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Focal myositis of the iliopsoas muscle--a benign pseudotumour: ultrasound appearance in correlation with CT and MRI.
[focal myositis]
Focal
myositis
of
the
iliopsoas
muscle
is
a
rare
condition
.
A
case
is
presented
,
emphasizing
the
value
of
ultrasound
for
detection
,
localisation
,
image-guided
biopsy
and
follow-up
in
correlation
with
CT
and
MRI
findings
.
A
58
-
year
-old
woman
was
referred
to
our
clinic
with
strong
left
sided
inguinal
pain
,
which
radiated
to
the
thigh
and
had
lasted
for
four
days
.
Ultrasound
,
CT
and
MRI
were
performed
.
Ultrasound-guided
biopsy
with
histological
correlation
was
obtained
and
US
-follow-ups
were
available
.
CT
showed
an
enlarged
iliopsoas
muscle
on
the
left
side
without
any
focal
pathology
or
enhancement
.
MRI
revealed
a
sharpely
delineated
lesion
,
which
was
hypointense
to
muscle
in
fat-suppressed
T
1
w
images
with
circumferential
enhancement
and
showed
a
hyperintense
appearance
in
T
2
w
images
.
Ultrasound
displayed
a
polylobulated
,
inhomogeneous
and
hypoechoic
tumour
within
the
iliopsoas
muscle
.
Ultrasound-guided
biopsy
was
found
to
be
compatible
with
myositis
.
After
oral
therapy
with
steroids
,
improvement
could
be
documented
by
serial
ultrasound
follow-up
as
the
size
of
the
tumour
was
definitely
regressing
.
Focal
myositis
of
the
iliopsoas
muscle
is
a
rare
entity
which
may
mimic
a
tumoural
lesion
.
Imaging
findings
may
not
be
conclusive
,
and
US
-guided
biopsy
is
recommended
to
rule
out
a
malignant
mass
.
Ultrasound
seems
to
be
the
most
cost-effective
method
for
diagnosis
,
image
guided
biopsy
and
follow-up
.
Diseases
Validation
Diseases presenting
"pain"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
aniridia
aromatase deficiency
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital diaphragmatic hernia
congenital toxoplasmosis
cushing syndrome
cutaneous mastocytosis
cystinuria
dedifferentiated liposarcoma
dentin dysplasia
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
focal myositis
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
junctional epidermolysis bullosa
kabuki syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
neuralgic amyotrophy
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
phenylketonuria
pleomorphic liposarcoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
scrub typhus
sneddon syndrome
systemic capillary leak syndrome
thoracic outlet syndrome
trochlear dysplasia
typhoid
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
wolf-hirschhorn syndrome
This symptom has already been validated