A 42-year-old pregnant woman was referred with massive fetal bilateral pleural effusions. Observation with serial ultrasound was made. The documented spontaneous resolution of fetal pleural effusion was recorded. Neonatal examination revealed a completely healthy infant with normal respiration. Fetal pleural effusion can cause fetal lung compression, abnormal neonatal respiration and finally, neonatal mortality. Regular ultrasounds are one of the supportive options due to spontaneous resolution that can occur in 9 to 22% of the cases.
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Medicine (Baltimore)
December 2024
Department of Perioperative Stress Management, Hirosaki, Japan.
Rationale: Mirror syndrome is a rare pregnancy condition in which maternal edema is associated with fetal hydrops. Because of its rarity and overlapping symptoms, this condition is often misdiagnosed as another pregnancy complication.
Patient Concerns: A 28-year-old pregnant Japanese woman presented with sudden 7.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
October 2024
Center for Medical Genetics and Prenatal Diagnosis, the Third Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China.
Int J Surg Case Rep
December 2024
University Tunis El Manar Medical school, Tunisia; Department of pediatric surgery A, Children's Hospital Bechir Hamza, Tunisia.
Introduction: Congenital diaphragmatic hernia (CDH) is a rare developmental anomaly where a defect in the diaphragm allows abdominal organs to migrate into the thoracic cavity, impairing lung function. While typically identified in neonates, delayed presentations, though uncommon, can complicate diagnosis and treatment. Early detection is vital to prevent severe complications such as organ strangulation or perforation.
View Article and Find Full Text PDFSurg Radiol Anat
December 2024
Department of Otolaryngology-Head and Neck Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
Purpose: An entire fascial configuration at the esophageal hiatus might not be demonstrated histologically. According to observations of human fetus histology, the aim of this study was to consider which factor is likely to make the individual variation in adults.
Methods: We observed frontal histological sections containing the esophageal hiatus from 12 midterm fetuses at 12-16 weeks (crown-rump length: CRL, 85-137 mm) and 10 near-term fetuses at 26-30 weeks (CRL, 214-250 mm).
Radiol Case Rep
January 2025
Department of Obstetrics and Gynecology, Dilla University, College of Medicine and Health Sciences, Dilla, Ethiopia.
Cystic hygroma is a congenital lymphatic malformation characterized by fluid-filled cysts, often located in the neck or axillary regions, and is associated with significant fetal morbidity and mortality. This case report details a 32-year-old gravida 7 para 6 at 15 weeks of gestation, diagnosed prenatally with a large cystic hygroma exhibiting septation in the cervicoccipital and axillary region, accompanied by bilateral pleural effusion, pericardial effusion and subcutaneous edema. This report underscores the importance of early diagnosis and the need to carefully consider management options in cases of cystic hygroma with fetal hydrops.
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