scholarly journals Prenatal diagnosis and conservative management of complex meconium peritonitis: a case report

2019 ◽  
Vol 4 (1) ◽  
pp. 48-52
Author(s):  
Gürcan Türkyılmaz ◽  
◽  
Didar Kurt ◽  
Tuğba Saraç Sivrikoz ◽  
İbrahim Kalelioğlu ◽  
...  
2020 ◽  
Vol 2020 (5) ◽  
Author(s):  
Marcella Schiavone ◽  
Damiano Pizzol ◽  
Anna Claudia Colangelo ◽  
Mario Antunes

Abstract Cantrell syndrome (CS) is defined as congenital combination of five anomalies: defects at the lower part of the sternum, anterior diaphragm, midline supraumbilical abdominal wall, diaphragmatic pericardium and ectopia cordis. Antenatal screening should be performed to make an accurate prenatal diagnosis. The prognosis is usually poor with a high mortality early in life. The gold standard management is surgery but its prognosis remains poor. In many low-income settings prenatal examinations and surgery treatment are not possible. In the present case, we report a not surgery managed baby affected by CS, with good clinical conditions after 5 months.


2014 ◽  
Vol 34 (1) ◽  
pp. 9-13 ◽  
Author(s):  
Uğur Keskin ◽  
Kazım Emre Karasahin ◽  
Mustafa Ozturk ◽  
Cüneyt Atabek ◽  
Suzi Demirbağ ◽  
...  

Author(s):  
I Staboulidou ◽  
K Miller ◽  
G Göhring ◽  
P Hillemanns ◽  
M Wüstemann

2019 ◽  
Vol 1 (23) ◽  
pp. 28
Author(s):  
Ioana Corina Gorgoi ◽  
Constantin-Alexandru Albu ◽  
Oana Eliza Creţu ◽  
Florina Magdalena Mihai ◽  
Adriana Mihaela Dan ◽  
...  

2019 ◽  
Vol 24 (4) ◽  
pp. 371-375
Author(s):  
Li-tal Pratt ◽  
Shelly I. Shiran ◽  
Ronit Precel ◽  
Liat Ben-Sira ◽  
Gustavo Malinger ◽  
...  

Mature teratomas (MTs) of the posterior fossa are extremely rare. The authors present a case of a prenatal diagnosis of an MT splitting the brainstem. Representative images as well as the clinical and surgical course are presented. Literature regarding “split brainstem” and MT of the posterior fossa is discussed.


Author(s):  
E.N. Glavatskaya , O.V. Pribushenya , N.A. Venchikova

Two clinical cases of meconium peritonitis in the fetuses are presented. The diagnosis was made prenatally at 30+5 and 20+1 weeks of gestation. The main ultrasound signs were ascites, loop expansion and thickening of the intestinal wall, peritoneal calcifications, meconium pseudocysts. In one case, pregnancy was complicated by polyhydramnios. In both cases, the pregnancy ended in premature birth, followed by surgical treatment during the first days of life. A review of the literature on the topic are discussed the etiology, the spectrum and frequency of ultrasound signs suggesting this condition in the fetus, the effectiveness of prenatal diagnosis, the prognosis for the life and health of the newborn, as well as the impact of the quality and timeliness of the prenatal diagnosis on the management of pregnancy and timeliness of surgical care for the newborn.


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