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[Pleuropericardial mesothelial cysts]

I Besznyák, Z Szabó, T Gyöngy

Acta Chirurgica Academiae Scientiarum Hungaricae

|January 1, 1978

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This study details the diagnosis and removal of 33 pleuropericardial mesothelial cysts, offering insights into their characteristics and treatment options. Findings compare clinical experience with existing literature on these rare cysts.

Area of Science:

Cardiovascular Surgery
Thoracic Surgery
Pathology

Background:

Pleuropericardial mesothelial cysts are rare congenital anomalies.
These cysts arise from the serosal lining of the pericardium or pleura.
They can present with diverse clinical manifestations or be asymptomatic.

Purpose of the Study:

To describe the clinical experience with 33 cases of pleuropericardial mesothelial cysts.
To compare these findings with existing literature.
To discuss the incidence, pathology, symptomatology, diagnostics, and therapeutic options.

Main Methods:

Retrospective review of 33 surgically treated cases.
Literature review of published data on pleuropericardial mesothelial cysts.

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Analysis of diagnostic imaging and pathological findings.

Main Results:

Detailed description of the 33 cases, including cyst location and size.
Comparison of patient demographics, symptoms, and treatment outcomes with literature data.
Discussion of diagnostic accuracy and challenges in differential diagnosis.

Conclusions:

Pleuropericardial mesothelial cysts require accurate diagnosis for appropriate management.
Surgical excision is often the definitive treatment.
Further research can refine diagnostic criteria and therapeutic strategies.