Archives of Medicine and Health Sciences (Jan 2014)

A rare case of primary mediastinal yolk sac tumor

  • Vinay Mahishale,
  • Prakash R. Malur,
  • Virupakshi Hattiholi,
  • Sindhuri Avuthu,
  • Ankit Rathi

DOI
https://doi.org/10.4103/2321-4848.133812
Journal volume & issue
Vol. 2, no. 1
pp. 54 – 56

Abstract

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Yolk sac tumor (endodermal sinus tumor) is a subtype of germ cell tumor and a highly malignant neoplasm. In addition to presenting in ovaries and testes, the tumor has been detected at several extragonadal sites, including the presacral area, the anterior mediastinum, face, uvula, and the pineal gland. Primary yolk sac tumor of the anterior mediastinum is rare and carries a grave prognosis, affecting mainly young men. Patients often present with advanced, bulky tumors that are unresectable. We present a 16-years-old young male patient with primary yolk sac tumor of mediastinum.

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