Myxomatous liposarcoma is an extremely rare type of mediastinal tumour that manifests in a manner comparable to other lung pathologies. Chest pain, shortness of breath, and dysphagia are the common presenting complaints. Radiological examinations or postoperative histological examinations provide the majority of the diagnostic evidence. The cornerstone of therapy consists of surgery and sometimes chemotherapy. Those who are afflicted have a better chance of experiencing favourable outcomes if they receive a diagnosis and treatment quickly.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512315PMC
http://dx.doi.org/10.7759/cureus.28438DOI Listing

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Article Synopsis
  • * A case study of a 36-year-old woman showed she had worsening shortness of breath and swelling, leading to a diagnosis of a large anterior mediastinal mass that was successfully surgically removed.
  • * The significance of this case highlights the need for early diagnosis of mediastinal liposarcoma in patients with respiratory symptoms, as prompt treatment can greatly improve patient outcomes.
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Liposarcomas account for about 20% of all sarcomas among mesenchymal neoplasms. Myxomatous liposarcoma is a rare mediastinal tumor that seems the same as other lung disorders. The most common presenting symptoms are chest pain, dyspnea, and dysphagia.

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Myxomatous liposarcoma is an extremely rare type of mediastinal tumour that manifests in a manner comparable to other lung pathologies. Chest pain, shortness of breath, and dysphagia are the common presenting complaints. Radiological examinations or postoperative histological examinations provide the majority of the diagnostic evidence.

View Article and Find Full Text PDF

Myxomatous liposarcoma in giant pleural cavity: case report and literature review.

Int J Clin Exp Pathol

March 2021

The First Affiliated Hospital Cardiothoracic Surgery Department, Guangdong Pharmaceutical University Guangzhou 510080, Guangdong, China.

Liposarcoma was mainly occurring in the lower extremities and deep retroperitoneal soft tissues, but rarely occurred in the thoracic cavity. Most cases were reported in the literature, and most of them were middle-aged and elderly people. It was even more rare in adolescents with tumors occupying the entire thoracic cavity.

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Myxoid Emboli.

Int J Surg Pathol

October 2018

1 Rashid Hospital, Dubai, United Arab Emirates.

Emboli are common clinicopathologic findings. Recognition of the type of arterial emboli could be the first clue to the original source. Emboli with myxomatous changes are rare.

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