Diane DeFriend Derriford Hospital, Plymouth
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1 Diane DeFriend Derriford Hospital, Plymouth
2 Ultrasound US remains primary imaging modality for investigation of an adnexal mass Aim to characterise Benign Malignant Indeterminate 90% adnexal masses characterised by ultrasound alone
3 Adnexal Masses- Why do we need to characterise Benign Conservative Management Discharge / Follow up imaging Surgery Minimally invasive Fertility sparing Malignant Staging laparotomy / Cytoreductive surgery Specialist gynaecological oncology surgeon Cancer Centre
4 AIMS RECOGNISE FEATURES MALIGNANCY Avoid need for repeat surgery RECOGNISE COMMON BENIGN MASSES Most adnexal masses benign May avoid unnecessary surgery INDETERMINATE MASSES Role of follow up / alternative imaging Different approaches to characterising adnexal masses Experienced examiner Subjective pattern recognition approach superior
5 Benign Ovarian Lesions BIG FIVE
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7 Corpus Luteum Crenellated cyst Low level echoes Circumferential flow Secretory endometrium
8 Benign Adnexal Masses Simple Cysts Virtually exclude malignancy Large cysts - ensure not missing small nodules serous cystadenoma occ present as simple cyst esp larger cysts / older women Most resolve 1-2 months - follow up pre-menopausal > 5cm Post-menopausal > 3cm
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10 Haemorrhagic Cysts Varied appearance change blood products over time Typical appearances reticular pattern (fibrin strands)-strong predictor Clot may simulate solid nodule concave border absence flow Atypical premenopausal Should resolve 1-2 cycles Follow -up
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12 Endometrioma Characteristic Well defined cyst Uni / multilocular Homogenous low level echoes - ground glass appearance Hyperechoic wall foci Atypical 15% mural irregularity Usually avascular clot Rarely flow endometrial tissue Diffuse echoes Dermoid Cyst Mucinous ovarian tumour Further imaging Characteristic - haemorrhage
13 MR T1 high signal Endometrioma FS more conspicuous excludes dermoid T2 low signal (SHADING) complete loss signal dependent layering
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15 Polycystic Ovary 2003 Consensus report defined PCOS 2 of 3 criteria Oligo and/or anovulation Hyperandrogenism Polycystic ovary US Polycystic Ovary 12+ follicles 2-9mm and/or Ovarian volume >10cc Follicle distribution/stromal echogenicity not included? 25 follicles - Dewailly et al follicles, yrs - Lujan et al 2013
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17 Germ Cell Tumours Cystic/Solid Mature Teratoma (Dermoid Cyst ) Variable appearance internal composition Often specific features Dermoid plug Tip of iceberg sign Rokitansky Nodule echogenic nodule / dense well defined shadowing Dermoid mesh Floating Balls Fat-Fluid level Echogenic mass (sebaceous material / hair ) ill defined shadowing obscures posterior border
18 Mature Teratoma ( Dermoid Cyst) Dermoid Mesh Multiple echogenic lines/dots Hair fibres Floating Balls Uncommon / Pathognomonic Sebaceous material around focus debris/hair Fat fluid Level non specific Often at least 2 characteristic features detected Further imaging Atypical - characteristic for fat Visualise other ovary
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20 T2 T1 T1 FAT SAT
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22 BIG FIVE Benign Ovarian Lesions Corpus Luteal Cysts Functional Cysts Haemorrhagic Cysts Endometriomas PCOS Dermoids
23 Benign Extra- Ovarian Lesions Hydrosalpinx Para-ovarian Cysts Peritoneal Inclusion cysts
24 Paraovarian cyst Broad ligament Paramesonephric, mesothelial, mesonephric remnants Usually simple
25 Hydrosalpinx Tubular Incomplete septations Indentations opposite sides of wall -waist sign Mural nodules cogwheel beads on a string Echoes - pyosalpinx
26 Peritoneal Inclusion Cyst Functioning ovary Adhesions surgery, endometriosis, PID Cystic mass + septa Shape conforms to adjacent pelvic structures NB normal ovary within/ periphery mass
27 Pseudocyst / Peritoneal Inclusion Cyst
28 Pitfalls
