Small Cell Carcinoma of the Ovary with Hypercalcemia A Case Report and Literature Review

  • Study Findings:
    • The patient, a 23-year-old female, presented with abdominal pain and a large ovarian mass. Following surgery, she underwent chemotherapy and has been disease-free for over 9 years.
    • SCCOHT is often associated with hypercalcemia, which can be used as a tumor marker.
    • Genetic studies revealed a SMARC-A4 mutation, a crucial diagnostic tool for SCCOHT.
  • Implications for Treatment
    • Surgical intervention followed by chemotherapy is the primary treatment approach.
    • The patient’s successful treatment highlights the importance of early detection and comprehensive care.
  • Clinical Relevance:
    • This case offers insights into the management of SCCOHT, especially in young women.
    • It underscores the need for genetic testing to improve diagnosis and prognosis.

Disclaimer: This content is generated using AI assistance and should be reviewed for accuracy and compliance before considering this article and its contents as a reference. Any mishaps or grievances raised due to the reusing of this material will not be handled by the author of this article