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Protocol for the Examination of Specimens from Patients with Ductal Carcinoma In Situ (DCI) of the Breast Protocol applies to DCI without invasive carcinoma or microinvasion. Based on JCC/ICC TNM,
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Begin by gathering all necessary medical records and documentation related to the patient's history and diagnosis of ductal carcinoma in situ.
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Who needs ductal carcinoma in situ?

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Ductal carcinoma in situ (DCIS) is a non-invasive form of breast cancer that is diagnosed through a biopsy. It is typically found during routine mammogram screenings or as a result of other breast-related concerns. As DCIS is a precancerous condition, anyone who has been diagnosed with it will require medical attention and treatment. The treatment aims to prevent the progression of the condition into invasive breast cancer. Therefore, anyone diagnosed with ductal carcinoma in situ needs medical intervention, including surgery, radiation therapy, or hormone therapy, to reduce the risk of the disease advancing.

What is Ductal Carcinoma In Situ (DCIS) of the Breast Form?

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Ductal carcinoma in situ (DCIS) is a non-invasive breast cancer where abnormal cells are found in the lining of the breast duct but have not spread outside the duct.
Typically, healthcare providers and cancer registries are required to report cases of ductal carcinoma in situ for monitoring and statistical purposes.
Filling out forms related to ductal carcinoma in situ generally involves providing patient information, diagnosis details, treatment plans, and any follow-up care notes.
The purpose of identifying and treating ductal carcinoma in situ is to prevent the progression of cancer, as it can develop into invasive breast cancer if left untreated.
Information that must be reported includes patient demographics, tumor characteristics, treatment details, and outcomes.
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