Indian Journal of Radiology and Imaging Indian Journal of Radiology and Imaging

: 2016  |  Volume : 26  |  Issue : 1  |  Page : 52--62

Fetal MRI: A pictorial essay

Sapna Rathee, Priscilla Joshi, Abhimanyu Kelkar, Nagesh Seth 
 Department of Radiodiagnosis, Bharati Hospital, Pune, Maharashtra, India

Correspondence Address:
Dr. Sapna Rathee
C/O SR Century Public School, Delhi Rohtak Road, Bahadurgarh - 124 507, Jhajjar, Haryana


Ultrasonography (USG) is the primary method for antenatal fetal evaluation. However, fetal magnetic resonance imaging (MRI) has now become a valuable adjunct to USG in confirming/excluding suspected abnormalities and in the detection of additional abnormalities, thus changing the outcome of pregnancy and optimizing perinatal management. With the development of ultrafast sequences, fetal MRI has made remarkable progress in recent times. In this pictorial essay, we illustrate a spectrum of structural abnormalities affecting the central nervous system, thorax, genitourinary and gastrointestinal tract, as well as miscellaneous anomalies. Anomalies in twin gestations and placental abnormalities have also been included.

How to cite this article:
Rathee S, Joshi P, Kelkar A, Seth N. Fetal MRI: A pictorial essay.Indian J Radiol Imaging 2016;26:52-62

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Rathee S, Joshi P, Kelkar A, Seth N. Fetal MRI: A pictorial essay. Indian J Radiol Imaging [serial online] 2016 [cited 2020 Apr 5 ];26:52-62
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USG has routinely been used in the evaluation of obstetrical andgynecological conditions since the late 1950s.However, due to its limitations of a small field of view, operator dependence, a need for an additional imaging modality has emerged, especially in cases of oligohydramnios and obese patients. As MRI does not involve radiation, is safe for the fetus, and provides detailed structural anatomy, it has emerged as a suitable adjunct to USG.

MRI was first performed in 1983 for evaluation of the placenta and fetus. [1] The main drawback of MRI was fetal motion which was overcome in the 1990s with the development of ultrafast sequences. [2] According to the Safety Committee of the Society for MRI, no known biological risks have so far been proven to be associated with MRI.Acoustic noise and biological effects are the main safety concerns for fetal MRI. The noise intensity produced by gradients in fetal MRI can reach 120 dB. Fetal hearing damage, which is a potential hazard, has still not been confirmed in practice. [3]

Fetal MRI is indicated in pregnant women when other non-ionizing diagnostic imaging methods are inadequate or when the examination provides important information that would otherwise require exposure to ionizing radiation. [4] The quality of fetal MRI is comparable to postnatal MRI, facilitating discussion of surgical treatment options. Relative advantages and disadvantages of antenatal USG and MRI are described in [Table 1].{Table 1}

Fetal MRI should be performed in the second or third trimester. As the teratogenic effects of MRI in early pregnancy are not confirmed and the multilayer structure of the cerebral parenchyma is appreciable after 16 weeks of gestation on a 1.5 T MR, MRI is best performed after completion of organogenesis (16 weeks). [5] The patients are advised to fast for 4 h prior to the study, to reduce bowel peristalsis artifacts and to prevent postprandial fetal motion. Patients are asked to empty the urinary bladder prior to the study and positioned feet first supine or in left lateral decubitus position. A single-body matrix coil is often used over the abdomen and pelvis to improve the spatial resolution. No medication or sedation is required.

 MR Protocol

MR studies are best performed on a MRI system with field strength of 1.5 T. Imaging is performed during free breathing with respiratory gating to avoid artifacts.

