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Testicular Cancer

NICE CKS Scrotal pain and swelling. Last revised: Aug 2024.

Overview of Testicular Cancer Types

This table provides a concise overview and allows direct comparison of various testicular cancer types. Further details are presented in the sections below.

 
Cancer type
Epidemiology
Specific clinical Features
Tumour Markers
Histology Findings
Germ cell tumour
 
 
 
Seminoma
Most common subtype
Majority of post-pubertal tumour
Best prognosis due to slow growth and late metastasis.
Some may secrete β-hCG, leading to gynaecomastia.
  • Normal AFP
  • ↑ β-hCG and ↑ LDH in ~30% of cases
“Fried-egg” appearance and lymphocytic stroma.
Yolk sac tumour
Majority of pre-pubertal tumour
  • ↑↑ AFP (highly significant)
  • Normal β-hCG
  • LDH may be elevated
Gross yellow mucinous cut surface (resemble primitive glomeruli)
Choriocarcinoma
Rare but considered the most aggressive subtype
Almost always secretes β-hCG, often leading to gynaecomastia
  • ↑↑ β-hCG
  • Normal AFP
  •  LDH may be elevated
Contains syncytiotrophoblasts and cytotrophoblasts
Teratoma
Common in children (typically benign)
Rare in adults (can be malignant)
  • Normal AFP
  • Normal β-hCG
  • LDH may be elevated
Contains various tissue types such as teeth, cartilage, bone, and hair
Non-germ cell tumour
 
Leydig cell tumour
Non-germ cell tumours make up ~5% of all testicular tumours (rare)
Secretes testosterone, which can cause precocious puberty in boys
  • NOT associated with elevated tumour marker
Sertoli cell tumour
Secretes oestrogen, which can lead to gynaecomastia

Aetiology

Testicular cancer is the most common solid malignant tumour in young males (15-44 y/o) [Ref]

 

Key risk factors:

  • Cryptorchidism (undescended testis) – most significant risk factor
    • There is an increased risk even after orchiopexy surgery
    • The risk is increased for both the undescended and the contralateral testis and persists after orchidopexy
    • ↑ Risk of germ cell tumour
  • Infertility / subfertility
  • Klinefelter’s syndrome

 

  • Hypospadias
  • Family history of testicular cancer
  • Contralateral testicular tumour

Types and Classification

Testicular cancer is divided into 2 main types, each with its own subtypes

Germ Cell Tumours (95%)

Germ cell tumours can be further divided into:

  1. Seminoma – most common (comparable to ovarian dysgerminoma in women)
  2. Non-seminomas:
    • Teratoma
    • Yolk sac tumour
    • Choriocarcinoma
    • Embryonal carcinoma
    • Mixed germ cell tumour

Non-Germ Cell Tumours (5%)

There are 2 main non-germ cell tumours

  • Leydig cell tumours
  • Sertoli cell tumours

Epidemiology

Testicular tumours are the most common solid malignancy in young men (15-34 y/o)

  • The majority of pre-pubertal tumours are yolk sac tumours (and teratomas)
  • The majority of post-pubertal tumours are seminomas

 

Some other information: [Ref1][Ref2]

  • Seminoma has the best prognosis (slow tumour growth and late metastases)
  • Choriocarcinoma is the most aggressive
  • Teratoma is common in children (typically benign), rare in adults (but can be malignant)

Clinical Features

Local Features

Unilateral testis enlargement / change in shape or texture

  • Classic presentation: hard, irregular mass fixed to the testis
  • Typically painless +/- dull ache or dragging sensation in the scrotum

 

An associated hydrocele is possible

  • In a hydrocele, the testis is typically not palpable, making it hard to feel for any tumours.
  • Therefore, scrotal ultrasound is essential in any new hydrocele in adults to exclude an underlying tumour

Metastasis

Lymphatic spread is most common:

  • Para-aortic (retroperitoneal) lymphadenopathy (→ abdominal mass / pain / discomfort)
  • Supraclavicular lymphadenopathy (Virchow node involvement) – only seen in advanced disease

High-yield anatomy + oncology fact:

  • The penis (and scrotum) primarily drains lymph to the inguinal lymph nodes
  • The testis primarily drains lymph to the para-aortic lymph nodes

Most common distant site of metastasis: lungs

Endocrine-Mediated Features

Only seen in certain tumours (mainly non-germ cell tumours):

  • Gynaecomastia is seen in:
    • Choriocarcinoma and embryonal carcinoma almost always secrete β-hCG, and sometimes seminomas
    • Sertoli cell tumours (secrete oestrogen)

 

  • Leydig cell tumours secrete testosterone → precocious puberty in boys (prominent external genitalia, pubic hair growth, mature masculine voice, accelerated skeletal and muscle growth)

Investigation and Diagnosis

Imaging

1st line: scrotal ultrasound [Ref]

  • A solid intratesticular mass is malignant until proven otherwise
  • Hypoechoic lesion compared with normal testicular tissue
  • Irregular margins

2nd line: MRI

Tumour Markers

Testicular cancer type AFP β-hCG LDH
Seminoma Normal ↑ in ~30% cases ↑ in ~30% cases
Yolk sac tumour ↑↑ Normal May be elevated
Choriocarcinoma Normal ↑↑ May be elevated
Teratoma Normal Normal May be elevated

Non-germ cell tumours (i.e. Sertoli and Leydig cell tumours) are NOT associated with elevated tumour markers

Key patterns:

  • ↑ AFP → yolk sac tumour
  • ↑ β-hCG → choriocarcinoma (marked elevation) and some seminomas
  • ↑ LDH → non-specific

Histology

Note that neither imaging nor tumour markers can provide a definitive diagnosis; orchiectomy for histology remains the primary diagnostic and therapeutic intervention [Ref]

 

Some key histological findings (simplified for exam purposes): [Ref]

  • Seminoma → fried-egg appearance (large cells with clear cytoplasm and round nucleus) + lymphocytic stroma
  • Teratoma → contains teeth, cartilage, bone, hair
  • Choriocarcinoma → contains syncytiotrophoblasts and cytotrophoblasts
  • Yolk sac tumour → gross yellow mucinous cut surface with Schiller-Durval bodies on microscopy, which resemble primitive glomeruli

Management

All patients require radical inguinal orchiectomy (for diagnostic and therapeutic purposes) [Ref1][Ref2]

 

Additional management: [Ref1][Ref2]

  • Stage 1 cases can be managed with active surveillance and no additional management
  • Higher-risk  / advanced disease may need adjuvant chemotherapy and retroperitoneal lymph node dissection

References

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