|Home | About | Journals | Submit | Contact Us | Français|
Infertility in females is multifactorial in origin. Though hysterolaparoscopy is the gold-standard investigation, USG is usually the first-line investigation. MRI has expanded the usefulness of imaging in female infertility. This pictorial essay reviews the role of imaging in the evaluation of female infertility.
Infertility is defined as failure to conceive a desired pregnancy after 12 months of unprotected intercourse. Approximately 10% of married couples are infertile. Males and females are equally affected. The causes of female infertility can be broadly categorized into the following:
Uterine causes – Congenital anomalies, infections, uterine synechiae, focal lesions, intrauterine scar, cervical stenosis, reduced uterine perfusion, and alterations in endometrial thickness and vascularity.
Ovarian causes – Follicular and ovulation abnormalities, stromal vascularity, and endometriosis.
Tubal causes – Infections, obstruction.
It is the first-line investigation and can be coupled with color Doppler and 3D/4D scans.[2,3] It is readily available, inexpensive, noninvasive, radiation-free, relatively less time consuming, and easily repeatable. Limitations include subjective errors, limited field of view, interference by obesity or by gaseous bowel loops, suboptimal visualization of fallopian tubes and broad ligament, failure to delineate small ovaries, and inability to obtain images in the surgical plane.
USG helps in determining the morphology of the uterus and ovaries, uterine and ovarian perfusion, and endometrial thickness, volume, and vascularity. It detects pathological lesions, including tubal lesions and abnormalities of follicular maturation and ovulation. Tubal patency can be confirmed through sonosalpingography. USG can guide oocyte retrieval and embryo transfer in in vitro fertilization procedures and drainage of pelvic collections or cystic lesions.
It is best for delineating the morphology and orientation of pelvic structures. Though it is noninvasive and radiation-free, it has limited availability and high cost, and hence cannot be repeated easily.[2,3] Longer examination time, failure to delineate sub-centimeter uterine lesions, and inability to characterize endometriomas at some stages are other limitations. MRI is contraindicated in patients with cardiac pacemakers and cochlear implants.
MRI also detects pathological lesions, including tubal lesions and pituitary adenoma. It helps in predicting the prognosis in conservatively treated cases of leiomyoma, adenomyosis, and endometriosis.
It is a less-preferred procedure used to visualize the uterine cavity and confirm tubal patency. It involves ionizing radiation and carries the risk of infection and injury.
It involves airless, sterile, saline infusion through a soft plastic catheter in the cervix with simultaneous endovaginal USG. It allows excellent visualisation of the endometrial cavity and its lining. The procedure can also confirm tubal patency by demonstrating spillage of saline from a distended tube into the pelvic cavity.
This is characterized by a combination of multiple clinical manifestations (i.e., hirsutism, menstrual disturbances, anovulatory cycles, and infertility) and hormonal imbalance (an abnormal luteinizing hormone / follicular stimulating hormone (LH/FSH) ratio and excessive androgen secretion).
USG characteristically reveals rounded ovaries with normal (30% case) or increased volume, multiple peripheral, sub-centimeter follicles (at least 15) with no dominant follicle (‘string-of-pearls’ appearance), thickened walls, and an echogenic and vascular stroma. Bulky and thick-walled ovaries with multiple, peripheral, sub-centimeter T2-hyperintense cysts and hypointense stroma are characteristic findings on MRI.
MRI is the modality of choice for detecting pituitary adenoma. Microadenoma (<1 cm) is usually hypointense to the normal pituitary on T1W images. Convex pituitary contour and deviations of the pituitary stalk are indirect signs. Dynamic postcontrast MRI reveals strong enhancement of the normal pituitary and its stalk in the early phase in contrast to the faint enhancement of a microadenoma. Macroadenomas (>1 cm) may compress/invade surrounding structures, including the optic chiasm, cavernous sinus, and bony sella.
These mainly include destruction or obstruction and peritubal adhesions.
HSG is useful for assessing tubal patency. Recently, MRI-based HSG has also been introduced. MRI is superior to USG for studying the tubes. Dilated tubes appear as fluid-filled, tortuous, sausage-shaped masses adjacent to the uterus with incomplete septae appearing as hyperechoic mural nodules (beads on string sign) and short linear projections (cogwheel appearance). The presence of partially effaced longitudinal folds inside the masses is specific for fallopian tubes on MRI. The presence of a normal-appearing ipsilateral ovary is a clue to the presence of a tubal mass.