Initially, multiplanarT2-weighted (T2W) scout images are often obtained using 5-7-mm-thick slices with a 1- to 2-mm gap and a large field of view, followed by a T2W_TSE sagittal sequence of the mother, to visualize the position of the fetus, placenta, and cervix as well as assess the uterus. Sequences should be performed in the coronal, sagittal, and axial planes through the region of interest for confirming/excluding the suspected fetal anomalies. This is followed by sequences through the rest of the fetus to rule out/detect associated anomalies. Ultrafast T2W sequences known as single-shot rapid acquisition with refocused echoes (i.e. single-shot fast spin-echo or half-Fourier acquired single-shot turbo spin-echo) are often used. Single images acquired in less than 1 s, decrease the artifacts from fetal motion. In addition to the regular T2W_TSE and balanced turbo field echo (BTFE) sequences for evaluating the fetus, T1-weighted image (T1WI) sequences of the fetal abdomen in the sagittal and coronal planes help to confirm the presence of meconium (which appears bright on T1WI) in the large bowel and rectum, up to the anal verge [Table 2]. It should be noted that BTFE, being a heavily T2W sequence, demonstrates fetal anatomy better at an early gestational age, as compared to the regular T2W sequence.{Table 2}

For detailed neurological evaluation, multiplanar T2W and BTFE sequences can be obtained. Ventricular atrial measurements are typically in the axial plane. Cavum septum pellucidum and corpus callosum (CC) must be identified. Age-appropriate sulcation and gyration is evaluated next. The tegmento-vermian angle [Figure 1] is measured on the midline sagittal image of the fetal brain. It is the angle formed by lines along the anterior surface of the vermis and the dorsal surface of the brainstem. The angle should be near zero. Large angles indicate elevation of the vermis due to the developmental anomalies of vermis.The cerebellar transverse diameter and cisterna magna are measured in axial images.{Figure 1}


The most important indications of fetal MRI are evaluation of the fetus in suspected chromosomal syndromes/familial genetic disorders where USG is normal, confirmation of anomalies/findings detected on USG, and detecting/excluding associated anomalies. Fetal MRI can also assist in planning prenatal/postnatal intervention where necessary [Table 3].{Table 3}

Spectrum of anomalies

CNS anomalies

The most common indication for CNS imaging was ventriculomegaly, followed by suspected CC abnormalities, cerebellar anomalies, congenital infections, malformations of cortical development, and posterior fossa anomalies. Ventriculomegaly is defined as atrial width equal to or more than 10 mm on the sonogram. [Figure 1] shows normal CC and brain anatomy.

CC anomalies

The CC is a midline cerebral structure consisting of white matter tracts connecting two cerebral hemispheres. Its formation starts at the 10 th week of gestation with genu formation and is completed by 18-20 th weeks with the formation of rostrum. [6] It is seen as a C-shaped, curved hypointense structure on T2W images in the midsagittal plane [Figure 1]. Cerebral ventriculomegaly raises the suspicion of CC agenesis. MRI is superior to prenatal USG for evaluation of CC at any gestational age as it actually shows the CC, whereas ultrasonography (USG) relies on indirect signs like absence of cavum septum pellucidum for diagnosing CC anomalies. MR imaging features suggestive of CC agenesis are parallelization of lateral ventricles (Viking helmet sign), colpocephaly, and a high riding third ventricle [Figure 2].{Figure 2}


It is characterized by lack of cleavage of prosencephalon. [7] There is incomplete separation of two cerebral hemispheres. MRI is complementary to USG for confirmation and further evaluation of the subtypes of holoprosencephy, i.e. alobar [Figure 3], semilobar, and lobar, in order of severity. The spectrum of findings in holoprosencephaly includes monoventricle, fusion of thalami, and absence of falx, CC, and optic tracts. Associated anomalies include cleft lip, hypertelorism, encephaloceles [Figure 4], andrenal and cardiac anomalies.{Figure 3}{Figure 4}

Neural tube defects

These are a group of anomalies due to incomplete closure of the neural tube in early pregnancy. They include spina bifida, meningocele, meningomyelocele, and lipomeningomyelocele.


