Oman Medical Journal (Sep 2016)

Primary Gastric Chorioadenocarcinoma

  • Bahaaeldin A. Baraka,
  • Suad S. Al Kharusi,
  • Bassim J. Al Bahrani,
  • Gunmala Bhathagar

DOI
https://doi.org/10.5001/omj.2016.75
Journal volume & issue
Vol. 31, no. 5
pp. 381 – 383

Abstract

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Primary gastric chorioadenocarcinoma (PGC) is a rare and rapidly invasive tumor. Choriocarcinoma is usually known to be of endometrial origin and gestational; however, it has been reported in other extragenital organs, such as the gall bladder, prostate, lung, liver, and the gastrointestinal tract. Human chorionic gonadotropin related neoplasms of the stomach are seldom discussed in the literature. We report a case of PGC in a 56-year-old man treated with a standard non-gestational choriocarcinoma chemotherapy regimen, EMA/CO (etoposide, methotrexate, actinomycin D, cyclophosphamide, vincristine), with a complete response and good tolerability.

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