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What Is Basal Breast Cancer

How To Spot A Bcc: Five Warning Signs

Pregnancy Obesity and Basal-like Breast Cancer Microenvironment

Check for BCCs where your skin is most exposed to the sun, especially the face, ears, neck, scalp, chest, shoulders and back, but remember that they can occur anywhere on the body. Frequently, two or more of these warning signs are visible in a BCC tumor.

  • An open sore that does not heal, and may bleed, ooze or crust. The sore might persist for weeks, or appear to heal and then come back.
  • A reddish patch or irritated area, on the face, chest, shoulder, arm or leg that may crust, itch, hurt or cause no discomfort.
  • A shiny bump or nodule that is pearly or clear, pink, red or white. The bump can also be tan, black or brown, especially in dark-skinned people, and can be mistaken for a normal mole.
  • A small pink growth with a slightly raised, rolled edge and a crusted indentation in the center that may develop tiny surface blood vessels over time.
  • A scar-like area that is flat white, yellow or waxy in color. The skin appears shiny and taut, often with poorly defined borders. This warning sign may indicate an invasive BCC.
  • Please note: Since not all BCCs have the same appearance, these images serve as a general reference to what basal cell carcinoma looks like.

    An open sore that does not heal

    A reddish patch or irritated area

    A small pink growth with a slightly raised, rolled edge and a crusted indentation in the center

    A shiny bump or nodule

    A scar-like area that is flat white, yellow or waxy in color

    Carcinoma In Situ Vs Cancer

    A million-dollar question lately, especially with controversy over the treatment of ductal carcinoma in situ or in situ breast cancer, is whether or not carcinoma in situ is really cancer. The answer is that it depends on who you talk to. Some physicians classify carcinoma in situ as non-invasive cancer and others may prefer calling it pre-cancer. The distinction would lie in knowing whether or not the CIS would progress to invasive cancer, and that, by definition, is not known. Nor are we apt to get answers soon, as it wouldn’t be ethical to simply watch large numbers of carcinoma in situ’s to see if they became invasive cancer and spread.

    Ifn Ifn And Tnf Pathways Are Up

    Activities of the IFN, IFN, TNF TGF and STAT3 pathways, which were predicted with corresponding signatures, were compared among five PAM50-based BC subtypes. The first four pathways showed different expression pattern among different BC subtypes . The IFN and IFN pathways showed higher levels in HER2-enriched BCs and BLBCs but lower levels in luminal A and B BCs. The TNF pathway activity increased gradually from luminal A, luminal B, Normal-like, HER2-enriched and basal-like subtypes. Conversely, the TGF pathway exhibited an opposite activity pattern with TNF pathway. Overall, the pathway activities of IFN, IFN, TNF were the highest, while that of TGF was the lowest in BLBC. No significant difference of the STAT3 pathway activity was observed among the five PAM50 subtypes .

    Figure 1

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    Subtype And Relapse Events

    Breast cancer subtype is associated with local and regional relapse. Voduc et al.90 studied 2985 women with PBC, diagnosed between 1986 and 1992 in British Columbia, Canada. Median age at diagnosis was 59 years, and median follow-up time was 12 years. Six subtypes were classified based on tissue microarrays constructed from archival tissue blocks of the PBCs. Factors used in classification included ER, PR, HER2, Ki-67, EGFR, and CK 5/6. Forty-two percent of patients received BCT including radiation therapy, and 58% received mastectomy, with 25% of mastectomy patients also receiving radiation therapy. Fifty-seven percent of patients received adjuvant systemic therapy, either chemotherapy , endocrine therapy , or both . No patients received trastuzumab.

    Similar results have been reported in the United States. Two studies examined women diagnosed with invasive breast cancer treated with breast conservation and radiation therapy, with Nguyen et al.âs91 study population being a subset of Arvold et al.âs subsequent study.92 Of 1434 consecutive patients diagnosed with invasive breast cancer from 1997 to 2006 in an academic comprehensive cancer center, five breast cancer subtypes were approximated from IHC analysis: Luminal A , Luminal B , Luminal-HER2 , HER2 , and Triple Negative . While 91% of patients received adjuvant systemic therapy, no patients received trastuzumab.

    Lakshmy Nair, Ana Maria Gonzalez-Angulo, in, 2015

    Answer: Timing For Squamous Cell Carcinoma On The Scalp


    A well differentiated SCC on an otherwise healthy person is not a high risk lesion. Most of these arise from actinic keratoses, and although they need to be removed, waiting for a week or two for an excision is not an issue.I dont know the size of the spot they biopsied, but in all probability, your doc will be able to have the site closed and it will heal nicely and your hair wont be an issue.