It is a type of neural defect comprising absence of cranial vault and cortical tissue [Figure 5]. It can be associated with spina bifida, congenital heart anomalies, skeletal anomalies, gastrointestinal anomalies, and diaphragmatic hernias.{Figure 5}


It is a neural tube defect, more common in females, with an incidence of 10 in 10,000. [8] It is characterized by retroflexion of head, absence of occipital bones, spinal deformities, fusion of cervicothoracic vertebrae, and absence of neck causing upward turning of chin and face [9] [Figure 6].{Figure 6}

Chiari malformations

These are a group of disorders associated with congenital downward displacement of the cerebellum and brainstem, showing peg-like tonsillar herniation into the upper cervical canal on T2W images with a small posterior fossa. Four types are known. Chiari I is the commonest type with tonsillar herniation. Type II is associated with lumbosacral spinal myelomeningocele [Figure 7]. Type III is associated with a cervical/occipital encephalocele, and type IV is a variation of cerebellar hypoplasia. [10] The limitation of USG in visualizing the posterior fossa and detecting tonsillar herniation has been overcome by fetal MRI.{Figure 7}

Genitourinary tract anomalies

MRI scores over USG as fetal kidneys are well visualized and can be evaluated in the early gestational period as well as in the presence of scanty liquor. Oligohydramnios limits the assessment of genitourinary anomalies on US due to the poor sonic window, thus making MRI a useful adjunct. Fetal ureters are not visualized on USG unless dilated. Hydronephrosis is the most common genitourinary abnormality detected on prenatal USG. [11] Commonest causes of hydronephrosis are pelviureteric junction obstruction, vesicoureteral reflux, megaureter, and posterior urethral valves (PUVs).

Posterior urethral valves

It is the commonest cause of hydronephrosis and obstructive uropathy in male infants. On antenatal USG, the urethra shows a "keyhole" appearance with a distended urinary bladder and urethra proximal to valve [Figure 8]. Three types of PUVs were described in the past; however, at present, only one type is accepted (type I). [12] Fetal MRI helps in diagnosing PUVs with associated hydronephrosis or renal dysplasia.{Figure 8}

Congenital megaureter

An infantile ureter measuring more than 7 mm, visualized as a hyperintense tubular structure posterior to the bladder on T2W sequences is termed as a megaureter. [13] It can be further classified as obstructed primary megaureter, refluxing primary megaureter (vesicoureteric reflux), and non-refluxing obstructed primary megaureter. [13]

Antenatally, this is seen as a dilated collecting system and ureter [Figure 9], as was seen in a 25-week pregnancy in our series. Reflux maybe excluded postnatally.{Figure 9}

Multicystic dysplatic kidney

In multicystic dysplastic kidneys [Figure 10], multiple small non-communicating cysts are seen dispersed throughout the renal parenchyma. It usually affects one kidney with associated renal abnormalities likes vesicoureteric reflux, pelviureteric junction obstruction, ureteral ectopia, and ureterocele in the contralateral kidney. [14] The non-communication of the cysts helps differentiating it from hydronephrosis.{Figure 10}

Chest anomalies

Fetal lungs appear hyperintense on T2W and BTFE images. Common fetal thoracic anomalies are congenital diaphragmatic hernia (CDH), congenital pulmonary airway malformations (CPAM), and bronchopulmonary sequestration (BPS). [15]

Lung volume is calculated on USG by lung to head ratio (LHR); if it is >1.6, survival is >83%. In MRI, total fetal lung volumes (TFLV) can be calculated. Cannie et al.[16] conducted a study in 200 fetuses without abnormalities at University Hospital Gasthuisberg (Belgium). Total lung volume correlated best with fetal body volume (FBV) than with all other biometric variables. The estimated lung volume ELV is calculated by the equation: ELV= [(2.0 × 10 -9 ) x FBV 3 ] - [(1.19 × 10 -5 ) x FBV 2 ] + (0.0508 × FBV) - 1.79. All fetuses with values < 14.3% have a 100% mortality rate and those with values >32.8 have a 100% survival rate. [16] Thus, MRI scores over USG in calculating the lung volume more accurately and, therefore, predicting the fetal outcome. [16]

