(1)
Department of Fetal Medicine and Obstetric & Gynecological Ultrasound, Manipal Hospital, Bangalore, Karnataka, India
14.1 Abnormal Uterine Bleeding
To investigate abnormal uterine bleeding, one must know what ‘normal’ bleeding is. Features of normal menstrual bleeding are:
Cyclical menstrual flow with cycle length varying from 21 to 35 days.
Duration of menstrual flow or bleeding up to 7 days.
Amount of flow is a subjective parameter (normally, patients change about 3–5 pads per day).
14.1.1 Common Forms of Abnormal Uterine Bleeding
Amenorrhoea – the absence of menstrual periods (for a period of 3 months or more)
Hypomenorrhoea – scanty flow during periods
Oligomenorrhoea – long menstrual cycles with period length of greater than 35 days
Menorrhagia – excessive flow or prolonged flow during periods
Polymenorrhoea – short menstrual cycles
Polymenorrhagia – short cycles with increased flow during periods
Metrorrhagia – acyclical bleeding which could be heavy or minimal
Intermenstrual bleeding – bleeding in between two periods
Postmenstrual bleeding – bleeding (often minimal) just after periods
Premenstrual bleeding – bleeding (often minimal) just before periods
Post-coital bleeding – bleeding following intercourse
Based on the nature of bleeding, one may be able to suspect the type of gynecological pathology leading to abnormal uterine bleeding:
Amenorrhoea and hypomenorrhoea – These are most often due to local endometrial pathology but could be secondary to hormonal disturbances.
Menorrhagia and polymenorrhagia – These patients usually have myometrial pathology (fibroids or adenomyosis). In some cases, endometrial pathology like hyperplasia may be noted.
Metrorrhagia and intermenstrual bleeding – Pathology involving the surface of the uterine cavity can cause irregular bleeding from the surface of the lesion. If it is heavy, one must think of neoplasia or an AV malformation or retained products of conception. If it is minimal, it could be due to an endometrial polyp or hormonal imbalance.
Post-coital bleeding – These patients are likely to have local pathology involving the cervix or vagina (like neoplasia, polyps or infection).
14.1.2 Abnormal Uterine Bleeding in the Reproductive Age Group
- 1.
Causes for decreased flow (amenorrhoea, hypomenorrhoea or oligomenorrhoea):
Pregnancy – This is a frequent cause of amenorrhoea in women of reproductive age group, and a simple urine pregnancy test or serum BhCG levels will help in the diagnosis. Ultrasound may show an intrauterine or an extrauterine pregnancy, which helps to confirm the diagnosis.
Premature menopause – That is, menopause occurring before the age of 40 can also cause amenorrhoea or oligomenorrhoea (in the few months preceding menopause). On ultrasound, the ovaries appear atrophic. Diagnosis can be further confirmed with the help of serum FSH and LH levels.
Asherman’s syndrome – In these cases, patients will often give history of instrumentation. On ultrasound, endometrial scarring can be seen (details in Chap. 4).
Hormonal causes like polycystic ovaries, hyperandrogenism, hormone-producing tumours, hormonal medication, etc., can also cause amenorrhea, hypomenorrhoea or oligomenorrhoea.
- 2.
Causes for increased flow (menorrhagia, polymenorrhagia and metrorrhagia):
Pregnancy related – This includes patients with threatened abortion (Fig. 14.1), incomplete abortion, retained products of conception, ectopic pregnancy, molar pregnancy and gestational trophoblastic disease (GTD). In these cases, ultrasound will help clinch the diagnosis (details in Chap. 10).
