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Accessory diaphragm associated with non-immune hydrops fetalis
Archana Priyadarshi1, Ella Sugo2, Daniel Challis3
1Division of Newborn Services, Royal Hospital for Women, Randwick, New South Wales, Australia.
BMJ Case Reports
|August 8, 2014
Summary
Congenital accessory diaphragm, a rare diaphragmatic duplication, can cause hydrops fetalis in newborns. Antenatal ultrasound may reveal key radiological features of this condition.
Area of Science:
- Medical Imaging
- Pediatric Surgery
- Fetal Medicine
Background:
- Accessory diaphragm (diaphragmatic duplication) is a rare congenital anomaly characterized by a fibromuscular membrane above the diaphragm.
- This anomaly divides the hemithorax, potentially trapping pulmonary parenchyma and leading to respiratory complications.
Observation:
- This report details a rare case of congenital accessory diaphragm diagnosed antenatally.
- The condition presented as hydrops fetalis, a severe form of fluid accumulation in the fetus.
Findings:
- Less than 40 cases of accessory diaphragm are documented, with only five diagnosed neonatally.
- This case highlights the antenatal presentation of accessory diaphragm, specifically its association with hydrops fetalis.
- Radiological features on antenatal ultrasound are described for this rare anomaly.
Implications:
- This case expands the understanding of congenital accessory diaphragm presentations.
- It emphasizes the importance of recognizing specific ultrasound findings for antenatal diagnosis.
- Early diagnosis can potentially guide management strategies for affected newborns.
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