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ColposcopicNomenclature
22.
JahrestagungderArbeitsgem
einschaft
fürZervixpathologie und
Kolposkopie AG CPC
walterprendiville
IFCPC
Evolution of terminology
 Progress evolves from clear understanding of
existing research and experience and clarity of
terminology is fundamental to this
 It is not possible to compare apples with oranges
or to understand precisely published evidence
where terminology is unclear
 cone biopsy (UK) with cone biopsy (US),
 Height
 Depth
 atypia
Practice variation in OB/GYN
 C Section, 3rd stage of labour
 Antenatal V/E
 Hysteroscopy
 Management of Endometrial Cancer
 Colposcopy
Evolution of colposcopy
 First colposcope :: Hamburg
 Early colposcopic skills
 image recognition,
 diagnosis of HSIL,
 recognition of microinvasion
 Late colposcopic skills =
 discriminating between normal and
abnormal
 facilitating precise treatment
MODERN COLPOSCOPY
Objective and easily achieved
skills through structured training as
part of a QA service
Risk assessment using biomarkers
and patient characteristics
Modified treatment techniques
Variation in colposcopy and
treatment
 Colposcopy is not a defined entity and performs
differently in different settings
 Treatment is not a defined entity and produces
different results and complications in different
settings
 Nomenclature varies in interpretation and we
therefore can not easily compare practice
Colposcopy is not a defined entity
and performs differently in
different settings
Colposcopy performed by variably
trained colposcopists who do not
adhere to strict quality assured
practice or self audit is completely
different to colposcopy in a region
where QA, adherence to best
evidence guidelines and CME are
the norm’
Why is there such a difference in
colposcopic reward
ALTS 11.5% CIN 2+ after a normal colposcopy
72.3% of CIN2+ found at original colposcopy
UK NHS study 5.3% CIN2+ after a normal colposcopy
94.6% of CIN2+ found at original colposcopy
Why is there such a difference in
colposcopic reward
In the UK NHS CSP colposcopy setting the risk of
missing high grade disease appears to be much lo
than in the equivalent US setting
Why is this?
Why is there such a difference in
colposcopic reward
In the UK there exists
A comprehensive training programme
Preceptor based
Strict number of cases under supervision
and subsequently unsupervised
Ongoing assessment during training
Exit exam (OSCE)
30% failure rate
Why is there such a difference in
colposcopic reward
In the UK
Colposcopy practice
Devoted colposcopy clinics
All women referred with a suspected
abnormality
Rate of CIN relatively high
Not rewarded according to
procedures performed
Comprehensive audit of practice
Treatment is not a defined entity
and produces different results and
complications in different settings
 The resection of a small type 1 TZ is easy and
associated with minimal morbidity
 The resection of a large Type 3 TZ is difficult
and associated with significant short and
long term morbidity
13
Preterm delivery (<37W): Excision vs no treatment ~heigth
Height < 10mm
Risk ratio
.1 .2 .5 1 2 5 10
Risk ratio (95% CI)
Raio, 1997 0.52 ( 0.06, 4.83)
Sadler, 2004 0.99 ( 0.57, 1.72)
Samson, 2005 3.02 ( 1.65, 5.53)
Nohr, 2007 0.83 ( 0.21, 3.25)
Overall 1.32 ( 0.59, 2.95)
Risk ratio
.1 .2 .5 1 2 5 10
Raio, 1997 4.64 ( 1.20, 17.88)
Sadler, 2004 1.64 ( 1.13, 2.37)
Samson, 2004 3.84 ( 1.66, 8.88)
Nohr, 2007 2.46 ( 1.45, 4.16)
Overall 2.39 ( 1.55, 3.69)
Height >= 10mm
Risk ratio (95% CI)
RiskofpretermlabourafterLLETZDoessizematter,
Aretrospectivestudy
Khalid S, Dimitriou E &Prendiville W
BSCCP (poster) 2009
Excision dimensions and preterm labour
