ArticleAME case reports2026
Hemothorax as an infrequent complication of aortic dissection in a young 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. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Acute aortic dissection (AAD) is a life-threatening condition with high mortality and a broad spectrum of clinical presentations. Hemothorax is an infrequent but catastrophic complication, particularly uncommon in young patients. Case Description: We report the case of a 39-year-old man with treated systemic arterial hypertension and obesity who presented with acute chest pain of approximately 50 minutes duration prior to hospital arrival. The initial clinical presentation was suggestive of acute coronary syndrome, leading to early management in that direction. Non-contrast chest computed tomography (CT) performed approximately 2 hours and 43 minutes after symptom onset revealed a massive left hemothorax, and subsequent contrast-enhanced imaging at approximately 10 hours and 19 minutes confirmed Stanford type B aortic dissection. No point-of-care ultrasound was performed during the initial evaluation. Diagnostic delay and limited access to specialized cardiovascular services contributed to the unfavorable outcome. Despite further diagnostic evaluation, the patient experienced progressive clinical deterioration and developed cardiac arrest approximately 28 hours after initial presentation, resulting in a fatal outcome. Conclusions: Hemothorax represents a rare but severe manifestation of AAD and should be considered in cases of non-traumatic hemothorax, even in young patients without known genetic disorders. Early recognition, appropriate imaging, and timely referral to specialized centers are critical to improve outcomes.
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.