ArticleJournal of medical cases2026
An Atypical Case of Superior Vena Cava Syndrome Due to Sarcomatoid Lung Cancer With Pericardial Metastasis.
Article in Journal of medical cases, 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
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Superior vena cava (SVC) syndrome is commonly caused by malignancies from lung cancers, thrombus, and indwelling intravascular devices. Specifically, SVC syndrome is mostly associated with malignancies such as small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC). Pulmonary sarcomatoid carcinoma (PSC), as a rare type of NSCLC, accounts for 0.1% to 0.4% of pulmonary tumors. PSC's rapid progression, aggressive growth, and complexity to diagnose help differentiate from other thoracic malignancies, yet due to its rarity, there is limited literature documenting an association between this entity and SVC syndrome. Here we present an atypical case of SVC syndrome with a history of tobacco use and chronic right upper extremity lymphedema who developed facial swelling, dyspnea, and worsening right upper extremity swelling. Imaging revealed a large mediastinal mass compressing both the SVC and pulmonary artery. Further workup and endobronchial ultrasound (EBUS) were performed, which led to a diagnosis of poorly differentiated sarcomatoid carcinoma. Additionally, pericardiocentesis revealed features consistent with adenocarcinoma. The case was further complicated with hypoxic respiratory failure and new-onset atrial fibrillation. With extensive intensive care unit (ICU) care, the patient was discharged with a medication regiment, and referred to oncology, cardiology, and palliative care. Patient declined chemotherapy and immunotherapy, opting for hospice care. Patient stay was complicated by hypoxia respiratory failure, pleural effusions, pericardial effusion, and atrial fibrillation with rapid ventricular response (RVR). This case emphasizes that SVC syndrome can be associated with poorly differentiated sarcomatoid carcinoma.
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.