This document discusses various imaging modalities used for breast cancer screening and diagnosis, including mammography, ultrasound, MRI, CT, and PET scans. It provides details on mammography techniques for screening and diagnostic purposes. Key findings from studies on screening mammography for different age groups are summarized. Guidelines on screening from organizations like ACS, NCCN, and NCI are also outlined. The use of ultrasound and MRI as supplemental tools for diagnosis is discussed.
Introduction to mammography and its equipment.
Different views on mammography & supplementary views.
Birads mammographic lexicon
Birads ultrasound lexicon
Imaging of suspicious mammary lymph nodes
Categories in BIRADS 2013.
A comprehensive study about new and upcoming modalities in imaging and screening of breast lesions with description about every new modalities with their advantages and pitfalls.
Sonographic evaluation of breast Dr. Muhammad Bin Zulfiqar
In this we will discuss role of high resolution Ultrasound in breast pathologies.
We will further discuss the role of Elastography in characterization of BIRADS.
This seminar slides were prepared by us for our own seminar with Consultant Surgeon Dato Imi from HRPZ II, Kelantan.
The information is extracted from CPG Breast Cancer 2nd edition, November 2010.
Supervised by DATO DR IMI SAIRI BIN AB HADI, General Surgeon, Breast and Endocrine
Introduction to mammography and its equipment.
Different views on mammography & supplementary views.
Birads mammographic lexicon
Birads ultrasound lexicon
Imaging of suspicious mammary lymph nodes
Categories in BIRADS 2013.
A comprehensive study about new and upcoming modalities in imaging and screening of breast lesions with description about every new modalities with their advantages and pitfalls.
Sonographic evaluation of breast Dr. Muhammad Bin Zulfiqar
In this we will discuss role of high resolution Ultrasound in breast pathologies.
We will further discuss the role of Elastography in characterization of BIRADS.
This seminar slides were prepared by us for our own seminar with Consultant Surgeon Dato Imi from HRPZ II, Kelantan.
The information is extracted from CPG Breast Cancer 2nd edition, November 2010.
Supervised by DATO DR IMI SAIRI BIN AB HADI, General Surgeon, Breast and Endocrine
Comprehensive review of Isolated Axillary lymph nodal metastasis of unknown origin- Clinically unknown primary axilla which includes detailed approach and management of inguinal lymph nodal metastasis also
For more information, visit https://www.timberlandmedical.com
Timberland Medical Centre is a private hospital that has been in operation since 1994. We are strategically located at the 3rd Mile roundabout on Jalan Rock, Kuching, Sarawak, East Malaysia. Our hospital is 10 minutes from the Kuching International Airport and 15 minutes from the Central Bus Terminal. We continually seek to improve and upgrade our services and facilities, as we strive to provide the best medical care for our patients and customers.
Original StudyType of Breast Cancer Diagnosis, Screening,a.docxvannagoforth
Original Study
Type of Breast Cancer Diagnosis, Screening,
and Survival
Carla Cedolini,1 Serena Bertozzi,1 Ambrogio P. Londero,2 Sergio Bernardi,3,4
Luca Seriau,1 Serena Concina,1 Federico Cattin,1 Andrea Risaliti1
Abstract
Organized, invitational breast cancer screening in our population succeeded in detecting early-stage tumors,
which have been consequently treated more frequently with breast and axillary conservative surgery, com-
plementary breast irradiation, and eventual hormonal therapy. The diagnosis of invasive cancer with screening
in our population resulted in a survival gain at 5 years from the diagnosis.
Introduction: Breast cancer screening is known to reduce mortality. In the present study, we analyzed the prevalence
of breast cancers detected through screening, before and after introduction of an organized screening, and we
evaluated the overall survival of these patients in comparison with women with an extrascreening imaging-detected
breast cancer or those with palpable breast cancers. Materials and Methods: We collected data about all women
who underwent a breast operation for cancer in our department between 2001 and 2008, focusing on type of tumor
diagnosis, tumor characteristics, therapies administered, and patient outcome in terms of overall survival, and re-
currences. Data was analyzed by R (version 2.15.2), and P < .05 was considered significant. Results: Among the 2070
cases of invasive breast cancer we considered, 157 were detected by regional mammographic screening (group A),
843 by extrascreening breast imaging (group B: 507 by mammography and 336 by ultrasound), and 1070 by extra-
screening breast objective examination (group C). The 5-year overall survival in groups A, B, and C were, respectively,
99% (95% CI, 98%-100%), 98% (95% CI, 97%-99%), and 91% (95% CI, 90%-93%), with a significant difference
between the first 2 groups and the third (P < .05) and a trend between groups A and B (P ¼ .081). Conclusion: The
diagnosis of invasive breast cancer with screening in our population resulted in a survival gain at 5 years from the
diagnosis, but a longer follow-up is necessary to confirm this data.