Fig. 14.1
A six-week live pregnancy, in a patient presenting with pain and bleeding. (a) Uterus with a gestational sac and subchorionic haemorrhage (arrow). (b) Subchorionic haemorrhage measured
Pregnancy unrelated:
If the flow is cyclical (i.e. the patient complains of excessive flow during periods – menorrhagia or polymenorrhagia), possibilities include myometrial pathologies like fibroid and adenomyosis or an endometrial pathology like endometrial hyperplasia or even an endometrial malignancy. Patients with fibroids and adenomyosis are likely to complain of dysmenorrhoea. On ultrasound, the uterus may be enlarged with fibroids and adenomyosis, or there may be thickened endometrium secondary to hyperplasia or malignancy. This may also be seen in women with bleeding disorders (e.g. Von Willebrand’s disease). Hormonal disorders like hormone-producing tumours or polycystic ovaries can also cause excessive bleeding.
If the flow is acyclical (i.e. metrorrhagia, intermenstrual bleeding or post-coital bleeding), one must think of pathologies involving the surface of the uterine cavity (polyps, malignancy and submucous fibroid) or pathologies of the cervix or vagina (polyps and malignancy). These lesions can be picked up on ultrasound (details of ultrasound diagnosis are available in Chaps. 2, 3, 4 and 5, respectively); those involving the uterine cavity may be better seen with sonohysterogram, while those involving the cervix and vagina may be better assessed with gel sonovaginography (unless the patient is actively bleeding). Sometimes in a patient with a deficient caesarean scar or an acutely retroflexed uterus, brownish postmenstrual spotting may be seen due to retention of menstrual blood in the deficient scar or upper uterine body, respectively.
Both cyclical and acyclical bleeding may coexist in a few conditions, for example, endometrial malignancy and AV malformations (this is a rare condition, and diagnosis has been discussed on Chap. 13), etc.
In patients with a thickened endometrium, possibilities include endometrial polyp, endometrial hyperplasia and endometrial carcinoma. The ultrasound features and their differentiation are discussed in Chap. 4.
Summary of Abnormal Uterine Bleeding
History: particularly menstrual history and history of hormonal intake are important.
Complaints: details of presenting complaint is important – whether it is cyclical or acyclical or intermenstrual or post-coital. Brownish flow indicates discharge of old collected blood.
Rule out pregnancy: an important cause in women of reproductive age group, particularly with unscheduled bleeding.
Per speculum examination is important in diagnosing local, cervical and vaginal pathology.
Ultrasound is the diagnostic modality of choice, particularly TVS.
Previous reports may be helpful in diagnosis.
Beyond the age of 40: think of the possibility of malignancy.
When in doubt, call the patient back for review.
Discussing with the referring gynecologist often helps in appropriate management.
14.2 Pelvic and Adnexal Masses
Pelvic and adnexal masses may arise from the uterus, ovary, tubes and a few other structures, both gynecological and non-gynecological. These patients may at times come with a history of abdominal distention, abdominal mass or pain. Most often, however, the mass is detected or suspected by the clinician on examination of the patient. Pelvic masses which are small can be felt on bimanual examination. Large masses, however, may be felt abdominally.
Ultrasound is the modality of choice for investigating these masses. TVS is ideal and is more accurate in evaluating these masses, not only because of better assessment of their morphology and Doppler flows, but also because TVS is interactive and one can move structures, which helps in knowing their origin, the presence of adhesions, tenderness, etc. TAS is more informative for large masses extending above the true pelvis and in those cases where visualisation may be suboptimal due to fibroids in lower corpus or cervix. Ideally, as mentioned throughout the book, a TAS and TVS should both be done in all cases.
For adnexal masses, the terminology used to describe the morphology of the masses should be based on the IOTA recommendations. In addition, the IOTA consensus group has come out with methodologies to help assess the nature of the mass, particularly whether it is likely to be benign or malignant. This includes a three-step strategy, logistic regression models LR1 and LR2 and the ADNEX model (details of the LR1, LR2 and ADNEX models may be obtained from the references).
