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1.
Curr Oncol ; 24(3): e205-e213, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28680288

ABSTRACT

BACKGROUND: Indications for breast magnetic resonance imaging (mri), a very sensitive but less-specific tool for breast investigation, remain controversial, and accessibility is limited. The purposes of our study were to determine the proportion of breast mri exams performed for various clinical indications, to assess the wait times for breast mri, and to create a list of evidence-based indications for breast mri. METHODS: The indications for breast mri exams performed in September 2013 at our academic centre were audited. A multidisciplinary meeting held in May 2014 established a list of evidence-based indications for breast mri, after which, in September 2014 and 2015, breast mri exams were re-audited for clinical indications, and pending requests were calculated. RESULTS: In September 2013, surveillance of women with a prior diagnosis of breast cancer represented 21% of breast mri exams (24 of 113), with preoperative staging representing 18% of exams (20 of 113) and high-risk screening representing 12% (13 of 113). Of pending mri requests, 230 were within the recommended delay period, and 457 exceeded the recommended delay. After elaboration of evidence-based guidelines, repeat audits in September 2014 and September 2015 showed that mri performed for women with a prior breast cancer diagnosis represented 23% (33 of 141) and 7% (10 of 143) of exams respectively, with preoperative staging having declined to 9% (13 of 141) and 11% (16 of 143) of exams, and high-risk screening having increased to 36% (51 of 141) and 46% (66 of 143) of exams. Overall, wait times were improved for all breast mri indications. CONCLUSIONS: Through multidisciplinary discussion, we actualized a list of breast mri indications, prioritized requests more adequately, and improved wait times.

2.
Curr Oncol ; 23(6): e615-e625, 2016 Dec.
Article in English | MEDLINE | ID: mdl-28050152

ABSTRACT

In recent years, risk stratification has sparked interest as an innovative approach to disease screening and prevention. The approach effectively personalizes individual risk, opening the way to screening and prevention interventions that are adapted to subpopulations. The international perspective project, which is developing risk stratification for breast cancer, aims to support the integration of its screening approach into clinical practice through comprehensive tool-building. Policies and guidelines for risk stratification-unlike those for population screening programs, which are currently well regulated-are still under development. Indeed, the development of guidelines for risk stratification reflects the translational aspects of perspective. Here, we describe the risk stratification process that was devised in the context of perspective, and we then explain the consensus-based method used to develop recommendations for breast cancer screening and prevention in a risk-stratification approach. Lastly, we discuss how the recommendations might affect current screening policies.

3.
Eur J Radiol ; 82(12): e790-800, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24055186

ABSTRACT

OBJECTIVE: To compare the accuracy of different MR sequences to measure tumor size. METHODS: Eighty-six women (mean age: 53 years (30-78)) who underwent preoperative MRI for breast cancer were included. Maximal diameters of the index tumor (IT) and of the whole extent of the tumor (WET) were measured on T2-weighted (T2W) sequences, on dynamic contrast-enhanced (DCE) T1-weighted (T1W) sequences and on Maximal Intensity Projection (MIP) reconstructions. Agreements with pathological size were evaluated using concordance correlation coefficient (k). RESULTS: Median pathological size of IT was 20mm (13-25 mm, interquartile range). Median pathological size of the WET was 29 mm (16-50mm, interquartile range). Measurement of IT showed a good concordance with pathological size, with best results using T2W (k = 0.690) compared to MIP (k = 0.667), early-subtracted DCE frame (k = 0.630) and early-native DCE frame (k = 0.588). IT was visible on T2W in 83.7% and accurately measured within 5mm in 69.9%. Measurement of WET was superior using early-subtracted DCE frame (k = 0.642) compared to late-native frame (k = 0.635), early-native frame (k = 0.631), late-subtracted frame (k = 0.620) and MIP (k = 0.565). However, even using early-subtracted frame, WET was accurately measured within 5mm only 39.3%. CONCLUSION: If visible, IT size is best measured on T2W with a good accuracy (69%) whereas WET is best estimated on early-subtracted DCE frame. However, when adjacent additional sites exist around IT, suspected surrounding disease components need to be proved by pathological analysis.


