OncologyDr. Niti RaizadaCommon Cancers & Blood Disorders

Principal Director, Medical Oncology & Hemato-Oncology, Fortis Hospital, Bannerghatta Road, Bengaluru, India

Part 6 of 12 in Diagnosing Common Cancers & Blood Disorders

Ovarian Cancer: The Silent Killer and Its Diagnostic Trail

August 28, 2026

A 63-year-old woman, para 3 with three live births, who had reached menopause at 52, went to her gynaecologist with abdominal distension of one month's duration. She had no family history of cancer and well-controlled hypertension. Alongside the distension, she described early satiety, a dragging pelvic pain, heaviness in the pelvis while walking, and breathlessness when lying down.

Why the symptoms alone are easy to miss

None of these symptoms, on their own, point clearly to a gynaecological cancer. Dr. Raizada calls ovarian cancer a silent killer precisely because its symptoms are usually mild and nonspecific, easily attributed to digestion, weight gain or ageing, until the disease has already advanced. That is why, in a postmenopausal woman with this symptom cluster, the workup needs to move quickly to imaging and a tumour marker rather than waiting to see if symptoms resolve.

CA-125, transvaginal ultrasound, and what they showed

The workup combined CA-125 testing with a transvaginal ultrasound. The scan showed a left adnexal mass measuring 10 centimetres, complex in structure with both solid and cystic components, internal septations, and papillary projections, a finding Dr. Raizada flagged as particularly characteristic of serous carcinoma. Mild to moderate ascites was present and was clinically palpable. The CA-125 came back markedly elevated at 745.

A CT scan confirmed the large left ovarian mass and additionally showed peritoneal deposits, including omental deposits with omental caking. The CT of the thorax was normal, indicating the spread was confined to the abdomen and pelvis.

A rule that matters: never biopsy the ovary directly

Dr. Raizada was unambiguous on this point: when an ovarian mass is suspected of malignancy, a needle should never be inserted directly into the ovary to obtain a biopsy. Instead, a guided biopsy is taken from a more accessible site with disease involvement, in this case the omentum. The biopsy from the omental mass showed high-grade serous carcinoma.

Because the peritoneal disease was extensive, upfront surgery was not feasible. The patient was started on chemotherapy first, with cytoreductive surgery and HIPEC, hyperthermic intraperitoneal chemotherapy, planned to follow once the disease had responded.

The red flag pattern for ovarian cancer

Dr. Raizada summarised the pattern that should raise suspicion of ovarian malignancy: a postmenopausal woman with a rapidly growing mass, often larger than 8 centimetres, which may be unilateral or bilateral. On imaging, the mass appears irregular, solid, or complex with both solid and cystic components, sometimes with thick or irregular walls. Papillary projections are especially characteristic of serous carcinoma. Ascites is commonly present, along with increased vascularity on imaging. CA-125 is frequently elevated, and CEA may also be checked to rule out a secondary Krukenberg tumour. Symptoms tend to be mild, and the histology is most often high-grade serous carcinoma.

Screening, and a note on the uterus

There is currently no routine population screening recommendation for ovarian cancer. Where family history is strong, a transvaginal ultrasound combined with CA-125 testing may be considered on an individual basis. Dr. Raizada also flagged endometrial, or uterine, cancer as a related and growing concern, where the key screening criterion is endometrial thickness on ultrasound in a postmenopausal woman: a thickness of 5 millimetres or more, in the presence of vaginal bleeding or in a patient on tamoxifen, warrants an endometrial biopsy. Without vaginal bleeding, a thickness of up to 8 millimetres is generally considered acceptable.

This guide is based on a live Jivo Masterclass — Dr. Niti Raizada taught doctors across Africa on February 1, 2026.

FROM THE LIVE Q&A

DR

Dr. Emmanuel

Are there any specific concerns in monitoring chronic liver disease, for example the frequency of ultrasound and the skill set of the radiographer?

NR

Dr. Niti Raizada

Ultrasound should be done once every 6 months for a chronic liver disease patient, along with alpha-fetoprotein testing every 6 months. The skill of the radiographer matters because ultrasound is a subjective, operator-dependent test. If there is any doubt on ultrasound, a triple-phase CT scan or a multiphasic MRI should be done immediately.

