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Diffuse large B cell lymphoma in wiskott-Aldrich syndrome: a case report and review of literature.
[wiskott-aldrich syndrome]
Wiskott-
Aldrich
syndrome
(
WAS
)
is
an
X
linked
rare
primary
immunodeficiency
syndrome
with
an
increased
propensity
for
infection
,
autoimmunity
and
malignancy
.
Here
we
report
a
male
child
,
who
was
diagnosed
with
WAS
at
1
year
of
age
following
evaluation
for
symptomatic
thrombocytopenia
and
eczematous
skin
lesions
.
He
presented
later
with
lymphadenopathy
,
which
was
consistent
with
diffuse
large
B
cell
lymphoma
on
histopathology
.
He
received
6
cycles
of
R-CHOP
chemotherapy
for
the
same
and
is
presently
in
remission
after
6
months
.
We
review
the
major
publications
of
lymphoma
in
WAS
and
discuss
the
pathological
findings
,
treatment
and
prognosis
of
lymphoma
in
WAS
.
Diseases
Validation
Diseases presenting
"thrombocytopenia"
symptom
22q11.2 deletion syndrome
adrenomyeloneuropathy
dedifferentiated liposarcoma
erythropoietic protoporphyria
esophageal adenocarcinoma
heparin-induced thrombocytopenia
hodgkin lymphoma, classical
holt-oram syndrome
homocystinuria without methylmalonic aciduria
liposarcoma
malignant atrophic papulosis
monosomy 21
oculocutaneous albinism
scrub typhus
sneddon syndrome
typhoid
waldenström macroglobulinemia
wiskott-aldrich syndrome
This symptom has already been validated
