J Korean Surg Soc.
2000 Mar;58(3):352-360.
Clinical Analysis of Phyllodes Tumor of the Breast
- Affiliations
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- 1Department of Surgery, Seoul National University College of Medicine.
- 2Department of Pathology, Seoul National University College of Medicine.
Abstract
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PURPOSE: Phyllodes tumor is a rare fibroepithelial tumor of the breast, first described by Johannes
Muller in 1838. Much has been written about phyllodes tumor, but very few widely accepted conclusions
about its clinical behavior, treatment modality, and prognosis have been reached. This study aims to
analyze the clinical, radiological, and pathological characteristics of phyllodes tumor of the breast.
METHODS
The medical records of 41 patients with phyllodes tumor who had been treated
between February 1982 and August 1998 at the Department of Surgery, Seoul National
University Hospital, were retrospectively reviewed for clinical, radiological and pathological
findings, treatment modalities, and follow-up results. RESULTS: Of these 41 cases, there were
28 cases (68.3%) of benign tumors and 13 cases (31.7%) of malignanat tumors. All patients
were females, and the mean ages of onset were 33.2 years for benign tumors and 40.8 years
for malignant tumors. Most patients, 100% of benign and 92.3% of malignant, presented with
a papable mass in the breast. The median duration of illness was 2 months for malignant tumors
and 8 months for benign tumors. The tumor size was greater than 10 cm in diameter in 5 cases
(38.5%) of malignant tumors and in 3 cases (10.7%) of benign tumors. Only 4 cases were
preoperatively diagnosed as having a phyllodes tumor by using radiological and fine needle
aspiration cytology. Out of the 10 malignant cases reviewed, 5 cases were confirmed as
malignant, and 5 cases were confirmed as borderline phyllodes tumors. Cellularity was moderate
or above in all 5 malignant and 5 borderline cases. Atypism above moderate degree was found
in 4 of 5 (80%) malignant tumors, in 3 of 5 (60%) borderline tumors, and in 4 of 24 (16.7%)
benign tumors. Mitotic counts in all 5 malignant cases were 5 or more per 10 high power field
while those in the 5 borderline tumors were 2-5 mitoses per 10 high power field. The most
commonly performed operative procedures were a simple mastectomy (50%) for malignant
tumors and a simple excision (64.3%) for benign tumors. Post-operative adjuvant therapy was
done for 4 cases; out of these, 1 case had been initially diagnosed as a malignant phyllodes
tumor, but the diagnosis was changed to a benign phyllodes tumor upon review. Of the 27
follow-up cases, recurrences developed in 3 cases (16.7%) of benign tumors. CONCLUSION: From
the above results, there were no specific clinical features for differentiating benign from
malignant phyllodes tumor preoperatively; therefore, we cannot help depending on the
pathologic findings. Pathologic reviews showed that among several criteria, atypism, cellularity,
and mitotic count were the most definite pathologic characteristics in differentiating benign
from malignant phyllodes tumor. But much more experience and long-term follow-up may be
needed to define optimal treatments and to analyze the prognosis for phyllodes tumors of the
breast.