The most common of these masses (particularly an adnexal mass) is of ovarian origin. Therefore, whenever one sees an adnexal mass, the first question that one needs to consider is whether it is of ovarian origin (Fig. 14.2). This can be assessed as follows:
Ovaries or ovarian tissue are identified very easily in women of reproductive age group by the presence of small cystic spaces within, i.e. the follicles (both developing and antral follicles). In postmenopausal women with atrophic ovaries, it is more challenging because follicles are not seen.
If both the ovaries are visualised separate from the mass, then it is of extra-ovarian origin.
If the mass is seen lying beside the ovary and there is intervening tissue between the ovary and the mass, or if the ovary, on pressure with the TVS probe, can be seen moving away from the mass or sliding along the mass, then the mass is not of ovarian origin.
If, on the other hand, the mass is seen lying beside the ovary but does not move away from the ovary on pressure, then it is likely to be an exophytic ovarian mass or an extra-ovarian mass adherent to the ovary. In these cases, deciding the site of origin can be challenging.
If the ovarian tissue is seen stretched around the mass (or cyst) as if it were hugging it, then the mass is of ovarian origin. This feature of stretched out ovarian tissue along the walls of the mass is called the ‘crescent sign’.
Sometimes, however, the mass is extremely large, and ovarian tissue may not be seen around it even when it is of ovarian origin. But in these cases, an ovary will not be seen separate from the mass.
Fig. 14.2
Assessing ovarian origin. (a) Ovarian tissue (arrow) seen beside the cyst and stretched around it (‘crescent sign’) – suggesting ovarian origin. (b) Ovarian tissue seen beside the cyst, with a wedge of intervening external tissue (arrow) – suggesting that the cyst may not be of ovarian origin. This can be further checked by applying external pressure with the probe when one will be seen sliding along the other (positive sliding sign) or they may move apart (splitting sign). (c) Both ovaries (small arrows) seen separate from the cyst with some tissue (long arrow) between the right ovary and cyst – suggesting extra-ovarian origin. (d) Both ovaries seen distinctly with the left ovary and cyst far apart in the left adnexa – suggesting the cyst is not of ovarian origin
14.2.1 Ovarian Masses
Ovarian masses can be broadly classified into functional cysts, neoplastic masses, endometriomas and masses of inflammatory origin. The ovary may also be enlarged due to other conditions like torsion, hyperstimulation, polycystic ovaries, ovarian ectopic pregnancy, etc. All these conditions have been dealt with in detail in their respective chapters.
A rare cause for enlarged cystic ovaries is the Van Wyk–Grumbach syndrome (VWGS), a condition associated with juvenile hypothyroidism (of long standing duration and with high levels of TSH), delayed bone age and isosexual precocious puberty. These return to normal on thyroid hormone replacement. These patients have bilateral enlarged multicystic ovaries secondary to stimulation of the gonadal FSH receptor by TSH, resulting in multiple follicular cysts. Histopathological analysis of resected ovaries showed cystic follicles and little, if any, luteinisation. Some reports have suggested myxoedematous infiltration of the ovaries. Awareness of this condition is important because of the high probability of this being diagnosed wrongly as a case of bilateral neoplastic ovaries with inadvertent surgical excision (in a young girl and one that can be treated with simple thyroid replacement). In the case described below, preoperative blood workup picked up the high TSH levels and led to the diagnosis (Fig. 14.3).