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    Luminal Narrowing Stricture Formation And Upstream Dilation

    Initially, when the disease is present, the bowel lumen is not significantly narrowed. However, as the disease progresses, the affected bowel lumen narrows . As noted, luminal narrowing in Crohnâs can be caused by spasm or proliferation of the smooth muscle and/or fibrous tissue. The two can be differentiated with MRE/CTE by the presence or absence of upstream dilation. Using dynamic, fluoroscopic MR techniques, one can also identify ballooning, upstream dilation caused by a fixed stricture. We define a stricture as an area of luminal narrowing associated with upstream dilation more than 3â¯cm . When the upstream segment is less than 4â¯cm, it is considered mild, 4cm to 5.9â¯cm is moderate, and more than 6â¯cm is severe.

    Natasa Snoj, … Christos Sotiriou, in, 2009

    Microscopic Characteristics And Histological Subtypes Of Blbc

    BLBCs originate from the outer cell layer of the ductal and lobular frames of the breast gland, nearby the basal membrane. BLBC cells are prevalently myoepithelial with epithelial and smooth muscle features, and consequently they express smooth muscle markers and myofilament proteins .

    General characteristics of BLBC are tumor size larger than 2 cm, histological grade of 3, and high mitotic rate . Tumor cells reveal vesicular chromatin pattern and prominent nucleoli. A central necrosis has been observed in about 65% of cases and a geographic necrosis in roughly 40% of BLBCs . Moreover, a marked lymphoplasmacytic infiltration is more frequent in BLBC than in non-basal-like cancers .

    BLBC involves almost all different histological types of BC, including invasive ductal carcinoma, invasive lobular carcinoma, mixed carcinoma, mucinous carcinoma, metaplastic carcinoma, papillary carcinoma, medullary carcinoma, tubular carcinoma, apocrine carcinoma, micropapillary carcinoma, signet ring cell carcinoma, pleomorphic carcinoma, cribriform carcinoma and more rarely neuroendocrine carcinoma and atypical medullary carcinoma .

    Figure 1

    Basal-like mucinous carcinoma is of epithelial tumor cells with moderate nuclear atypia surrounded by abundant extracellular mucus . Basal-like neuroendocrine tumor cells are characterized by small, round or spindle cells, organized in alveolar, nest, trabecular, and rosette patterns .

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    Management Of Metastatic Triple

    A cohort study of more than 1600 Canadian women with breast cancer quantified the prognostic significance of triple-negativity. Of the 1601 patients, 180 had triple-negative breast cancer. At a median follow-up of 8.1 years, women with triple-negative breast cancer had an increased likelihood of distant recurrence and death within 5 years of diagnosis but not thereafter compared with other women with breast cancer. The pattern of recurrence was also qualitatively different in the triple-negative group, the risk of distant recurrence peaked at 3 years and declined rapidly thereafter. In the remaining 89% of patients, the recurrence risk seemed to be constant over a longer time period.201

    Multicenter clinical trials are currently investigating the role of new agents in triple-negative breast cancer. Investigation in the neoadjuvant setting not only allows for the assessment of clinical response but also for repeat pathologic testing at the completion of therapy. These “window studies” allow for the rapid evaluation of efficacy and mechanism. For these reasons, the antiangiogenic agent bevacizumab is currently under investigation in combination with platinum in the preoperative setting. Other treatments being tested in women with these tumors include EGFR inhibitors and drugs that stimulate the tumor suppressor protein PPAR-gamma, which could be used to prevent or delay progression of these tumors.

    Shailendra Dwivedi, … Sanjeev Misra, in, 2019

    Gabarapl1 Is Associated With Dip G

    Basal cell carcinoma is present? Watch for other cancers

    Our previous study reported that Dip G-induced myeloid differentiation of AML cells. To investigate the unique molecular mechanism underlying Dip G-induced luminal differentiation of basal-like breast cancer cells, we compared gene expression changes in Dip G-treated MDA-MB-231 and the AML cell line HL60. Among the common differentially regulated genes, the most significantly regulated gene was found to be GABARAPL1 . Dip G upregulated the mRNA expression of GABARAPL1 in a dose- and time-dependent manner in both MDA-MB-231 and SUM1315 cells . Western blotting results confirmed the GABARAPL1-inducing function of Dip G . In addition, analysis of the transcriptional profiles of 1097 breast tumors collected from The Cancer Genome Atlas revealed that the expression of GABARAPL1 was substantially lower than that in normal breast tissues , indicative of an essential role of GABARAPL1 downregulation during breast cancer progression.

