Testicular cancer is the most common malignancy affecting men aged 20 – 30 years. Most are germ cell tumours (>95%), of which there are two main types: seminomas and teratomas. Recent classification divides testicular cancer into seminoma (50%) and non-seminoma germ cell tumours (including teratomas). Both types can occur together.
Testicular cancer accounts for 1 – 2% of all tumours. They mostly occur between 14 – 40 years of age.
Teratoma vs Seminoma
Teratoma
Seminoma
Age of onset
20 – 30
30 – 40
Peak incidence
25 years
35 years
aFP
Produced
Not produced
B-hCG
Produced
Produced
5-year survival if stage I
85%
95%
Risk factors for testicular cancer
Cryptorchidism
Klinefelter’s syndrome
Male infertility (3 times risk)
Low birth weight
Infantile hernia
Height (taller men are at a greater risk)
History of testicular cancer (in the contralateral testis)
Family history of testicular cancer (50 times increased risk with TCGT1 gene which is carried by 20% of the population)
Mumps orchitis
Signs and symptoms
Firm lump on the testes
Painless (rarely painfull)
“Stuck on” to the side of the testes
Hard
Testicular “ache” or abdominal pain
Sensation of “dragging” or “anchoring” on the scrotum
Hydrocele
Gynaecomastia (due to B-hCG produced by the tumor)
Differentials
Hernia
Hydrocele
Varicocele
Testicular torsion
Epididymo-orchitis
Investigations
Ultrasound
Thoraco-abdominal CT scan: for staging after diagnosis
Tumour markers
a-fetoprotein. (AFP)
B-human chorionic gonadotrophin (hCG)
Lactate dehydrogenase (LDH)
Treatment
Radical orchidectomy: The affected testes and spermatic cord are removed preferably through the inguinal route to minimise risk of seeding into the scrotum
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