Testicular cancer
Appearance
Risk factors
[edit | edit source]- 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
[edit | edit source]- 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
- Seminoma
- 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.
- Subtypes: (multiple types may exist within a single tumour)
- 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
- Leydig cell tumours
- Lymphoma (3-7%)
- Other tumours
History
[edit | edit source]- 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
[edit | edit source]- 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
[edit | edit source]- USS
- Staging once confirmed - CT C/A/P
- AFP and hCG and LDH (reassess a week after orchidectomy if elevated)
Staging
[edit | edit source]- TNM
Management
[edit | edit source]- 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
[edit | edit source]- Seminoma - 95% five year survival if stage I, 70% if higher stage
- NSGCT - >90% five year survival in early stage, 60% later stage