    Fig. 3: Upregulation of GABARAPL1 expression by Dip G in basal-like breast cancer cells.Fig. 4: Knockdown of GABARAPL1 attenuates Dip G-induced cell differentiation.

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    Taking Care Of Yourself

    After you’ve been treated for basal cell carcinoma, you’ll need to take some steps to lower your chance of getting cancer again.

    Check your skin. Keep an eye out for new growths. Some signs of cancer include areas of skin that are growing, changing, or bleeding. Check your skin regularly with a hand-held mirror and a full-length mirror so that you can get a good view of all parts of your body.

    Avoid too much sun. Stay out of sunlight between 10 a.m. and 2 p.m., when the sun’s UVB burning rays are strongest.

    Use sunscreen. The suns UVA rays are present all day long — thats why you need daily sunscreen. Make sure you apply sunscreen with at least a 6% zinc oxide and a sun protection factor of 30 to all parts of the skin that aren’t covered up with clothes every day. You also need to reapply it every 60 to 80 minutes when outside.

    Dress right. Wear a broad-brimmed hat and cover up as much as possible, such as long-sleeved shirts and long pants.


    What Is The Prognosis For Basal Breast Cancer

    Basal tumors are frequently assimilated to triple-negative breast cancers. They display epidemiological and clinico-pathological features distinct from other subtypes. Their pattern of relapse is characterized by frequent and early relapses and visceral locations. Despite a relative sensitivity to chemotherapy, the prognosis is poor.

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    Molecular Subtyping Of Tnbc

    The first attempt to molecularly distinguish TNBC subtypes was a direct comparison of 374 TNBC samples extracted from 14 datasets where investigators sought to determine the relationship between the PAM50 intrinsic and TNBC molecular subtypes. The majority of the TNBC samples were indeed classified as basal-like followed by HER2 , normal-like , luminal B , and luminal A by PAM50 .

    Using gene expression analyses, distinct TNBC subtypes have been recently identified, each displaying a unique biology. In this pivotal study, Lehman et al. analyzed gene expression profiles from 21 breast cancer data sets with a total of 3,247 breast cancers and identified 587 TNBC cases representing 18% of all breast cancers. The 6 TNBC subtypes in this study included 2 basal-like , 1 immunomodulatory , 1 mesenchymal , 1 mesenchymal stem-like , and 1 luminal androgen receptor subtype, the last being characterized by androgen receptor signaling. Masuda et al. confirmed the classification of Lehmann et al. in an independent analysis, and they classified TNBC with high correlation into 7 subtypes including 1 unstable subtype .

    Very recently, an expression algorithm reduced to 101 genes was describedwith the power to subtype TNBC tumors similarly to the original 2,188-gene expression algorithm and predict patient outcomes .

    Survival Rates For Triple A Collection of Surgical Pathology Images

    Triple-negative breast cancer is considered an aggressive cancer because it grows quickly, is more likely to have spread at the time its found, and is more likely to come back after treatment than other types of breast cancer. The outlook is generally not as good as it is for other types of breast cancer.

    Survival rates can give you an idea of what percentage of people with the same type and stage of cancer are still alive a certain amount of time after they were diagnosed. They cant tell you how long you will live, but they may help give you a better understanding of how likely it is that your treatment will be successful.

    Keep in mind that survival rates are estimates and are often based on previous outcomes of large numbers of people who had a specific cancer, but they cant predict what will happen in any particular persons case. These statistics can be confusing and may lead you to have more questions. Talk with your doctor about how these numbers may apply to you, as he or she is familiar with your situation.

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    Definition Of The Basal Subtype

    A/ Hierarchical clustering of 353 breast cancer samples profiled in our institution with 12.304 genes. Each row is a gene andeach column a sample. The expression level of each gene in each sample is relative to its median abundance across thesamples and is depicted according to the color scale shown under the matrix. Red and green indicate expression levelsrespectively above and below the median. Above the matrix, the dendrogram shows the degree of similarity between samples.To the right, vertical colored bars indicate gene clusters zoomed in C. B/ Dendrogram of samples. The branches are color-codedaccording to the molecular subtype: red for basal and black for the other subtypes. Under the dendrogram, the subtypesare color-coded as follows: dark blue, lulinal A light blue, luminal B pink, ERBB2 red, basal green, normal-like. The basalsubtype is the most homogeneous subtype. C/ Gene clusters of interest: luminal/ER-related, ERBB2, basal, proliferation andimmune clusters. Some genes of interest of four clusters are noted .

