Case report
Uptake of 2-[
18
F]fluoro-2-deoxy-D-glucose in uterine
leiomyoma: imaging of four patients by coincidence positron
emission tomography
I
˙
lknur Ak
a
, Sinan O
¨
zalp
b
,O
¨
mer T. Yalc ¸ in
b
, Evren Zor
a
and Erkan Vardareli
a
Uterine leiomyomas, benign tumours of the human uterus,
are the most common uterine neoplasm and are composed
of smooth muscle with varying amounts of fibrous
connective tissue. As a functional imaging modality,
2-[
18
F]fluoro-2-deoxy-D-glucose (
18
F-FDG) positron
emission tomography can be used to obtain information
about glucose metabolism in tissues. In this study, the
findings of the
18
F-FDG scans of four patients who were
suspected of having malignant gynaecological tumours
because of clinical and radiological findings and
finally diagnosed as uterine leiomyoma based on
histopathological examination were evaluated. Moderately
intense
18
F-FDG accumulation was detected in uterine
mass localization in lower pelvis. The reason for the
accumulation of
18
F-FDG in uterine leiomyomas is not
known. It may be explained by the existence of higher
levels of growth factors, including basic fibroblast growth
factor, transforming growth factor beta,
granulocyte-macrophage colony-stimulating factor and
receptors, and proliferation of smooth muscle cells
in leiomatous uterus. Nucl Med Commun 25:941–945
c
2004 Lippincott Williams & Wilkins.
Nuclear Medicine Communications 2004, 25:941–945
Keywords: uterine leiomyoma,
18
F-FDG, coincidence PET
Departments of
a
Nuclear Medicine and
b
Obstetrics and Gynecology, Osmangazi
University Faculty of Medicine, Eski ¸ sehir, Turkey.
Correspondence to Dr I
˙
lknur Ak, Osmangazi University Medical Faculty,
Department of Nuclear Medicine, 26480 Eski ¸ sehir, Turkey.
Tel: +90 222 239 2979 or 3450; fax: +90 222 229 1150;
e-mail: ilknur_ak@yahoo.com
Received 14 November 2003 Accepted 11 March 2004
Introduction
Uterine leiomyomas (fibroids or myomas), benign tu-
mours of the human uterus, are the most common uterine
neoplasm and are composed of smooth muscle with
varying amounts of fibrous connective tissue. They are
clinically apparent in about 25% of women and the most
common solid pelvic tumours [1]. With newer imaging
techniques, the true clinical prevalence may be higher.
Careful pathological examination of surgical specimens
suggests that the prevalence is as high as 77% [2].
Although most leiomyomas are asymptomatic, patients
may present with abnormal uterine bleeding, pressure on
adjacent organs, pain, infertility, or a palpable abdominal–
pelvic mass. The size of uterine leiomyomas is variable,
ranging from microscopic to large tumours that fill the
abdomen. The diagnosis of myomas is often suspected on
the basis of palpation of an enlarged irregular uterine
contour on pelvic examination. Ultrasonography (USG) is
typically used to confirm the diagnosis and exclude the
possibility of ovarian neoplasm. Magnetic resonance
imaging (MRI) gives better visualization of individual
myomas and it is currently considered the most accurate
imaging technique for detection and localization of
leiomyomas [3,4]. Their typical appearances at MRI have
been well established. Because of its ability to clearly
demonstrate individual tumours, MRI has been shown to
be more sensitive than USG in detection of leiomyomas
[5]. However, cases that are extremely difficult to
differentiate from other conditions are occasionally
encountered. Unlike with MRI, accurate assessment of
an enlarged, myomatous uterus ( > 140 cm
3
) is not
consistently possible with USG because of the limited
field of view [6].
Positron emission tomography (PET) with 2-[
18
F]fluoro-
2-deoxy-D-glucose (
18
F-FDG) has opened a new field in
clinical imaging, thereby differing from the more
conventional morphological or anatomical imaging meth-
ods, including radiography, USG, computed tomography
(CT), MRI and even single photon emission tomography
(SPET). It has been used successfully for assessing the
large variety of primary tumours and metastases, prog-
nosis, and planning and for monitoring tumour therapy as
well as for early detection of recurrent tumour growth. As
a functional imaging modality,
18
F-FDG PET represents
the information about glucose metabolism of tissues. The
glucose analogue 2-deoxy-D-glucose is transported into
the cell in the same way as glucose. In the cell, it is
phosphorylated to deoxyglucose-6-phosphate by hexo-
kinase, like normal glucose. However, in contrast with
glucose, glucose-6-phosphate isomerase does not react
with deoxyglucose-6-phosphate, so further metabolism is
not possible. In addition, deoxyglucose-6-phosphate
shows slow clearance from the cell, which is caused by
low membrane permeability. Thus, deoxyglucose-6-phos-
phate is trapped in the cell [7].
18
F-FDG imaging can be
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