AI Article Synopsis

  • Primitive neuroectodermal tumors (PNETs) are small tumors classified into peripheral or central types based on location, typically found in young adults, but can rarely occur in organs like the lungs.
  • A case study details a 37-year-old woman with a peripheral PNET in her lung, who presented with respiratory symptoms and underwent extensive treatment including surgery, chemotherapy, and radiotherapy.
  • After treatment, the patient remains alive without signs of tumor recurrence and continues with regular follow-up care.

Article Abstract

Primitive neuroectodermal tumors (PNETs) are small, round cell tumors that may be classified as peripheral or central, based on their site of origin. PNETs often arise in the soft tissue or bone of young adults. Although not common, PNETs have been described in other organs, including the gonads, kidneys, myocardium and pancreas, but rarely in the lungs without chest wall or pleural involvement. The present study reports a rare case of peripheral PNET (pPNET), which originated in the lung. A 37-year-old female patient presented at Xuzhou Central Hospital (Xuzhou, China) with a history of a dry cough, mild dyspnea and slight pain in the left chest. Histopathological and immunohistochemical analyses permitted the diagnosis of a pPNET. The patient was treated with surgical resection, followed by chemotherapy (including cyclophosphamide, cisplatin and vincristine), radiotherapy and traditional Chinese medicine (including Kanglaite and Shenqi Fuzheng injections). At the time of writing, the patient was alive with no sign of recurrence and under regular follow-ups at the Outpatient Clinic of Xuzhou Central Hospital.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038617PMC
http://dx.doi.org/10.3892/ol.2016.4973DOI Listing

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