Testicular cancer (module 5 cont.) Flashcards

1
Q

epidemiology of testicular cancer

A

most common cancer for aged 15-34 men

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2
Q

major risk factors of testicular cancer

A

cryptorchidism (increases risk x6)
previous Hx of testicular cancer)
atrophy eg. mumps, orchitis, trauma
genetic syndromes especially Klinefelter’s disease

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3
Q

is secondary testicular cancer common?

A

no, it is rare
most testicular cancers are primary

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4
Q

types of testicualr cancer (classification)

A

Germ cell tumours (GCT)
1. seminoma (half of cases)
2. non seminomatous germ cell tumours (NSGCT)
Non Germ Cell Tumours (Non-GCTs)
1. lymphoma (common in >50yo)
2. leydig cell tumours
3. Sertoli cell tumours
4. other

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5
Q

which cells produce testosterone

A

leydig cells

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6
Q

which cells nourish the sperm

A

Sertoli cells

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7
Q

which type of testicualr cancer represents half of all cases

A

GCT Seminoma

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8
Q

what are the Non-GCT testicular tumours

A
  1. lymphoma (common in >50yo)
  2. leydig cell tumours (cells that make testosterone)
  3. Sertoli cell tumours (cells that nourish the sperm)
  4. other
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9
Q

What are the Non Seminomatous Germ Cell Tumours (NSGCTs)

A
  • yolk sac
  • embryonal
  • teratoma
  • choriocarcinoma
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10
Q

clinical features of testicular cancer presentation

A

usually presents as a painless lump
patient will frequently recall a non-significant testicular trauma or event (this is a red herring)
occasionally may present with acute testicular pain, hydrocoele, or metastatic disease

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11
Q

associated signs and symptoms of testicular cancer

A

weight loss
seizures
cough/haemoptysis
abdominal distension/pain
swelling of ankles
occasionally may have features of hormone production (eg. choriocarcinoma, leydig)

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12
Q

what are features of hormone production?

A

gynaecomastia
altered libido etc.

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13
Q

when will tumour markers be raised

A

50% of tumours
90% of advanced tumours

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14
Q

when should tumour markers be monitored

A

before, during and after treatment

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15
Q

alpha feto protein (a-FP)

A

half life of 5-7 days
produced by foetal gut, liver and yolk sac
elevated in liver, pancreatic, stomach and lung tumours also
also raised in normal pregnancy and benign liver disease

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16
Q

b-HCG

A

half life of 24-36 hours
it implies syncytiotrophoblastic component (choriocarcinoma)
produced by placental tissue
is produced by many subtypes especially choriocarcinoma
elevated in upper GI, lung and bladder tumours also

17
Q

LDH

A

non specific tumour markers
measures burden of metastatic disease

18
Q

CT chest/abdomen/pelvis

A

used to stage the disease/check for mets and nodes

19
Q

LDH used for testicular cancer is best used for measuring

A

burden of metastatic disease

20
Q

b-HCG is especially raised by

A

choriocarcinoma

21
Q

staging of testicular cancer

A

uses Tumour Node Metastasis (TNM)
testicualr cancer is the only malignancy that also uses S stage (Serum markers) by measuring both the presence and level of serum markers

22
Q

what are the serum markers for testicualr cancer

A

a-FP
b-HCG
LDH

23
Q

treatment for testicular cancer

A

removal of the affected testicle is urgent

24
Q

why is it so urgent to remove the cancer affected testicle

A

Cancer of the testis has one of the fastest doubling times of all malignancies
patient should be referred to a urologist without delay

25
process of removing the testicle
urologist removes testicle and cord through inguinal canal, rather than the scrotum enables early control of venous drainage prior to manipulating avoids seeding the scrotal tissues with cancer cells removes initial lymphatic drainage pathway of testicle(via cord)
26
orchidectomy
removal of testicle
27
most patients have _ after orchidectomy
chemotherapy or radiotherapy seminoma are very radiosensitive and chemosensitive non-seminomas are very chemosensitive
28
prior to treatment patents should be offered
sperm banking patient may be offered a prosthesis (artificial testicle) by their urologist
29
prior to treatment what else should be done
serum markers should be sent patients disease should be staged (CT abdominal/pelvis/chest)
30
after orchidectomy
patients require prologued follow up (10y+) recurrence can occur many years down the track
31
prognosis of testicular cancer
follows from tumour subtype and staging advances in chemo have improved survival high cure rates
32
what type of testicular cancer has the poorest prognosis
non-seminoma with high markers and visceral metastasis fare poorest
33
long term effects of testicular cancer treatment
bleomycin chemotherapy may cause long fibrosis etoposide chemotherapy may cause hair loss radiotherapy is associated with secondary malignancy risk orchidectomy may have psychological impact
34
main risk factor of testicular cancer
undescended testes