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Prof. M.C.Bansal
    Ovarian Malignancy
       MBBS,MS,MICOG,FICOG
          Professor OBGY
      Ex-Principal & Controller
 Jhalawar Medical College & Hospital
Mahatma Gandhi Medical College, Jaipur.
Epidemology
   2nd most common of all genital      cancers , accounts for 10-15 %
incidence.
In last 2 decades its incidence as well as survival rate has increased.
The risk of woman developing ovarian cancer in her life time is 1:70
to 1: 100.
Women with low parity, infertility and delayed child bearing
predisposes higher chances.
5-10% ovarian tumors are genaticaly affected ---BRACE_1&@
mutations on chromosome 17 & 13 respectively . if one family
member is affected, the life long risk is 2.7% but it goer up to 13%
with2 or more sibblings. They develop at earlier age < 40 years.
. Inheritance pattern is autosomal dominant. The risk increases with
advancing age up to 70 years.
Induction of ovulation, industrial pollution, talc use at perineum, High
dietary fat , western world have increased incidences
streak ovaries, mums infection at puberty leading to premature
ovarian failure.
Epidemology----
 Protective factors Multiparity , ocs ,Breast feeding
,anovulation ,Prophylactic oopherectomy.
Late diagnosis and early metastasis are responsible for
poor prognosis.
80% malignancies are of epithelial origion,.almost 80%
report in late stage iii or iv .
80% are primary carcinoma.
20% are secondary form.
Before menarche 10% are malignant.
During reproductive period15% are malignant., but rises
to > 50% after menopause.
Pathology
• Epitehelial ovarian carcinoma---80-90%
  Papillary cystadenocarcinoma
  Mucinous cystadenocarcnoma
• Nonepethelial carcinoma---10-20% these
  include malignancy of (A) Germcells (2)Sex
  cord stromal(3)Metastatic (4) Rare malignancy
  like Sarcoma, lipoid cell carcinoma.
Coincidence of uterine and ovarian
                cancer
• In some cases primary lies in uterus and direct spread to
  ovaries
• Primary in ovary and secondaries in uterus.
• Estrogen / and progesteron producing tumor of ovary and
  primary cancer endometrium.
• Cancer present in uterus and cancer in ovary are histologicaly
  different.
• Theerfore extended hysterectomy along with bilateral
  oopherectomy should always be done in either case’
Spread
• Lymphatic--- Para -aortic Lymph Nodes and
  superior gastric , mediastinal---pleural effusion
  , supra-clavicular.
• Blood spread---uncommon---lungs
• Direct spread through peritoneum----Rupture
  capsule—exfoliation of malignant cells,
  peritoneal irritation---ascites, omental cake.,
  intestine, parietal, visceral peritoneum---- liver
  spleen, dome of diaphragm, uterus, tubes.
STAGING CARCINOMA OVAARY FIGO
STAGING CARCINOMA OVAARY FIGO
FIGO STAGING OVARIAN CANCERS
FIGO STAGING OVARIAN CANCERS
OMENTAL CAKING AT STAGING LAPROTOMY
Management
• Laparotomy and maximal removal of cancer tissue----intra
  operative staging, cytology of ascitic fluid, pan hysterectomy,
  partial or complete omantectomy, enucleation of cancer
  growth on parietal and visceral peritoneum with out
  perforating the viscera.
• If non operable---intra peritoneal instillation of radioisotopes
  (p34)or chemotherapeutic agent.
• Chemotherapy---followed by second look laparotomy to
  remove uterus ,ovaries ,omantum and any residual cancer
  tissue.
• Radiotherapy for nodal metastasis.
• Stem cell Therapy.
• Immunotherapy.
• Palliative therapy –to relieve pain(opiates/NSAIDs, nutritional
  supplimentaton(callories, proteins to keep Hb > 10 gm% and
  wt loss < 10 %), psychological support , symptomatic
Role of Laparoscopy in the Clinical Management of Ovarian
   Cancer
At present, the role of laparoscopy in the management of
   ovarian cancer is evolving. There are several clinical settings
   in which the potential for this surgical modality has been
   investigated
(a) primary surgery for early-stage ovarian cancer
(b) restaging of unstaged ovarian cancer
(c) primary cytoreductive surgery for advanced-stage ovarian
cancer
(d) assessment of resectability
(e) intra-peritoneal catheter placement
(f) second-look surgery
(g) secondary cytoreductive surgery.
