ArticleAME case reports2026
Spontaneous intramural small bowel hematoma: unusual cause of intestinal subocclusion in an anticoagulated patient-a case report.
Article in AME case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Spontaneous intramural small bowel hematoma (SISBH) is a rare complication of long-term oral anticoagulation, particularly with vitamin K antagonists (VKAs). SISBH diagnosis is based on oral anticoagulation history associated with acute abdominal symptoms and suggestive radiological findings. Experience with this condition is still limited in the literature. This report highlights the clinical presentation and management of this rare condition, including the first known use of total-body positron emission tomography/computed tomography (PET/CT) scan in the diagnostic workup of SISBH. Case Description: A 53-year-old male on long-term oral anticoagulation with VKA for mechanical mitral valve replacement due to rheumatic heart disease presented to the emergency department for abdominal pain and nausea. Physical examination was remarkable for abdominal distension, increased bowel sounds and rebound tenderness, a presentation compatible with intestinal subocclusion. At admission, the international normalized ratio was 8.3, indicating VKA intoxication. Abdominal CT revealed significant jejunal parietal thickening, suggestive of SISBH. PET/CT findings were also consistent with a possible hematoma, although an inflammatory or neoplastic process could not be excluded. We opted for conservative treatment with temporary warfarin suspension and vitamin K infusion. The patient's intestinal subocclusion gradually improved, and he was discharged after seven days with full recovery. Conclusions: SISBH, although rare, should be considered in the differential diagnosis of acute abdominal symptoms in patients receiving long-term oral anticoagulation, particularly with VKAs. Conservative treatment is the preferred initial option. A high index of suspicion, followed by prompt abdominal CT, is key to early diagnosis. PET/CT provided minimal diagnostic value beyond CT. Conservative management with anticoagulation reversal and supportive care is generally the primary therapeutic strategy adopted in the literature, demonstrating favorable short-term outcomes, as was the case with our patient.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.