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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
"immunodeficiency"
symptom
adrenal incidentaloma
allergic bronchopulmonary aspergillosis
cushing syndrome
dracunculiasis
hirschsprung disease
hodgkin lymphoma, classical
homocystinuria without methylmalonic aciduria
kabuki syndrome
legionellosis
malignant atrophic papulosis
oculocutaneous albinism
omenn syndrome
papillon-lefèvre syndrome
primary effusion lymphoma
primary hyperoxaluria type 1
pyomyositis
severe combined immunodeficiency
sneddon syndrome
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
This symptom has already been validated
