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A random Abstract
Our Project
Our Team
Evaluation of the WHO criteria for the classification of patients with mastocytosis.
[cutaneous mastocytosis]
Diagnosis
and
classification
of
mastocytosis
is
currently
based
on
the
World
Health
Organization
(
WHO
)
criteria
.
Here
,
we
evaluate
the
utility
of
the
WHO
criteria
for
the
diagnosis
and
classification
of
a
large
series
of
mastocytosis
patients
(
n
=
133
)
,
and
propose
a
new
algorithm
that
could
be
routinely
applied
for
refined
diagnosis
and
classification
of
the
disease
.
Our
results
confirm
the
utility
of
the
WHO
criteria
and
provide
evidence
for
the
need
of
additional
information
for
(
1
)
a
more
precise
diagnosis
of
mastocytosis
,
(
2
)
specific
identification
of
new
forms
of
the
disease
,
(
3
)
the
differential
diagnosis
between
cutaneous
mastocytosis
vs
systemic
mastocytosis
,
and
(
4
)
improved
distinction
between
indolent
systemic
mastocytosis
and
aggressive
systemic
mastocytosis
.
Based
on
our
results
,
a
new
algorithm
is
proposed
for
a
better
diagnostic
definition
and
prognostic
classification
of
mastocytosis
,
as
confirmed
prospectively
in
an
independent
validation
series
of
117
mastocytosis
patients
.
Diseases
Validation
Diseases presenting
"and"
symptom
achondroplasia
adrenomyeloneuropathy
aniridia
carcinoma of the gallbladder
cutaneous mastocytosis
cystinuria
esophageal squamous cell carcinoma
harlequin ichthyosis
hodgkin lymphoma, classical
hydrocephalus with stenosis of the aqueduct of sylvius
kallmann syndrome
liposarcoma
locked-in syndrome
neonatal adrenoleukodystrophy
omenn syndrome
oral submucous fibrosis
pleomorphic liposarcoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
sneddon syndrome
triple a syndrome
trochlear dysplasia
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