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Table 2 Clinical and radiological findings of tumor mimickers in the male genital tract (part-2)

From: Identifying the deceiver: the non-neoplastic mimickers of genital system neoplasms

Disease

Imaging findings

Auxiliary clinical information

Testicular hematoma

Acute phase (US): Iso-hyperechoic mass with no apparent internal vascularity

Resolution phase (US): Hypoechoic lesion with gradual decrease in size

Single or multiple lesions can be seen. Concomitant imaging findings of scrotal trauma such as hematocele

MRI: T1 hyperintensity (subacute phase), T2 hypointensity (chronic phase), no internal enhancement

History of trauma is suggestive. Resolution during follow-up is expected. May complicate with testicular necrosis, compression atrophy or secondary infections. Incidental diagnosis of testicular tumors after scrotal trauma should also be kept in mind

Segmental testicular infarction

US: Solid-appearing wedge-shaped heterogeneous lesion without apparent vascularity

MRI: Well-defined heterogeneous parenchymal areas with absence of enhancement. Hemorrhagic changes may be seen as T1 hyperintense areas. Rim enhancement may be observed

Testicular pain. Young adults. Underlying causes may be infection, trauma, vasculitis, or hematologic diseases. Follow-up imaging is required to rule out malignancy

Leydig’s cell hyperplasia

US: Small, multifocal, frequently bilateral parenchymal nodules with internal vascularity and variable echogenicity

MRI: T2 hypointense nodules with avid contrast enhancement

Rare. Mostly seen in asymptomatic patients with normal serum tumor markers. May coexist with Klinefelter syndrome

Testicular adrenal rests

US: Bilateral, multiple, well-defined hypoechoic nodular lesions with no apparent mass effect located in the mediastinum testis. Tend to appear as heterogeneous hyperechoic masses as they get larger. Internal vascularity is variable. Posterior acousting shadowing may be observed

MR: T1 iso-hyperintense, T2-hypointense lesions with avid enhancement

History of congenital adrenal hyperplasia or Cushing’s syndrome. May cause infertility. Regression after glucocorticoid therapy can be seen

Tubular ectasia of rete testis

US: Multiple cystic-tubular anechoic structures replacing the mediastinum testis. Internal vascularity, calcification, presence of solid component are not expected. Bilateral involvement is common

MRI: T2-hyperintense cystic structure with no internal enhancement

Over the age of 45. History of previous scrotal surgery and vasectomy. It should be kept in mind that testicular tumors may also cause post-obstructive rete testis dilation

Cystic dysplasia of rete testis

Unilateral, multicystic lesion compressing the surrounding parenchyma in the mediastinum testis

It may be useful to control ipsilateral renal anomalies such as renal agenesis or multicystic dysplastic kidney

Seen in the pediatric age group. Unilateral painless scrotal swelling. May coexist with ipsilateral renal anomalies. Testicular compression atrophy may develop

Negative serum tumor markers

Paratesticular inflammatory pseudotumor

US: Paratesticular lesions with variable echogenicity and mild-to-moderate internal vascularity. Posterior acoustic shadowing and intralesional calcifications may be seen

MRI: T1 and T2 hypointense lesions with gradual contrast enhancement

Uncommon. May be related to previous surgery, trauma, infection or inflammation. Could be secondary to the IgG4-RD

Paratesticular tuberculoma

US: Well-circumscribed hypoechoic lesions with calcifications and mild internal vascularity. Extension to the scrotal wall or testicular parenchyma may be seen

MRI: T1-hyperintense and T2-hypointense paratesticular lesions

Rare. History of immunosuppression or intravesical BCG instillation. Histopathological examination is required for definitive diagnosis

Polyorchidism

US: Solid nodular lesion with similar echogenicity and echotexture to the normal testes

MRI: Homogeneous solid lesions with intermediate T1 and high T2 signal intensity similar to testes

Rare congenital anomaly. More common on the-left side. Extra testis is smaller than normal testes, and mostly located within the scrotum adjacent to the lower pole

Splenogonadal fusion

Continuous form: Long parenchymal or fibrous cord extending from the spleen to the testis

Discontinuous form: Homogeneous solid iso-hypoechoic lesion with internal vascularity

In case of suspicion, Tc99m-sulfur colloid scintigraphy can help detection and prevent orchiectomy

Rare congenital anomaly. More common on the left-side. Commonly associated with inguinal hernia and cryptorchidism