Hydronephrosis Index: A Better Physiological Reference in Antenatal Ultrasound for Assessment of Fetal Hydronephrosis

2009 ◽  
Vol 154 (1) ◽  
pp. 116-120 ◽  
Author(s):  
Vivian Yee-fong Leung ◽  
Winnie Chiu-wing Chu ◽  
Constantine Metreweli
2020 ◽  
Vol 9 (1) ◽  
Author(s):  
Anupam Nanda ◽  
Rajinder Nanda ◽  
Seema Thakur ◽  
Tej Prakash Gupta ◽  
Sudhir Jain ◽  
...  

AbstractObjectivesLung tissue choristoma is a very rare disorder where mature lung tissues develop in the site not normal to the lung.Case presentationWe hereby report a first case of fetal pulmonary choristoma in a 23–24 weeks fetus where antenatal ultrasound showed a mass in posterior fossa with severe ventriculomegaly. The mass extended inferiorly in cervical spinal column and thereafter extended in the skin over the back of fetus. Fetal autopsy confirmed these findings. Pathologic findings showed mature lung tissues with bronchi, bronchioles, and alveoli. Clinical exome sequencing showed normal results.ConclusionsWe describe the antenatal ultrasound, fetal autopsy and pathologic findings of an intracranial and cutaneous pulmonary choristoma.


Diagnosis ◽  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Elham Kebriyaei ◽  
Ali Davoodi ◽  
Seyed Alinaghi Kazemi ◽  
Zahra Bazargani

Abstract Objectives Renal anomalies are the most common fetal abnormalities that occur during prenatal development, and are typically detected by observing hydronephrosis on fetal ultrasound imaging. Follow-up with post-natal ultrasound is important to detect clinically-important obstruction, because many of the pre-natal abnormalities resolve spontaneously. This study aimed to evaluate the postnatal hydronephrosis follow-up rate, and reasons for non follow-up in affected neonates. Methods In this cross-sectional study all neonates born during a period of one year at Ayatollah Mousavi Hospital with hydronephrosis on fetal ultrasound imaging were recruited. All mothers were also given face-to-face information about fetal hydronephrosis and its postnatal outcomes, and follow-up with at least a postnatal ultrasound was recommended from the fourth day of their neonates’ birth until the end of the fourth week. The neonates were subsequently observed for one month to determine the postnatal ultrasound follow-up rate and to reflect on diagnostic test results, reasons for failure to follow-up, as well as causes of hydronephrosis. Results In this study, 71 cases (1.2%) out of 5,952 neonates had fetal hydronephrosis on prenatal ultrasound images. The postnatal ultrasound imaging showed kidney involvement in 18 neonates (25%), particularly in the left kidney (61.1%). Seven neonates had no follow-up at one month (10%). No significant relationship was found between lack of follow-up and the neonates’ place of residence (p=0.42), maternal education (p=0.90), number of siblings (p=0.33), or gender (p=0.64). Conclusions Postnatal ultrasound follow-up rate in these neonates with a history of fetal hydronephrosis was incomplete even though parents had been provided with education and advice at their birth time. Accordingly, it is recommended to perform postnatal ultrasound once neonates are discharged from hospitals.


2003 ◽  
Vol 22 (S1) ◽  
pp. 22-22
Author(s):  
K. Marsal ◽  
J. Brodszki ◽  
H. M. Gardiner ◽  
A. Hellstr�m ◽  
L. Martin ◽  
...  

2021 ◽  
Vol 15 (8) ◽  
pp. 2080-2082
Author(s):  
Nuzhat Rafeeq ◽  
Ayesha Niaz ◽  
Lubna Noor ◽  
Anum Sultan ◽  
Durre-E-Shahwar Hayat ◽  
...  

Objective: The aim of this study was to compare the fetal biometric growth measurements (Head Circumference, Bi-Parietal Diameter, and Femur Length) between male and female fetuses on antenatal ultrasound in our population. Methodology: This was an observational study carried out in the Department of Radiology CMH Malir, Karachi and Ziauddin hospital, Karachi from July 2016 till July 2018 using non-probability sampling technique. A total of 510 pregnant women with second and third trimester were enrolled for the study. The biometric parameters of fetus i.e., Bi-Parietal Diameter, Head Circumference, and Femur Length were established through two-dimensional ultrasound. Chi-square and t tests were used to analyze differences in biometric parameters in both genders. Results: The study results showed significant differences in the Bi-Parietal Diameter and Head Circumference between male and female fetuses (p=0.006 and p=0.003, respectively). Mean Bi-Parietal Diameter in males was 71.47±13.70 and in females it was68.30±11.90cm, mean Head Circumference in males was 264.23±47.87and in females it was 252.03±44.91cm. It has also been observed that there was an insignificant difference in the femur length between male and female fetuses (p= 0.605). Mean femur length was 52.74±12.39 in males and 52.19±11.38 in females. Conclusion: This study concluded that male fetuses have considerably larger bi-parietal diameter and head circumference as compared to female fetuses however, no variation in femur length is observed in both genders. Keywords: Fetal Gender, Bi-Parietal Diameter, Head Circumference, Femur Length.


2010 ◽  
Vol 19 (4) ◽  
pp. 383-386 ◽  
Author(s):  
Timur Gürgan ◽  
Hakan Yarall ◽  
Hulusi Zeyneloglu ◽  
Osman Develioglu ◽  
Bülent Urman

1989 ◽  
Vol 142 (2 Part 2) ◽  
pp. 661-662 ◽  
Author(s):  
Stephen W. Dejter ◽  
M. David Gibbons
Keyword(s):  

2012 ◽  
Vol 2 ◽  
pp. 5
Author(s):  
Nischal G. Kundaragi ◽  
Kishor Taori ◽  
Chetan Jathar ◽  
Amit Disawal

Fibrochondrogenesis is a rare, neonatally lethal osteochondrodysplasia, with autosomal recessive inheritance. It differs from other lethal dwarfisms in that it leads to broad, long-bone metaphyses (dumb-bell shaped) and pear-shaped vertebral bodies. We report a case of fibrochondrogenesis with severe pear-shaped platyspondyly, suspected antenatally, and give a comprehensive pictorial review of the antenatal ultrasound and postnatal radiographic findings. Only few cases of fibrochondrogenesis are diagnosed before the termination of pregnancy.


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