STRATEGIES TO REDUCE THE INCIDENCE OF GENITAL TRACT
                       MALIGNANCIES

• First injection at elected time.
• Second injection 2 months later.
• Third injection 6 months after the first injection.
• The cost of each injection is $200, and immunity is expected to last 5 years.
  The only benefit as seen today is a longer interval of screening in HPV-
  negative women. page 429 page 430 There have been advances in strategies
  evolved to reduce the incidence of genital cancers. The following are
  notable amongst these: 1. The role and value of periodic 'Pap smear' tests is
  well-established in reducing the incidence of invasive carcinoma of the
  cervix.
• 2. Evaluation of abnormal Pap tests with colposcopy-directed biopsies has
  enabled the diagnosis of intraepithelial cancers and diagnosis of early
  invasive cancer of the cervix.
• 3. The practice of preferring total over subtotal
  hysterectomy for benign diseases (fibroids, adenomyosis,
  dysfunctional uterine bleeding-DUB) protects against risk
  of future cervical stump carcinoma estimated to occur in
  2% of cases.
• 4. Early diagnosis of sexually transmitted diseases (STDs)
  and their eradication. Herpes and HPV infections render
  an individual prone to cancer of vulva and the cervix.
  Barrier contraceptives protect against STD as well as
  cervical cancer.
• 5. HPV vaccine is now available which may eradicate
  lower genital tract malignancies in young women. The
  available vaccine is type specific and therefore protective
  in only 60-70%.
• 6. The treatment of cervical dysplasia by CO2
  laser/conization for CIN lesions.
• 7. Addition of progestogens to oestrogens in
  hormone replacement therapy (HRT) reduces the
  risks of uterine endometrial cancer.
• 8. Thorough investigation of a woman with
  postmenopausal bleeding often brings to light
  early unsuspected endometrial/ovarian/tubal
  cancers.
• 9. The practice of routine removal of both ovaries
  when performing hysterectomy for benign
  conditions after the age of 50 years is a
  prophylaxis against risk of future ovarian cancer.
  Prophylactic oophorectomy in a genetically
  predisposed woman is recommended, though
  premature menopause remains a risk. This also
  reduces breast cancer by 50%.
• 10. Early diagnosis of ovarian cancer is the
  primary objective for long-term survival, though
  this is not obtained as of today. Seventy-five per
  cent tumours are advanced when diagnosed.
• 11. Oral combined pills reduce the incidence of
  uterine and ovarian cancer by 40-50%. Barrier
  contraceptives prevent cervical cancer.
• 12. Gene study can select women at high risk
  for cancer.
• 13. Evaluation of adnexal masses with scans,
  Doppler velocimetric studies, and CA-125 tumour
  marker to diagnose ovarian cancer.
• 14. Hysteroscopy/laparoscopy/selective biopsies of
  suspicious lesions.
• 15. Routine mammography for all women over the
  age of 40 years, earlier whenever clinical
  examination reveals a doubtful lump, or in women
  with strong family history of breast cancer.
• For many women the obstetrician-gynaecologist is
  likely to be the only physician to provide them
  healthcare. Hence the importance of developing
  skills for evaluation and counselling for genital
  cancers and adopting clinical practices which
  reduce the future risks of genital cancers lies with
  the gynaecologists.
KEY POINTS
• Vulval intraepithelial neoplasia (VIN) is a well-recognized
  entity which can be effectively treated by conservative
  surgery.
• Vulval cancer, mostly squamous cell carcinoma, is
  encountered in 2-4% of all genital tract malignancies. An
  elderly woman of low parity and associated with previous STD
  is the high-risk case.
• The treatment of vulval cancer is based on the age of the
  woman, type and extent of the lesion and involvement of the
  regional lymph nodes. Local wide excision, skinning
  vulvectomy with split skin graft, laser therapy and simple or
  radical vulvectomy have improved the survival rate without
  increasing the surgical morbidity.
