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Meconium pseudocyst presenting as massive ascites in a new-born
Suhail A Khan1, Manjiri Khare2, Haitham Dagash3
1Addenbrookes Hospital, Hills road, Cambridge CB20QQ, UK.
Radiology Case Reports
|November 28, 2018
Summary
Meconium pseudocyst (MPC) is a rare surgical condition. This case highlights that massive ascites and absence of calcifications do not rule out MPC, even with prenatal bowel perforation.
Area of Science:
- Neonatal surgery
- Pediatric surgery
- Gastrointestinal surgery
Background:
- Meconium pseudocyst (MPC) is a recognized surgical complication of prenatal bowel perforation.
- It typically presents in newborns, often requiring surgical intervention.
Observation:
- A unique case of MPC secondary to prenatal bowel perforation is presented.
- This case involved massive ascites necessitating peritoneal drainage for respiratory support.
- Notably, prenatal intra-abdominal calcifications were absent.
Findings:
- Massive ascites requiring peritoneal drainage is a previously unreported presentation of MPC.
- The disappearance of prenatal intraperitoneal calcifications has not been previously associated with MPC.
- Absence of prenatal calcifications does not exclude the diagnosis of MPC.
Implications:
- Neonatal care providers should consider MPC in cases of massive fetal ascites.
- Imaging findings, including the absence of calcifications, should not preclude MPC diagnosis.
- Early recognition and intervention are crucial for managing MPC and associated complications.
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