See all 9 questions from this masterclass →

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Frequently Asked Questions

We had a case where a gentleman with no history of alcohol or hepatitis could not get preliminary triple-phase CT staging done. The plan was hepatectomy, but he developed a crisis from bile build-up and passed away during the consultation and visa process. How could such cases be managed by a local doctor with limited information?

The key is always the right diagnosis at the right time. Liver cancer carries a real risk of coagulopathy and bleeding, so any patient with chronic liver disease should have regular PT, PTT and INR testing. If there is any bleeding diathesis, it needs to be treated, including with vitamin K and blood products if needed. Chronic liver disease patients also commonly have low white cell counts and low platelets, so basic blood counts should be checked regularly alongside liver and kidney function tests.

Could you recap the management of leukemia, including the case you discussed earlier?

Leukemias are broadly acute or chronic. Acute leukemias have a short history with low hemoglobin, white cell count and platelets, presenting with fever and bleeding. Chronic leukemias, chronic myeloid leukemia (CML) or chronic lymphocytic leukemia (CLL), generally occur in older age groups and are often managed with tablets alone. Acute leukemias are either AML or ALL. Genetic testing subcategorises each: CML needs confirmation of Philadelphia chromosome or BCR-ABL positivity; CLL needs a FISH panel to check p53 status and risk category; AML is categorised as good, intermediate or high risk. ALL is the most common leukemia in children and young adults and is treated with steroids followed by chemotherapy based on T-cell or B-cell type. AML M3, acute promyelocytic leukemia, is rare but very curable with ATRA or arsenic trioxide tablets; non-M3 AML needs chemotherapy.

What comfort or guidance can you give the doctor partners here, who may not always have clarity because of diagnostic challenges? When should a case trigger further action?

Please write in with any questions, over WhatsApp or text, at any time. Many patients cannot travel to India, so the goal is to help diagnose and treat them on time wherever they are. Prepare a doctor's note with the relevant clinical details and share it; if the picture is clear, specific pointers on managing the case can be given from that.

Can a general practitioner also perform a clinical breast examination, or does it need to be a specialist?

Self-examination should be done by the woman herself, using the opposite hand on the opposite breast with three fingers held flat, including the axilla and neck. Clinical breast examination should be done by anyone properly trained, which can include nurse practitioners, physician assistants, internal medicine doctors, general surgeons, gynaecologists and oncologists. Training, not job title, is what matters, since missing lesions is common when the examiner has not been trained. GPs and internal medicine doctors should learn the technique and offer it to every woman who comes to the clinic.

What further investigations are needed to assess disease extension before starting management of this cervical cancer case?

Once the diagnosis is confirmed by biopsy, a staging scan, often a PET scan, establishes the exact stage, including whether the bladder, rectum, parametrium or lymph nodes are involved. Fitness for treatment is then assessed with kidney function testing (GFR) and audiometry, since some chemotherapy agents can affect hearing. Weekly chemotherapy is then given alongside radiation, with the potential radiation side effects explained to the patient beforehand.

Why is ovarian cancer often described as a silent killer?

Its symptoms, such as abdominal distension, early satiety, and pelvic heaviness, are usually mild and nonspecific, and are easily mistaken for digestion problems, weight gain, or normal ageing. By the time these symptoms prompt an evaluation, the disease has often already advanced.

Which ultrasound and blood test findings point to ovarian malignancy?

A complex adnexal mass with both solid and cystic components, internal septations, and papillary projections on transvaginal ultrasound, combined with ascites and a markedly elevated CA-125, together form a strong red flag pattern for ovarian cancer, particularly in a postmenopausal woman.

Why should a suspected ovarian mass never be biopsied directly?

A needle should never be inserted directly into the ovary when malignancy is suspected. Instead, a guided biopsy is taken from a more accessible site with disease involvement, such as the omentum, which avoids the risks associated with direct ovarian puncture.

When is chemotherapy given before surgery in ovarian cancer rather than after?

When peritoneal disease is extensive enough that upfront surgery is not feasible, chemotherapy is started first, with cytoreductive surgery and HIPEC planned to follow once the disease has responded to treatment.

What endometrial thickness on ultrasound should prompt a biopsy in a postmenopausal woman?

A thickness of 5 millimetres or more, in the presence of vaginal bleeding or in a patient on tamoxifen, warrants an endometrial biopsy. Without vaginal bleeding, a thickness of up to 8 millimetres is generally considered acceptable.

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