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Pre-transplant manipulation processing of umbilical cord blood units: Efficacy of Rubinstein's thawing technique used in 40 transplantation procedures.
[omenn syndrome]
Umbilical
cord
blood
(
UCB
)
is
a
valid
alternative
to
be
used
in
transplanted
patients
.
Limitations
of
the
use
of
stem
cells
depends
on
the
small
number
of
cells
available
;
this
is
the
reason
why
UCB
can
be
used
only
in
very
low
-weight
patients
.
In
this
study
we
have
evaluated
the
efficacy
of
cellular
manipulation
before
transplant
and
in
particular
,
before
thawing
the
units
through
the
Rubinstein
method
.
We
have
evaluated
the
results
obtained
after
thawing
40
UCB
to
be
used
for
as
many
patients
affected
by
several
pathologies
(
21
ALL
,
6
AML
,
3
MDS
,
2
LNH
,
2
histiocytosis
,
2
β-thalassemia
,
1
Chédiak-
Higashi
syndrome
,
1
Fanconi
anemia
,
1
Wiskott-
Aldrich
syndrome
and
1
Omenn
syndrome
)
.
After
thawing
,
nucleated
cells
(
NC
)
mean
recovery
was
76
.
81
%
(
SD
±
15
.
41
)
.
The
quantity
of
NC
obtained
was
124
.
29
×
107
(
SD
±
43
.
18
)
and
in
only
5
cases
the
number
of
NC
after
the
procedure
was
lower
than
the
requested
graft
dose
.
Among
the
last
ones
,
in
two
cases
only
we
did
not
achieve
the
target
after
manipulation
.
The
post-manipulation
cellular
viability
was
83
.
48
%
(
SD
±
10
.
6
)
.
For
all
the
units
shipment
complied
with
all
the
necessary
procedures
;
in
fact
the
temperature
never
rose
above
-
120
°
C
.
In
our
study
we
highlighted
the
efficacy
of
UCB
thawing
technique
,
with
the
same
method
defined
in
1995
at
the
New
York
Blood
Centre
that
guarantees
an
excellent
NC
recovery
and
maintains
a
high
level
of
cell
viability
.
Diseases
Validation
Diseases presenting
"high level"
symptom
22q11.2 deletion syndrome
aniridia
cadasil
carcinoma of the gallbladder
cohen syndrome
congenital toxoplasmosis
cutaneous mastocytosis
cystinuria
dedifferentiated liposarcoma
dentinogenesis imperfecta
erdheim-chester disease
erythropoietic protoporphyria
esophageal carcinoma
esophageal squamous cell carcinoma
familial hypocalciuric hypercalcemia
familial mediterranean fever
hodgkin lymphoma, classical
inclusion body myositis
liposarcoma
lymphangioleiomyomatosis
omenn syndrome
oral submucous fibrosis
pyomyositis
scrub typhus
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
x-linked adrenoleukodystrophy
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