Abstract
The incidence of ovarian cysts in pregnancy appears to be rising, especially with the increased use of routine antenatal ultrasounds. Most of them are benign and tend to resolve spontaneously. It is rare to diagnose malignant ovarian tumours during pregnancy. Evaluating the adnexa during routine antenatal ultrasound is considered opportunistic screening. Even though several factors can make ultrasound less reliable during pregnancy, it is the preferred initial imaging method. MRI is also a safe option during pregnancy for further evaluation of ovarian lesions. Surgery is recommended for larger, symptomatic cysts or those suspected of malignancy. Laparoscopic management of ovarian cysts is possible between 14 and 16 weeks of gestation but requires advanced laparoscopic skills. Due to the risk of adverse fetal and maternal outcomes associated with surgery during pregnancy, conservative management is preferred when it is deemed safe. Multi-disciplinary team approach is recommended for complicated and malignant adnexal masses.
Introduction
Ovarian cysts or adnexal masses during pregnancy are a frequent occurrence, with reported prevalence ranging from 1% to 5.3%. The occurrence of cancer in pregnancy is an uncommon event, with an overall estimated incidence of 0.02 to 1%. Before the widespread use of ultrasonography, these masses were typically identified only when symptomatic or palpable due to their size. The increased utilization of ultrasound scans for pregnant women has led to the discovery of asymptomatic ovarian cysts in a significant number of cases. Although most of the adnexal masses observed during pregnancy are benign, it is crucial to thoroughly investigate, monitor, and treat them as needed.
Types of ovarian cyst in pregnancy
See Table 1 .
Benign | Physiological | Follicular cyst |
Corpus luteum | ||
Haemorrhagic cyst | ||
Pathological | Serous cystadenoma | |
Mucinous cystadenoma | ||
Mature cystic teratoma (Dermoid cyst) | ||
Fibroma | ||
Endometrioma | ||
Fibroid (pedunculated) | ||
Borderline ovarian tumours | Serous borderline tumours | |
Mucinous borderline tumours | ||
Endometrioid borderline tumours | ||
Clear cell borderline tumours | ||
Brenner borderline tumours | ||
Malignant | Epithelial ovarian tumours | Serous cystadenocarcinoma |
Mucinous cystadenocarcinoma | ||
Clear cell carcinoma | ||
Endometroid | ||
Germ cell tumours | Dysgerminoma | |
Immature teratoma | ||
Endodermal sinus tumour | ||
Embryonal carcinoma | ||
Sex cord stromal cell tumours | Granulosa cell tumour | |
Sertoli-Leydig cell tumour | ||
Mesenchymal tumour sarcoma | ||
Lymphoma | ||
Metastatic deposits from other primary tumours | ||
Specific to pregnancy | Theca lutein cysts | |
Luteoma of pregnancy | ||
Decidualised endometrioma |
Physiological cysts
Physiological cysts tend to regress spontaneously without any intervention in most cases.
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Follicular Cysts : Follicular cysts typically occur due to the failure of ovulation or the failure of a mature follicle to rupture, resulting in the formation of a follicular cyst. Generally simple and measuring less than 6 cm, the majority of these cysts resolve by 16 weeks of gestation.
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Corpus Luteal Cyst : The corpus luteum is responsible for secreting progesterone in the early 1st trimester of pregnancy until the placenta assumes this role. Corpus luteal cysts generally regress by 8 weeks of gestation. Failure to recognize a corpus luteal cyst can lead to unnecessary intervention and an increased risk of miscarriage in the early first trimester if it is mistakenly removed.
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Haemorrhagic Cyst : Acute bleeding into a cyst can lead to the formation of a haemorrhagic cyst, often accompanied by abdominal pain. In the majority of cases, symptoms are brief and temporary, and if the patient is stable, conservative management is advisable.
Pathological cysts
Pathological cysts generally do not resolve over time. They can be benign, borderline or malignant.
Mature cystic teratoma (dermoid cyst): These are the most common benign ovarian cysts found in pregnancy. They are generally asymptomatic when <6 cm but are prone to torsion if larger. Various distinctive sonographic features have been identified to facilitate their diagnosis, including:
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A focal or diffuse hyperechoic component.
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Areas displaying acoustic shadowing, known as the “tip of the iceberg” sign.
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Echogenic lines and dots, also termed the dermoid “mesh” or “dot-dash” sign.
The hyperechoic component, referred to as a Rokitansky nodule, usually corresponds to a mixture of hair and sebaceous material or, on occasion, calcification, potentially associated with bone or tooth elements. While the presence of floating echogenic globules within a large mass is an uncommon characteristic, it is reportedly a strong indicator of a dermoid cyst.
Malignant transformation is a serious potential complication of mature cystic teratomas, occurring in up to 2%, with 80% of cases being squamous cell carcinomas. Additional potential complications include hyperthyroidism resulting from teratomas with thyroid hormone-secreting tissue and chemical peritonitis following spontaneous or iatrogenic dermoid rupture.
