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Pneumatosis cystoides intestinalis in systemic sclerosis
The British Journal of Dermatology
|January 1, 1976
Summary
Pneumatosis cystoides intestinalis (PCI) is a rare gastrointestinal condition. This case highlights its association with systemic sclerosis, suggesting a need for consideration in such patients with obstructive abdominal symptoms.
Area of Science:
- Gastroenterology
- Internal Medicine
- Rheumatology
Background:
- Pneumatosis cystoides intestinalis (PCI) is a rare condition with gas-filled cysts in the intestinal wall.
- PCI is often linked to chronic obstructive pulmonary disease and various gastrointestinal disorders.
- Previous associations with systemic sclerosis have been occasionally reported.
Observation:
- This report focuses on a patient with severe systemic sclerosis.
- The patient presented with abdominal symptoms suggestive of intestinal obstruction.
- The symptoms were not readily explained by other common causes.
Findings:
- The patient was diagnosed with pneumatosis cystoides intestinalis.
- This finding is of particular interest due to the co-existing severe systemic sclerosis.
- The association between PCI and systemic sclerosis is rare but significant.
Implications:
- Clinicians should consider PCI in patients with systemic sclerosis presenting with unexplained abdominal symptoms.
- Early recognition of PCI in systemic sclerosis patients can aid in timely diagnosis and management.
- This association warrants further investigation into the underlying mechanisms linking systemic sclerosis and gastrointestinal manifestations.