Showing posts with label Breast Cancer. Show all posts
Showing posts with label Breast Cancer. Show all posts

Thursday, September 23, 2010



The Spy technology is an intraoperative Flouresence Imaging System that captures real-time images of blood flow in vessels and tissue perfusion. This allows Plastic and Reconstructive Surgeons to evaluate perfusion of perforator flaps.



www.drbriandickinson.com

Sunday, May 2, 2010

Oncotype DX: Reading Notes


Oncotype DX is a diagnostic test that helps identify which women with early-stage, lymph node negative and estrogen receptor-positive breast cancer are more likely to benefit from adding chemotherapy to their hormonal treatment.
The Oncotype DX test measures the activity of different genes in a woman's breast tissue tumor tissue.

Women with lower (RS) recurrence scores have a lower risk that their cancer will return. These women also have a cancer that is less likely to benefit from chemotherapy. A lower recurrence score does not necessarily mean that there is no chance that the breast cancer will return.

Women with a higher (RS) recurrence score have a stronger chance that their breast cancer will return, but may also benefit largely from chemotherapy. A higher recurrence score does not mean that a woman's breast cancer will definitely return.

Sunday, December 27, 2009

Self Study:Book Chapter Review & Reading Notes


Chapter 4: Pathology of Breast Disorders

Functional unit of the breast is the terminal ductal lobular unit.

The entire lobular and ductal structure of the breast is lined by two layers of cells:the inner epithelial layer and the outer myopepithelial layer.

“Breast cancer” typically refers to breast carcinoma that arises by preferential growth of the inner epithelial layer.

Benign Disorders:
Fibrocystic change-pathologic condition that correlates with ‘lumpy’ breasts.

This term is applied to a plethora of benign changes in the breast, which are best categorized based on the subsequent risk of development of breast carcinoma.

Three categories:

Non-proliferative lesions:
Proliferative lesions without atypia
Atypical hyperplasia

Nonproliferative Lesions

This is the most common category of breast disorders and includes cysts, papillary apocrine change, mild hyperplasia of the usual type, and epithelial-related calcifications.

Women with these lesions do not incur a higher risk of development of breast carcinoma than that of women who had no breast biopsy (relative risk, 0.89)

Proliferative Lesions without Atypia
Women with these lesions have a slight risk of developing breast carcinoma, 1.5 to 2 times greater than the general population. This category includes moderate or florid hyperplasia of the usual type, sclerosing adenosis, small duct papillomas, and fibroadenomas.

Sclerosis adenosis is the most common lesion and refers to expanded lobular units with a proliferation of both acini and intervening stroma. Microcalcifications are frequently seen and correspond to “benign calcifications” seen on mammography.
Atpical Hyperplasia

Atypical hyperplasia confers a risk of development of breast cancer that is 3.5-5 times that of the reference population. This category includes both atypical ductal hyperplasia (ADH) and atypical lobular hyperplasia (ALH).

Radial Scars and Complex Sclerosing Lesions

Radial scars are typically small areas of scarring (less than 1 cm) surrounded by glandular elements.

Benign Neoplasms

Fibroadenoma

Fibroadenomas typically present as painless, mobile, rubbery masses. They are usually solitary but occasionally multiple. Most often present in the upper-outer quadrant and slightly more common in the left breast.

Solitary (Large Duct) Intraductal Papilloma
These tumors typically arise in a large duct in the subareolar region and present with unilateral hemorrhagic discharge.

Phyllodes Tumor

Character may be benign to malignant. Phyllodes tumors tend to have local recurrences and should be widely excised.

Lobular Carcinoma in Situ (LCIS)
LCIS is a rare multicentric entity that can not be identified clinically or on gross examination.

The invasive carcinoma that may develop may be either ductal or lobular.

LCIS is more common in younger, premenopausal women, and the mean age of diagnosis is 44 to 46 years.

LCIS is commonly bilateral and multicentric (present in more than one quadrant).

LCIS is typically an incidental finding in a breast biopsy done for a mammographically detectable lesion, which may be calcifications in adjacent sclerosing adenosis or other proliferative lesions.

Estrogen receptor (ER) is typically over expressed in cells of LCIS, whereas Her-2/neu is not. E-cadherin is a useful marker to distinguish lobular and ductal proliferations because it is preferentially expressed in ductal proliferations.

