Invasive cribriform carcinoma of the breast
Invasive Cribriform Carcinoma of the Breast (ICC) is a rare and distinct subtype of breast cancer characterized by its unique histological appearance. It falls under the broader category of invasive carcinoma, which signifies a cancer that has spread beyond the initial site of development into surrounding breast tissues. ICC is distinguished by its cribriform pattern, a term derived from the Latin cribrum, meaning sieve, which describes the tumor's perforated or sieved appearance under microscopic examination.
Epidemiology[edit | edit source]
Invasive Cribriform Carcinoma is relatively rare, accounting for approximately 0.3% to 0.8% of all breast cancers. It tends to occur more frequently in postmenopausal women, although it can present at any age.
Pathophysiology[edit | edit source]
The hallmark of ICC is the presence of distinctive cribriform architecture within the invasive component of the tumor. This architecture is characterized by nests of tumor cells punctuated by round, uniform holes or spaces, resembling a sieve. These spaces are not true lumina but are artifacts of the tumor's growth pattern. The cells themselves tend to be low grade, indicating a slower growth rate and a lesser tendency to spread compared to more aggressive forms of breast cancer.
Clinical Presentation[edit | edit source]
Patients with Invasive Cribriform Carcinoma typically present with a palpable mass in the breast, although the tumor can also be detected incidentally through mammography or other imaging studies. Unlike some other forms of breast cancer, ICC does not usually present with skin changes or nipple discharge.
Diagnosis[edit | edit source]
Diagnosis of ICC is confirmed through a combination of imaging studies and histopathological examination. Mammography and ultrasound are useful in detecting the presence of a mass, but a definitive diagnosis requires a biopsy. Microscopic examination of the biopsy specimen reveals the characteristic cribriform pattern that defines this cancer subtype.
Treatment[edit | edit source]
The treatment for Invasive Cribriform Carcinoma generally follows the guidelines for other types of invasive breast cancer. Surgery, in the form of a lumpectomy or mastectomy, is typically the first line of treatment, often followed by radiation therapy. The role of chemotherapy and hormone therapy is determined on a case-by-case basis, depending on the hormone receptor status of the tumor and other factors.
Prognosis[edit | edit source]
The prognosis for patients with Invasive Cribriform Carcinoma is generally favorable, especially when compared to more aggressive forms of breast cancer. This is attributed to the tumor's low grade and the tendency for early detection. However, as with all cancers, outcomes depend on a variety of factors, including the stage at diagnosis, treatment modalities, and individual patient characteristics.
Conclusion[edit | edit source]
Invasive Cribriform Carcinoma of the Breast is a rare subtype of breast cancer with distinct histological features. Its prognosis is relatively favorable, but early detection and appropriate treatment are crucial for optimal outcomes. Ongoing research into the molecular and genetic underpinnings of this cancer subtype may provide further insights into its pathogenesis and potential therapeutic targets.
NIH genetic and rare disease info[edit source]
Invasive cribriform carcinoma of the breast is a rare disease.
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