Clinical Breast Cancer, Vol. 14, No. 4, 235-40 ª 2014 Elsevier Inc. All rights reserved.
Keywords: Breast cancer, Breast cancer screening, Invasive breast cancer, Mammographic screening, Overall survival
Introduction
Because of the detection of early-stage tumors, breast cancer
screening reduced breast cancer mortality in Europe by 25%-31%
in patients who were invited for screening and by 38%-48% in
those who were actually screened during the last decade of the
twentieth century and the first decade of the twenty-first.1 In our
region of Italy, an organized breast cancer screening was firstly intro-
duced in 2005, but despite the high compliance of invited women
1Clinic of Surgery
2Clinic of Obstetrics and Gynecology
University of Udine, Udine, Italy
3Department of Surgery, Ospedale Civile di Latisana, Udine, Italy
4 ...
breast cancer
cancer
epidemiology
community medicine
awareness of breast cancer
سرطان الثدي
وبائيات سرطان الثدي
epidemiology of breast cancer
prevention of breast cancer
risk factors of breast cancer
epidemiology of breast cancer in iraq
sign and symptoms of breast cancer
location of breast cancer
http://link.com The main keyword for cancer http://link.com The main keyword for cancerhttp://link.com The main keyword for cancerhttp://link.com The main keyword for cancerhttp://link.com The main keyword for cancerhttp://link.com The main keyword for cancerhttp://link.com The main keyword for cancerhttp://link.com The main keyword for cancerhttp://link.com The main keyword for cancerhttp://link.com The main keyword for cancerhttp://link.com The main keyword for cancer
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
2. Imaging modalities in breast cancer are used for
screening as well as diagnosis.
-Mammography
-Ultrasonography
- MRI scan
-CT scan
-PET scan
-Bone scan
3. Mammography
Is used both as a screening as well as diagnostic tool in
breast cancer
4. Screening Mammogram
Before 1977, no formal guidelines existed for
screening women for occult breast cancer.
The publication of the Health Insurance Plan
(HIP) of Greater New York Screening Project, in
the 1960s, led the National Cancer Institute and
the American Cancer Society to support a breast
cancer screening project to evaluate further the
efficacy of screening by mammography and
physical examination.
5. At 5 years, the HIP study found a 50% decrease in
mortality rate in women older than 50 years of
age, but only a 5% decrease in mortality rate in
women younger than 50 years of age.
With follow-up, the mortality rate in women
younger than 50 years of age showed a 23.5%
Women who refused screening had no reduction
in mortality rate.
6. Screening Mammogram
Although an active area of debate
Several authors agree that screening mammography in
women 40-49 years of age may reduce mortality from
breast cancer
Health insurance plan study, (1963-1969)
Taber et al (1988-1996)
{Canadian study- addition of annual mammography screening had no effect on breast cancer
mortality}
7. National Organizations' Screening Guidelines for
Mammography
ACS (American college of surgeons)
For women for normal risk, yearly mammograms
are recommended starting at age 40.
CBE suggested about every three years for women
in the 30′s and every year for women age 40 and
above.
BSE is suggested for women starting in their 20s.
8. NCCN
Women at normal risk are recommended to have
CBE every 1–3 years;
periodic SBE is encouraged.
Beginning at age 40, annual CBE and
mammograms are recommended, and periodic
SBE is encouraged.
9. NCI
Women who are age 40 and above should be
screened with mammograms every 1–2 years.
10. For age group <50 years
The National Cancer Institute, American Cancer
Society, and the American College of Radiology
recommend a baseline mammogram at the age of 35
years (30 years in high-risk groups).
Repeat examinations should be carried out every 2
years beginning at 40 years of age.
In women older than 50 years, mammograms should
be performed annually.