29 Pitfalls
30 Bladder - TVS
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33 Classification of Ovarian Neoplasms EPITHELIAL TUMOURS 65-70% Serous Cystadenoma/Carcinoma Mucinous Cystadenoma/Carcinoma Endometrioid Clear Cell Brenner Tumour GERM CELL TUMOURS 15-20% SEX CORD STROMAL TUMOURS 5-10% Mature Teratoma (Dermoid) / Immature Teratoma Dysgerminoma Granulosa Cell Sertoli Leydig Fibroma Thecoma Metastases 5-10 %
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35 Classification of Ovarian Neoplasms EPITHELIAL TUMOURS 65-70% Serous Cystadenoma / Carcinoma Mucinous Cystadenoma / Carcinoma Endometrioid Clear Cell Brenner Tumour 85% malignant ovarian neoplasm Serous / Mucinous Benign Peak years Malignant - Peak 6-7 th decade Cystic and Solid - varying amounts solid tissue +/-Differentiation
36 Epithelial Tumours - Cystic/Solid - Serous Predominantly cystic Largely echo-free fluid Unilocular/multilocular Papillary projections single best predictor of epithelial neoplasm 60% benign (cystadenoma) few/small papillary nodules 25% malignant (cystadenocarcinoma) Malignant more projections / solid tissue 15% borderline (resemble benign or malignant) Serous cystadenocarcinoma
37 Epithelial Tumours - Cystic/Solid - Mucinous Multilocular Cystadenoma Echogenic fluid mucin Benign thin septa Malignant thick enhancing septa / solid elements Mucinous Cystadenocarcinoma 20-25% ovarian tumours 80% benign 10% borderline 10% malignant
38 Serous Bilaterality Ca2 + common psammomatous Peritoneal carcinomatosis Mucinous Rarely bilateral Ca2+ rare linear Pseudomyoma peritonei
39 Epithelial - Cystic / Solid Endometrioid 10-15% all ovarian cancers Almost always malignant 15-30% assoc endometrial Ca / hyperplasia Clear Cell 5% all ovarian cancer Malignant Assoc with endometriosis Most common neoplasm assoc with endometriosis
40 Pitfalls
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45 Decidualised Endometriotic Cyst Hypertrophy stromal cells endometrium during pregnancy Decidual change ectopic endometrium Vascularised rounded papillary projections in cyst with low level echoes Major contributory factor to incorrect diagnosis in pregnant women Resoving at follow up - surgically proven
46 Classification of Ovarian Neoplasms EPITHELIAL TUMOURS 65-70% Serous Cystadenoma/Carcinoma Mucinous Cystadenoma/Carcinoma Endometrioid Clear Cell Brenner Tumour GERM CELL TUMOURS 15-20% SEX CORD STROMAL TUMOURS 5-10% Mature Teratoma (Dermoid) / Immature Teratoma Dysgerminoma Granulosa Cell Sertoli Leydig Fibroma Thecoma Metastases 5-10 %
47 Solid Masses - Regular Regular solid masses often benign Pedunculated fibroid Typically solid Picket fence shadowing Ovarian fibroma Solid mass Marked acoustic shadowing (18-52%)
48 Solid Masses Regular Fibroma SEX CORD STROMAL TUMOURS 5-10% Granulosa Cell Sertoli Leydig Fibroma Thecoma Almost always benign Middle age women Heterogenous/homogen ous solid mass Marked acoustic shadowing (18-52%) Differential Pedunculated fibroids Brenner Tumour Brenner Tumour Rarely malignant
49 Solid Masses Regular Fibroma Further imaging Large fibroids / shadowing may limit TVS Atypical Characteristic for fibrous tissue Visualise ovaries / relationship to uterus
50 Solid Masses Regular MEIGS Syndrome Ascites Pleural Effusion Benign ovarian tumour - Fibroma
51 Solid masses - Malignant Irregular solid mass suggests malignancy Epithelial neoplasms cystic/solid rarely completely solid Solid/nearly solid malignancies Metastases Rare Tumours Sex Cord Stromal Tumours Malignant teratoma Dysgerminoma Bilateral solid masses raise concern for metastases further imaging? primary Krukenberg - gastric
52 Sex Cord Stromal - Granulosa Cell Tumours SEX CORD STROMAL TUMOURS 5-10% Granulosa Cell Sertoli Leydig Fibroma Thecoma Hormone secreting - oestrogen Rare 3% ovarian malignancies Peri /postmenopusal Unilateral - 95% US appearances non specific Cystic/solid - Solid 1/3 endometrial hyperplasia Up to 25% endometrial Ca
53 Sex Cord Stromal - Fibrothecoma SEX CORD STROMAL TUMOURS 5-10% Granulosa Cell Sertoli Leydig Fibroma Thecoma