Khalid S, Dimitriou E & Prendiville W2009
 1999 - 2002
 Obstetric &Colpo
databases
 353 pregnancies in
women after LLETZ
Excision dimensions and preterm labour
Khalid S, Dimitriou E & Prendiville W2009
Increased risk of
preterm labour if
specimens larger
than 6 cubic cms
RR 3.17, 95%CI 1.56 -
6.38
Excision dimensions and preterm labour
Khalid S, Dimitriou E & Prendiville W2009
Increased risk of
preterm labour if
specimens thicker
than 12 mms
RR 3.05, 95%CI 1.37 -
7.08
2011 IFCPC colposcopic terminology of the cervix(draft – May 2011)
SCJ visualization: complete/partial/none
Adequate/inadequate for the reason … (i.e.: cervix
obscured by inflammation, bleeding, scar)
Basic definitions
Deciduosis in
pregnancy,
Atrophic epithelium,
Nabothian cyst,
Gland (crypt)
openings
Original squamous epithelium,
Columnar epithelium
including ectopy,
Transformation zone types 1,2,3
Normal colposcopic
findings
Inside or outside the T-zone,
Numberof cervical quadrantsthe l esioncovers ,
Size of the lesion in percentage of cervix,
Lugol’s staining (Schiller’s test): stained/non-stained
General
principles
Abnormal
colposcopic
findings
Fine mosaic,
Fine punctation
Fine aceto-white epitheliumGrade 1
(Minor)
Rapid appearance of
acetowhitening,
Cuffed gland (crypt)
openings
Sharp border,
Exophytic
lesion,
Inner border
sign,
Ridge sign
Dense aceto-
white
epithelium,
Coarse mosaic,
Coarse
punctuation,
Leukoplakia
Grade 2
(Major)
Atypical vessels, fragile vessels, Irregular surface,
Necrosis, Ulceration (necrotic), tumor/gross neoplasm
Suspicious for invasion
Stenosis,
Congenital anomaly,
Post treatment
consequence
Endometriosis,
Condyloma,
Polyp
(Ectocervical/
endocervical)
Erosion
(traumatic)
Inflammation
Miscellaneous finding
Nomenclature committee 2011
 Jim Bentley - Canada
 Jacob Bornstein – Israel (Chairman of the
Committee)
 Peter Bosze – Hungary
 Frank Girardi – Austria
 Hope Haefner - USA
 Michael Menton – Germany
 MyriamPerrota – Argentina
 Walter Prendiville – Ireland
 Peter Russell - Australia
 Mario Sideri – Italy
ThenewIFCPCnomenclatureforcervix,
(vaginaandvulva)WWW.IFCPC.ORG
Bornstein et al
Amer J Obstet Gynecol
Vol 120 No 1 July 2012
2011 committee considerations
 Establish an evidence base
 KeratosisvLeukoplakia
 Inside/outside TZ
 Size of lesion
 Inner border and ridge signs
 Treatment types
Abnormal vessel
Coarse punctation
Colposcopic features suggestive of
highgrade disease (major change)
 A generally smooth surface with an sharp outer border.
 Dense acetowhite change, that appears early and is slow to resolve; it may
appear oyster white.
 Iodine negativity, a yellow appearance in a previously densely white
epithelium.
 Coarse punctation and wide irregular mosaics of differing size.
 Dense acetowhite change within columnar epithelium may indicate
glandular disease.
New S C Junction
Columnar
Original
squamous epithelium
Crypt openings
Dr SC Quek
Polyps
Size of cervical lesions
 Kierkegaard 1995: lesion size has independent
predictive value
 Ferris 2005: Size of cervical lesions correlates directly with
the severity of disease.
 Hopman et al. 1995 reported an inter-observer
agreement rate of 68% when evaluating colposcopic
photographs for lesion size.
 Hammes 2007: Lesions >50% of cervix had higher
probability for high-grade lesion / carcinoma (OR, 3.45).
Prof Jacob Bornstein
New colposcopic sign- Ridge sign
An opaque acetowhite ridge
at the squamocolumnar junction
Prof Jacob Bornstein
Scheungraber C, Koenig U, Fechtel B, Kuehne-Heid R, Duerst M, Schneider A. The colposcopic feature ridge sign is associated with the
presence of cervical intraepithelial neoplasia 2/3 and human papillomavirus 16 in young women. J Low Genit Tract Dis. 2009;13(1):13-
16.
