MRI contrast agents during lactation and pregnancy are categorized as group C according to the FDA (food and drug administration) classification. Therefore, contrast agents are not recommended during pregnancy, although some guidelines such as the European Society of Urogenital Radiology find this harmless since the proven teratogenic effects have not been reported in humans (
25). Gadolinium crosses the placenta and some of it is contained in the amniotic fluid by excreting from fetal kidneys; hence, the toxic effects of free gadolinium cannot be ruled out on the fetus (
26) routinely intravenous gadolinium should be avoided during pregnancy and used only if it is judged absolutely essential. Gadolinium may cause a high blood level in the fetus; this condition in adults causes the nephrogenic systemic fibrosis (NSF) syndrome. The probability of this condition in the fetus and infants under the age of 1 is low due to underdeveloped kidney function. However, in some academic sources, the use of gadobenate demeglumine and gadoterate megluminine (dotareme) are recommended because it has not been reported any case of NSF by injecting these two drugs until now (
8). The national radiological protection board in the United Kingdom stipulates in its principles for the protection of patients and volunteers during MRI that it “might be prudent to exclude pregnant woman during the first 3 months of pregnancy,” whereas the latest American College of Radiology guidelines for safe MRI practices does not differentiate among the pregnancy trimesters, and states that all pregnant patients could undergo MRI as long as the benefits outweigh the risks. Because of theoretical concerns, we advocate a cautious approach to using obstetrical MRI in the first trimester and in this trimester, MRI should be restricted to maternal indications (
27). There are no published studies of the long-term effects in children and significant acoustic impairment resulting from exposure to prenatal MRI even with at magnetic field strengths of 3 T or more (
27). In lactating patients with newly diagnosed cancers, MRI with contrast is safe and helps to determine the spread of the disease. Breastfeeding before obtaining MRI sequences is recommended. It should be noted that the similarity of lactation changes with suspicious findings can reduce the sensitivity of MRI (
28). Gadolinium is secreted very little in milk; however, according to the American college of radiology guidelines, it is not necessary to stop lactation after the contrast injection (
26). By the way, the patient can be depending on his desire, stop breastfeeding for up to 24 hours until Gadolinium is completely removed from milk. For screening of high-risk patient in lactating phase, MRI has limitations because of some controversies in the interpretation. Unfortunately, little studies about MRI findings of PABC have been done. In a study of 7 patients in the lactation phase with the final histological report of PABC, 5 had a clear appearance of their cancer in T2 without contrast that could be due to increasing water content of fibroglandular tissue causing increase the intensity of T2 (
21). In surveys, MRI images of PABC have been reported similar to those of non-PABC, and the most common findings are masses with homogeneous, heterogeneous, or rim enhancement as well as nonmass lesions with segmental enhancement or one-sided diffuse enhancement. Lactation agents, unlike non-PABC, have a rapid parenchymal background enhancement with the type B kinetic curve (early plateau enhancement), which may be misleading to malignancy, although malignancies usually show more rapid and severe enhancement. MRI is important in detecting the spread of disease (
21,
28).