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Infradiaphragmatic extralobar pulmonary sequestration: masquerading as suprarenal mass
Kiran V Kalenahalli1, Navneet Garg, Lakshmikantha N Goolahally
1Department of Radiology and Imaging, Sagar Hospitals, Bangalore, Karnataka, India.
This case report highlights an extremely rare instance of infra-diaphragmatic pulmonary sequestration, a congenital lung malformation. Early detection and imaging are crucial for accurate diagnosis and to avoid unnecessary surgery for suspected suprarenal masses.
Area of Science:
- Pediatric Surgery
- Medical Imaging
- Congenital Malformations
Background:
- Pulmonary sequestration is a rare congenital lung malformation characterized by non-functional lung tissue separate from the normal tracheo-bronchial tree.
- It can be intralobar (within the lung lobe) or extralobar (separate from the lung).
- Infra-diaphragmatic pulmonary sequestration is an extremely rare extralobar variant, often associated with other congenital anomalies.
Observation:
- A case of isolated infra-diaphragmatic pulmonary sequestration was detected antenatally.
- Postnatal CT scan revealed the malformation mimicking a suprarenal mass.
- The patient underwent surgical treatment for the condition.
Findings:
- This case represents an extremely rare instance of isolated infra-diaphragmatic pulmonary sequestration.
- The malformation presented as a suprarenal mass on imaging, highlighting a diagnostic challenge.
- The lesion was stable in size and appearance, suggesting a non-neoplastic origin.
Implications:
- This case underscores the importance of considering congenital malformations, such as pulmonary sequestration, in the differential diagnosis of antenatal and postnatal suprarenal masses.
- Stable suprarenal masses detected antenatally warrant careful evaluation and may not require immediate surgical intervention.
- Accurate imaging and diagnostic workup are essential to differentiate sequestration from other suprarenal pathologies, potentially avoiding unnecessary surgeries.
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