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Year : 2013  |  Volume : 23  |  Issue : 4  |  Page : 379-385
Magnetic resonance imaging of placenta accreta

1 Department of Radiodiagnosis, Amala Institute of Medical sciences and Mediscan, Thrissur, Kerala, India
2 Department of Radiodiagnosis, Jubilee Mission Medical College and Research Institute, Thrissur, Kerala, India
3 Department of Gynaecology and Obstetrics, Jubilee Mission Medical College and Research Institute, Thrissur, Kerala, India

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Date of Web Publication21-Jan-2014


Placenta accreta (PA) is a severe pregnancy complication which occurs when the chorionic villi (CV) invade the myometrium abnormally. Optimal management requires accurate prenatal diagnosis. Ultrasonography (USG) and magnetic resonance imaging (MRI) are the modalities for prenatal diagnosis of PA, although USG remains the primary investigation of choice. MRI is a complementary technique and reserved for further characterization when USG is inconclusive or incomplete. Breath-hold T2-weighted half-Fourier rapid acquisition with relaxation enhancement (RARE) and balanced steady-state free precession imaging in the three orthogonal planes is the key MRI technique. Markedly heterogeneous placenta, thick intraplacental dark bands on half-Fourier acquisition single-shot turbo spin-echo (HASTE), and disorganized abnormal intraplacental vascularity are the cardinal MRI features of PA. MRI is less reliable in differentiating between different degrees of placental invasion, especially between accreta vera and increta.

Keywords: Abnormal placental vascularity; dark intraplacental bands; magnetic resonance imaging; placenta accreta

How to cite this article:
Varghese B, Singh N, George RA, Gilvaz S. Magnetic resonance imaging of placenta accreta. Indian J Radiol Imaging 2013;23:379-85

How to cite this URL:
Varghese B, Singh N, George RA, Gilvaz S. Magnetic resonance imaging of placenta accreta. Indian J Radiol Imaging [serial online] 2013 [cited 2021 Mar 1];23:379-85. Available from:

   Introduction Top

Placenta accreta (PA) occurs when the chorionic villi (CV) invade the myometrium abnormally due to defect in the decidua basalis. [1] PA is used as an umbrella term for invasive placentation and is classified on the basis of the degree of myometrial invasion [Figure 1] as shown in [Table 1].
Figure 1 (A-D): Diagrammatic illustration showing different degrees of placental invasion (P, placenta; M, myometrium). Arrow shows stratum basalis of endometrium. (A) Low-lying placenta showing normal stratum basalis of endometrium (arrow). (B) Placenta accreta vera showing invasion of stratum basalis of endometrium and in contact with myometrium. (C) Placenta increta showing partial invasion of myometrium. (D) Placenta percreta showing invasion of myometrium and extension beyond serosa

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Table 1: Classification of placenta accreta

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Prevalence of PA is approximately 1 in 1000 deliveries, with a reported range from 0.04 to 0.9%. Differences in the study population and definition account for this wide range. [1] Major risk factors for PA are placenta previa and previous cesarean section. The risk of developing PA is 3% in women with only placenta previa and increases to 24% in those with placenta previa and one prior cesarean delivery. [2] The risk increases with the number of previous cesarean deliveries. [3] Other risk factors are increasing maternal age and history of uterine surgery. [4]

Placenta previa refers to abnormal low position of the placenta, near to or overlying the internal cervical os. The occurrence is 1 in 200 pregnancies at the time of delivery. The presence of placenta previa in at-risk pregnancies warrants detailed evaluation to exclude the PA. Normally, the lower margin of placenta is seen at least 2 cm away from the margin of the internal cervical os. The placenta previa is divided into four types depending on the relationship and distance to the internal os as follows:

  • low-lying placenta - lower placental edge is within 2 cm from the internal os
  • marginal previa - placental edge extends to the margin of the internal os, but does not cover it
  • complete previa - placenta completely covers the internal os
  • central previa - midportion of the placenta (not the edge) completely covering the internal os.
The consequence of PA is massive hemorrhage at the time of placental separation and complications of blood loss. Hysterectomy is usually required, leading to complications like adjacent organ injuries and serious co-morbidities. Placenta percreta can also lead to disruption of adjacent organs, most often the urinary bladder.