A New Scoring System
Strander et al 2005
 Designed to evaluate a scoring system for high
grade lesions
 297 examinations of women referred for
colposcopy, Department of Obstetrics and
Gynecology, Göteborg, Sweden
 First Scoring system to incorporate lesion size as a
variable
 Subsequently validated at the Royal Free
Aceto-white
colour
Iodine stainingVascular Pattern
Peripheral Margins
0 1 2 Score
ACETO UPTAKE Zero or transparent Shady, Milky
(not transparent
not opaque)
Distinct, opaque
white
MARGINS/
SURFACE
Diffuse Sharp but
irregular, jagged,
“geographical”
Satellites
Sharp and even,
difference in
surface level incl
“cuffing”
VESSELS Fine, regular Absent Coarse or atypical
LESION SIZE <5mm 5-15mm or 2
quadrants
>15mm or 3-4
quadrants or
endocervically
undefined
IODINE STAINING Brown Faintly or patchy
yellow
Distinct yellow
Total score 10
The transformation zone
 A Type 1 transformation zone is completely
ectocervical and fully visible, and may be small
or large
 A Type 2 transformation zone has an
endocervical component, is fully visible, and
may have an ectocervical component that may
be small or large
 A Type 3 transformation zone has an
endocervical component that is not fully visible
and may have an ectocervical component that
may be small or large
Type 1
• Completely
ectocervical
• Fully visible
• small or large
Transformation Zone
Classification
SBX1739_3
Histology CIN1
Cytology LSIL,CIN 1;Atyp
endocerv,
neopl
Carcinogenic
HPV
16, 58, 66
Age 28
Category Mario Walter
SCJ visibility Fully Visible Fully Visible
TZ type Type 1 - Small Type 1 - Small
TZ pattern Abnormal Grade 1 Abnormal Grade 2
Image quality Good Good
Jim Usha
Partially Visible Partially Visible
Type 2 - Large Type 1 - Large
Abnormal Grade 2 Normal
Good Limited
SBX1759_3
Histology CIN3
Cytology LSIL,CIN 1;Atyp
endocerv,
neopl
Carcinogenic
HPV
16, 51
Age 25
Category Mario Walter
SCJ visibility Partially Visible Fully Visible
TZ type Type 2 - Small Type 1 - Small
TZ pattern Abnormal Grade 2 Abnormal Grade 1
Image quality Good Limited
Jim Usha
Fully Visible Fully Visible
Type 1 - Small Type 1 - Small
Abnormal Grade 1 Normal
Good Good
Type 2
• has
endocervical
component
• Fully visible
• may have
ectocervial
component
which may be
small or large
Transformation Zone
Classification
SBX1842_1
Histology CIN3
Cytology HSIL,CIN
3;Adeno, NOS
Carcinogenic
HPV
16, 18
Age 30
Category Mario Walter
SCJ visibility Partially Visible Partially Visible
TZ type Type 3 - Small Type 2 - Small
TZ pattern Abnormal Grade 2 Suspicious for invasion
Image quality Limited Limited
Jim Usha
Fully Visible Fully Visible
Type 2 - Small Type 1 - Small
Abnormal Grade 2 Abnormal Grade 2
Good Limited
Transformation Zone
Classification
Type 3
• has endocervical
component
• is not fully visible
• may have
ectocervial
component which
may be small or
large
SBX1216_2
Histology CIN3
Cytology HSIL,CIN 2;Adeno
in situ (AIS)
Carcinogenic HPV 31
Age 21
Category Mario Walter
SCJ visibility Not Visible Partially Visible
TZ type Type 3 - Small Type 2 - Small
TZ pattern Abnormal Grade 1 Abnormal Grade 2
Image quality Good Good
Jim Usha
Not Visible Fully Visible
Type 3 - Small Type 1 - Large
Abnormal Grade 2 Abnormal Grade 1
Good Good
SBX1774_1
Histology CIN3
Cytology HSIL,CIN
3;Adeno, NOS
Carcinogenic
HPV
16
Age 47
Category Mario Walter
SCJ visibility Not Visible Partially Visible
TZ type Type 3 - Small Type 2 - Small
TZ pattern Abnormal Grade 2 Suspicious for invasion
Image quality Good Good
Jim Usha
Not Visible Not Visible
Type 3 - Small Type 3 - Large
Suspicious for invasion Suspicious for invasion
Good Good
SBX1928_1
Histology CIN3
Cytology HSIL,CIN
3;Adeno, NOS
Carcinogenic
HPV
16, 39
Age 30
Category Mario Walter
SCJ visibility Not Visible Not Visible
TZ type Type 3 - Small Type 3 - Small
TZ pattern Abnormal Grade 2 Abnormal Grade 2
Image quality Good Good
Jim Usha
Partially Visible Fully Visible
Type 3 - Small Type 1 - Small
Abnormal Grade 1 Abnormal Grade 1
Good Good
The BSCCP invites
you to the
15th World
Congress
On behalf of
IFCPC
In London
26-30th May 2014
www.IFCPC2014.
www.IFCPC2014.com
Bemvindo a Londres al 26de30 de Mayo
Queen Elizabeth II conference centre
Westminster Hall for the plenary sessions
Up to 2160 delegates
2070 m2 exhibition space
¡NosvemosemLondres ! 2014
St James’s Park – 5 minutes walk from venue
Shopping...................
