Testicular Cancer Flashcards

1
Q

What kind of tumours are testicular tumours predominantly?

A

germ cell tumours.

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2
Q

Where do other germ cell tumours commonly arise?

A
  • retroperitoneum

- mediastinum

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3
Q

What is the predominant age bracket for testicular cancer?

how many new cases every year

A
  • 15 to 45 years old

- 2000 cases in the UK

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4
Q

what is the risk factors?

A
  • maldescent of the testes predisposes germ cell tumours
  • testicular atrophy
  • family history
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5
Q

Describe the aetiology of the tumour

A
  • pre-invasive lesion called an “intratubular germ cell neoplasia”
  • when contralateral testis is small it should be biopsied
  • treat with radiotherapy as it eventually turns into cancer
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6
Q

1) Describe the histology in 60% of cases

2) Describe the histology of the other 40%

A
  • Non-seminomatous germ cell tumours (NSGC1)
  • Seminomas

Note that rare ones include combined (seminoma / non-seminoma), yolk sac tumours,

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7
Q

where is the common spread of seminomas? and how?

A
  • via lymphatics to para-aortic nodes (reflects the embryological origin from para-renal tissue)
  • Blood borne spreads to lungs, liver, bone, brain
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8
Q

How might the patient present?

A
  • painless testicular swelling
  • in metastasis:
    > cough/ dyspnoea due to lung mets
    > low- back pain due to para- aortic involvement
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9
Q

What imaging/ bloods?

A
  • testicular ultrasound mandatory (differentiates solid from fluid filled masses)
  • beta- HCG and AFP
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10
Q

which marker is raised in both seminomatous and non-seminomatous tumours?

A
  • B-HCG (in 75% of patients)

- AFP only raised in presence of non- seminomatous elements

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11
Q

What other marker can be used and how useful is it?

A
  • Lactate dehydrogenase useful in assessing prognosis, response to treatment and detect relapse
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12
Q

What kind of surgery should be done? and why?

A
  • Orchidectomy done for diagnosis and therapy for localised disease
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13
Q

Why would you do a biopsy of the other testicle? (2)

A
  • cryptorchidism patients
  • history of maldescent
    (increase risk of bilateral disease)
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14
Q

What kind of imaging should be done?

A
  • CT chest, abdo and pelvis

- usually done post- op

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15
Q

Describe the staging system

A

Royal Mardsen staging system:

Stage 1- confined to testicle

Stage 2- involves para-aortic lymph nodes below diaphragm

Stage 3- involves para- aortic lymph nodes above diaphragm

Stage 4- involves visceral mets

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16
Q

Why is the royal marsden grouping system not good?

A
  • does not incorporate useful information from tumour markers
  • led to formation of prognostic grouping
17
Q

Describe the IGCCC

A
  • split into seminoma and non- seminoma
  • Divided into good, medium and poor prognosis
  • incorporating tumour markers, LDH, and the RMG staging system
18
Q

Describe the nature of germ cell tumours

A
  • highly malignant with rapid growth and high metastatic potential
  • generally chemo/ radiosensitive
  • The clinical distinction between a seminoma and a tumour with non-seminomatous elements determines management
19
Q

What is the normal surgical protocol?

A
  • Orchidectomy required for definitive treatment of localised disease
  • should be performed via inguinal canal to stop spread through scrotal tissue planes
20
Q

In metastatic teratoma when is surgery performed?

A
  • surgery performed after chemotherapy for resection of residual mass
  • careful examination of edges is performed to see no tumour, removal prevents regrowth
21
Q

How is adjuvant chemotherapy given?

A
  • Stage 1: carboplatin (seminoma), Non seminoma two cycles of BEP (Bleomycin, etoposide, cisplatin)
    some low risk patients for stage 1 do not have chemo
  • 3-4 cycles of BEP are used in those with more extensive disease
22
Q

What is BEP?

A

Bleomycin, etoposide, cisplatin.

It is very intensive and gives expected rates of neutropenia

23
Q

What is the role of radiotherapy in testicular cancer?

A
  • can be used in conjunction with adjuvant chemotherapy

- for malignant teratoma, radiotherapy to sites of bulky mets used in conjunction with chemotherapy

24
Q

Describe prognostic factors.

A
  • bulky tumour sites carry a worse prognosis
    (the presence of pulmonary mets does not affect prognosis)
  • presence of yolk sac/ vascular/ lymphatic invasion
  • tumour markers (AFP BHCG and LDH associated with poor prognosis)