• Endometrial cancer is the disease of the perimenopausal and
  postmenopausal women with low parity.
• Endometrial cancer is fast becoming the more common
  cancer in women. Early menarche, late menopause, small
  family size, obesity, carbohydrate intolerance, PCOD-related
  infertility and unsupervised HRT in menopausal women
  contribute to its occurrence.
• Oestrogen therapy, tamoxifen cause hyperplasia and
  endometrial cancer over a period of time. Oral combined pills
  have a protective effect and reduce the incidence by 40-50%.
• CT and MRI help in preoperative staging and determine the
  extent of spread of malignancy. Hysteroscopic evaluation and
  biopsy improve the diagnostic accuracy.
• Abdominal hysterectomy with bilateral salpingo-
  oophorectomy, peritoneal washing and omental biopsy form
  the primary surgical therapy in early stages.
• Radiotherapy and chemotherapy are recommended in the
  advanced stage of the disease and are also adjuvants to
  surgery.
• Progestogens are beneficial in advanced stages of endometrial
  cancer and pulmonary metastasis.
• Carcinoma of the cervix is the most common genital tract
  cancer in women and ranks second to the breast cancer. It
  occurs in younger women.
• Late marriage, contraception, small family size, improved
  personal hygiene, avoidance of extramarital relationships and
  regular gynaecological check-ups inclusive of a Pap test and
  colposcopy have contributed to the lowering of its incidence.
• Endometrial cancer developing in a woman following
  unopposed oestrogen uptake is well-differentiated and less
  invasive with better prognosis. It also responds well to
  progestogens.
• Endocervical cancer has different aetiology and requires
  chemotherapy with radiotherapy, followed by radical
  surgery.
• Fallopian tube cancer is rare, and is often mistaken for
  ovarian cancer. It is treated the same way as ovarian cancer.
• Ovarian cancer is the second most common genital cancer.
  It remains asymptomatic for a long time. Many cases are
  already far advanced at the time of diagnosis. Germ cell
  tumours and mesenchymomas are known to occur in
  younger women. Epithelial tumours occur in older women.
  Surgical removal is adequate treatment for cases of
  borderline malignancy. Surgery followed by chemotherapy
  is indicated in advanced cases.
• The gold standard is abdominal hysterectomy and bilateral
  salpingo-oophorectomy with omentectomy in the early and
  operative cases of ovarian cancer. Debulking, radiotherapy
  and chemotherapy prolong life and duration of remission.

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Malignancy of ovary

  • 1. Prof. M.C.Bansal Ovarian Malignancy MBBS,MS,MICOG,FICOG Professor OBGY Ex-Principal & Controller Jhalawar Medical College & Hospital Mahatma Gandhi Medical College, Jaipur.
  • 2. Epidemology 2nd most common of all genital cancers , accounts for 10-15 % incidence. In last 2 decades its incidence as well as survival rate has increased. The risk of woman developing ovarian cancer in her life time is 1:70 to 1: 100. Women with low parity, infertility and delayed child bearing predisposes higher chances. 5-10% ovarian tumors are genaticaly affected ---BRACE_1&@ mutations on chromosome 17 & 13 respectively . if one family member is affected, the life long risk is 2.7% but it goer up to 13% with2 or more sibblings. They develop at earlier age < 40 years. . Inheritance pattern is autosomal dominant. The risk increases with advancing age up to 70 years. Induction of ovulation, industrial pollution, talc use at perineum, High dietary fat , western world have increased incidences streak ovaries, mums infection at puberty leading to premature ovarian failure.
  • 3. Epidemology---- Protective factors Multiparity , ocs ,Breast feeding ,anovulation ,Prophylactic oopherectomy. Late diagnosis and early metastasis are responsible for poor prognosis. 80% malignancies are of epithelial origion,.almost 80% report in late stage iii or iv . 80% are primary carcinoma. 20% are secondary form. Before menarche 10% are malignant. During reproductive period15% are malignant., but rises to > 50% after menopause.