Covent Garden, London
National Institute of Medical Research- The biology of HPV and molecular markers
Wolfson Institute of Preventive of Medicine- Screening across the world
St Thomas’s Hospital – Improving Cytology
Institute of Women’s Health
Imperial College
Post Congress Seminars
See you in London

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3 prof walter colposcopic

  • 2. Evolution of terminology  Progress evolves from clear understanding of existing research and experience and clarity of terminology is fundamental to this  It is not possible to compare apples with oranges or to understand precisely published evidence where terminology is unclear  cone biopsy (UK) with cone biopsy (US),  Height  Depth  atypia
  • 3. Practice variation in OB/GYN  C Section, 3rd stage of labour  Antenatal V/E  Hysteroscopy  Management of Endometrial Cancer  Colposcopy
  • 4. Evolution of colposcopy  First colposcope :: Hamburg  Early colposcopic skills  image recognition,  diagnosis of HSIL,  recognition of microinvasion  Late colposcopic skills =  discriminating between normal and abnormal  facilitating precise treatment
  • 5. MODERN COLPOSCOPY Objective and easily achieved skills through structured training as part of a QA service Risk assessment using biomarkers and patient characteristics Modified treatment techniques
  • 6. Variation in colposcopy and treatment  Colposcopy is not a defined entity and performs differently in different settings  Treatment is not a defined entity and produces different results and complications in different settings  Nomenclature varies in interpretation and we therefore can not easily compare practice
  • 7. Colposcopy is not a defined entity and performs differently in different settings Colposcopy performed by variably trained colposcopists who do not adhere to strict quality assured practice or self audit is completely different to colposcopy in a region where QA, adherence to best evidence guidelines and CME are the norm’
  • 8. Why is there such a difference in colposcopic reward ALTS 11.5% CIN 2+ after a normal colposcopy 72.3% of CIN2+ found at original colposcopy UK NHS study 5.3% CIN2+ after a normal colposcopy 94.6% of CIN2+ found at original colposcopy
  • 9. Why is there such a difference in colposcopic reward In the UK NHS CSP colposcopy setting the risk of missing high grade disease appears to be much lo than in the equivalent US setting Why is this?
  • 10. Why is there such a difference in colposcopic reward In the UK there exists A comprehensive training programme Preceptor based Strict number of cases under supervision and subsequently unsupervised Ongoing assessment during training Exit exam (OSCE) 30% failure rate
  • 11. Why is there such a difference in colposcopic reward In the UK Colposcopy practice Devoted colposcopy clinics All women referred with a suspected abnormality Rate of CIN relatively high Not rewarded according to procedures performed Comprehensive audit of practice
  • 12. Treatment is not a defined entity and produces different results and complications in different settings  The resection of a small type 1 TZ is easy and associated with minimal morbidity  The resection of a large Type 3 TZ is difficult and associated with significant short and long term morbidity
  • 13. 13 Preterm delivery (<37W): Excision vs no treatment ~heigth Height < 10mm Risk ratio .1 .2 .5 1 2 5 10 Risk ratio (95% CI) Raio, 1997 0.52 ( 0.06, 4.83) Sadler, 2004 0.99 ( 0.57, 1.72) Samson, 2005 3.02 ( 1.65, 5.53) Nohr, 2007 0.83 ( 0.21, 3.25) Overall 1.32 ( 0.59, 2.95) Risk ratio .1 .2 .5 1 2 5 10 Raio, 1997 4.64 ( 1.20, 17.88) Sadler, 2004 1.64 ( 1.13, 2.37) Samson, 2004 3.84 ( 1.66, 8.88) Nohr, 2007 2.46 ( 1.45, 4.16) Overall 2.39 ( 1.55, 3.69) Height >= 10mm Risk ratio (95% CI)