Fig. 14.3
Van Wyk–Grumbach syndrome – Bilateral multicystic enlarged ovaries with a very high TSH level of 1980 micIU/ml in a 14-year-old girl with short stature, who presented with the complaint of irregular periods. Both ovaries were enlarged and multicystic. (a) Right ovarian volume – 503 ml. (b) Left ovarian volume – 87 ml. (c) 3D-rendered image showing multiple locules. (d) Flow in septa with RI of 0.48. (e, f) Six weeks after thyroid replacement treatment, the ovaries had reduced in size with lesser number of locules – the right ovarian volume was 129 ml and the left ovarian volume was 74 ml
14.2.2 Uterine Masses
An enlarged uterus presenting as a pelvic mass may be seen in both adenomyosis and fibroids. In adenomyosis, of course, the uterus is usually globular in shape, with distinctive features making diagnosis very simple. With fibroids, the uterus may be irregularly enlarged or there may at times be confusion about the origin of the mass. This is particularly so when the mass is a subserous/pedunculated fibroid. Fibroids have typical ultrasound features but can be confused with adnexal masses, particularly when they show degenerative changes. Fibroids are usually masses within the uterus, but the subserous pedunculated ones can be diagnosed to be of uterine origin by tracing their attachment to the uterus through a pedicle or blood flow. The pedicle may not be well seen unless there is surrounding fluid. Doppler flows are very helpful in assessing the origin of any mass as vessels are seen passing between the mass and the source of origin. Exceptions to this, of course, are true broad ligament fibroids orfibroids seen in cases with disseminated leiomyomatosis. In such cases, however, the ovaries will be seen separate from the mass.
Occasionally, in patients with unicornuate uterus, the adjoining rudimentary horn (particularly when non-cavitary) may present as an adnexal mass, but these masses are attached to the main uterine body and their echotexture is similar to that of the myometrium (Fig. 14.4).
Fig. 14.4
Rudimentary horn presenting as an adnexal mass. (a) Well-defined, isoechoic mass seen in the left adnexa, raising the suspicion of a solid adnexal mass. (b) This mass, on further evaluation, was found to be connected to the main uterine body of a right-sided unicornuate uterus. (c) 3D-rendered image of the unicornuate right uterus
14.2.3 Tubal Masses
The normal fallopian tube is difficult to identify, unless it is surrounded by fluid. It appears as an elongated undulating isoechoic or hyperechoic structure. Tubal masses may be of inflammatory or neoplastic nature or secondary to a tubal ectopic pregnancy. These have been dealt with in their respective chapters. Tubal masses may be seen continuous with the uterine cornua, but often they are not, because the pathological segment of the tube is away from its attachment to the uterus. The distal part of the tube has a broader lumen, and most collections (hydrosalpinx, pyosalpinx or haematosalpinx) are, therefore, seen at its distal end. Cystic tubal masses are generally easy to identify because of their elongated shape and incomplete septa.
14.2.4 Tubo-ovarian Masses
Tubo-ovarian masses are typically secondary to PID. At times, one may be able to differentiate between the tubal and ovarian component; however, often (like in some tubo-ovarian abscesses) this may not be possible. These have been dealt with in the section on PID in Chap. 9.
14.2.5 Paraovarian Masses
These are typically cystic masses seen in the adnexa separate from the ovary. Occasionally, they may be adherent to the ovary, when distinguishing them from an exophytic ovarian cyst can be challenging. They are usually small, unilocular and anechoic but can be large, septate and even undergo torsion. They have been dealt with in the section on paraovarian cysts in Chap. 9.
14.2.6 Pseudoperitoneal or Peritoneal Inclusion Cysts
Pseudoperitoneal cysts are nothing but areas of loculated fluid with adhesions. They may be secondary to chronic infection, endometriosis or previous surgery. They can pose a diagnostic challenge in a patient in whom ovarian cystectomy or ovariotomy has been done for a neoplastic ovarian cyst, where these may be considered as a recurrence of pathology. This has also been dealt with in Chap. 9.
14.2.7 Pelvic Hematomas and Pelvic Abscess
These may be seen to be associated with ectopic pregnancies or infection. They may present as pelvic masses when localised to an area. These are avascular masses, and correlation with other findings helps in diagnosis.
14.2.8 Non-gynecological Masses (Fig. 14.5)
These are rarely seen and most often are either appendicular masses or malignant masses arising from the small or large intestine (e.g. gastrointestinal stromal tumour of the small bowel and anorectal masses). The ovaries are seen distinct from these masses, and they do not originate from the uterus (i.e. no flow is seen between the uterus and the mass).