Frisell J, Lidbrink E. The Stockholm Mammographic Screening Trial: risks and benefits in age group 40-49
years. J Natl Cancer Inst Monogr 1997:49–51.
UK Trial Group. 16-year mortality from breast cancer in the UK trial of early detection of breast cancer. Lancet
1999;353:1909–1914
Kerlikowske K, Grady D, Rubin SM, et al. Efficacy of screening mammography. A meta-analysis. JAMA
1995;273:149–154.
Feig SA. Estimation of currently attainable benefit from mammographic screening of women aged 40-49 years. Cancer
1995;75:2412–2419
11. Diagnostic mammogram
most critical component of diagnostic imaging in
breast cancer patients
bilateral mammograms should be performed routinely
in the work-up of the breast cancer patient
12. Special x-ray machines
developed exclusively for
breast imaging
produce mammography
films.
use very low doses of
radiation and produce
high-quality x-rays
13. The patient wears an
open wrap and
undress above the
waist
14. Breast is briefly compressed
between 2 plates attached
to the mammogram
machine– an adjustable
plastic plate on top and a
fixed plate on bottom which
holds the x-ray film
15. We should be familiar with the difference between
diagnostic and screening mammogram.
Screening mammogram-
Routine mammogram, done in asymptomatic women
2 views- craniocaudal, mediolateral
16. Diagnostic mammogram-
To characterise abnormalities detected at screening or
in women with palpable masses
Additional magnification views
Done in presence of radiologist generally to determine
need for additional views or follow up studies
-lateromedial(from side towards center of chest)
- mediolateral(from the center of the chest out)
- Spot compression view
17.
18.
19.
20. Mammographic abnormalities
Mammographic signs of cancer consist of two primary
findings:
(1) a mass with ill-defined, irregular, or spiculated
edges and/or
(2) irregular, pleomorphic calcifications
22. IDC- mass with illdefined ,
spiculated margins
Benign masses- well defined, with
sharp margins, and have little effect on
the surrounding breast architecture
29. In ductal carcinoma in situ (DCIS), there is
normally no mass but just an area of
calcification
30. CC and MLO mammographic views
show a large and relatively
circumscribed ovalar lesion in the
upper outer quadrant.
On US scan it consists on a complex
cyst with a parietal ill-defined mass
(arrows).
US-guided core needle biopsy of the
intracystic mass revealed a
malignant phyllodes tumor
31. The BIRADS ( Breast Imaging and Reporting Data
System) classification system is widely adopted in
classifying mammograms with respect to appropraite
follow up and intervention
32. Nothing to comment on.
Breasts are symmetric ; no masses,
architectural disturbances, or suspect
calcifications are present.
Category 1
Negative
33. Negative mammogram, but the interpreter
may wish to describe a finding.
Involuting, calcified fibroadenomas,
multiple secretory calcifications, fat-
containing lesions such as oil cysts, lipomas,
galactoceles, and mixed-density
hamartomas all have characteristic
appearances, and may be labeled with
confidence.
The interpreter might wish to describe
intramammary lymph nodes, implants, and
the like, while still concluding that there is
no mammographic evidence of malignancy
Category 2
Benign finding
34. A finding placed in this category should
have a very high probability of being benign
Not expected to change over the follow-up
interval, but the radiologist would prefer to
establish its stability.
(Data are becoming available that shed light
on the efficacy of short-interval follow-up.
At present, most approaches are intuitive.
These will likely undergo future
modification as more data accrue as to the
validity of an approach)
Category 3
Probably benign
finding ---short-interval
follow-up suggested
35. lesions that do not have the
characteristic morphologies of
breast cancer but have a definite
probability of being malignant.
The radiologist has concern to urge a
biopsy.
Category 4
Suspicious abnormality--
----biopsy should be
considered
36. These lesions have a high
probability of being cancer
Category 5
Highly suggestive of
malignancy----appropriate
action should be taken
37. Finding for which additional
imaging evaluation is needed.
almost always used in a screening
situation and should rarely be used
after a full imaging workup.
Perez , 6th edition , pg-1058
Category 0
Need additional
imaging evaluation
39. Screening USG
In a randomised trial of USG and Mammography of
2809 women with dense breasts from ACRIN,
Adding a single screening USG yielded and additional
1.1 to 7.2 additional cancers found in high risk women
But a substantial increase in false positives
Role of USG as a screening tool is therefore limited
40. Diagnostic USG
But is a useful tool to complement physical
examination and mammography in diagnosis and
treatment of cancer.
