AI Article Synopsis

  • - Benign tumors of the chest wall are uncommon and can develop from various types of chest tissues, including vessels, nerves, and bones, though they usually don’t affect life expectancy.
  • - While these tumors can cause symptoms like pain, over 20% of patients may not show any symptoms and might be diagnosed incidentally through imaging tests.
  • - Diagnosis often requires a thorough medical history and imaging assessment, and while surgery is a common treatment, it may not be suitable for all cases due to the tumor's size or location, with limited guidelines available for treatment.

Article Abstract

Benign tumors of the chest wall are rare tumors that might arise from all the tissues of the chest: vessels, nerves, bones, cartilage, and soft tissues. Despite benign features, these tumors can have several histological characteristics and different behaviors. Even if they do not influence life expectancy, rarely they may have a potential risk of malignant transformation. They can cause several, oft, unspecific symptoms but more than 20% of affected patients are asymptomatic and are being diagnosed incidentally on chest radiograph or computed tomography scan. Pain is the most common described symptom. Together with a detailed medical history, a rigorous and meticulous clinical and radiological assessment is mandatory. If radiological features are unclear or in case surgery could not be performed, a biopsy should be indicated to establish a diagnosis. Radical surgical resection can often be offered to resect and cure these neoplasms, but this is might not be true for all types of tumors and, in some cases, their dimension or position might contra-indicate surgery. Given the rarity of these tumors, there is a lack of treatment's guidelines and prospective trials that include a significant number of patients. This review discusses, according to the latest evidence, the histological features and the best treatment of several chest wall benign tumors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10894435PMC
http://dx.doi.org/10.21037/jtd-23-464DOI Listing

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