Endometrioma: Endometriomas are seen as cystic lesions with diffuse low-level internal echoes, often described as “ground glass,” which is present in 95% of endometriomas. When observed through MRI scanning, endometriotic cysts typically display homogeneous high-signal intensity on T1-weighted images and low-signal intensity on T2-weighted images. Asymptomatic endometriomas can be monitored using ultrasound after pregnancy. In cases where concerns exist about the cyst’s potential malignant transformation, MRI can be a valuable tool for assessment.
Borderline and malignant ovarian tumours in pregnancy
Borderline ovarian tumours (BOTs)
Borderline ovarian tumours (BOTs), also known as atypical proliferative tumours, are a distinct subset of epithelial ovarian tumours that exhibit abnormal cell proliferation but lack the invasive characteristics typically seen in malignant ovarian cancers. They have a better prognosis compared to fully malignant ovarian cancers, with a generally low risk of spreading or recurrence.
Borderline ovarian tumours are primarily classified based on their histological subtype, similar to invasive epithelial ovarian cancers. The classification includes:
- 1.
Serous borderline tumours (SBT):
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The most common type of BOT.
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Characterized by papillary structures and serous fluid-filled spaces.
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Can have non-invasive or micro-invasive implants in the peritoneum.
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Rarely, serous BOTs can progress to low-grade serous carcinoma.
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- 2.
Mucinous borderline tumours (MBT):
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Second most common type.
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Composed of mucin-producing epithelial cells.
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Can be intestinal-type (more common) or endocervical-type.
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Less likely to spread beyond the ovary, but occasionally associated with pseudomyxoma peritonei if rupture occurs.
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- 3.
Endometrioid borderline tumOURS:
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Less common.
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Resemble the endometrial tissue of the uterus.
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Often associated with endometriosis.
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- 4.
Clear cell borderline tumours:
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Rare and resemble the clear cell type of invasive ovarian cancers.
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Their biological behaviour and clinical relevance are less well understood.
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- 5.
Brenner borderline tumours:
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Extremely rare.
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Composed of transitional cells resembling the bladder epithelium.
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Malignant ovarian tumours
Malignant ovarian tumours are cancerous growths that arise from different cells within the ovaries. These tumours are categorized based on the type of cell they originate from. Types of malignant ovarian tumour are as follows.
- 1.
Epithelial tumours:
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Most Common: Over 90% of ovarian cancers are epithelial in origin.
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Types:
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Serous : The most common and aggressive form.
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Mucinous : Can grow large and is less aggressive but harder to treat once metastasized.
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Endometrioid and Clear Cell : Often associated with endometriosis.
- •
- ○
- 2.
Germ cell tumours:
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Rarer (5–10%): Typically found in younger women, these tumours arise from the cells that produce eggs.
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Types:
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Dysgerminoma : The most common germ cell malignancy.
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Yolk sac tumour, Teratoma : Other forms, each with varying prognosis and treatment approaches.
- •
- ○
- 3.
Stromal tumours:
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Rare (1–2%): These originate from the ovarian tissue that produces hormones. Examples include granulosa cell tumours and Sertoli-Leydig tumours.
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Hormonal Impact: These can sometimes cause symptoms related to oestrogen or testosterone overproduction.
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Ovarian cysts unique to pregnancy
Theca lutein cysts
These cysts are commonly linked to gestational trophoblastic disease. Additionally, they might be present in pregnancies complicated by fetal hydrops. Resembling ovarian neoplasms, these cysts frequently exhibit a multiseptated or multiple adjacent cyst appearance. The diagnosis is often suggested by the bilateral nature of these cysts and their recognized clinical associations. In cases where ovulation induction or gestational trophoblastic disease is absent, the term “hypereactio lutinalis” may be used to characterize these cysts.
Decidualized endometrioma
Although rare, it is crucial to diagnose these lesions as they can unnecessarily raise concerns about ovarian malignancy. Typically cystic, these lesions often feature small solid components with detectable internal blood flow through Doppler studies. Unfortunately, colour Doppler imaging is unable to distinguish between a decidualized endometrioma and ovarian malignancy. Therefore, awareness of this entity, comparison with scans of a known pre-pregnancy endometrioma, monitoring changes in size or appearance during pregnancy, and employing additional imaging modalities such as MRI are all crucial for accurate diagnosis and management.
Luteoma of pregnancy
This uncommon benign ovarian cyst during pregnancy lacks distinctive sonographic characteristics. Diagnosis may be supported by the presence of maternal virilization, and hirsutism along with elevated serum androgens can aid in the diagnostic process.
Diagnosis of ovarian cysts and cancer in pregnancy
Most of the ovarian cyst in pregnancy are incidentally detected at the time of dating or detailed anomaly scans. Occasionally, the patients would present with symptoms ( Box 1 ). Symptoms are non-specific and overlap with common ailments of pregnancy.

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