Sensitivity of 73%
specificity of 95%
41. USG Breast is most useful in
differentiating cysts from
solid tumors
Identification and
characterisation of palpable
and non palpable
abnormalities of breast
detected by physical
examination or
mammography.
42. USG breast---
very accurate (>95%) in diagnosing breast cysts.
Cysts have well-demarcated, smooth margins and
an echo-free center ; usually rounded and thin-
walled and produce distal shadowing.
Clear cysts require no further evaluation.
Complex cysts that contain evidence of tissue or
debris may be aspirated to clarify whether they are
simply cysts or represent cystic degeneration of a
tumor.
43. USG as a guide
in core biopsies
FNA
Cyst aspirations
Presurgical localizations
44. NCCN recommends- USG breast for patients with
- a dominant mass
- assymetric thickening
- nodularity
46. Screening MRI
Role of MRI screening is rapidly evolving
But unlikely to replace mammography
47. Its use in screening high risk populations has recently
been supported in several studies.
Lehman et al ( MRI detected 4 contralateral breast
{MMG – none} cancers in 103 women with unilteral
breast cancer)
Kriege et al ( MRI is more sensitive than
mammography in detecting tumors in women at high
risk for familial breast cancer)
48. Diagnostic MRI
Routine use is controversial
Use to supplement mammography in breast cancer
diagnosis is rapidly increasing.
49. Upponi and Warren – MRI resulted in an increase in
confidence or change in clinical plan in 46% of
diagnostic group, 72 % of chemotherapy group, 80 %
of screening group.
In 44/283 of these MRI resulted in a beneficial change
in plan.
• Esserman etal – MRI detected cancer in 55/58 cases;
anatomic extent was correctly identified in 98%
,(MMG-55%)
50. In a woman with dense breasts, the mammogram was normal
but the MRI showed the cancer
51. NCCN recommends Breast MRI for women with
With early stage disease whose breasts cannot be
imaged adequately with mammography and
ultrasound
Who receive NACT in occult breast cancer to assess
response
With genetic mutations leading to a higher risk of
bilateral or contralateral breast cancer
52. Role of MRI in Occult Breast Cancer
MRI has a clear role in evaluation of patients with
axillary metastasis with no evidence of primary tumor
in breast by physical examination or mammography.
Buchanan et al – breast MRI detects mammographically occult cancer in half of women
with axillary metastasis and is a valuable tool for patients with occult primary breast
cancer.
53. Computed Tomography
No established role for CT scans in routine staging in
patients of early breast cancer
Its role in initial evaluation is minimal
Need of iodine contrast material to differentaiate benign
from malignant lesions
High radiation dose
Cost per study
Inability to detect small lesions
54. NCCN recommends an abdominopelvic CT if
Abnormal lab values
Positive findings on physical examination
For stage IIIA ( T3N1M0 ) or greater.
55. Bone Scan
Not routinely used for initial evaluation of early stage
breast cancer.
Koizumi et al reviewed records from 5538 patients of
breast cancer.
The overall incidence of metastasis to bone was 2.13%
In stage I– 0.08 %
In stage II- 10.9%
In stage III-9.96%
In stage IV- 34.04%
56. Therefore bone scans are more commonly
recommended in patients with
Stage II large tumors (>3cm)
Aggressive histopathological features
Stage III or Stage IV cancer
Perez 6th edition
57. PET scan
Not a routine component of staging
NCCN guidelines
Recommend against routine PET scans in stage 0 to IIIA
disease
May be useful in patients with locally advanced disease
or in situations where standard imaging results are
suspicious.
58. Schirrmeister et al ---
For interpreting results as being breast cancer , FDG
PET has sensitivity of 93%, specificity of 78%, accuracy
of 89%, PPV 92%, NPV- 96%
For detecting multifocal lesions , FDG-PET was twice
as sensitive (63%) as combination of mammography
and ultrasonography
High false-negative rate of 20% for detection of lymph
node metastases, this imaging method cannot replace
histologic evaluation of axillary nodes.
Frisell J, Lidbrink E. The Stockholm Mammographic Screening Trial: risks and benefits in age group 40-49 years. J Natl Cancer Inst Monogr 1997:49–51.