  • 15. Excision dimensions and preterm labour Khalid S, Dimitriou E & Prendiville W2009  1999 - 2002  Obstetric &Colpo databases  353 pregnancies in women after LLETZ
  • 16. Excision dimensions and preterm labour Khalid S, Dimitriou E & Prendiville W2009 Increased risk of preterm labour if specimens larger than 6 cubic cms RR 3.17, 95%CI 1.56 - 6.38
  • 17. Excision dimensions and preterm labour Khalid S, Dimitriou E & Prendiville W2009 Increased risk of preterm labour if specimens thicker than 12 mms RR 3.05, 95%CI 1.37 - 7.08
  • 18. 2011 IFCPC colposcopic terminology of the cervix(draft – May 2011) SCJ visualization: complete/partial/none Adequate/inadequate for the reason … (i.e.: cervix obscured by inflammation, bleeding, scar) Basic definitions Deciduosis in pregnancy, Atrophic epithelium, Nabothian cyst, Gland (crypt) openings Original squamous epithelium, Columnar epithelium including ectopy, Transformation zone types 1,2,3 Normal colposcopic findings Inside or outside the T-zone, Numberof cervical quadrantsthe l esioncovers , Size of the lesion in percentage of cervix, Lugol’s staining (Schiller’s test): stained/non-stained General principles Abnormal colposcopic findings Fine mosaic, Fine punctation Fine aceto-white epitheliumGrade 1 (Minor) Rapid appearance of acetowhitening, Cuffed gland (crypt) openings Sharp border, Exophytic lesion, Inner border sign, Ridge sign Dense aceto- white epithelium, Coarse mosaic, Coarse punctuation, Leukoplakia Grade 2 (Major) Atypical vessels, fragile vessels, Irregular surface, Necrosis, Ulceration (necrotic), tumor/gross neoplasm Suspicious for invasion Stenosis, Congenital anomaly, Post treatment consequence Endometriosis, Condyloma, Polyp (Ectocervical/ endocervical) Erosion (traumatic) Inflammation Miscellaneous finding
  • 19. Nomenclature committee 2011  Jim Bentley - Canada  Jacob Bornstein – Israel (Chairman of the Committee)  Peter Bosze – Hungary  Frank Girardi – Austria  Hope Haefner - USA  Michael Menton – Germany  MyriamPerrota – Argentina  Walter Prendiville – Ireland  Peter Russell - Australia  Mario Sideri – Italy
  • 21. 2011 committee considerations  Establish an evidence base  KeratosisvLeukoplakia  Inside/outside TZ  Size of lesion  Inner border and ridge signs  Treatment types
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  • 27. Colposcopic features suggestive of highgrade disease (major change)  A generally smooth surface with an sharp outer border.  Dense acetowhite change, that appears early and is slow to resolve; it may appear oyster white.  Iodine negativity, a yellow appearance in a previously densely white epithelium.  Coarse punctation and wide irregular mosaics of differing size.  Dense acetowhite change within columnar epithelium may indicate glandular disease.
  • 28. New S C Junction Columnar Original squamous epithelium Crypt openings
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  • 35. Size of cervical lesions  Kierkegaard 1995: lesion size has independent predictive value  Ferris 2005: Size of cervical lesions correlates directly with the severity of disease.  Hopman et al. 1995 reported an inter-observer agreement rate of 68% when evaluating colposcopic photographs for lesion size.  Hammes 2007: Lesions >50% of cervix had higher probability for high-grade lesion / carcinoma (OR, 3.45). Prof Jacob Bornstein
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  • 38. New colposcopic sign- Ridge sign An opaque acetowhite ridge at the squamocolumnar junction Prof Jacob Bornstein Scheungraber C, Koenig U, Fechtel B, Kuehne-Heid R, Duerst M, Schneider A. The colposcopic feature ridge sign is associated with the presence of cervical intraepithelial neoplasia 2/3 and human papillomavirus 16 in young women. J Low Genit Tract Dis. 2009;13(1):13- 16.