Accurate prenatal diagnosis is the most important factor affecting outcome, as underdiagnosing or overdiagnosing PA can create major problems. It gives opportunity for, timing and site of delivery. It also enables the obstetrician to ensure the availability of blood products, and the presence of a multidisciplinary surgical team. Definitive therapy is an elective cesarean hysterectomy at 34-36 weeks, [1],[2] although hysterectomy is not required or desirable in every case.

USG and MRI are the modalities for prenatal diagnosis of PA, although limitations exist for each technique. As it is relatively inexpensive and easily available, USG remains the primary diagnostic tool for the diagnosis of abnormal placentation. In addition, routine USG examination at 18-20 weeks gestation affords an ideal opportunity to screen for the disorder. Placental lacunae with turbulent flow and abnormal areas of hypervascularity with dilated blood vessels at the placenta-myometrial interphase are the most useful USG markers for PA.

In recent years, there has been an increased interest in the use of MRI for evaluation of suspected PA. MRI should be reserved primarily for equivocal USG findings of abnormal placentation or posterior placenta with risk factors. It also has a complementary role in specifically delineating the extent of an USG-diagnosed placenta percreta.

The reported accuracies for diagnosis of PA by USG (including color Doppler) and MRI showed no statistically significant difference. [5],[6],[7],[8],[9],[10] In high-risk patients, a normal ultrasound at 18-20 weeks of gestational age does not completely exclude PA, and these patients should be reevaluated in the third trimester. MRI is typically not indicated after a negative screening ultrasound due to relatively high negative predictive value of USG.

The purpose of this article is to describe the MRI technique and features of normal placentation and accreta.

Technique of MRI Scanning

Key guidelines

  1. Supine or left lateral decubitus position depending on patient tolerability
  2. Use of multichannel surface coil and oxygen supplementation
  3. Urinary bladder should be moderately distended
  4. T2-weighted half-Fourier RARE and balanced steady-state free precession sequences in the axial, sagittal, and coronal planes
  5. Breath-hold T1-weighted gradient-echo sequence in one plane.
The optimal timing of MRI is not established and usually follows an incomplete or inconclusive USG. Usually second trimester patients can tolerate supine positioning. Left lateral decubitus positioning is preferred for third trimester patients, as it decreases the risk of impaired venous return from caval compression by the gravid uterus. A phased-array surface coil is used whenever possible to maximize signal. Oxygen via a nasal cannula should be given routinely to patients to reduce fetal motion. Urinary bladder should be only moderately full to avoid patient discomfort and for better assessment of potential bladder invasion. A radiologist should be present at the time of the examination and should guide the technologist when repeat sequences or oblique images are needed.

MRI was performed with a 1.5-T scanner (Magnetom Vision, Siemens Medical Systems, Erlangen, Germany). T2-weighted half-Fourier RARE sequence (HASTE or half-Fourier single-shot fast spin-echo) acquired in the axial, sagittal, and coronal planes is the key technique employed for evaluation of placenta. Balanced steady-state free precession (True FISP) sequence in three orthogonal planes and T1-weighted gradient-echo sequence in any one plane are also acquired. HASTE and True FISP sequences are relatively resistant to maternal and fetal motion artifacts and provide reasonable differentiation between the placental tissue and underlying myometrium. T1-weighted gradient-echo sequence is useful in visualizing any high-signal-intensity subchorionic hemorrhage, and use of fat suppression in conjunction improves the conspicuity of blood products. Ideally, all these sequences are acquired during maternal breath holding. If placental accretion is suspected on the basis of preliminary survey, additional images in planes perpendicular to the placenta-myometrium or myometrium-bladder interface are obtained.

Some investigators used gadolinium-based contrast agents to improve the specificity of MRI for diagnosis of PA by better defining the outer placental surface and myometrium. [8] They employed dynamic gadolinium-enhanced (dose up to 0.1 mM/kg) imaging in the arterial, venous, and equilibrium phases over the identical slices, perpendicular to the plane of the placenta-uterine interface, after the plane imaging. This shows early intense lobular enhancement of placenta and subsequent enhancement of myometrium. Although no detrimental effects of gadolinium-based contrast agents on the human fetus were shown, these agents do cross the placenta. [2] Therefore, the accepted practice in pregnancy is the gadolinium-based contrast agents can only be used when the potential risks to the patient are outweighed by the potential benefits of contrast-enhanced imaging.

