ArticleJournal of medical case reports2026
Scimitar syndrome and horseshoe lung presenting with syncope and hemoptysis in late childhood, management challenges, and outcomes: a case report.
Article in Journal of medical 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
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundHorseshoe lung (HL) and scimitar syndrome are rare congenital cardiopulmonary anomalies that may coexist, posing complex diagnostic and management challenges. The following case presents the clinical manifestation of repeated hemoptysis episodes and syncope, a combination that has rarely been reported in this context. Moreover, there were treatment challenges regarding the utility of minimally invasive techniques in the iatrogenic occlusion of aberrant vessels, which has more recently been suggested in the literature to yield comparable outcomes compared with open surgeries. CASE PRESENTATION: We described the case of a 15-year-old Iranian boy who presented with syncope and hemoptysis following physical activity. Imaging findings were consistent with concomitant HL, partial anomalous pulmonary venous return (PAPVR), right lung hypoplasia, and scimitar syndrome. The patient successfully underwent transcatheter arterial embolization (TAE); however, another episode of hemoptysis occurred after three weeks. This recurrence indicated the failure of TAE and necessitated a right lower lobe segmentectomy. After the surgical excision, the patient showed improvement in respiratory status, with no further episodes of hemoptysis. He was discharged on postoperative day seven. At the 2-month follow-up, there were no signs of recurrence or complications. Nonetheless, the patient was scheduled for subsequent open-heart repair of the PAPVR defect.
conclusionsThis case highlights that when HL or scimitar syndrome is identified, clinicians should be aware of associated congenital cardiopulmonary and vascular anomalies and perform a comprehensive clinical exam and multimodality imaging. Moreover, although TAE may yield outcomes comparable to open surgery with faster recovery and fewer postoperative complications, its effectiveness is questionable in patients with complex underlying conditions. Therefore, although the choice between the minimally invasive and invasive managements requires a multidisciplinary approach, it is recommended that patients with complications such as infections, bronchiectasis, large lumen aberrant vessels, multiple aberrant vessels, or unusual anatomies be planned for surgical resection of sequestrated lung tissue to avoid potentially less effective interventions.
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.