    A/ Distribution of molecular subtypes within TN tumors. B/ Distribution of IHC groups within basaltumors. Our database was combined with publicly available MDA data .

    What Are The Treatments For Basal Cell Carcinoma

    BCC is treated by removing it. The choice of treatment depends on many things, including patient health and age, the location of the tumor, and the extent and type of the cancer. Treatment may occur in many ways:

    • Scratching off with a curette, an instrument that may end in a ring or a spoon, and then burning with a special electric needle. This method is called electrodessication and curettage.
    • Surgical removal
    • Mohs surgery: This is a specialized technique. The doctor first removes the visible cancer and then begins cutting around the edges. The tissues are examined during the surgery until no more cancer cells are found in tissues around the wound. If necessary, a skin graft or flap might be applied to help the wound heal.
    • Excisional surgery: The growth and a bit of surrounding skin is removed with a scalpel.
  • Freezing
  • Applying chemotherapy medication to the skin
  • Using lasers
  • Using blue light and a light-sensitive agent applied to the skin
  • Using radiation
  • If the BCC has advanced locally or spread to another location, which is very rare for BCC, the FDA has approved two medicines: vismodegib and sonidegib . These drugs are of a class called hedgehog inhibitors.

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    Histologic Analysis And Immunohistochemistry

    For histologic analysis, lung sections were stained with hematoxylin and eosin and photographed using a light microscope . Immunostaining of GABARAPL1 and ER of tumor sections was performed using a Real Envision Detection kit according to the manufacturer s instruction. Data analysis was performed blindly.

    Treatment Details And Outcomes

    Advancing Our Understanding of Basal-Like, Luminal A, and Luminal B Breast Cancers

    As for treatment modalities, Eighty five patients received surgery . Forty patients had conservative surgery . The remaining patients received radical mastectomy with axillary lymph nodes dissection . All patients with local disease, who were operated, received optimal surgery with free histological margins. Twenty-three patients with advanced tumors or inflammatory breast cancer have received neoadjuvant chemotherapy before surgery. Nineteen patients had Anthracycline based chemotherapy and four patients received Anthracycline and taxane based protocol. Only three patients had pathologic complete response to neoadjuvant chemotherapy according to Sataloff and Chevalier classification. Seventeen patients over 68 received adjuvant chemotherapy, 17 had Anthracycline based chemotherapy, 35 had sequential Anthracycline and taxane. Eight patients with metastatic disease received anthracycline-based regimen in the first line metastatic chemotherapy.

    Radiation therapy was indicated in 69 non-metastatic patients. Palliative radiotherapy was delivered in two patients with painfull bone metastasis.

    After a median follow up of 49 months, twelve among the 82 non metastatic patients experienced locoregional relapse and nineteen patients had metastatic recurrence. The maximum of recurrence occurred between the first and second year from diagnosis with a median of 21 months and 24 patients died.

    Figure 2: Population distribution by relapse period. View Figure 2

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    Pattern Of Relapse And Survival

    The prognosis of basal subtype is poorer than that of other subtypes . Most of gene profiling studies have repeatedly reported a shorter metastasis-free survival and overall survival among basal breast cancer patients . According to three different multigene expression signatures most of the tumors predicted as poor-prognosis were basal . In our pooled series of 480 luminal A and 227 basal breast cancers, the 5-year OS was 88% for patients with luminal A subtype and 58% for patients with basal subtype, and the 5-year MFS was of 82% and 66%, respectively . Data are less consistent with the IHC definitions. Most studies showed that the clinical outcome of TN breast cancers is less favorable than that of non-TN cancers. However, some studies did not find such association . This discrepancy of outcome for basal subtype between the gene and IHC definitions is well evidenced by our study in which the basal subtype was defined using the intrinsic gene set . No difference for MFS existed among the 160 basal tumors between those with and those without the TN status. Conversely, there was a significant difference between 123 TN samples defined as basal and 49 TN samples defined as non-basal. This observation was confirmed using an IHC definition of basal within a series of TN samples . A confrontation of two IHC definitions of basal breast cancers in a series of 3744 cases revealed that the five-biomarker definition had superior prognostic value than the TN one.


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