Subject(s)
Algorithms , Breast Neoplasms/pathology , Image Interpretation, Computer-Assisted/methods , Imaging, Three-Dimensional/methods , Magnetic Resonance Imaging/methods , Subtraction Technique , Tumor Burden , Adult , Aged , Female , Humans , Image Enhancement/methods , Middle Aged , Reproducibility of Results , Sensitivity and Specificity
4.
Clin Radiol ; 68(7): e378-83, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23522486

ABSTRACT

AIM: To investigate current practice regarding clip placement after breast biopsy. MATERIALS AND METHODS: In June 2011, an online survey instrument was designed using an Internet-based survey site (www.surveymonkey.com) to assess practices and opinions of breast radiologists regarding clip placement after breast biopsy. Radiologists were asked to give personal practice data, describe their current practice regarding clip deployment under stereotactic, ultrasonographic, and magnetic resonance imaging (MRI) guidance, and describe what steps are taken to ensure quality control with regards to clip deployment. RESULTS: The response rate was 29.9% in France (131 respondents) and 46.7% in Quebec (50 respondents). The great majority of respondents used breast markers in their practice (92.1% in France and 96% in Quebec). In both countries, most reported deploying a clip after percutaneous biopsy under stereotactic or MRI guidance. Regarding clip deployment under ultrasonography, 38% of Quebec radiologists systematically placed a marker after each biopsy, whereas 30% of French radiologists never placed a marker in this situation, mainly due to its cost. Finally, 56.4% of radiologists in France and 54% in Quebec considered that their practice regarding clip deployment after breast percutaneous biopsy had changed in the last 5 years. CONCLUSION: There continues to be variations in the use of biopsy clips after imaging-guided biopsies, particularly with regards to sonographic techniques. These variations are likely to decrease over time, with the standardization of relatively new investigation protocols.


Subject(s)
Breast Neoplasms/pathology , Breast/pathology , Fiducial Markers , Professional Practice , Radiology , Adult , Aged , Attitude of Health Personnel , Biopsy, Needle/instrumentation , Biopsy, Needle/methods , Female , France , Humans , Image-Guided Biopsy/instrumentation , Image-Guided Biopsy/methods , Magnetic Resonance Imaging, Interventional , Middle Aged , Quebec , Stereotaxic Techniques , Surgical Instruments , Ultrasonography, Interventional
5.
Eur J Radiol ; 82(3): 435-43, 2013 Mar.
Article in English | MEDLINE | ID: mdl-22658868

ABSTRACT

The aim of this paper is to review all clinical applications of diffusion weighted MR imaging (DWI) for breast pathology. The challenge of DWI is to obtain the best compromise between lesion detection and characterization. Technical factors affecting lesion characterization and detection are detailed including the effect of contrast administration, the choice of number of b and of b(max), the variation of diagnostic performance according to the type and the size of lesion studied.


Subject(s)
Breast Neoplasms/pathology , Diffusion Magnetic Resonance Imaging/methods , Image Interpretation, Computer-Assisted/methods , Female , Humans , Image Enhancement/methods , Reproducibility of Results , Sensitivity and Specificity
6.
Diagn Interv Imaging ; 93(11): 828-39, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23084072

ABSTRACT

The standard breast MRI protocol includes T2 sequences (anatomy and signal analysis), T1 gradient-echo sequences which can detect markers placed after biopsy, and injected dynamic 3D sequences for performing volume and multiplanar reconstructions, which are particularly useful for locating lesions well. Good patient positioning is essential and is obtained by using foam wedges for small breasts, ensuring there are no folds, and the correct position of the nipples. These aspects limit movement artefacts which alter subtraction sequences, so that it must always be possible for reading these sequences to be assisted by comparing them with the native sequences. New functional imaging sequences are now appearing in an attempt to increase the specificity of MRI, which is one of its main limitations. Of these, magnetic resonance spectroscopy appears to be the most promising, highlighting an abnormal choline peak in malignant lesions. This molecular signature provides early information (24 hours after beginning neoadjuvant treatment) on the chemosensitivity of a breast tumour.


