ArticleThoracic cancer2017
Primary pulmonary myxoid sarcoma located in interlobar fissure without parenchymal invasion.
Article in Thoracic cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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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.
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Who cites it
9 citing papers in PubMed, 16 citations in OpenAlex.
- Primary mucinous sarcoma of the lung with EWSR1 translocation: a case report.Frontiers in medicine · 2025Article
- Primary Pulmonary Myxoid Sarcoma Located in the Left Lung Parenchyma: Case Report with a Review of Literature.Surgical case reports · 2025Article
- Primary pulmonary myxoid sarcoma in the interlobar fissure of the left lung lobe: a case report.BMC pulmonary medicine · 2024Article
- Primary pulmonary myxoid sarcoma with EWSR1::CREB1 fusion: a literature review.Journal of cancer research and clinical oncology · 2024Review
- CT findings of a large primary pulmonary myxoid sarcoma: A case report.Radiology case reports · 2022Article
- Distinct clinicopathological features of pulmonary primary angiomatoid fibrous histiocytoma: A report of four new cases and review of the literature.Thoracic cancer · 2021Review
- Primary pulmonary myxoid sarcoma: report of one case and literature review.International journal of clinical and experimental pathology · 2021Article
- Primary pulmonary myxoid sarcoma with an unusual gene fusion between exon 7 of EWSR1 and exon 5 of CREB1.Virchows Archiv : an international journal of pathology · 2020Article
- Primary pulmonary myxoid sarcoma with EWSR1-CREB1 fusion: a case report and review of the literature.Diagnostic pathology · 2020Review
Corrections and comments
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Primary pulmonary myxoid sarcoma (PPMS), classified as low to intermediate grade malignant myxoid endobronchial tumor, is rarely reported. Most reported cases occurred in lung parenchyme with an endobronchial component. Herein, we report a case of PPMS in a 29-year-old woman that developed in a major fissure of the left lung without parenchymal invasion. Histopathologically, the diagnosis was compatible to PPMS with EWSR1-CREB1 translocation.
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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.