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Carcinoma of the ovary and Fallopian tube doc
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c It a pi e r
Carcinoma of the ovary and
Fallopian tube
CanDEr of Ihe ovary 143 Cance<ofrliG Fallopian lube 152
OVERVIE W
of tha ovary is mosl common ii1
the 'ijeamiyridtirjri:.c-t 111 fc world There die lustundsr 6000 case!, each ysar in Ibs UK
Wb ilfl ffiB incidence of ovarian cancer is si mi l&r to thai of endometri urn aridcf cervix, more women die from ovar&n cancer than
fro-;1
^drtinnma nl fl>E.cerm anfl body of fbe ut?rue combined.
Most wanan temours are ol epithelial (irigm. Tlie&E jre Mre befure Hit age of 35'years buttle incider-DE increases i<iitb age
IG a peak in tbe 5Q-7Q-ypar-i;ld aae gmup (Fig. 13.1 j. Mo^tspltlieli?! amours art not discovered until they hava spread widely
Some at fiiesE "nvariai'' lumouis prnoabiy arise frnm the fallopian ^bo.tumnurF of whmh arn .Dually racogriized only v/tien at a
relatively early ^tage Surely and rjhemufherapy. mdirily v<A\\ carboplafir, DI cisplalm and paciilaxel, form lire mapnsfay nf iiBafDnJv 3 pEri:Hnln;nvanan cjnggrs are seen mwnm fin you ngerthan 35 yea rs and most of these are non ^jjltnelial cancers
a& yerm ^11 luinuurs ^n conlrasf To epithelial fumpurs. germ DE!! lumouis can be Ireaterjvpry successfully 'Vifh
Ferlilitycanoffen bu^jnaerved
CANCER OF THE OVARY
Aeliology "
Incessant uunlation' theory
Epithelial liimaura arc mosl trcqucntlv
wilb nulli|iari[y, jr) t&tly rncnjrdic, ^ late age at
menopju*,e and j high esrimjTeJ number of vewri
ol o^iiliition. Grill contraceptive use reduces the rkk
iouifuld (The Cancer and Steroid Hormont Sludy,
1997). lk>ive\er, even without urdl Lonlidceplives,
inciej<.ingage at first birtli reduces tht risk of ovarian
cancer. This and other anomialici ca^ldcubt upon the
'incessant ovulalicii* theor,1
.
Suhfertititylreatmenr
Subfertiliry, especially when il is unexplained, isassoaaccd with buth ovarian and cnddmdrial canitr.
r, 1,-ist-coiii rolled Siiudies have sujy>eMed
1 1 Carcinoma of the ovary antf Fallopian lube
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1 20-
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10-14 25-33 40-44 55-74 >94
.Age iy£arsj
Figure 13.1 The Incidence D! ovarian cancers England anO
Wales iQffice of Population Censuses and Surveys, 1985|.
there might possibly bed link between ovarian cancer
and prolonged attempts at induction of ovulalion
(VenneraL,
Genetic factors
F3inilial ovarian cancer
• Familial ovarian cancer is rarfl -5-10%
• Suggflstive history
• fttlea5tt'"ofir&t-rtogree relatives mill u.'diidn
or ti)loretlal carcmama
• Casss usually diaynoaed before 50 vFarsotagH
» Defective genss include 0flC4f and 8RCA2
t Th* risk of ovarian cancfii 1.40%) in Ihese lamilles is
less than the r&k of breast cancer {80%|
» Genetic testing cannot guarantee to defect all
genes
Familial ovarian cancer
There is a family hinor? in between 5 and HI per cent
of ^omtn ivith epithelial nvarian tantcrs -
serous adenocardoornas (Kafipr/^k ul jl.t
Av-umaii with one affectf d dose relati\r
e has a lifetime
ctsk of 2-5 per cent, twice tht ribk in the general
popuklion. With two affected clost reldLivt^ lhiL
litetime risk increases to 30-10 per cent iPonder, 19y4|.
A partieular feature of familial unciT:> is the i elativelv
early age dl ™hich thcv occur
Most of these families rtl>o have ia&C;> of breast or
(.olorectal cancer in the family. 'Itie defective gt;ne
in (he breast/ovary families is most commonly the
luinoiir-s.uppn:$ior gene BRCAl (#1 pei cent).
BRCA2 is defective in aboiil 14 ntr^unl. Families Wffl
i.olorettal cancer have defects in the J3NA repair genes
but this is seldom found m association with tamilial
ovarian cancer (Kaflpr/ak el al., 1999). A woman
who has inheuied a detective RK.CA1 gene hi a weJlducumenlctl [dmilv ha;> a 60 per cent risk of breast
cancer by .'ill years nl a^ and an &0 pel cent lifetime
risk. However, the risk of ovarian earlier is much
lower, he ing nearer JO per cent
Management ot women with a family
history of Dvarian cancer
Genetic testing for BKCAl is. now pos&iblc bill is
impracticable and unreliable because mutations are
found far lesi often than expected, even in
with a strong family bislorv. There jre very
able problems in interpreting the resulis in
with only one or li^o aftected relatives There maybe
a spectrum of inulaliyrii, isith verv different lei'els of
risk. Ei'en a negative test resnlr nid\ nol provide ihe
expflded reassurance.
Once idenlilied vvilh the help or a clinical geneticist,
women with a hiph ri^k of ovarian and" bica&t cancer
arc difiitult to advise. The main risk is bre&sl i-uiLerh
but prophyldclk, bilalcral mastectoniy ifl a very drastic
s^tep for any 'voilian 10 Lake. None of the available
&tre.emng tests for ovarian cancer is vurv effective, and
false-positive result* can result in unnecessary surgery.
Annual ovarian ullrasonography with colour-flow
Doppler studies and serum CA 1Z5 estimation evert
6-12 months are recommended, bui it is unierlaJB
how much pro Let Lion this offei^. Prophylactic hilat
eral oopho recto in y, iiiually combined v-nth hv^itereclomy, i> recommended for dejrh ilelinuil h^h-rnt
women aflcr Completion of their family at aN«*]
45 years of age (K,ii|ir^Hk ul al., 1999). This does, nol
recnyvt the nsi; entirely, as c.lrcillonn of the pcrfl
toneum has occurred after this procedure.
Class if i callon of nujrian tumouis
Ovarian inmoiirb lan be solid or cystic. They nuyhf
benign r>r ma%nanl antl [n addition there are thc«
that, while having
lack am' evidence ol
called borderline lurai
ovarian |lin
orig
coid gonadal tyj>e laiso
Oi sex cord me.senchyi
«A cord iTie^nchmal
Simplified hi stole
ovarian tumours
I Connirnii apfilielial hi
A Serous rumour
B MuGifious tumour
C. EniJumetmid lumui
D Clear cell
f U ill 'fferpniiated care
II Sex cord stromal turn
A Grgnulo&dsn'niiac
fl Andrablas'Oma: SH
III Germ cell
A Dy&ngrniincma
C Embiyonalcelltumi
E. Teratuma
F Mlx
IV MaiasiaLc
Pathology of ep it he
cpid
ofteji rfM^i
ihe dfgr.ee of dif
vival, fflfLt-pt in the mo
mniuui-3 tend [o be a^s<i
and a bedii progrn
Hin'rv^l between differa
• .c i n on i and
ajsociated with an