Summary
Imaging studies play a vital role in the diagnosis and
management of testicular cancer. Ultrasound is primarily used for initial diagnosis,
and CT is the standard for cancer staging. MRI provides an equally powerful diagnostic
alternative to CT for use in certain circumstances. The use of PET is limited
in tumor characterization, but, with the advent of new tracers, PET is gaining acceptance for the
evaluation of treatment response as well as recurrence.
Diagnosis
Sonographic imaging of the testes represents the reference
standard imaging evaluation, with sensitivity of near 100% when combined with
physical examination (Fig. 1).
Ultrasound can distinguish intra- and extra-testicular
lesions and is undertaken in most cases before orchiectomy [9]. Testicular tumors
are typically well defined and hypoechoic compared with normal testicular
tissue but can be heterogeneous with calcification or cystic changes [10]. Increased vascularity of a lesion is
not specific to testicular tumors.
In cases in which the diagnosis is in question, additional
information can be gained with MRI. Solid testicular tumors have lower signal
intensity on T2-weighted MRI in contrast with the high signal intensity of
normal testicular parenchyma. One study evaluated MRI of the testes before
orchiectomy in 33 patients with T1- and T2-weighted images using a 1.5-T MRI
unit.
The sensitivity and specificity of MRI in differentiating
benign from malignant intratesticular lesions were 100% and 87.5%,
respectively.
Furthermore, the accuracy of MRI for assigning pathologically
confirmed T category was 92.8% [11]. The role of MRI of the testis in place of ultrasound
remains to be clearly determined. However, it offers reliable and detailed
information in the case of equivocal ultrasound findings or in the absence of a
skilled sonographer. On occasion, the initial presentation may be a
retroperitoneal mass, with testicular imaging not revealing an evident lesion.
In these cases, a testicular malignancy must be considered because the
primary testicular tumor may have “burned out” and no longer be evident or it
may appear more subtle on imaging [12, 13] (Fig. 2). A more unusual presentation
would be that of an extragonadal GCT. Extragonadal GCTs are essentially of the
same histology as testicular malignancies but develop outside of the testis,
commonly in the pineal gland, mediastinum, retroperitoneum, or sacrum [14, 15].
In either of these situations, tumor markers or biopsy may provide insight to
the diagnosis.
The finding of testicular microlithiasis (Fig. 3) is
commonly present on ultrasound imaging in patients with testicular malignancy.
Historically, the contribution of testicular microlithiasis to the risk of
malignancy has been controversial; however, more recent data have shown that the presence of microlithiasis on an otherwise normal
testicular ultrasound does not predispose the patient to testicular malignancy
[16]. One study of sonographic screening in 1504 healthy United States Army
Reserve recruits revealed an incidence of testicular microlithiasis of 5%, or 1000 times greater than the incidence of
testicular malignancy [17]. It appears the presence or absence of testicular microlithiasis
is not significantly associated with risk for malignancy, and there is no good
evidence to support a role for imaging surveillance in the absence of
additional risk factors [18, 19].
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