urology,

Testicular cancer

May 10, 2020

Epidemiology

  • Most common malignancy in males aged 15-44 yo
  • 10% occur in undescended testes, even after orchidopexy

Risk factors:

  • Cryptorchidism
  • infertility
  • family history
  • Klinefelter’s syndrome
  • mumps orchitis

Classification

Classification of testicular tumours including germ cell tumours and sex cord-stromal tumours

Classification of Testicular tumour

Presentation:

  • Usually painless lump
  • Painful lump if bleeds inside or infection
  • Rarely, changes in testicular volume or consistency
  • Longer history in seminoma pt than non-seminoma
  • Signs of metastasis
    • supraclavicular lymph node
    • Dyspnoea from pulmonary mets

Investigations:

  • Bloods: AFP, B-hCG, Lactate dehydrogenase
  • Imaging
    • 1st line: Ultrasound colour Doppler
    • Other: CT abdomen and chest for staging

Seminomous Germ cell tumour

  • Older patients (avg. 40 years)
  • 25% metastasise at presentation
  • Excellent prognosis even with advanced disease (5 year survival of 73%)
  • Tumour marker not typically raise: AFP normal, ↑ HCG (10%), ↑LDH (10%)
  • Strong association with cryptorchidism
  • May present with mass in the undescended testes in the inguinal region or the abdomen

Non-seminomatous germ cell tumours

  • Younger patients (20-30 year olds)
  • Advanced disease = poor prognosis (48% at 5 years)
  • Biomarkers
    • Embryonal carcinoma: ↑AFP /↑B-hCG
    • Yolk sac tumour: ↑AFP characteristic
    • Choriocarcinoma:↑B-hCG characteristic
    • Teratoma: ↑AFP /↑B-hCG

Sex cord-stromal tumour

  • Arise from supportive connective tissue around germ cells
  • Rare, less than 5% of testicular cancer
  • Excellent prognosis after surgical resection
  • Two types of tumour: Leydig cell tumour, Sertoli cell tumour

Lymphoma

  • Most common cause of a testicular mass in males > 60 years old; often bilateral
  • Usually of diffuse large B-cell type

Staging

  • Stage 1: No evidence of metastasis
  • Stage 2: Infradiaphragmatic node involvement (spread via para-aortic nodes)
  • Stage 3: Supradiaphragmatic node involvement
  • Stage 4: Lung involvement (haematogenous)

Management

  • SGCT
    • Orchidectomy (via inguinal approach to prevent lymphatic spread)
    • Extremely radiosensitive
    • NOTE: orchidectomy and radiotherapy cures 95% in stage 1
  • NSGCT
    • Orchidectomy (inguinal approach)
    • 3 cycles of Bleomycin + Etoposide + Cisplatin
  • Follow-up
    • Do close follow up using biomarkers, reviews and self-examination