Subject(s)
Breast Neoplasms/diagnosis , Diffusion Magnetic Resonance Imaging/methods , Image Interpretation, Computer-Assisted , Imaging, Three-Dimensional/methods , Magnetic Resonance Imaging/methods , Mammography/methods , Artifacts , Breast/pathology , Breast Neoplasms/drug therapy , Breast Neoplasms/pathology , Breast Neoplasms/surgery , Combined Modality Therapy , Female , Humans , Magnetic Resonance Spectroscopy/methods , Neoadjuvant Therapy , Patient Positioning , Prognosis , Sensitivity and Specificity
8.
Curr Oncol ; 17(3): 28-36, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20567624

ABSTRACT

BACKGROUND: Women with a predisposition for breast cancer require a tailored screening program for early cancer detection. We evaluated the performance of mammography (MG), ultrasonography (US), and magnetic resonance imaging (MRI) screening in these women. PATIENTS AND METHODS: In asymptomatic women either confirmed as BRCA1/2 carriers, or having a greater than 30% probability of being so as estimated by brcapro [Berry D, Parmigiani G. Duke SPORE (Specialized Program of Research Excellence) in Breast Cancer. 1999], we conducted a prospective comparative trial consisting of annual MRI and MG, and biannual US and clinical breast examination. All evaluations were done within 30 days of one another. For each screening round, imaging tests were independently interpreted by three radiologists. RESULTS: The study enrolled 184 women, and 387 screening rounds were performed, detecting 12 cancers (9 infiltrating, 3 in situ), for an overall cancer yield of 6.5%. At diagnosis, 7 infiltrating cancers were smaller than 2 cm (T1); only 1 woman presented with axillary nodal metastases. All tumours were negative for the human epidermal growth factor receptor 2. Of the 12 cancers, MRI detected 10, and MG, 7; US did not identify any additional cancers. The overall recall rate after MRI was 21.8%, as compared with 11.4% for US and 16.1% for MG. Recall rates declined with successive screening rounds. In total, 45 biopsies were performed: 21 as a result of an US abnormality; 17, because of an MRI lesion; and 7, because of a MG anomaly. INTERPRETATION: In high-risk women, MRI offers the best sensitivity for breast cancer screening. The combination of yearly MRI and MG reached a negative predictive value of 100%. The recall rate is greatest with MRI, but declines for all modalities with successive screening rounds.

11.
Top Magn Reson Imaging ; 12(1): 3-17, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11215714

ABSTRACT

The development of ultrafast sequences has revolutionized fetal magnetic imaging (MRI). Fetal anatomy can be characterize precisely by MRI. This is particularly true for evaluation of the central nervous system, for which magnetic resonance (MR) evaluation is superior to ultrasound evaluation. MR allows analysis of development of the cerebrum as well as posterior fossa structures. Awareness of the normal sequence of maturation as well as the approximate timing of development of key structures is useful for evaluating the developing fetus. MRI also permits evaluation of the oropharynx, lungs, diaphragm, and intra-abdominal and retroperitoneal structures. Occasionally, beautiful depiction of smaller structures, including extremities and details of the face and neck may be obtained, but this is dependent on the orientation of the fetus and the plane of imaging as well as the section thickness. MRI is useful in assignment of fetal gender as well as in evaluation of the chorionicity of twin gestations. This report illustrates the normal appearance of the developing fetus as seen on fast sequences during the second and third trimesters.


Subject(s)
Fetus/anatomy & histology , Magnetic Resonance Imaging/methods , Embryonic and Fetal Development/physiology , Female , Humans , Pregnancy , Prenatal Diagnosis/methods , Reference Values , Sensitivity and Specificity
12.
Radiology ; 212(3): 841-5, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10478255

ABSTRACT

PURPOSE: To describe the diagnostic features, appearance, and vascularization pattern of venous malformations (VMs) at Doppler ultrasonography (US). MATERIALS AND METHODS: Between February 1991 and May 1997, 51 soft-tissue VMs were studied with Doppler US in patients between 1 day and 21 years of age (mean age, 9 years). These VMs were located in the maxillofacial region (n = 19), trunk (n = 5), and upper (n = 10) and lower (n = 17) extremities. Twenty-three VMs had venographic confirmation, seven had only histologic confirmation, and 21 had both venographic and histologic confirmation. US was performed with 7.5- or 7-10-MHz linear transducers, a low pulse repetition frequency (mean, 1,680 Hz), and the lowest wall filter (25-50 Hz). RESULTS: At gray-scale US, VMs appeared as hypoechoic, heterogeneous lesions in 82% of cases. All lesions displayed compressibility. In eight lesions (16%), phleboliths were identified, thus confirming the diagnosis of VM. Analysis of vascular flow revealed monophasic, low-velocity flow in 40 VMs (78%), with an average flow velocity of 0.22 kHz. Biphasic flow was noted at the periphery of three lesions, which is indicative of a mixed capillary-venous malformation. The remaining eight lesions did not display any flow. CONCLUSION: In pediatric patients, Doppler US is a noninvasive, easily available, and rapid mode of investigation of vascular lesions and can help confirm the diagnosis of VM when it shows a characteristic flow pattern.