Congenital diaphragmatic hernia

In CDH, the diaphragm is incompletely formed resulting in a defect through which the contents of the abdomen can enter the thoracic cavity [Figure 11]. Left-sided diaphragmatic hernias are more common than right-sided ones, with omental fat, stomach, and small bowel loops being the commonest structures to herniate.In addition to more accurate evaluation of residual lung volume, MRI assesses the contents of the hernia more accurately than USG, hence determining the outcome.{Figure 11}

Congenital pulmonary airway malformations

They are abnormal pulmonary solid/cystic masses vascularized by the pulmonary artery and drained via pulmonary veins.Stocker et al.[17] classified them as: Type I (one or more cysts >2 cm), type II (multiple cysts 2-0.5 cm), and type III (large microcystic lesion <0.5 cm). CPAMs appear hyperintense on T2WI than the normal lung parenchyma.

Bronchogenic cysts

These are congenital malformations of the bronchial tree (type of bronchopulmonary foregut malformation) appearing as large solitary cystic lesions. Most bronchogenic cysts appear as single lesions typically located in the mediastinum [Figure 12], in the carinal region, but can also be found in the lung parenchyma or extend below the diaphragm as dumbbell-shaped cysts. [18]{Figure 12}

Cystic hygromas

They are known as vasculolymphatic origin anomalies. [19] They can arise anywhere along the lymphatic system; however, in most cases, they are located in the head and neck region. Cystic hygromas are multilobulated, thin-walled, lymph-containing sacs [Figure 13].{Figure 13}

Other anomalies

Amniotic band syndrome

These are a group of congenital anomalies affecting the limbs and internal organs due to early rupture of amnion leading to fibrous bands with entrapment and herniation of the fetal parts [20] [Figure 14]. Multiple amniotic bands maybe associated with colpocephaly due to CC dysgenesis.{Figure 14}

Congenital vascular malformations

These are a group of congenital dysplasias affecting the arterial, capillary, or venous system, presenting at birth. Sturge Weber, Klippel-Trenaunay, Maffucci, and Proteus syndromes are a few of these complex malformations.

Klippel-Trenaunay syndrome [Figure 15] comprises bony or soft tissue hypertrophy (localized gigantism), venous malformations, and port wine hemangiomas. [21]{Figure 15}

Twin pregnancies

Miscellaneous conditions were seen in twin pregnancies including conjoint twins, genitourinary anomalies (renal agenesis) involving one twin [Figure 16], dilated PUVs [Figure 17], and twin reversed arterial perfusion sequence (TRAP) syndrome.{Figure 16}{Figure 17}

TRAP sequence

It is seen in multifetal monochorionic pregnancies. It consists of abnormalities resulting from entrapment of various fetal parts from a disrupted amnion.The condition results in one normal (pump) twin and abnormal (acardiac) co-twin [22] [Figure 18]. The acardiac twin is further classified as acardiusanceps (when the head is poorly formed), acardiusacephalus (if the head is absent), acardiusacormus (presence of head only), and acardiusamorphous (unrecognizable amorphous mass). [23]{Figure 18}

Placental anomalies

Placenta previa, accreta, increta, and hydatiform molar pregnancy with live fetus [Figure 19] were few of the placental indications for performing fetal MRI.{Figure 19}


The main role of MRI was to confirm/exclude lesions suspected on USG, as well as to define their extent and demonstrate associated abnormalities.

Fetal MRI scored over USG due to its higher spatial resolution, larger field of view, and ability to visualize fetal anatomy well, despite scanty liquor. Maternal factors such as echogenic abdominal wall and obesity are also not deterrents.

Fetal MRI is increasingly used in clinical practice, partly because of the increasing interest in fetal surgery and fetal medicine. [24] It allows simultaneous imaging of different organ systems with reproducibility of images, producing images akin to postnatal scans, thus facilitating surgical planning and intervention. It helps predict postnatal management and in genetic counseling.

Sequences such as DWI, Apparent Diffusion Coefficient, MRI spectroscopy, functional imaging, and volumetric data acquisition are still under research and show future promise.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.


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