Phylloides tumor of the breast: a rare neoplasm, though not that innocent
2009

Cystosarcoma Phylloides: A Rare Breast Tumor

Sample size: 22 publication Evidence: low

Author Information

Author(s): Stamatakos Michael, Tsaknaki Sofia, Kontzoglou Konstantinos, Gogas John, Kostakis Alkiviades, Safioleas Michael

Primary Institution: Department of Propedeutic Surgery, Medical School, University of Athens, Laiko General Hospital, Athens, Greece

Conclusion

Cystosarcoma phylloides is a challenging tumor to treat, requiring careful follow-up to manage potential recurrences.

Supporting Evidence

  • 16 out of 22 patients did not show any signs of local recurrence or metastases.
  • One patient with metastatic cystosarcoma phylloides died three months after diagnosis.
  • Histological examination revealed benign lesions in 15 cases and malignant tumors in 4 cases.

Takeaway

Cystosarcoma phylloides is a rare type of breast tumor that can be tricky to treat, and doctors need to keep a close eye on patients to catch any problems early.

Methodology

The study involved a retrospective analysis of 22 patients diagnosed with cystosarcoma phylloides over a 38-year period, focusing on their treatment and follow-up.

Limitations

The study is limited by its small sample size and retrospective nature.

Participant Demographics

The participants were 22 women with a mean age of 38 years, presenting with cystosarcoma phylloides.

Digital Object Identifier (DOI)

10.1186/1477-7800-6-6

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