Mistakes We All Make: Breast Imaging - CAR Lifelong Learning/Meetings/ASM201… · Mistakes We All...
Transcript of Mistakes We All Make: Breast Imaging - CAR Lifelong Learning/Meetings/ASM201… · Mistakes We All...
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Mistakes We All Make:Breast Imaging
Dr. Kalesha HackSunnybrook Health Sciences CentreDivision of Women’s Imaging
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Mistakes We All Make:Breast Imaging
Dr. Kalesha HackSunnybrook Health Sciences CentreDivision of Women’s Imaging
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DISCLOSURE
• I have no financial conflicts of interest to disclose
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OBJECTIVES
• Identify common pitfalls in multi-modality breast imaging screening
• Identify common pitfalls in multi-modality breast imaging work-up
• Apply methods as a medical expert to avoid these common pitfalls
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BACKGROUND
v “The important question isn’t how to keep bad physicians from harming patients; it’s how to keep good physicians from harming patients… The deeper problem with medical malpractice is that by demonizing errors they prevent doctors from acknowledging & discussing them publicly.”
v “Not only do all human beings err, but they err frequently and in predictable, patterned ways”
Dr. Atul Gawande, author of Complications, Better and Being Mortal
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CASE 1RCC2013
RMLO 2013
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CASE 1RCC2012
RMLO2012
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CASE 1RCC2011
RMLO2011
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CASE 12013 2012 2011
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CASE 1
• “Right breast requires additional imaging for an enlarging circumscribed mass in the right upper outer quadrant. It is favored to be benign but further evaluation with additional views and targeted ultrasound is recommended.”
• BIRADS 0
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CASE 1
DX: INVASIVE DUCTAL CARCINOMA
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DISCUSSION FROM CASE 1
• What were potential pitfalls?
• Slow interval growth is hard to recognize
• Slow interval growth not as worrisome as rapid interval growth
• Potential to assume UOQ masses are intramammary nodes
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DISCUSSION FROM CASE 1
• What can we do to help?
• Compare to remote priors (ie. 2 years or more)
• “Oldest mammogram in the bag”
• Remember not all UOQ masses are lymph nodes
• Consider using hanging protocol where multiple priors displayed side-by-side
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CASE 2OBSP Screening MRI May 2012
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CASE 2
• Asymmetric right retroareolar enhancement . This would not be amenable to MRI guided biopsy given the position. Suggest right subareolar magnification views and ultrasound for further evaluation.
• If no suspicious features on magnification views/ultrasound, suggest clinical correlation and 6 month followup MRI could be performed.
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CASE 2
Cluster of indeterminatecalcs in retroareolar region. Recommend stereo bx.
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CASE 2
• Pathology result:
• Proliferative FCC with usual hyperplasia
• Microcalcifications seen
• CONCORDANT
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CASE 2MRI February 2013
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CASE 2MRI July 2013
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CASE 2MRI July 2014
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CASE 2MRI February 2015
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CASE 2
• Right subareolar enhancement surrounding the postbiopsy clip is increased in prominence compared to remote previous.
• Suggest right mammogram, magnification views of the subareolar region and second look ultrasound.
• If no suspicious findings, suggest 6 month followup MRI.
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CASE 2
DX: INVASIVE DUCTAL CARCINOMA
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CASE 2MRI February 2015MRI May 2012
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DISCUSSION FROM CASE 2
• What were the potential pitalls?
• Difficult area to perform MRI biopsy on initial study
• Potential for discordance when MR findings biopised under different modality
• False reassurance because of biopsy clip location
• Failure to recognize or act on slow interval growth
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DISCUSSION FROM CASE 2
• What can we do to help?
• Remember interval growth is a predictor of malignancy
• Do not be afraid to rebiopsy lesions that are growing, changing or that look suspicious
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CASE 3Left MLO2015 Left CC
2015
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CASE 3• Focal
asymmetry posterior central on the CC view, probably parenchyma
• Added views +/- US
Screening January 2013 Screening January 2015
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CASE 3CC spot CC spot
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CASE 3
• “Persistent left posterior asymmetry on the CC view which may have been present in 2013 and only partially imaged at that time due to far posterior location. No suspicious ultrasound findings. This is felt to likely represent parenchymal tissue and a 6 month follow up left breast mammogram can be performed to ensure stability.”
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CASE 3Aug 2015
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CASE 3Jan 2015 Aug 2015
Again seen only on the CC view, is an asymmetry in the posterior 3rd of the left breast. This appears denser than on the previous imaging. This was not seen on the previous ultrasound. Impression:
Asymmetry left breast for which additional mammographic views again suggested.
Biopsy may be required under stereotactic guidance but the need for biopsy will bedetermined after the additional views.
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CASE 3
DX: INVASIVE DUCTAL CARCINOMA WITH LOBULAR GROWTH PATTERN
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DISCUSSION FROM CASE 3
• What were the potential pitfalls?
• Initial mammogram report may have biased reader
• Allowing ultrasound to ‘trump’ mammogram
• False reassurance because only seen well on 1 view
• Recommending 6 month follow up instead of stereotactic biopsy
• Not correlating initial ultrasound finding to mammogram
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DISCUSSION FROM CASE 3
• What can we do to help?