  • 39. A New Scoring System Strander et al 2005  Designed to evaluate a scoring system for high grade lesions  297 examinations of women referred for colposcopy, Department of Obstetrics and Gynecology, Göteborg, Sweden  First Scoring system to incorporate lesion size as a variable  Subsequently validated at the Royal Free
  • 41. 0 1 2 Score ACETO UPTAKE Zero or transparent Shady, Milky (not transparent not opaque) Distinct, opaque white MARGINS/ SURFACE Diffuse Sharp but irregular, jagged, “geographical” Satellites Sharp and even, difference in surface level incl “cuffing” VESSELS Fine, regular Absent Coarse or atypical LESION SIZE <5mm 5-15mm or 2 quadrants >15mm or 3-4 quadrants or endocervically undefined IODINE STAINING Brown Faintly or patchy yellow Distinct yellow Total score 10
  • 42. The transformation zone  A Type 1 transformation zone is completely ectocervical and fully visible, and may be small or large  A Type 2 transformation zone has an endocervical component, is fully visible, and may have an ectocervical component that may be small or large  A Type 3 transformation zone has an endocervical component that is not fully visible and may have an ectocervical component that may be small or large
  • 43. Type 1 • Completely ectocervical • Fully visible • small or large Transformation Zone Classification
  • 44. SBX1739_3 Histology CIN1 Cytology LSIL,CIN 1;Atyp endocerv, neopl Carcinogenic HPV 16, 58, 66 Age 28 Category Mario Walter SCJ visibility Fully Visible Fully Visible TZ type Type 1 - Small Type 1 - Small TZ pattern Abnormal Grade 1 Abnormal Grade 2 Image quality Good Good Jim Usha Partially Visible Partially Visible Type 2 - Large Type 1 - Large Abnormal Grade 2 Normal Good Limited
  • 45. SBX1759_3 Histology CIN3 Cytology LSIL,CIN 1;Atyp endocerv, neopl Carcinogenic HPV 16, 51 Age 25 Category Mario Walter SCJ visibility Partially Visible Fully Visible TZ type Type 2 - Small Type 1 - Small TZ pattern Abnormal Grade 2 Abnormal Grade 1 Image quality Good Limited Jim Usha Fully Visible Fully Visible Type 1 - Small Type 1 - Small Abnormal Grade 1 Normal Good Good
  • 46. Type 2 • has endocervical component • Fully visible • may have ectocervial component which may be small or large Transformation Zone Classification
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  • 48. SBX1842_1 Histology CIN3 Cytology HSIL,CIN 3;Adeno, NOS Carcinogenic HPV 16, 18 Age 30 Category Mario Walter SCJ visibility Partially Visible Partially Visible TZ type Type 3 - Small Type 2 - Small TZ pattern Abnormal Grade 2 Suspicious for invasion Image quality Limited Limited Jim Usha Fully Visible Fully Visible Type 2 - Small Type 1 - Small Abnormal Grade 2 Abnormal Grade 2 Good Limited
  • 49. Transformation Zone Classification Type 3 • has endocervical component • is not fully visible • may have ectocervial component which may be small or large
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  • 51. SBX1216_2 Histology CIN3 Cytology HSIL,CIN 2;Adeno in situ (AIS) Carcinogenic HPV 31 Age 21 Category Mario Walter SCJ visibility Not Visible Partially Visible TZ type Type 3 - Small Type 2 - Small TZ pattern Abnormal Grade 1 Abnormal Grade 2 Image quality Good Good Jim Usha Not Visible Fully Visible Type 3 - Small Type 1 - Large Abnormal Grade 2 Abnormal Grade 1 Good Good
  • 52. SBX1774_1 Histology CIN3 Cytology HSIL,CIN 3;Adeno, NOS Carcinogenic HPV 16 Age 47 Category Mario Walter SCJ visibility Not Visible Partially Visible TZ type Type 3 - Small Type 2 - Small TZ pattern Abnormal Grade 2 Suspicious for invasion Image quality Good Good Jim Usha Not Visible Not Visible Type 3 - Small Type 3 - Large Suspicious for invasion Suspicious for invasion Good Good
  • 53. SBX1928_1 Histology CIN3 Cytology HSIL,CIN 3;Adeno, NOS Carcinogenic HPV 16, 39 Age 30 Category Mario Walter SCJ visibility Not Visible Not Visible TZ type Type 3 - Small Type 3 - Small TZ pattern Abnormal Grade 2 Abnormal Grade 2 Image quality Good Good Jim Usha Partially Visible Fully Visible Type 3 - Small Type 1 - Small Abnormal Grade 1 Abnormal Grade 1 Good Good
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  • 58. The BSCCP invites you to the 15th World Congress On behalf of IFCPC In London 26-30th May 2014 www.IFCPC2014.
  • 59. www.IFCPC2014.com Bemvindo a Londres al 26de30 de Mayo Queen Elizabeth II conference centre
  • 60. Westminster Hall for the plenary sessions Up to 2160 delegates 2070 m2 exhibition space
  • 61. ¡NosvemosemLondres ! 2014 St James’s Park – 5 minutes walk from venue
  • 63. National Institute of Medical Research- The biology of HPV and molecular markers Wolfson Institute of Preventive of Medicine- Screening across the world St Thomas’s Hospital – Improving Cytology Institute of Women’s Health Imperial College Post Congress Seminars
  • 64. See you in London