  • 4. Pathology • Epitehelial ovarian carcinoma---80-90% Papillary cystadenocarcinoma Mucinous cystadenocarcnoma • Nonepethelial carcinoma---10-20% these include malignancy of (A) Germcells (2)Sex cord stromal(3)Metastatic (4) Rare malignancy like Sarcoma, lipoid cell carcinoma.
  • 5. Coincidence of uterine and ovarian cancer • In some cases primary lies in uterus and direct spread to ovaries • Primary in ovary and secondaries in uterus. • Estrogen / and progesteron producing tumor of ovary and primary cancer endometrium. • Cancer present in uterus and cancer in ovary are histologicaly different. • Theerfore extended hysterectomy along with bilateral oopherectomy should always be done in either case’
  • 6. Spread • Lymphatic--- Para -aortic Lymph Nodes and superior gastric , mediastinal---pleural effusion , supra-clavicular. • Blood spread---uncommon---lungs • Direct spread through peritoneum----Rupture capsule—exfoliation of malignant cells, peritoneal irritation---ascites, omental cake., intestine, parietal, visceral peritoneum---- liver spleen, dome of diaphragm, uterus, tubes.
  • 11. OMENTAL CAKING AT STAGING LAPROTOMY
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  • 16. Management • Laparotomy and maximal removal of cancer tissue----intra operative staging, cytology of ascitic fluid, pan hysterectomy, partial or complete omantectomy, enucleation of cancer growth on parietal and visceral peritoneum with out perforating the viscera. • If non operable---intra peritoneal instillation of radioisotopes (p34)or chemotherapeutic agent. • Chemotherapy---followed by second look laparotomy to remove uterus ,ovaries ,omantum and any residual cancer tissue. • Radiotherapy for nodal metastasis. • Stem cell Therapy. • Immunotherapy. • Palliative therapy –to relieve pain(opiates/NSAIDs, nutritional supplimentaton(callories, proteins to keep Hb > 10 gm% and wt loss < 10 %), psychological support , symptomatic
  • 17.
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  • 21. Role of Laparoscopy in the Clinical Management of Ovarian Cancer At present, the role of laparoscopy in the management of ovarian cancer is evolving. There are several clinical settings in which the potential for this surgical modality has been investigated (a) primary surgery for early-stage ovarian cancer (b) restaging of unstaged ovarian cancer (c) primary cytoreductive surgery for advanced-stage ovarian cancer (d) assessment of resectability (e) intra-peritoneal catheter placement (f) second-look surgery (g) secondary cytoreductive surgery.
  • 22. STRATEGIES TO REDUCE THE INCIDENCE OF GENITAL TRACT MALIGNANCIES • First injection at elected time. • Second injection 2 months later. • Third injection 6 months after the first injection. • The cost of each injection is $200, and immunity is expected to last 5 years. The only benefit as seen today is a longer interval of screening in HPV- negative women. page 429 page 430 There have been advances in strategies evolved to reduce the incidence of genital cancers. The following are notable amongst these: 1. The role and value of periodic 'Pap smear' tests is well-established in reducing the incidence of invasive carcinoma of the cervix. • 2. Evaluation of abnormal Pap tests with colposcopy-directed biopsies has enabled the diagnosis of intraepithelial cancers and diagnosis of early invasive cancer of the cervix.
  • 23. • 3. The practice of preferring total over subtotal hysterectomy for benign diseases (fibroids, adenomyosis, dysfunctional uterine bleeding-DUB) protects against risk of future cervical stump carcinoma estimated to occur in 2% of cases. • 4. Early diagnosis of sexually transmitted diseases (STDs) and their eradication. Herpes and HPV infections render an individual prone to cancer of vulva and the cervix. Barrier contraceptives protect against STD as well as cervical cancer. • 5. HPV vaccine is now available which may eradicate lower genital tract malignancies in young women. The available vaccine is type specific and therefore protective in only 60-70%. • 6. The treatment of cervical dysplasia by CO2 laser/conization for CIN lesions.
  • 24. • 7. Addition of progestogens to oestrogens in hormone replacement therapy (HRT) reduces the risks of uterine endometrial cancer. • 8. Thorough investigation of a woman with postmenopausal bleeding often brings to light early unsuspected endometrial/ovarian/tubal cancers. • 9. The practice of routine removal of both ovaries when performing hysterectomy for benign conditions after the age of 50 years is a prophylaxis against risk of future ovarian cancer. Prophylactic oophorectomy in a genetically predisposed woman is recommended, though premature menopause remains a risk. This also reduces breast cancer by 50%.
