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http://dx.doi.org/10.1016/0002-9343(88)90443-3 | DOI Listing |
J Cardiothorac Surg
January 2025
Department of Cardiothoracic Surgery, The First People's Hospital of Neijiang, No. 1866, West Section of Hanan Avenue, Shizhong District, Neijiang, Sichuan, 641000, P.R. China.
Background: Primary mediastinal liposarcomas (PLMs) are extremely rare. Patients typically present with symptoms caused by tumor size, as the mass can compress surrounding tissues and organs. Here, we report a case of a large primary mediastinal liposarcoma that was successfully resected thoracoscopically.
View Article and Find Full Text PDFJACC Case Rep
November 2024
Northwell, New Hyde Park, New York, USA.
A 61-year-old woman presented to our team with giant mediastinal liposarcoma causing compression of the esophagus, bronchus, and left atrium. Given the patient's advanced presentation and reduced cardiac reserve, rescue venoarterial extracorporeal membrane oxygenation was used in addition to standard robotic-assisted thoracic surgery for mass resection.
View Article and Find Full Text PDFMedicine (Baltimore)
December 2024
Department of Ultrasound, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Int J Surg Case Rep
December 2024
Adama Hospital Medical College, Adama, Ethiopia.
Cureus
September 2024
Department of Cardiothoracic and Vascular Surgery, Westpfalz-Klinikum, Kaiserslautern, DEU.
Liposarcomas (LPSs) are rare malignant tumors of adipocytic origin, primarily occurring in the extremities and retroperitoneum, with thoracic involvement being exceptionally rare. This case report details the surgical management and outcomes of a recurrent intrathoracic LPS in a 65-year-old male with a history of previous mediastinal tumor resection. CT imaging revealed a recurrent tumor extending into the left pleura.
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