[Pneumatosis cystoides intestinalis: a rare illness in adults]
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Date of Publication
2007
Publication Type
Article
Division/Institute
Author
Vetter, Ch | |
Robert-Tissot, L | |
Bielecki, W J |
Series
Praxis - schweizerische Rundschau für Medizin
ISSN or ISBN (if monograph)
1661-8157
Publisher
Huber
Language
English
PubMed ID
18065049
Description
Pneumatosis cystoides intestinalis (PCI) is a rare illness in adults with gas filled blebs found in the submucosa or subserosa of the bowel wall. The main localization is the terminal ileum although all parts of the intestine can be affected. Clinical symptoms can vary from aqueous-slimy, bloody diarrhea to constipation and/or vague abdominal pain. Patients can also be completely asymptomatic. In symptomatic patients the therapy of PI is based on the assumed pathogenesis, so that a combined treatment of metronidazole 1500 mg daily during a period of 6-8 weeks additionally and oxygen application (PaO2 of 200-350 mmHg) for 7 days is suggested. In addition, elemental diets are recommended. Complications are indicated in the literature with 3%. In particular mechanical ileus, invagination and perforation as well as substantial intestinal bleeding up to the volvolus lead to further diagnostic and therapeutic steps. A surgical intervention is reserved for rare cases.