PID is a common cause of infertility and can manifest as pelvic collections, tubo-ovarian collections, uterine or broad ligament infection.
USG and MRI are equally sensitive in detecting tubo-ovarian collections. The presence of peripheral vascularity of high-resistance type on color Doppler USG is suggestive of an infective mass. The presence of a high-signal-intensity inner rim on T1W images and enhancement on postcontrast images are helpful signs. MRI is superior to USG for revealing an infected uterus and broad ligament which appear hyperintense on T2W images.
Other signs of PID include probe tenderness, thickening of the tubes (mural thickness more than 5 mm) and tubo-ovarian masses (tube and ovary identifiable but inseparable).
This condition mostly involves the ovaries but can secondarily involve other pelvic structures. USG is the preferred technique and shows a typical endometrioma located in the ovary as a well-defined cystic lesion with homogeneous low-level internal echoes (chocolate cyst) (more than 95%). It may also appear as an anechoic cyst, cystic mass with fluid-debris level or as a solid-appearing mass with or without thick septae. The presence of hyperechoic wall foci is characteristic on USG. MRI is more sensitive in detecting an endometrioma which appears hyperintense on T1W images and hypo- to hyperintense on T2W images. Fat-suppressed T1W images are very useful for detecting peritoneal implants.
The tubes may be involved in the form of a hematosalpinx or with peritubal adhesions, while uterine involvement appears as adenomyosis. Adhesions are seen on MRI as hypointense strands within the adjacent fat, obscuring adjacent interfaces. A posteriorly displaced uterus, kissing ovaries (both ovaries lying in the pouch of Douglas (POD) inseparable from each other), elevated posterior vaginal fornix, angulated small bowel loops, hydro-/hematosalpinx, and multilocular fluid collections are indirect indicators of pelvic adhesions.
It infrequently causes infertility by interfering with transportation of sperms or implantation due to distortions of the uterine contour and cavity. Endovaginal USG is as sensitive as MRI in the detection of leiomyoma. MRI however is superior in the preoperative evaluation of the site, number, and size of leiomyomas.
A typical leiomyoma on USG appears as a well-defined, hypoechoic to heteroechoic solid lesion with variable posterior acoustic shadowing located in a submucosal, intramural, or subserosal location. Color Doppler reveals peripheral vascularity of mild to moderate resistance, differentiating it from an adenomyoma which reveals moderate central and peripheral vascularity of relatively low resistance. Leiomyoma appears hypointense to myometrium on both T1W and T2W images.
MRI can monitor post-treatment changes and recurrences in patients treated with uterus-conserving methods of treatment.
It uncommonly causes infertility possibly by reducing uterine/endometrial receptivity. Both endovaginal USG and MRI are equally sensitive for making a diagnosis.
USG findings include a diffusely enlarged or globular uterus, asymmetric walls (>2.5 cm), ill-defined areas or diffusely altered uterine echogenicity, myometrial or subendometrial cysts, indistinct endometrial-myometrial interface, subendometrial echogenic nodules or strands with surrounding hypoechoic myometrium, and undulating outer margin of endometrium. MRI findings include hypointense masses with poorly defined margins on both T1W and T2W images; focal or diffuse, symmetric or asymmetric, widening of the junctional zone (>12 mm) of the uterus; presence of hyperintense foci representing ectopic endometrium on T2W images. MRI can be used for monitoring patients undergoing conservative gonadotropin-releasing hormone (GnRH) analogue therapy.
These are considered as causes of infertility when all other causes have been excluded. Multiplanar MRI is diagnostic. These are classified according to the American Fertility Society criteria as follows:
USG is the investigation of first choice in infertile females, as it is highly accurate in determining common causes of infertility.
MRI should be used as a second-line tool in patients with complex clinical manifestations with normal USG; equivocal, atypical, or multiple USG findings; or when a particular question cannot be answered on USG. It serves as a useful adjunct to diagnostic hysterolaparoscopy, especially in patients with tubal diseases and endometriosis.
The author likes to acknowledge the role of Dr. Neetu Rastogi, Consultant Gynecologist and Obstetrician, Yash Hospital & Research Center for her selfless efforts in making this study a success. The author also likes to acknowledge the role of his team of technicians, Mr. T.S. Rajput, Mr. Shivam, Miss Anju, and Miss Deepali for their kind help in this study.
Source of Support: Nil
Conflict of Interest: None declared.