AssessmentsOvarian cysts and tumors: Pathology review
USMLE® Step 1 style questions USMLE
A 61-year-old woman, gravida 2 para 2, comes to the clinic due to pelvic discomfort and fatigue over the past 6 months. The patient was previously healthy, other than a history of polycystic ovarian syndrome. Menarche occurred at age 12, and menopause occurred 2 years ago. Both of the patient’s children were delivered via Cesarean sections due to personal preference. Family history is significant for breast cancer in her cousin at age 56 and colon cancer in her father at age 55. Vitals are within normal limits. BMI is 35 kg/m2. On physical examination, the abdomen is bloated, and shifting dullness is present. Pelvic examination reveals a left-sided adnexal mass. The patient undergoes a hysterectomy and bilateral salpingo-oophorectomy, followed by adjuvant chemotherapy. A pathohistological analysis is consistent with serous cystadenocarcinoma of the ovary. Which of the following is the most significant risk factor for this patient’s condition?
Content Reviewers:Yifan Xiao, MD
Contributors:Robyn Hughes, MScBMC, Sam Gillespie, BSc, Samantha McBundy, MFA, CMI, Antonia Syrnioti, MD
Menarche was at age 10 and menopause at age 57. On physical examination, a slightly painful nodule is palpated around the umbilicus. Transvaginal ultrasound showed a large, irregular cyst with heterogeneous fluid in her right ovary.
Later that day, 6-year-old Gloriana is brought to the office by her mother, who is worried that her daughter is more “womanly” and taller than the other girls her age. Over the last few months, she has also occasionally complained of vague abdominal pain. Physical examination reveals coarse pubic hair and significant breast enlargement. The child’s height is also in the 96th percentile. Laboratory studies also showed increased inhibin b levels.
Based on the initial presentation, Rebecca and Gloriana’s symptoms are caused by some form of ovarian mass. Broadly speaking, ovarian masses include ovarian cysts and tumors. Starting with ovarian cysts, these are fluid-filled sacs on or in the ovaries and can be classified into simple and complex cysts. Simple cysts are generally small, they contain a clear serous liquid, and have a smooth internal lining. The classic example is a follicular cyst which is a dominant follicle that fails to rupture before ovulation and keeps growing. This can happen, if say, the normal surge of LH that causes ovulation just doesn’t happen during a given menstrual cycle. In fact, follicular cysts are the most common type of ovarian mass in young individuals. For your test, remember that if you encounter multiple follicular cysts, they are usually associated with polycystic ovary syndrome, or PCOS. This is caused by a dysfunction in the hypothalamic-pituitary-ovarian axis that causes chronic anovulation, which may lead to amenor rhea, or absent menstruation, and excess androgen production, which may lead to hirsutism.
Another type of simple cysts are the corpus luteum cysts. Normally, after ovulation, the follicle remnants become the corpus luteum, which regresses during the luteal phase. If instead of regressing, the corpus luteum continues to grow, then the arteries nourishing it can rupture and hemorrhage into the cyst. So a high-yield fact to know is that corpus luteum cysts are also called hemorrhagic cysts. The last kind of simple cysts are theca lutein cysts. These are caused by overstimulation by human chorionic gonadotropin, or hCG, a hormone that’s produced by the placenta, so they’re only seen in pregnancy. For your test, keep in mind that since hCG stimulates growth of the follicular theca cells and resting follicles can be found on both ovaries, these cysts are usually bilateral. Another important thing is that theca lutein cysts are much more likely to develop when there’s more hCG than usual, so the scenario will usually include multiple fetuses, or gestational trophoblastic disease, like hydatidiform mole, or choriocarcinoma.
Okay, now, the second category of cysts are complex cysts. These are generally large, have irregular borders, internal septations creating a multilocular appearance and the fluid inside these cysts tends to be heterogeneous, meaning there’s something other than fluid inside it. In many cases, a complex cyst could be part of an ovarian tumor. Speaking of ovarian tumors, they can be divided into three categories: epithelial ovarian tumors, which derive from the surface epithelium of the ovary, germ cell tumors, which derive from primordial germ cells which are the cells that can give rise to all other tissues and organs, and sex cord-stromal tumors, which derive from sex cord-stromal cells that originate from the connective tissue of the ovary. For your exams, remember that epithelial tumors account for over seventy percent of all ovarian tumors.
The other thirty percent comes from germ cell and sex cord-stromal tumors. Epithelial ovarian tumors can then be subdivided into four types: serous, mucinous, endometrioid and transitional. Serous tumors are usually cystic and full of watery fluid. Mucinous-type tumors are similar to the serous type, but they’re full of a mucus-like fluid, which is where they get their name. Both serous and mucinous tumors can be benign, malignant, or borderline, meaning that they have a mix of benign and malignant characteristics.
The benign type is called serous or mucinous cystadenoma. Cystadenomas are usually a single cyst lined with simple cuboidal and columnar cells. On your test, they most commonly arise in premenopausal women who are between thirty and forty years old. What sets them apart is that serous cystadenomas, which are the most common type of ovarian cyst, tend to be bilateral and are lined with fallopian tube-like epithelium. On the other hand, only five to ten percent of mucinous cystadenomas are bilateral, and they are lined with mucous secreting epithelium. The malignant type is called serous or mucinous cystadenocarcinoma. Cystadenocarcinomas have a thick, shaggy lining due to inflammation, edema and overcrowding of the epithelial cells. They are also more common in postmenopausal women. The serous type is the most common malignant ovarian neoplasm and they tend to be bilateral. Another high-yield fact to remember is that, serous cystadenocarcinomas contain psammoma bodies which are circular plaques of calcium deposits around necrotic or dead cells.
On the other hand, an important clue to the mucinous type is that it can cause pseudomyxoma peritonei, pseudo meaning false, myxoma meaning mucinous tumor, and peritonei telling us its location. So the mucinous material can leak from the ovary into the peritoneum, resulting in metastasis to the appendix or other parts of the GI tract. Finally, there is a borderline type of both serous and mucinous tumors and it has a mix of characteristics from both benign and malignant types.
The one thing to keep in mind here is that it usually has a better outcome than the malignant type since it is not as likely to metastasize. So then we’ve got tumors from endometrial cells, which are called endometriomas. These are benign cysts within the ovary that occur in endometriosis, which is when endometrial tissue from the uterus grows on the ovary. Because they’re functionally the same as the endometrial tissue inside the uterus, endometriomas respond to hormones just like the uterus would. And because of this, endometriomas tend to bleed within the cyst cavity during menstruation, and over time, they fill up with old blood that turns a dark brown color. Hence examiners love to call them “chocolate cysts”. If these cysts get too large, they can rupture and spill their “chocolate-like” contents inside the peritoneal cavity. Another commonly tested fact is that there’s a very rare subclass of endometriomas, the endometrioid tumor, which is malignant and composed of endometrial-like glands. The last type of epithelial tumors come from transitional cells, and these are better known as Brenner tumors. They are benign and made up of bladder-like tissue which gives them a pale yellow tan color. A high-yield fact here is that under the microscope, the cell n