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a Department of Surgery, National Cancer Institute, Cairo, Egypt
b Department of Pediatric Oncology, National Cancer Institute, Cairo, Egypt
c Department of Pathology, National Cancer Institute, Cairo, Egypt
d Department of Pathology, General Thoracic Section, Emory University, Atlanta, Georgia
e Department of Surgery, General Thoracic Section, Emory University, Atlanta, Georgia
Accepted for publication October 21, 2008.
* Address correspondence to Dr Mansour, Cardiothoracic Surgery, The Emory Clinic, 1365 Clifton Road, NE, Atlanta, Georgia 30322 (Email: kamal.mansour{at}emoryhealthcare.org).
Yolk-sac tumor mimics the yolk sac of the embryo, and the presence of alpha fetoprotein in the tumor cells is highly characteristic. We present an 18-year-old boy with primary pulmonary yolk-sac tumor diagnosed postoperatively. A computed tomographic scan revealed a huge intrathoracic soft tissue mass 20 x 25 cm occupying most of the left hemithorax. Two trials of computed tomographic-guided needle biopsy were nonconclusive. A left upper lobectomy was performed with a complete tumor resection. Postoperatively, the patient's alpha fetoprotein (AFP) was 10,512 IU/mL with gradual decline under chemotherapy. The patient is alive 10 months after surgery and is disease free.
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