54 Solid masses Malignant GERM CELL TUMOURS 15-20% Mature Teratoma (Dermoid) / Immature Teratoma Dysgerminoma Dysgerminoma 17 yr old Immature Teratoma 27 yr old Dysgerminoma Most common < 30 years Usually solid Immature Teratoma Most common first two decades Predominantly solid, cystic/solid Raised AFP/Beta-hCG/LDH in some malignant germ cell tumours
55 Features of Malignancy Solid Component within cystic mass Irregular solid mass / wall Thick Septations Presence of Flow Borderline Ascites Peritoneal nodules Metastases /Nodes
56 Solid Component Most important predictor of malignancy Malignant Several nodules solid tissue Echogenicity similar to cyst wall Often convex / irregular Flow Benign Solitary / small papillary nodule serous cystadenoma Hyperechoic with shadowing dermoid Clot concave border / avascular
57 Septations Septa in cystic mass suggest neoplasm Increased risk malignancy > 2-3mm flow Fibrin strands Thin weak reflectors Numerous Do not traverse entire cyst Adjacent cysts may mimic
58 Doppler Colour doppler qualitative Flow in solid component / septum Power doppler increased sensitivity / similar specificity Spectral doppler Confirm presence flow Malignant tumours Low resistance flow lower PI & RI s, higher velocity RI < 0.4; PI <1.0 prev cited as cut-off for malignancy Overlap with benign little role characterisation
59 Ascites Indirect indicator of malignancy Small amount fluid in Pouch of Douglas normal in premenopausal women >15mm AP diameter Pre-existing illness eg cirrhosis Echogenic fluid - ruptured cyst/torsion Meig s Syndrome ascites + pleural effusion + fibroma
60 Indeterminate Masses Ultrasound Typical benign lesions Sensitive malignancy Many benign lesions demonstrate features malignancy Solid areas / septations / flow Tubo-ovarian abscess Cystadenofibroma Borderline tumours
61 Risk of Malignancy Index U Score M score Feature RMI 1 Score Ultrasound features: Multilocular cyst Solid areas Bilateral lesions Ascites Intra-abdominal metastases Pre-menopausal 1 Post menopausal 3 CA125 0=none 1=one abnormality 3=2 or more abnormalities U/ml RMI score = ultrasound x menopausal x CA125 level in U/ml Sensitivity 85% Specificity 97%
62 Triage using RMI Risk RMI Women (%) Risk of cancer (%) Low <25 40 <3 Moderate High > High RMI score > referral to specialist centre (SIGN Guidelines 2012) Intermediate RMI score MRI often considered appropriate RMI heavily influenced by CA 125 CA 125 may be elevated by benign disease esp pre-menopausal RMI recommended by RCOG and systematic review 2009 Geomini P et al The Accuracy of Risk Scores in Predicting Ovarian Malignancy: A Systematic Review Obstetrics & Gynecology; Volume 113 : 2, (Part 1), February 2009, pp
63 Simple Rules Developed as part of the IOTA (International Ovarian Tumour Analysis) study Prospective, multicentre, European study patients with adnexal masses, 21 centres, 9 countries Simple rules based on clearly defined US features BENIGN - B RULES Unilocular cyst Presence solid components where largest solid component < 7mm Presence acoustic shadowing Smooth multilocular tumour with largest diameter <100mm No blood flow MALIGNANT - M RULES Irregular solid tumour Ascites At least four papillary structures Irregular multilocular solid tumour with largest diameter 100mm Very strong blood flow
64 Ultrasound in Obstetrics & Gynecology Volume 41, Issue 1, pages 9-20, 25 DEC 2012 DOI: /uog Slides Ligita Jokubkiene Jan 2013 UOG Journal club
65 A mass is unclassifiable if no M or B features or both
66 Simple Rules Could be applied in 77% 2 step strategy Simple Rules + subjective assessment by experienced examiner if unclassifiable ( MDT ) 90% sensitivity and 93% specificity to detect ovarian malignancy Equivalent to expert subjective assessment in all (sensitivity 90% /specificity 93%) misclassified fewer stage 1 malignancies than did RMI and measurement of CA125. UK - RCOG included simple rules in 2011 guideline for evaluating ovarian pathology in premenopausal women
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68 Conclusion Clinical, Pre/Post Menopausal CA125 US Adnexal Mass Likely Malignant Adnexal Mass Indeterminate Adnexal mass Likely benign Staging Characterisation Follow up
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