Subject(s)
Arteriovenous Malformations/diagnostic imaging , Ultrasonography, Doppler , Adolescent , Adult , Blood Flow Velocity/physiology , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Veins/abnormalities , Veins/diagnostic imaging
14.
AJNR Am J Neuroradiol ; 19(6): 1025-33, 1998.
Article in English | MEDLINE | ID: mdl-9672006

ABSTRACT

PURPOSE: Although MR findings in multiple sclerosis (MS) are well known, the relationship between MR-detected lesions and clinical activity has not been studied in the spinal cord. The purpose of this study was to determine whether serial MR imaging provides evidence of disease activity unsuspected on clinical examination and to determine whether it is useful in monitoring patients with MS primarily affecting the spinal cord. METHODS: Twenty-five consecutive patients with MS and with signs and symptoms of myelopathy underwent a full neurologic examination and contrast-enhanced MR imaging of the spinal cord at intervals of 0, 2, 6, and 12 months. Disability was rated according to Kurtzke's functional systems and the expanded disability status scale (EDSS). Clinical status of myelopathy (improved, deteriorated, or stable) was also assessed. Hyperintense lesions were counted on T2-weighted images and a weighted lesion load was calculated for each patient. The number of enhancing lesions was also determined. RESULTS: We found a moderate correlation between lesion load and sensory function and EDSS. Seventy percent of patients with new clinical manifestations of myelopathy had one or more enhancing lesions. Agreement between MR findings and clinical examination in evincing disease activity was found in 60% of follow-up examinations. MR images showed lesion progression in seven (44%) of 16 occurrences of clinical deterioration and in 21 (35%) of 60 occurrences of clinical improvement or stability. CONCLUSION: Serial MR imaging provides evidence of disease activity unsuspected on clinical examination and could be useful in monitoring patients with MS primarily affecting the spinal cord.


Subject(s)
Image Enhancement , Magnetic Resonance Imaging , Multiple Sclerosis/diagnosis , Spinal Cord Diseases/diagnosis , Adult , Brain/pathology , Female , Follow-Up Studies , Humans , Male , Middle Aged , Neurologic Examination , Sensitivity and Specificity , Spinal Cord/pathology
15.
AJNR Am J Neuroradiol ; 19(3): 583-6, 1998 Mar.
Article in English | MEDLINE | ID: mdl-9541323

ABSTRACT

We report a case of craniocervical dural arteriovenous fistula with perimedullary venous drainage associated with cervical myelopathy in which spinal angiography showed a normal venous phase after injection of the artery of Adamkiewicz. We conclude that because of the complex venous drainage of the spinal cord, a dural arteriovenous fistula with spinal drainage cannot be ruled out solely because a normal venous phase is seen in the lower part of the cord, as has previously been suggested.


Subject(s)
Arteriovenous Malformations/complications , Arteriovenous Malformations/diagnosis , Dura Mater/blood supply , Spinal Cord Diseases/etiology , Spinal Cord/blood supply , Aged , Humans , Lumbosacral Region , Magnetic Resonance Imaging , Male , Neck , Phlebography , Reference Values , Regional Blood Flow/physiology , Spinal Cord Diseases/diagnosis , Spinal Cord Diseases/physiopathology , Thorax , Veins/physiopathology
16.
Med Parazitol (Mosk) ; (1): 48-51, 1996.
Article in Russian | MEDLINE | ID: mdl-8700015

ABSTRACT

Among zoonotic infections with natural foci in the Republic of Sakha (Yakutia), leptospiroses have assumed greater importance. Their morbidity is sporadic, mainly afflicting rural adults. The serogroups pomona, grippotyphosa, and icterohaemorrhagiae are prevalent in the etiological structure of leptospiras. An epizootiological survey has revealed natural and anthropurgic leptospirosis foci which present a hazard primarily to rural inhabitants who deal with animal husbandry, fur-bearer breeding, hunting, and fishing. The vole (Microtis) and root vole (Microtis oeconomus) serve as the major reservoir and source of leptospiroses in the natural foci, while cattle and caged Arctic foxes do in the anthropurgic ones. High sizes of house and grey mice which are carriers of the Leptospira javanica and icterohaemorrhagiae, have been recorded in the residential and domestic constructions of localities. A complex of antileprospirotic measures that limits the influence of the leading factors of infection transmission and the risk of human infection is substantiated.


