Siêu thị PDFTải ngay đi em, trời tối mất

Thư viện tri thức trực tuyến

Kho tài liệu với 50,000+ tài liệu học thuật

© 2023 Siêu thị PDF - Kho tài liệu học thuật hàng đầu Việt Nam

Carcinoma of the ovary and Fallopian tube doc
MIỄN PHÍ
Số trang
23
Kích thước
1.4 MB
Định dạng
PDF
Lượt xem
700

Carcinoma of the ovary and Fallopian tube doc

Nội dung xem thử

Mô tả chi tiết

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 iiBaf￾DnJv 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, isasso￾aaccd with buth ovarian and cnddmdrial canitr.

r, 1,-ist-coiii rolled Siiudies have sujy>eMed

1 1 Carcinoma of the ovary antf Fallopian lube

UL>-

Cn

sc. 4C —

& 3D

6

1 20-

O

10

n-

,»"» • "--• \

/ \

pf

/

y

'

.....

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

lite￾time 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 weJl￾ducumenlctl [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^iterec￾lomy, 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

Tải ngay đi em, còn do dự, trời tối mất!