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Pneumatosis cystoides intestinalis: lung window setting on CT
Yosuke Kunishi1, Mitsuyasu Ota2, Yoshio Kato1
1Department of Gastroenterology Kanagawa Prefectural Ashigarakami Hospital Kanagawa Japan.
Clinical Case Reports
|November 21, 2017
Summary
Pneumatosis cystoides intestinalis, a rare condition, presents nonspecific symptoms. CT imaging using lung window settings can clearly define air collection in the ileum wall, aiding diagnosis.
Area of Science:
- Gastroenterology
- Radiology
- Medical Imaging
Background:
- Pneumatosis cystoides intestinalis (PCI) is a rare gastrointestinal condition characterized by the presence of gas-filled cysts in the intestinal wall.
- PCI often presents with nonspecific symptoms, making diagnosis challenging.
- Accurate imaging is crucial for identifying and characterizing PCI.
Purpose of the Study:
- To highlight the utility of specific CT imaging parameters in diagnosing pneumatosis cystoides intestinalis.
- To emphasize the importance of evaluating CT scans with lung window settings for subtle findings of PCI.
Main Methods:
- Case presentation of a patient with suspected pneumatosis cystoides intestinalis.
- Review of computed tomography (CT) imaging findings, including standard and lung window settings.
- Correlation of imaging findings with the diagnosis of PCI.
Main Results:
- CT imaging revealed air collection within the wall of the ileum.
- The air collection was significantly more clearly defined using the lung window setting compared to standard abdominal windows.
- Lung window settings enhanced the visualization of the cystic structures characteristic of PCI.
Conclusions:
- CT imaging, particularly when utilizing lung window settings, is a valuable tool for diagnosing pneumatosis cystoides intestinalis.
- Radiologists and clinicians should consider employing lung window settings when evaluating patients with suspected PCI.
- Optimizing CT window settings can improve the detection of rare conditions like PCI.
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