia
This symptom has already been validated