Breast cancer is the most common malignancy in women worldwide (
1). Globally, the incidence rate of breast cancer is high, identifying 2 million new cases in 2018. In Iran, the prevalence of breast cancer is also high, with an annual incidence rate of 33.21 per 100,000 women and the mortality rate associated with this cancer is 14.2 per 100,000 women, with a mean age of 49.84 years old (
2). Breast cancer, the most prevalent type of neoplasm among Iranian women, is often diagnosed when it reaches the advanced or metastatic stages. Therefore, the quality of life in these patients is profoundly disrupted due to the physical and psychological burden associated with the disease; however, it could be restored to some extent via prognostic factors. The rate of lymph node metastasis and the number of positive lymph nodes are prognostically important, particularly in some subtypes of breast carcinoma including invasive micropapillary cancer (IMPC). IMPC is a rare and aggressive subtype of breast cancer, initially described in 1980 (
3), and histologically distinguished from other subtypes. Micropapillary structures are clusters of tumor cells settled in the clear vascular-free space derived from polarity inversion of tumor cells (
4). Beside pure IMPC, which is a distinct subtype, mixed IMPC is present in which the micropapillary component is observed in association with other subtypes of breast cancer, particularly invasive ductal carcinoma (IDC) (
4). Tumors with any proportion of micropapillary components are aggressive and associated with a high rate of lymph node involvement and poor prognosis and outcome. Lymph node dissemination is common in IMPC due to its angioinvasive characteristics. The mechanisms by which a tumor can metastasize are various and generally comprised of several steps. Following the loss of connections, tumor cells can penetrate the vessel wall, enter new tissues, and perform angiogenesis. Numerous studies have attempted to clarify the main cause of increased lymph node metastasis in IMPC, but the answer remains unclear. However, previous studies have shown that heat shock protein 27 (Hsp27) and Leukocyte 1 cell adhesion molecule (L1CAM) can explain pathogenic features of IMPC and the high rate of lymph node involvement observed in this cancer (
5,
6). Furthermore, the level of CD24 expression in IMPC should be considered since the role of CD24 in the metastasis of other cancers has been previously confirmed (
7). Higher expression of CD24 in IMPC compared to invasive ductal carcinoma, not otherwise specified (IDC-NOS), was reported in a study by Reyal et al. This can explain the higher rate of invasion observed in IMPC and also make CD24 a potential therapeutic target (
8).