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Published on: March 17, 2014
Air filled, inflammatory, lung pseudo-cyst: etio-pathogenesis and management
Nishith Kumar Jetley1, Mahmoud Rezk Abd El-Wahed Hussein, Abdul Lateef Softha
1Department of Pediatric Surgery, Assir Central Hospital, Abha, Saudi Arabia. nkjetley@hotmail.com
Insights
Acquired lung cysts in children, often congenital, can present as pneumothorax. This case highlights an inflammatory pseudocyst, diagnosed via immunohistochemistry, expanding differential diagnoses for pediatric lung lesions.
Area of Science:
- Pediatric Pulmonology
- Thoracic Surgery
- Pathology
Background:
- Congenital lung cysts are common in children.
- Acquired cysts can result from infections, trauma, cystic fibrosis, or poisoning.
- Pneumothorax in children necessitates investigation for underlying lung pathology.
Observation:
- A child presented with pneumothorax, revealing a right lung cyst.
- Surgical resection and histological examination identified an inflammatory pseudocyst lacking epithelial lining.
- Immunohistochemical staining confirmed predominant histiocytes (CD68 positive) in the cyst wall.
Findings:
- The pseudocyst wall stained negative for S-100, cytokeratins, and smooth muscle actins.
- These negative markers excluded diagnoses such as Langerhans cell histiocytosis, epithelial cysts, and congenital cysts.
- The findings indicate an acquired pulmonary pseudocyst of inflammatory origin.
Implications:
- This case expands the understanding of acquired pulmonary pseudocysts in children.
- Pulmonary pseudocysts should be considered in the differential diagnosis of pediatric pneumothorax.
- Further research may elucidate the specific etiologic agents for such acquired pseudocysts.
Abstract:
Lung cysts in children are usually of congenital origin. Necrotising pneumonias, trauma, cystic fibrosis and kerosene poisoning may be the cause of acquired cysts in the lungs during childhood. We describe a child who presented with pneumothorax and was later discovered to have a cyst in his right lung. The cyst was resected and on histology found to be of inflammatory origin with no epithelial cell lining i.e. a pseudo-cyst. The immuno-histochemical staining of the inflammatory cells from the pseudo-cyst wall showed them to be predominantly histiocytes i.e:, CD68 antigen positive. The cells showed negative staining for S-100 (marker for Langerhans cells), cytokeratins (epithelial markers) and smooth muscle actins excluding the possibility of histiocytosisX, epithelial and congenital cysts respectively. This case illustrates the occurrence of acquired pulmonary pseudocysts unrelated to known etiologic agents which should be considered in the work-up for pneumothoraces.
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