Rare Diseases Symptoms Automatic Extraction
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Bullous mastocytosis in a 3-month-old infant.
[cutaneous mastocytosis]
Mastocytosis
is
a
rare
myeloid
neoplasm
characterized
by
abnormal
proliferation
and
accumulation
of
mast
cells
in
one
or
more
organ
systems
including
the
skin
,
bone
marrow
,
liver
,
spleen
,
lymph
nodes
and
gastrointestinal
tract
.
An
infant
presenting
with
bullous
lesions
is
an
even
rarer
clinical
presentation
of
cutaneous
mastocytosis
.
The
symptoms
and
complications
are
mostly
in
proportion
to
the
mast
cell
degranulation
in
tissues
.
Management
is
focused
on
preventing
and
treating
this
event
.
We
report
a
three
-
month
-old
infant
with
bullous
mastocytosis
to
enhance
awareness
about
this
rare
diagnosis
.
Diseases
Validation
Diseases presenting
"bone marrow"
symptom
adrenomyeloneuropathy
allergic bronchopulmonary aspergillosis
cohen syndrome
cushing syndrome
cutaneous mastocytosis
erdheim-chester disease
erythropoietic protoporphyria
focal myositis
hodgkin lymphoma, classical
krabbe disease
legionellosis
liposarcoma
monosomy 21
oculocutaneous albinism
omenn syndrome
papillon-lefèvre syndrome
pyomyositis
scrub typhus
severe combined immunodeficiency
systemic capillary leak syndrome
waldenström macroglobulinemia
werner syndrome
wiskott-aldrich syndrome
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