Rare Diseases Symptoms Automatic Extraction
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A random Abstract
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Littoral cell angioma: review of the literature and case report.
[alpha-thalassemia]
Littoral
cell
angioma
(
LCA
)
,
a
primary
vascular
neoplasm
originating
from
splenic
red
pulp
littoral
cells
,
was
initially
thought
to
be
an
extremely
rare
pathology
.
There
have
been
an
increasing
number
of
cases
reported
in
the
literature
.
However
,
the
etiology
and
prevalence
of
LCA
is
still
unclear
,
partly
due
to
the
rarity
of
cases
.
The
association
of
LCA
with
internal
organ
cancers
,
specifically
lymphoma
,
has
also
been
reported
.
In
the
patients
with
a
history
of
cancer
/
lymphoma
,
the
accurate
diagnosis
of
LCA
as
the
cause
of
the
splenomegaly
is
challenging
.
Here
we
present
a
case
of
LCA
in
a
patient
with
non-
Hodgkin
B-
cell
lymphoma
and
alpha-thalassemia
trait
.
To
our
knowledge
,
this
is
the
first
report
of
the
coexistence
of
LCA
and
thalassemia
and
only
the
second
report
of
LCA
and
marginal-zone
non-
Hodgkin
B-
cell
lymphoma
.
We
review
the
literature
and
discuss
the
radiologic
and
pathologic
findings
of
this
case
compared
with
the
previously
reported
cases
.
Diseases
Validation
Diseases presenting
"cancer"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
benign recurrent intrahepatic cholestasis
cadasil
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
hirschsprung disease
hodgkin lymphoma, classical
inclusion body myositis
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
This symptom has already been validated