Subject(s)
Leptospirosis/epidemiology , Leptospirosis/veterinary , Adult , Animals , Animals, Domestic , Animals, Wild , Disease Reservoirs/statistics & numerical data , Disease Reservoirs/veterinary , Female , Humans , Male , Middle Aged , Retrospective Studies , Siberia/epidemiology
17.
J Otolaryngol ; 24(2): 102-4, 1995 Apr.
Article in English | MEDLINE | ID: mdl-7602669

ABSTRACT

Usher syndrome is a heterogeneous group of disorders of autosomal recessive inheritance characterized by retinitis pigmentosa and congenital sensorineural hearing loss. Two types are accepted clinically: type I is associated with profound congenital deafness with progressive pigmentary retinopathy and total loss of vestibular function. Type II is a milder form, with moderate-to-profound hearing loss and a milder form of retinitis pigmentosa. Vestibular function is preserved. A total of five loci have been identified as accounting for the two distinct phenotypic presentations. We describe a consanguineous family of Pakistani origin whose four children all are affected with Usher syndrome type I. DNA analysis showed non-linkage to any of the loci already identified as tightly linked to the Usher syndrome type I.


Subject(s)
Consanguinity , Hearing Loss, Sensorineural/complications , Retinitis Pigmentosa/complications , Canada/ethnology , Child , Chromosome Aberrations , Chromosome Disorders , Female , Hearing Loss, Sensorineural/congenital , Hearing Loss, Sensorineural/genetics , Humans , Male , Pakistan , Parents , Retinitis Pigmentosa/genetics , Syndrome
19.
Hum Mutat ; 1(1): 35-9, 1992.
Article in English | MEDLINE | ID: mdl-1301189

ABSTRACT

The mutation causing juvenile Tay-Sachs disease (TSD) in two sibs of Lebanese-Maronite origin is described. An mRNA-containing extract of cultured fibroblasts obtained from one of the probands was used as a template to amplify the coding sequence of the hexosaminidase A (Hex A) alpha-subunit. Sequencing of amplified cDNA fragments revealed a single alteration, guanine to adenine at nt 749 creating a G250D mutation. The mutation introduces a new recognition site for the restriction enzyme Eco RV, permitting identification of heterozygotes for this allele following PCR amplification and Eco RV digestion of exon 7 sequences from genomic DNA templates. In order to test the effect of this substitution, an in vitro mutagenized cDNA construct was introduced into a mammalian expression vector and transfected into monkey Cos-1 cells separately or along with a beta-cDNA expression vector. When the mutant alpha-cDNA was the only gene introduced into COS cells no enzymatic activity above endogenous COS cell activity was detected. Cotransfection of normal alpha-cDNA and beta-cDNA followed by immunoprecipitation of human Hex A resulted in 20-fold increase in the ratio between positive and negative (mock transfection) control values. This allowed the detection of some residual activity (12% of the positive control) when the mutant alpha-cDNA replaced its wild-type counterpart. The predicted protein environment in which the mutation occurs is compared to that of the adult-onset Tay-Sachs disease mutation caused by a Gly269-->Ser substitution in exon 7.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Aspartic Acid , Glycine , Mutation , Tay-Sachs Disease/genetics , beta-N-Acetylhexosaminidases/genetics , Amino Acid Sequence , Animals , Base Sequence , Canada , Cell Line , Chlorocebus aethiops , Consanguinity , Female , Hexosaminidase A , Humans , Kidney , Lebanon/ethnology , Macromolecular Substances , Male , Molecular Sequence Data , Mutagenesis, Site-Directed , Oligodeoxyribonucleotides , Pedigree , Polymerase Chain Reaction/methods , Protein Structure, Secondary , Recombinant Proteins/chemistry , Recombinant Proteins/metabolism , Tay-Sachs Disease/enzymology , Transfection , beta-N-Acetylhexosaminidases/chemistry , beta-N-Acetylhexosaminidases/metabolism
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