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Transaxillary First Rib Resection for Treatment of the Thoracic Outlet Syndrome
Published on: September 13, 2020
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A Rare Case of Thoracoschisis
Jamie Harris1, Yanmin Zhang2, Saurabh Patel3
1Department of Surgery, Rush University Medical Center, 1750 W. Harrison St, Suite 785, Chicago, IL, 60612, USA.
Journal of Neonatal Surgery
|September 19, 2017
Summary
A rare congenital chest wall mass in a newborn was identified as protruding liver tissue. Surgical excision confirmed normal liver tissue, resolving the condition.
Area of Science:
- Pediatric Surgery
- Congenital Abnormalities
- Diagnostic Imaging
Background:
- Congenital chest wall masses are rare in newborns.
- Differentiating between various chest wall lesions requires accurate diagnostic approaches.
Purpose of the Study:
- To report a unique case of a congenital liver herniation through the chest wall in a neonate.
- To highlight the diagnostic and surgical management of this rare condition.
Main Methods:
- Clinical presentation of a term male infant with a left-sided chest wall mass.
- Radiological imaging (e.g., CT, MRI) to determine the mass origin and relationship to internal organs.
- Diagnostic laparoscopy to confirm intra-abdominal connection and diaphragmatic integrity.
- Surgical excision of the mass using electrocautery.
Main Results:
- A 3 cm beefy-red mass was observed protruding from the left chest wall.
- Imaging suggested the mass originated from the left lateral liver segment.
- Laparoscopy confirmed an isolated liver connection, elevated left hemidiaphragm, and protrusion between ribs.
- Pathologic examination revealed the excised mass was normal liver tissue.
Conclusions:
- Congenital hepatic herniation through the chest wall is a rare but treatable condition.
- Multimodal diagnostic imaging and minimally invasive surgical techniques are crucial for successful management.
- Complete excision of the herniated liver tissue is curative.
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