3-T MRI has attained interest recently because of its increased signal to noise ratio, faster sequences, and higher spatial resolution, in comparison with 1.5-T scanners. 3-T MRI of placenta is acceptable and no proven reproducible harmful effects have been reported so far. Normal intraplacental septi are well delineated on 3-T MRI. It is claimed that 3-T MRI can stage the grade of abnormal placentation more accurately, but tends to overstage in real practice. [9]

MRI appearance of normal placentation and accreta

Knowledge about the normal placental anatomy is essential in understanding the imaging appearances of the normal and invasive placentation.

Anatomy [4]

The placenta has two surfaces - fetal and maternal. It is limited at the fetal surface by the chorionic plate and amniotic membrane. The maternal surface is limited by the basal plate. Also, in between these two surfaces lies the villi, intervillous spaces, and placental septi. The placental septi are projections from the basal plate into the intervillous spaces.

Umbilical cord is attached to the fetal surface (chorionic plate). From the cord insertion, branches of the umbilical vessels (chorionic vessels) radiate beneath the amnion. Chorionic vessels send their branches in a perpendicular direction deep into the placenta and form vascular network of villous trees. The maternal spiral arteries open into the intervillous spaces by piercing the basal plate. Uterine veins drain these spaces also by piercing the basal plate and run parallel to the decidua. This venous network forms the retroplacental echolucent zone described in USG.

Relevant pathological anatomy of PA [11],[12]

Relevant pathological anatomy also needs attention at this context, because of its diagnostic value in PA - intraplacental lacunae (IPL) and placental or venous lakes (VL). IPL refer to intraparenchymal vascular spaces with ill-defined margins, irregular shape, and turbulent flow. They correspond to the increased volume of blood flow and high flow rate of the adherent placenta. Significant number of IPL at 15-20 weeks of gestation is the earliest reliable USG sign (sensitivity 79% and positive predictive value 92%) of PA in at-risk patients. Increase in the number and size of lacunae is associated with increased risk for PA.

VL refer to intraplacental sonolucent space. These appear usually rounded and show laminar flow. These include decidual septal cysts, intervillous thrombosis, and placental infarction (depending on chronicity). IPL sonologically differ from VL by their more indistinct margins and turbulent flow. Intervillous thrombi and placental infarctions are the potential causes of false positives in MRI diagnosis of accreta, due to their T2 hypointensity.

MR imaging appearance of normal placentation [2],[13]

Key imaging features of normal placentation

  1. Homogeneous T2-intermediate signal intensity of placenta
  2. Subtle thin, regularly spaced placental septi
  3. Normal subplacental vascularity
  4. Triple-layered sandwich appearance of myometrium
  5. Pear-shape of normal gravid uterus with smooth contour.
The placenta shows homogeneous intermediate signal intensity on T2-weighted images and is usually clearly distinct from the underlying myometrium [Figure 2]A-C. Subtle thin, linear areas of decreased T2 signal intensity running through the placenta may be seen in high-Tesla MR images, which represent normal placental septi [Figure 2]A, [Figure 3]B and C, and [Figure 4]A and B. These normal septi are usually regularly spaced and uniformly thin. Normal subplacental vascularity is seen as numerous flow voids just under placenta [Figure 2]B. Few intraplacental flow voids can also be seen, usually in the region of umbilical cord insertion.
Figure 2 (A-D): Marginal placenta previa in a 32-year-old woman at 35 weeks of gestation. (A) Sagittal T2 HASTE MR image shows a homogeneous placenta (+) with thin linear areas of decreased signal
intensity (arrows) representing normal placental septa. (B) Sagittal T2 HASTE MR image shows normal subplacental vascularity (arrows) appearing as small hypointensities underneath the placenta. (C,
D) Axial and coronal T2 HASTE MR images show a homogeneous placenta (+) and triple-layered appearance of normal myometrium – peripheral thin hypointense bands (arrowheads) and thickened vascular hyperintense middle layer (arrow)

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Figure 3 (A-C): Varying MRI appearances of normal placentation at different gestational ages. (A) Axial T2 HASTE MR image shows a homogeneous placenta (p) at 23 weeks of gestational age. (B) Axial T2 HASTE MR image shows a slightly lobulated placenta (p) due to visualization of faint sporadic septi (arrows) at 30 weeks of gestational age. (C) Axial T2 HASTE MR image shows a mildly heterogeneous stratified placenta (p) due to multiple placental septi (arrows) at 37 weeks of gestational age (mature)