• Try not to ‘over characterize’ lesions on screening
• Consider all modalities together when forming opinion
• Remember stereotactic biopsy for masses not seen on US
• Ensure sonographic findings ‘fit’ with the mammogram
• Low threshold to check diagnostic ultrasounds
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CASE 4Preoperative evaluation known left breast cancer September 2012
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CASE 4
“Solitary nonspecific lesion in right breast lower outer quadrant with time intensity curves similar to the cancer lesion seen on the left side but overall less maximum relative enhancement. We could attempt to localize the right breast nodule sonographically with a plan to biopsy it if we can identify it.”
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CASE 4
• Second look ultrasound October 2012:
• “Enhancing nodule seen on the prior MRI scan was not identified on this examination. This could represent an incidental fibroadenoma. A MR guided biopsy could be attempted.”
• Right breast ultrasound December 2012:
• “Targeted right breast ultrasound lower outer quadrant was performed. There is a 4 mm cyst at 6:00. No other abnormality is seen.”
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CASE 4MRI Feb 2013
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CASE 4MRI Feb 2013MRI Sept 2012
Patient started chemotherapy October 2012
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CASE 4
• MRI March 2014:
• Interval growth of solitary nodule right lower outer quadrant with interval development of increased signal intensity on theT2-weighted imaging. These are both worrisome findings, particularly given that the patient has had chemotherapy during this time interval which one would expect to impact any neoplastic lesion.
• Second-look right breast ultrasound April 2014:
• No correlate for MRI lesion
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CASE 4
DX: DCIS with no invasion
MRI May 2014 Ultrasound May 2014
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CASE 4Pre-operative MRISept 2012
MRI during chemotherapyFeb 2013
MRI post chemotherapyApril 2014
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DISCUSSION FROM CASE 4
• What were the potential pitfalls?
• Not recommending MRI biopsy more strongly on pre-operative report
• Not recommending MR biopsy when no US correlate seen
• Not recognizing disappearance of lesion as potentially worrisome finding
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DISCUSSION FROM CASE 4
• What can we do to help?
• Ensure each breast MRI centre has biopsy capability
• Better coordination between sites when MR biopsy is not available
• Remember malignant lesions may become less apparent or disappear on treatment
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CASE 5
Which one is the cancer? Red or yellow?
Screening MRI May 2013
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CASE 5Screening MRI May 2013
Screening MRI May 2014
Screening MRI May 2014
Now which one is the cancer?
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CASE 5
DX: INVASIVE DUCT CA
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DISCUSSION FROM CASE 5
• What were the potential pitfalls?
• Not finding the cancer on the first study
• Underestimating small focus with washout
• What can we do to help?
• Biopsy both lesions on initial study
• Biopsy all foci that washout
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DISCUSSION FROM CASE 5
• Screening MRI is a screening study
• Goal is to identify findings suspicious for malignancy
• Balance between detection and over intervention
• Interval growth is a predictor of malignancy
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CASE 6
Right Magnification ViewsAugust 2014
Right Magnification ViewsAugust 2014
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CASE 6
“The right central breast shows predominantly linear calcifications that show branching and extend over a distance of approximately 4 cm.”
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CASE 6Stereotactic guided core needle biopsy 8/22/14
Pathology: Benign breast tissue. Rare calcifications are identified. See full pathology report.
Result is concordant. Recommend 6 month follow up right breast mammogram with magnification views of the biopsy site.
Right Breast Specimen RadiographAugust 2014
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CASE 6
6 month follow up post biopsy:
Right breast central biopsied calcifications have a slightly different configuration, likely due to interval biopsy, but do not appear increased compared to previous.
Follow-up bilateral mammogram in 6 months with right magnification views recommended.
Right magnification viewsFeb 2015
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CASE 6Right magnification viewsAug 2015
Right magnification viewsAug 2014
Increasing suspicious right breast calcifications at the previously biopsied site. A repeat biopsy is recommended, with vacuum assistance.
DX: Ductal Carcinoma in Situ
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DISCUSSION FROM CASE 6
• What were the potential pitfalls?
• Undersampling
• Calling suspicious calcifications concordant with benign result
• Few calcifications on specimen but not rebiopsied
• Not recommending re-biopsy on first follow up
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DISCUSSION FROM CASE 6
• What can we do to help?
• Careful re-evaluation of images and level of suspicion for concordance
• Do not be afraid to re-biopsy if there is interval change
• Consider vacuum biopsy when diagnosis is unclear/discordant or calcifications may be challenging to target
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CASE 7Right mammogramJuly 2015
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CASE 7Last Friday April 15
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CASE 7
DX: INVASIVE DUCTAL CARCINOMA
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DISCUSSION FROM CASE 7
• What were the potential pitfalls?
• Edge of the film abnormality
• Unable to position breast properly because of tethering from cancer
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DISCUSSION FROM CASE 7
• What can we do to help?
• Routinely assess positioning of breast
• Tech sheet where it should be noted if positioning was challenging
• Routine search pattern (including blocking, magnification) to ensure each area of film is examined
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SUMMARY OF KEY POINTS
• Interval growth is an important predictor of malignancy
• All breast imaging modalities should be integrated when formulating opinion
• When there is interval change in a lesion, re-biopsy may be required
• Role of screening is to detect findings suspicious for cancer not necessarily to detect every cancer at earliest stage
• Remember to check technique and edge of films
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IN CONCLUSION
“No matter what measures are taken, doctors will sometimes falter, and it isn’t reasonable to ask that we achieve perfection. What is reasonable is to ask that we never cease to aim for it.”
wDr. Atul Gawande