  • 25. • 10. Early diagnosis of ovarian cancer is the primary objective for long-term survival, though this is not obtained as of today. Seventy-five per cent tumours are advanced when diagnosed. • 11. Oral combined pills reduce the incidence of uterine and ovarian cancer by 40-50%. Barrier contraceptives prevent cervical cancer. • 12. Gene study can select women at high risk for cancer.
  • 26. • 13. Evaluation of adnexal masses with scans, Doppler velocimetric studies, and CA-125 tumour marker to diagnose ovarian cancer. • 14. Hysteroscopy/laparoscopy/selective biopsies of suspicious lesions. • 15. Routine mammography for all women over the age of 40 years, earlier whenever clinical examination reveals a doubtful lump, or in women with strong family history of breast cancer. • For many women the obstetrician-gynaecologist is likely to be the only physician to provide them healthcare. Hence the importance of developing skills for evaluation and counselling for genital cancers and adopting clinical practices which reduce the future risks of genital cancers lies with the gynaecologists.
  • 27. KEY POINTS • Vulval intraepithelial neoplasia (VIN) is a well-recognized entity which can be effectively treated by conservative surgery. • Vulval cancer, mostly squamous cell carcinoma, is encountered in 2-4% of all genital tract malignancies. An elderly woman of low parity and associated with previous STD is the high-risk case. • The treatment of vulval cancer is based on the age of the woman, type and extent of the lesion and involvement of the regional lymph nodes. Local wide excision, skinning vulvectomy with split skin graft, laser therapy and simple or radical vulvectomy have improved the survival rate without increasing the surgical morbidity.
  • 28. • Endometrial cancer is the disease of the perimenopausal and postmenopausal women with low parity. • Endometrial cancer is fast becoming the more common cancer in women. Early menarche, late menopause, small family size, obesity, carbohydrate intolerance, PCOD-related infertility and unsupervised HRT in menopausal women contribute to its occurrence. • Oestrogen therapy, tamoxifen cause hyperplasia and endometrial cancer over a period of time. Oral combined pills have a protective effect and reduce the incidence by 40-50%.
  • 29. • CT and MRI help in preoperative staging and determine the extent of spread of malignancy. Hysteroscopic evaluation and biopsy improve the diagnostic accuracy. • Abdominal hysterectomy with bilateral salpingo- oophorectomy, peritoneal washing and omental biopsy form the primary surgical therapy in early stages. • Radiotherapy and chemotherapy are recommended in the advanced stage of the disease and are also adjuvants to surgery.
  • 30. • Progestogens are beneficial in advanced stages of endometrial cancer and pulmonary metastasis. • Carcinoma of the cervix is the most common genital tract cancer in women and ranks second to the breast cancer. It occurs in younger women. • Late marriage, contraception, small family size, improved personal hygiene, avoidance of extramarital relationships and regular gynaecological check-ups inclusive of a Pap test and colposcopy have contributed to the lowering of its incidence. • Endometrial cancer developing in a woman following unopposed oestrogen uptake is well-differentiated and less invasive with better prognosis. It also responds well to progestogens.
  • 31. • Endocervical cancer has different aetiology and requires chemotherapy with radiotherapy, followed by radical surgery. • Fallopian tube cancer is rare, and is often mistaken for ovarian cancer. It is treated the same way as ovarian cancer. • Ovarian cancer is the second most common genital cancer. It remains asymptomatic for a long time. Many cases are already far advanced at the time of diagnosis. Germ cell tumours and mesenchymomas are known to occur in younger women. Epithelial tumours occur in older women. Surgical removal is adequate treatment for cases of borderline malignancy. Surgery followed by chemotherapy is indicated in advanced cases. • The gold standard is abdominal hysterectomy and bilateral salpingo-oophorectomy with omentectomy in the early and operative cases of ovarian cancer. Debulking, radiotherapy and chemotherapy prolong life and duration of remission.