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Figure 4 (A, B): Normal mature placenta at upper segment of uterus at 37 weeks of gestation. (A, B) Coronal and sagittal T2 HASTE MR images show a mildly heterogeneous placenta with normal placental septi (white arrows) and triple-layered appearance of normal myometrium (white and black arrowheads)

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Placenta appears as a regular homogeneous structure at 19-23 weeks [Figure 3]A. Subsequently, placenta appears slightly lobulated at 24-31 weeks [Figure 3]B due to visualization of faint sporadic septi. This appearance progresses on advancing gestational age. Universal appearance of septi and stratification of placenta into lobules are seen after 36 weeks [Figure 3]C. [13]

The myometrium shows variable thickness and thins as pregnancy progresses. It can be seen as triple layer of signal intensity [Figure 2]C and D, [Figure 4]A and B, [Figure 5]A and B, and [Figure 6]A and B. The inner and outer layers are seen as thin bands of decreased T2 signal intensity. The middle layer is seen as thick intermediate signal intensity and frequently shows multiple vascular flow voids. Uterine contractions can cause transient focal T2-hypointense myometrial thickening [Figure 7]. The gravid uterus usually shows a smooth contour and a wider body and fundus than the lower segment.
Figure 5 (A, B): (A, B) Complete placenta previa in a 30-year-old woman at 36 weeks of gestation. Sagittal and coronal T2 HASTE MR images show normal stratification of placenta (+) into lobules with a smooth continuous curved myometrial interface and layered appearance of myometrium (arrows)

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Figure 6 (A-C): Partial placenta previa in a 28-year-old woman at 34 weeks of gestation. (A, B) Sagittal True FISP and T2 HASTE MR images show a homogeneous placenta (+) with smooth distinct placenta– myometrium interphase (arrows) and triple-layered appearance of normal myometrium. The clarity and sharpness of the interphase is superior in the TrueFISP images. (C) Coronal T2 HASTE MR image shows a homogeneous placenta (+) with multiple normal chorionic vessels subamniotically at fetal surface (arrowheads) and increased subplacental vascularity (arrows)

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Figure 7 (A, B): Axial T2 HASTE and True FISP MR images show focal transient hypointense myometrial thickening (white arrow) at the regions of uterine contraction. Note the normal trilaminar myometrial architecture (black arrow) and myometrial thickening at different locations in the images, denoting the transient nature of contractions

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However, the myometrium can normally appear thin and homogeneous beneath the placenta. This appearance is particularly common at sites where the gravid uterus is compressed by the maternal spine or aorta, just proximal to the bifurcation [Figure 8]. On nonenhanced T1-weighted images, both placenta and myometrium show homogeneous intermediate signal intensity and is not useful for assessment of abnormal placental invasion [Figure 9].
Figure 8: Axial T2 HASTE MR image shows loss of normal trilaminar myometrial architecture and mild focal thinning of placenta at the site of compression of myometrium in front of aorta (black arrow), just proximal to the bifurcation. Normal trilaminar signal pattern of myometrium can be seen at other regions (white arrows)

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Figure 9 (A, B): T1 WI showing normal placentation posteriorly at the upper segment of uterus. Both placenta and myometrium show homogeneous intermediate signal intensity (P, placenta; arrow, myometrium): (A) spin echo image (SE); (B) FLASH 2D image

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Imaging signs predictive of abnormal placentation

Various MR imaging features of PA with differing sensitivities and specificities are described in literature. Earlier MR criteria, which focused on primary signs of direct invasion of placenta into myometrium were nonspecific. The most acceptable secondary signs [4],[14],[15] with good inter-rater reliability are listed below.

Imaging findings of PA

Cardinal signs

  1. Dark intraplacental bands on T2-weighted images
  2. Heterogeneity within the placenta
  3. Abnormal disorganized placental vascularity
    Others - less sensitive signs
  4. Uterine bulging
  5. Focal interruptions of the myometrial wall (high specificity for increta and percreta)
  6. Tenting of urinary bladder (highly specific for percreta)
Dark intraplacental bands [Figure 10]A, [Figure 11], and [Figure 12] appear as nodular or linear areas of low signal intensity on T2-weighted images (HASTE and True FISP) and typically extend within the placenta from the placenta-myometrium interface. These bands are thicker than the normally fine placental septa and show a random distribution. They represent areas of fibrin deposition within the placenta.
Figure 10 (A-E): Low-lying anterior placenta percreta in a 32-year-old woman at 34 weeks of gestation. (A, B) Coronal and axial T2 HASTE MR images show a heterogeneous placenta with thick, dark intraplacental bands (black arrows). Focal interruption of the left inferolateral myometrium and subserosal extension of placental tissue (white arrows). (C, D) Sagittal T2 HASTE and T2 fast spin echo (FSE) MR images show focal interruption of anterior myometrium (black arrowheads), anterosuperior to the internal os and extending subserosally (white arrowheads). Marked heterogeneity of the anterior myometrium, just superior to the invasion noted, represents abnormal vascularity (arrow). (E) Surgical photograph showing the placenta extending through uterine wall (+) and covered by thin serosal layer (arrow). No features of bladder invasion

