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Testicular cancer

From Surgopaedia

Risk factors

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  • Seminomas peak in 4th decade, while non-seminomatous germ cell tumours peak in 3rd decade
  • Testicular mal-descent
  • Contra-lateral testicular tumour
  • Klinefelter's syndrome

Pathophysiology

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  • Germ cell tumours (90-95%)
    • Seminoma
      • Homogenous, pinkish cream cut surface
      • Appears to compress neighbouring testicular tissue
      • Oval cells with clear cytoplasm and large, rounded nuclei with predominant acidophilic nucleoli. Sheets of cells resembling spermatocytes are separated by a fine fibrous stroma. Active lymphocytic infiltration suggests a good host response and a better prognosis.
      • Two histological variants:
        • Anaplastic, or
        • Cells that closely resemble different phases of maturing spermatogonia (spermatocytic seminoma)
      • Mainly metastasise via the lymphatics (to para-aortic nodes near the origin of the gonadal vessels), but rarely haematogenous. Inguinal nodes only involved if scrotal skin is involved too.
      • Beta-hCG and LDH can be used as tumour markers, but not AFP
  • Non-seminomatous germ cell tumours
    • Subtypes: (multiple types may exist within a single tumour)
      • Embryonal cell carcinoma - highly malignant tumours that occasionally invade cord structures
      • Yolk sac tumour - secrete AFP
      • Teratoma - contain more than one cell type, with components from ectoderm, endoderm and mesoderm. 'Mature' - well-differentiated tissue elements. 'Immature' - undifferentiated primitive tissues.
        • Testicular tumours in children are usually anaplastic teratomas, presenting before the age of 3. Mostly fatal.
  • Choriocarcinoma - often produces hCG. Highly malignant. Metastasises via both lymphatics and blood.
  • These tumours are generally tiny but can reach the size of a coconut. May not even distort tunica albuginea.
  • Interstitial tumours (1-2%)
    • Typically small, well-circumscribed tumours with a yellow cut surface
    • Uniform and closely-packed cells
    • About 10% are malignant
    • Subtypes:
      • Leydig cell tumours
        • Masculinises
      • Sertoli cell tumours
        • Feminises
  • Lymphoma (3-7%)
  • Other tumours

History

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  • Usually painless lump
  • Heaviness can occur, but pain is rare
  • May simulate epididymo-orchitis/torsion due to acute haemorrhage into the tumour
  • Rarely symptoms of metastatic disease - abdo or chest

Examination

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  • Intra-testicular solid mass
  • Can be a/w hydrocoele
  • Vas never thickened
  • May have gynaecomastia - interstitial tumour
  • 1-2% have bilateral disease at diagnosis

Investigation

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  • USS
  • Staging once confirmed - CT C/A/P
  • AFP and hCG and LDH (reassess a week after orchidectomy if elevated)

Staging

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  • TNM

Management

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  • Radical orchidectomy
    • Inguinal incision
    • Dissect down to inguinal canal
    • Soft clamp across cord
    • Mobilise testis into wound
    • Double transfix and divide at the level of internal ring
  • Seminomas
    • Radiosensitive
    • Also sensitive to platinum-based chemotherapy
  • NSGCT
    • Not radiosensitive, but highly sensitive to bleomycin/etoposide and cis-platinum (BEP)

Prognosis

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  • Seminoma - 95% five year survival if stage I, 70% if higher stage
  • NSGCT - >90% five year survival in early stage, 60% later stage