An extremely rare case of postpartum gestational choriocarcinoma with long-term survival

Tumori. 2017 Nov 15;103(Suppl. 1):e16-e18. doi: 10.5301/tj.5000660.

Abstract

Gestational choriocarcinomas are highly malignant tumors with elevated serum human chorionic gonadotropin (hCG) levels. We report an extremely rare case of a 27-year-old woman who presented 4 months after normal delivery, with pulmonary, renal and intracardiac metastases of a choriocarcinoma. No primary uterine tumor was found. She was surgically treated for the renal and cardiac metastases as well as with cisplatin-etoposide chemotherapy. No recurrence has been observed 16 years after initial diagnosis, and the patient was able to have a second child. This case report shows that appropriate treatment of metastatic gestational choriocarcinoma can cure the patient without compromising her fertility.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Choriocarcinoma / mortality*
  • Choriocarcinoma / pathology
  • Choriocarcinoma / therapy
  • Combined Modality Therapy
  • Female
  • Gestational Trophoblastic Disease / mortality*
  • Gestational Trophoblastic Disease / pathology
  • Gestational Trophoblastic Disease / therapy
  • Heart Neoplasms / mortality*
  • Heart Neoplasms / secondary
  • Heart Neoplasms / therapy
  • Humans
  • Kidney Neoplasms / mortality*
  • Kidney Neoplasms / secondary
  • Kidney Neoplasms / therapy
  • Lung Neoplasms / mortality*
  • Lung Neoplasms / secondary
  • Lung Neoplasms / therapy
  • Pregnancy
  • Pregnancy Complications, Neoplastic / mortality*
  • Pregnancy Complications, Neoplastic / pathology
  • Pregnancy Complications, Neoplastic / therapy
  • Prognosis
  • Rare Diseases / mortality*
  • Rare Diseases / pathology
  • Rare Diseases / therapy
  • Survival Rate