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Figure 11 (A, B): Complete placenta previa and increta in a 27-year-old woman with history of previous two cesarean deliveries and at 33 weeks of gestation. Hysterectomy specimen showed placental invasion at the lower anterior uterine segment and histopathology was suggestive of increta. (A, B) Sagittal and coronal T2 HASTE MR images show complete previa with a heterogeneous placenta (arrows) due to few thick, dark intraplacental bands and abnormal vascularity

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Figure 12 (A, B): Complete placenta previa and accreta vera in a 30-year-old woman with history of previous two cesarean deliveries and at 36 weeks of gestation. Hysterectomy specimen and histopathology showed placenta accreta vera. (A) Sagittal T2 MR image shows complete previa and heterogeneity of the placenta due to the presence of multiple dark bands (arrows). (B) Coronal STIR MR image also shows marked heterogeneity of placenta due to the presence of dark bands (arrows)

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Heterogeneous signal intensity in the placenta [Figure 10]A, [Figure 11], and [Figure 12] depends primarily on the presence or absence of abnormal T2 dark bands. It may also represent areas of hemorrhage in the placenta or increased vascularity. Homogeneous placenta can exclude abnormal placentation with high levels of confidence.

Abnormal disorganized placental vascularity is described as hypertrophied, tortuous disorganized vessels deep within the placenta, located in some of the areas of dark bands. These areas of signal void on T2 HASTE images show hyperintensity on flow-sensitive True FISP images. This corresponds with IPL described earlier.

A focal outward contour bulge [Figure 10]A-D or disruption of the normal pear shape of the uterus, with the lower uterine segment being wider than the fundus, can be seen in PA. Focal interruptions of the myometrial wall [Figure 10]C and D or extension through the myometrium [Figure 10]E with occasional invasion of adjacent structures can also be seen. Placenta directly invading or tenting the urinary bladder is highly specific for placenta percreta. MRI is particularly useful in showing parametrial extension which is not apparent on USG.

Focal thinning and indistinctness of the myometrium and loss of thin T2 dark uteroplacental interface [Figure 13] are unreliable signs of PA. MRI is less reliable in differentiating between different degrees of placental invasion, especially between accreta vera and increta.
Figure 13 (A, B): Complete placenta previa in a 30-year-old woman with history of previous cesarean delivery and at 35 weeks of gestation. (A, B) Sagittal T2 HASTE MR and True FISP images show a homogeneous placenta (p) with triple-layered appearance of normal myometrium (white arrow) and marked focal thinning of myometrium (black arrows) at the region of cesarean scar

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Common pitfalls in the diagnosis of PA

Dark intraplacental bands are also seen in placental infarction and intervillous thrombus. Placental infarcts are common in term placentas and in patients with risk factors for placental insufficiency. These confounding factors should be kept in mind while diagnosing PA.

Heterogeneity of the placenta is a subjective finding, and the spectrum of normal appearance varies with gestational age. Hence, a good degree of clinical experience is needed for appropriate interpretation of placental heterogeneity. Even though abnormal intraplacental vascularity denotes placental invasion, the increased pelvic vascularity is not a reliable indicator of adherent placentation.

The lower segment widening of gravid uterus may result in more of an hourglass shape to uterus. Even though it is described as a reliable sign of PA, this appearance is seen occasionally in healthy gravid uterus. Imaging in oblique planes, where uterus has rounded contours at uteroplacental interphase, may give rise to pseudo impressions regarding the signs. So, additional imaging perpendicular to the suspicious interphase and localization of abnormality in at least two orthogonal planes are suggested.

   Conclusion Top

MRI is a complementary diagnostic modality in patients with high risk for PA and should be considered when USG is inconclusive or incomplete. Familiarity with MRI technique to assess the placenta and experience with imaging appearances of normal and invasive placentation will help the radiologist in contributing to an optimal outcome.

