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PH-RO08

Testicular tumours

How most testicular cancers arise from germ cells that failed to mature before birth, how seminoma and non-seminomatous tumours differ in appearance and markers, and why they spread first to the para-aortic nodes.

By the end, you can

  • Describe the cells of the testis and explain why its lymph drains to the para-aortic nodes.
  • Explain how germ cell neoplasia in situ arises and the main risk factors for testicular germ cell tumours.
  • Compare the gross and microscopic features of seminoma and the non-seminomatous germ cell tumours.
  • Relate AFP, hCG and LDH to the tumour components that make them, and explain gynaecomastia.
  • Describe lymphatic and blood-borne spread and the findings they cause.
  • Recognise the classic microscopic features, classifications, staging and tests of testicular tumours, including why the testis is removed through the groin, and explain how orchidectomy, platinum chemotherapy, radiotherapy and sperm banking act.

What it is

About 95% of testicular tumours are germ cell tumours, the commonest solid cancer in young men. Most arise from germ cell neoplasia in situ (GCNIS) and are either seminomas or non-seminomatous germ cell tumours (embryonal carcinoma, yolk sac tumour, choriocarcinoma, teratoma, often mixed). The rest are sex cord-stromal tumours (Leydig and Sertoli cell tumours) and, in older men, lymphoma.

5 types to tell apart
Seminoma
Sheets of uniform germ cells resembling primordial germ cells; a fleshy, well-demarcated mass. Peak in the fourth decade; AFP is not raised.
Non-seminomatous germ cell tumours
Embryonal carcinoma, yolk sac tumour, choriocarcinoma and postpubertal-type teratoma, usually mixed; a varied, haemorrhagic mass. Peak in the third decade; AFP or hCG often raised.
Germ cell tumours not derived from GCNIS
Spermatocytic tumour (formerly spermatocytic seminoma) in older men, and prepubertal-type teratoma and yolk sac tumour in young children.
Sex cord-stromal tumours
Leydig cell and Sertoli cell tumours, mostly benign; Leydig cell tumours can secrete androgens or oestrogens.
Lymphoma
Usually diffuse large B-cell lymphoma; the commonest testicular tumour in men over about 60.

US spelling: tumours → tumors, tumour → tumor.

Normal function

Germ cells, Sertoli cells and Leydig cells

Each lies in the scrotum inside a tough capsule, the tunica albuginea, and is divided into lobules of coiled seminiferous tubules. Along the basement membrane of each tubule, spermatogonia divide and mature towards the lumen into spermatocytes, spermatids and sperm, supported by Sertoli cells. Between the tubules, Leydig cells make testosterone under the control of luteinising hormone (LH).

Sperm pass from the tubules through the rete testis into the and on along the .

The testis develops on the back wall of the abdomen and descends into the scrotum before birth, bringing its vessels with it. The still arises from the aorta, and the testis’s lymph runs back up beside the testicular vessels to the para-aortic (lumbar) nodes near the kidneys, not to the inguinal nodes that drain the scrotal skin.

Point to it on the model
Testis and scrotal skin: different lymph routesSchematic
FeatureTestisScrotal skin
Where it developsBack wall of the abdomen, then descendsSkin of the perineum
ArteryTesticular artery from the aortaExternal pudendal arteries
First lymph nodesPara-aortic (lumbar) nodes near the kidneysSuperficial inguinal nodes

Lymph and blood vessels keep the route set by where an organ first developed.