Breast sarcoma is a rare and aggressive cancer. The usual presentation is a unilateral painless fast-growing mass (
14). Skin and nipple changes or axillary lymphadenopathy are not common. They have no pathognomonic imaging features and mammographic and sonographic findings are non-specific (
15). Diagnosis is usually made by core needle biopsy.
There are different subtypes of breast sarcoma. Our study revealed that after malignant phyllodes tumor, the most common subtypes are sarcoma NOS type, angiosarcoma, and fibrosarcoma, respectively. The most common mesenchymal malignancies of the breast are phyllodes tumor, followed by angiosarcoma (
2,
3,
16-
20). Yin et al. utilized a US population database to analyze a large series of women diagnosed with primary breast sarcoma, excluding phyllodes tumor (
16). In their study, angiosarcomas, sarcoma NOS, spindle cell sarcoma, and fibrosarcoma were the most prevalent (
16).
Some authors do not include malignant phyllodes tumors in their study. Wang et al. conducted a retrospective review of 35 cases with primary breast sarcoma (PBS) and 70 cases with malignant phyllodes tumor (MPT) (
21). They concluded that MPT and PBS may be considered together because these two diseases have similar behavior, disease-free survival (DFS), and overall survival (OS). Moreover, both diseases should be treated with the same strategy (
5,
21). Compared to other sarcomas, phyllodes tumor occurs in younger women. As this subtype of sarcoma composed 55.4% of our cases that could affect the average age, ASR was calculated both for all cases together and for phyllodes and other cases separately. This study revealed that the highest incidence rate for malignant phyllodes tumor in Iran is in 55- to 59-year-old women, which is higher than the literature (35 to 55 years) (
7,
17,
22). Excluding phyllodes tumor, the highest incidence rate for other sarcomas was between the 70- to 74-year-old group. This is higher than the literature as well (the 5th and 6th decades) (
4,
16). Patients with primary breast sarcoma have a lower age compared to the secondary breast sarcoma patients (
23,
24). However, if all cases are calculated together, the highest ASR will be in the 55- to 59-year-old group that is compatible with the literature.
Pediatric breast cancer (19 years old and younger) is rare and comprises less than 0.1% of all breast cancers (
25,
26). About 5% of phyllodes tumors occur in girls younger than 20 years. Low-grade forms of sarcoma have been reported in children in their second decade of life (
25-
27). In a population-based study in the United States, it was shown that 35.1% of all pediatric breast malignancies were fibroepithelial tumors and 14.2% were sarcoma (
21). In this study, 13 patients were 19 years old or younger consisting of 5% of all patients. Two of these patients were in the age group of 0 - 4 and both of them had malignant phyllodes tumor.
In data compiled from the Surveillance, Epidemiology and End Results (SEER) Program of the National Cancer Institute, the annual incidence of breast sarcomas was 4.48 cases per million women in the United States (
3-
5). May and Stroup used the SEER data from 1973 to 1986 and calculated the annual incidence rate of 4.48 cases per million women (
28). In this study, the annual incidence rate in Iran was 1.17 per million, which is lower than in western countries.
Al-Benna et al. reviewed major sarcoma series and found that only 1.5% of breast sarcomas occur in men (
3). In another review conducted by Lim et al., 2.4% of patients were male (
29). However, our study revealed that 2.7% of breast sarcoma patients in Iran are male. We have no clear explanation that why while the overall incidence of breast sarcoma is lower in Iran, it has a higher incidence in men.
The ASR was highest in Ahwaz. The reason is unknown and could be an interesting field for further studies. External beam radiation, chronic lymphedema, hereditary diseases like Neurofibromatosis or Li-Fraumeni-syndrome, and long-standing contact with vinyl chloride are known risk factors for developing sarcoma (
3,
30). However, the risk factors for developing breast sarcoma are mostly unknown and most the sarcomas have no demonstrable cause (
31). In this study, most of the sarcoma was grade 3, which is compatible with other studies that high-grade sarcoma has been more prevalent.
In this timeframe, 11 cases of carcinosarcoma were registered as well. This is a rare neoplasm that accounts for 0.08 to 0.2% of all breast malignancies (
32). This tumor is composed of both malignant epithelial (carcinomatous) components and malignant non-epithelial (sarcomatous) components with a clear-cut boundary between them (
32-
34). Carcinosarcoma, as defined by WHO, is a subtype of metaplastic carcinoma (
12), and their behavior and treatment strategy is more like a carcinoma; therefore, they were not included in this study.
A faster and more accurate diagnosis, as well as a more comprehensive registration, are essential for improving cancer registration. Cancer centers should be able to provide everyone with rapid identification and accurate diagnosis of cancer at an affordable price. Moreover, software and hardware resources should be encouraged to register cancer data comprehensively and precisely. Furthermore, individuals and staff who will be recording data should be well-informed and fully aware of the importance of accurate data recording.
4.1. Conclusions
Breast sarcoma is a rare disease with remarkable heterogeneity. Compared to western countries, Iran has a lower incidence of breast sarcoma in women, a higher incidence rate in men, and older onset age. As in other countries, malignant phyllodes tumors and angiosarcomas are the most common subtypes. In addition, breast sarcoma incidence rates in different grades are similar across countries. Geographically, it is more common in Ahwaz. Additional research in this area may be warranted.