   Acknowledgement Top

We would like to extend our sincere thanks to Dr. Kaleem Ulla and Dr. Lola Ramachandran, Jubilee Mission Medical College for providing the surgical photograph and to Mr Ratheesh and Mr Jithin, technologists, Mediscan for providing us some excellent images.

   References Top

1.Garmi G, Salim R. Epidemiology, etiology, diagnosis, and management of placenta accreta. Obstet Gynecol Int 2012;2012:873-929.  Back to cited text no. 1
2.Baughman WC, Corteville JE, Shah RR. Placenta accreta: Spectrum of US and MR imaging findings. RadioGraphics 2008;28:1905-16.  Back to cited text no. 2
3.Lim PS, Greenberg M, Edelson MI, Bell KA, Edmonds PR, Mackey AM. Utility of ultrasound and MRI in prenatal diagnosis of placenta accreta: A pilot study. AJR Am J Roentgenol 2011;197:1506-13.  Back to cited text no. 3
4.Derman AY, Nikac V, Haberman S, Zelenko N, Opsha O, Flyer M. MRI of placenta accreta: A new imaging perspective. AJR Am J Roentgenol 2011;197:1514-21.  Back to cited text no. 4
5.Mohamed AG, Nadia FE, Mohamed AI, Ahmed K. Placenta accreta in women with prior uterine surgery: Diagnostic accuracy of Doppler ultrasonography and MRI. Egypt J Radiol Nucl Med 2012;43:473-80.  Back to cited text no. 5
6.Dwyer BK, Belogolovkin V, Tran L, Rao A, Carroll I, Barth R, et al. Prenatal diagnosis of placenta accreta: Sonography or magnetic resonance imaging? J Ultrasound Med 2008;27:1275-81.  Back to cited text no. 6
7.Levine D, Hulka CA, Ludmir J, Li W, Edelman RR. Placenta accreta: Evaluation with color Doppler US, power Doppler US, and MR imaging. Radiology 1997;205:773-7.  Back to cited text no. 7
8.Warshak CR, Eskander R, Hull AD, Scioscia AL, Mattrey RF, Benirschke K, et al. Accuracy of ultrasonography and magnetic resonance imaging in the diagnosis of placenta accreta. Obstet Gynecol 2006;108:573-81.  Back to cited text no. 8
9.Dehdari A, Williams J. Role of 3T MRI in staging of placenta accreta. Paper presented at: ASM 2010. Royal Australian and New Zealand College of Radiologists, Annual Scientific Meeting; 2010 Oct 14-17; Perth, Western Australia.  Back to cited text no. 9
10.Masselli G, Brunelli R, Casciani E, Polettini E, Piccioni MG, Anceschi M, et al. Magnetic resonance imaging in the evaluation of placental adhesive disorders: Correlation with color Doppler ultrasound. Eur Radiol 2008;18:1292-9.  Back to cited text no. 10
11.Comstock CH, Love JJ Jr, Bronsteen RA, Lee W, Vettraino IM, Huang RR, et al. Sonographic detection of placenta accreta in the second and third trimesters of pregnancy. Am J Obstet Gynecol 2004;190:1135-40.  Back to cited text no. 11
12.Finberg HJ, Williams JW. Placenta accreta: Prospective sonographic diagnosis in patients with placenta previa and prior Cesarean section. J Ultrasound Med 1992;11:333-43.  Back to cited text no. 12
13.Blaicher W, Brugger PC, Mittermayer C, Schwindt J, Deutinger J, Bernaschek G, et al. Magnetic resonance imaging of the normal placenta. Eur J Radiol 2006;57:256-60.  Back to cited text no. 13
14.Lax A, Prince MR, Mennitt KW, Schwebach JR, Budorick NE. The value of specific MRI features in the evaluation of suspected placental invasion. Magn Reson Imaging 2007;25:87-93.  Back to cited text no. 14
15.Teo TH, Law YM, Tay KH, Tan BS, Cheah FK. Use of magnetic resonance imaging in evaluation of placental invasion. Clin Radiol 2009;64:511-6.  Back to cited text no. 15

Correspondence Address:
Binoj Varghese
Department of Radiodiagnosis, Amala Institute of Medical Sciences (AIMS), Thrissur, Kerala - 680 055
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0971-3026.125592

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  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8], [Figure 9], [Figure 10], [Figure 11], [Figure 12], [Figure 13]

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