Uterine compression suturing was found to be associated with a risk of postpartum uterine synechiae formation, which may subsequently affect future fertility.

Background: Methotrexate is widely used chemotherapy especially in pediatric hematological malignancy. It may associate with acute neurotoxicity. We evaluate the role of the diffusion-weighted imaging (DWI) in the early detection of the acute methotrexate neurotoxicity. Methods: Seventeen pediatric patients receiving high-dose methotrexate with clinical manifestation of neurotoxicity (seizures, headache, aphasia, hemiparesis or altered mental status) were included in our study. MRI was obtained in all cases within 48 h of onset of symptoms. DWI was done as a part of the routine MRI study. Results: In all patients, initial MRI showed abnormal restricted diffusion in the centrum semiovale. FLAIR is positive in 9 cases showing bright signal. All patients had follow-up MR (within two weeks); in all cases there was resolution of the diffusion abnormality and interval development of abnormal signal intensity on FLAIR and T2WI. Conclusion: Methotrexate can result in reversible neurotoxicity in the form of white matter injury. DWI may be used in early detection of such changes; therefore, it provides a rapid, noninvasive readily available tool by which neurotoxicity can be early detected and treated. It has the potential to alert the oncologist to this event and provide a technique by which neurotoxicity can be monitored. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).

Background: The objective of this study was to assess variation in number, size, shape, and location of greater and lesser palatine foramina using multiple anatomical landmarks through data obtained from adult head CT scans. CT skulls of 200 adult persons were included in this study. There were 100 males and 100 females, aged from 22 to 65 years old. An e-film DICOM viewer version 2 was applied to estimate morphological parameters and to calculate the linear measurements related to the greater palatine foramen. Results: On the basis of CT findings, regarding the position of GPF in relation to maxillary molar teeth, the most frequent location was opposite the third maxillary molar (41%). Regarding the dimensions of the GPF, the mean AP diameter was 3.94 ± 1.13 mm on the right side and 4.22 ± 1.21 mm on the left. The mean LM diameter was 2.17 ± 0.59 mm on the right side and 2.28 ± 0.74 mm on the left. It was concluded that the GPF was AP elongated in 90.5% and circular in 9.5% of the examined CT scans. Linear measurements from the center of GPF to surrounding anatomical landmarks were done and showed no statistically significant difference existed between sides, but a statistically highly significant difference existed between males and females. Conclusions: Proper localization of GPF is important to facilitate therapeutic, local anesthetic, and surgical manipulation in the maxillofacial region. Based on CT findings, we demonstrated that the GPF is most often located opposite the M3 in the majority of the cases. The maxillary molars are the best landmarks for locating the GPF.

No abstract

IntroductionWe studied the frequencies of the 3′ and 5′-end vitamin D receptor (VDR) gene polymorphisms and their correlation with bone mineral density (BMD) in Egyptian pediatric acute lymphoblastic leukemia (ALL) patients receiving calcium and vitamin D supplements. The purpose of this study is to find out the relation between VDR polymorphism and the response to vitamin D intake in pediatric ALL cases who receive corticosteroid therapy which predispose to osteoporosis. This study might shed the light on some genetic variants that are effect the response of individuals to vitamin D therapy.MethodsForty newly diagnosed pediatrics ALL cases were studied. Three SNPs at the 3′-end of the VDR gene (BsmI rs1544410, ApaI rs739837and TaqI rs731236) and two SNPs at the 5′-end (Cdx-2 rs11568820 and GATA rs4516035) were analyzed by Allelic discrimination assay. Of those twenty-six cases with initial BMD data available were further analyzed with regards to the effect of various VDR genotypes/haplotypes on BMD.ResultsThe genotype frequencies at 3′-end of VDR gene were, TaqI TT 23%, Tt 54% and tt 23%, BsmI bb 19.2%, Bb 65.4% and BB 15.4% and ApaI AA 12%, Aa 27% and aa 61%. The frequencies at the 5′-end were Cdx-2 GG 34.5%, GA 54% and AA 11.5% and GATA AA 8%, AG 50% and GG 42%. Eight and four possible haplotypes were observed at the 3′ and 5′-ends of the VDR gene respectively. The Tt genotype was significantly correlated with high BMD as compared to other TaqI genotypes (P = 0.0420). There was a trend towards higher BMD with the genotype Bb as compared to other BsmI genotypes. No statistical significance was found between the other VDR genotypes or haplotypes studied and BMD.ConclusionsThis is the first report on VDR gene polymorphisms in Egyptian pediatric ALL patients. The Tt genotype was associated with increased BMD. Our study showed marked genetic heterogeneity in VDR gene in Egyptian pediatric ALL patients.