Most women with LCIS do not develop invasive carcinoma on follow-up, but it does confer a relative risk from 6.9 to 12. The carcinomas that develop are mostly invasive ductal carcinoma.

LCIS is best considered to be a risk factor rather than a precursor of invasive carcinoma. Thus, the surgical management of LCIS does not aim for negative margins, and radiation therapy has no role in management of LCIS.

Ductal Carcinoma in Situ

Ductal carcinoma in situ (DCIS) comprises lesions in which the neoplastic growth of ductal cells is restricted within the ductal system.

DCIS is considered to be a direct precursor of invasive carcinoma.

The incidence of carcinoma in patients with DCIS varies from 11% to 53% and occurs in the ipsilateral breast.

Mammographic abnormalities, which commonly show microcalcifications, are the most common presentation of DCIS.

Comedo DCIS refers to central necrosis in the ducts that are lined by poorly differentiated cells. Comedo DCIS is invariably associated with calcifications.

Comedo necrosis was the only factor found to correlate with ipsilateral recurrence in a multivariate analysis of nine histologic features of DCIS.

The distinction between LCIS and DCIS can usually be made with E-cadherin staining. E-cadherin shows no staining in lobular proliferations.

Low Grade DCIS tends to be ER and PR positive and Her2/neu negative.
High Grade DCIS tends to be ER/PR positive and Her2/neu positive.

Tamoxifen decreases recurrence rates in patients with DCIS.

DCIS specimens should be inked for margins. In NSABPB-17, only the presence of a tumor-filled duct in contact with the inked margin was categorized as a positive margin.

Silverstein et al. showed that quantification of the distance of DCIS from the margin is useful, and greater than 1 cm is deemed to be a negative margin.

Paget’s Disease of the Nipple

Association of eczematous changes in the nipple with underlying mammary carcinoma. Paget’s disease of the nipple refers to the extension of underlying breast cancer to the skin of the nipple.

Paget’s disease presents as scaling and erythema of the nipple-areola complex.

95% of cases of Paget’s have underlying carcinoma, invariably ductal, and often associated with comedo-type DCIS.

Immunohistochemical stains are useful to distinguish Paget’s from melanoma and clear cells of the epidermis.

Her2/neu, epithelial membrane antigen, and polyclonal CEA are expressed in Paget’s CK 7 is positive in both Toker cells and Paget’s disease.

Saturday, December 19, 2009

Article Review


Review of "Breast Cancer Diagnosis and Prognosis in Augmented Women" Plastic & Reconstructive Surgery 118: 587-593, 2006 by Neal Handel & Melvin J. Silverstein."

Frequently in my practice I am asked by many women who desire breast augmentation or who have already had a breast augmentation and now want a lift, removal and replacement, or surgery for capsular contracture the following question:

Do breast implants impair my ability to detect breast cancer or increase my risk of getting breast cancer?

To answer this question and as part of my own self study, I read and reviewed an article in Plastic & Reconstructive Surgery 118: 587-593, 2006 by Neal Handel & Melvin J. Silverstein. I present here notes which are helpful for my own self study as well as for patient education during consultation:

Background:
--Breast enlargement surgery is popular. More than 334,000 women underwent elective breast augmentation in 2004.
--A woman in the United States has a 1 in 7 (13.4 percent) lifetime risk of developing breast cancer.
--There is no etiologic link between implants and breast tumors. Numerous studies show that the rate of breast cancer is not increased among augmented women, and some studies demonstrate lower than expected rates.
--However, because of the large number of women undergoing augmentation, there have been persistent concerns about possible adverse effects of implants on cancer detection and treatment.

Methods:
The authors reviewed their database of women with breast cancer and determined if there was a difference in breast cancer between augmented and non-augmented women.

Results:
--There was no statistically significant difference in stage of disease between augmented and non-augmented patients. The mean tumor size, recurrence rates, and breast cancer- specific survival were virtually identical in both groups.--Augmented patients were more likely to present with palpable lesions.

Conclusion:
Augmented and nonaugmented patients are diagnosed at a similar stage of breast cancer and have a comparable diagnosis. While implants may impair mammography, they appear to facilitate detection of palpable breast cancers on physical examination.