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3T MRI Whole-Brain Microscopy Discrimination of Subcortical Anatomy, Part 1: Brain Stem
Hoch, M J; Bruno, M T; Faustin, A; Cruz, N; Crandall, L; Wisniewski, T; Devinsky, O; Shepherd, T M
BACKGROUND AND PURPOSE/OBJECTIVE:The brain stem is compactly organized with life-sustaining sensorimotor and autonomic structures that can be affected by numerous pathologies but can be difficult to resolve on conventional MR imaging. MATERIALS AND METHODS/METHODS:We applied an optimized TSE T2 sequence to washed postmortem brain samples to reveal exquisite and reproducible brain stem anatomic MR imaging contrast comparable with histologic atlases. This resource-efficient approach can be performed across multiple whole-brain samples with relatively short acquisition times (2 hours per imaging plane) using clinical 3T MR imaging systems. RESULTS:< .10). CONCLUSIONS:Compared with traditional atlases, multiplanar MR imaging contrast has advantages for learning and retaining brain stem anatomy for clinicians and trainees. Direct TSE MR imaging sequence discrimination of brain stem anatomy can help validate other MR imaging contrasts, such as diffusion tractography, or serve as a structural template for extracting quantitative MR imaging data in future postmortem investigations.
PMID: 30705073
ISSN: 1936-959x
CID: 3626902
Automatic segmentation of the spinal cord and intramedullary multiple sclerosis lesions with convolutional neural networks
Gros, Charley; De Leener, Benjamin; Badji, Atef; Maranzano, Josefina; Eden, Dominique; Dupont, Sara M; Talbott, Jason; Zhuoquiong, Ren; Liu, Yaou; Granberg, Tobias; Ouellette, Russell; Tachibana, Yasuhiko; Hori, Masaaki; Kamiya, Kouhei; Chougar, Lydia; Stawiarz, Leszek; Hillert, Jan; Bannier, Elise; Kerbrat, Anne; Edan, Gilles; Labauge, Pierre; Callot, Virginie; Pelletier, Jean; Audoin, Bertrand; Rasoanandrianina, Henitsoa; Brisset, Jean-Christophe; Valsasina, Paola; Rocca, Maria A; Filippi, Massimo; Bakshi, Rohit; Tauhid, Shahamat; Prados, Ferran; Yiannakas, Marios; Kearney, Hugh; Ciccarelli, Olga; Smith, Seth; Treaba, Constantina Andrada; Mainero, Caterina; Lefeuvre, Jennifer; Reich, Daniel S; Nair, Govind; Auclair, Vincent; McLaren, Donald G; Martin, Allan R; Fehlings, Michael G; Vahdat, Shahabeddin; Khatibi, Ali; Doyon, Julien; Shepherd, Timothy; Charlson, Erik; Narayanan, Sridar; Cohen-Adad, Julien
The spinal cord is frequently affected by atrophy and/or lesions in multiple sclerosis (MS) patients. Segmentation of the spinal cord and lesions from MRI data provides measures of damage, which are key criteria for the diagnosis, prognosis, and longitudinal monitoring in MS. Automating this operation eliminates inter-rater variability and increases the efficiency of large-throughput analysis pipelines. Robust and reliable segmentation across multi-site spinal cord data is challenging because of the large variability related to acquisition parameters and image artifacts. In particular, a precise delineation of lesions is hindered by a broad heterogeneity of lesion contrast, size, location, and shape. The goal of this study was to develop a fully-automatic framework - robust to variability in both image parameters and clinical condition - for segmentation of the spinal cord and intramedullary MS lesions from conventional MRI data of MS and non-MS cases. Scans of 1042 subjects (459 healthy controls, 471 MS patients, and 112 with other spinal pathologies) were included in this multi-site study (n = 30). Data spanned three contrasts (T1-, T2-, and T2∗-weighted) for a total of 1943 vol and featured large heterogeneity in terms of resolution, orientation, coverage, and clinical conditions. The proposed cord and lesion automatic segmentation approach is based on a sequence of two Convolutional Neural Networks (CNNs). To deal with the very small proportion of spinal cord and/or lesion voxels compared to the rest of the volume, a first CNN with 2D dilated convolutions detects the spinal cord centerline, followed by a second CNN with 3D convolutions that segments the spinal cord and/or lesions. CNNs were trained independently with the Dice loss. When compared against manual segmentation, our CNN-based approach showed a median Dice of 95% vs. 88% for PropSeg (p ≤ 0.05), a state-of-the-art spinal cord segmentation method. Regarding lesion segmentation on MS data, our framework provided a Dice of 60%, a relative volume difference of -15%, and a lesion-wise detection sensitivity and precision of 83% and 77%, respectively. In this study, we introduce a robust method to segment the spinal cord and intramedullary MS lesions on a variety of MRI contrasts. The proposed framework is open-source and readily available in the Spinal Cord Toolbox.
PMID: 30300751
ISSN: 1095-9572
CID: 3334942
Accelerated Internal Auditory Canal Screening Magnetic Resonance Imaging Protocol With Compressed Sensing 3-Dimensional T2-Weighted Sequence
Yuhasz, Mikell; Hoch, Michael J; Hagiwara, Mari; Bruno, Mary T; Babb, James S; Raithel, Esther; Forman, Christoph; Anwar, Abbas; Thomas Roland, J; Shepherd, Timothy M
BACKGROUND AND PURPOSE/OBJECTIVE:High-resolution T2-weighted sequences are frequently used in magnetic resonance imaging (MRI) studies to assess the cerebellopontine angle and internal auditory canal (IAC) in sensorineural hearing loss patients but have low yield and lengthened examinations. Because image content in the Wavelet domain is sparse, compressed sensing (CS) that uses incoherent undersampling of k-space and iterative reconstruction can accelerate MRI acquisitions. We hypothesized that an accelerated CS T2 Sampling Perfection with Application optimized Contrasts using different flip angle Evolution (SPACE) sequence would produce acceptable diagnostic quality for IAC screening protocols. MATERIAL AND METHODS/METHODS:Seventy-six patients underwent 3 T MRI using conventional SPACE and a CS T2 SPACE prototype sequence for screening the IACs were identified retrospectively. Unilateral reconstructions for each sequence were separated, then placed into mixed folders for independent, blinded review by 3 neuroradiologists during 2 sessions 4 weeks apart. Radiologists reported if a lesion was present. Motion and visualization of specific structures were rated using ordinal scales. McNemar, Wilcoxon, Cohen κ, and Mann-Whitney U tests were performed for accuracy, equivalence, and interrater and intrarater reliability. RESULTS:T2 SPACE using CS reconstruction reduced scan time by 80% to 50 seconds and provided 98.7% accuracy for IAC mass detection by 3 raters. Radiologists preferred conventional images (0.7-1.0 reduction on 5-point scale, P < 0.001), but rated CS SPACE acceptable. The 95% confidence for reduction in any cerebellopontine angle, IAC, or fluid-filled inner ear structure assessment with CS SPACE did not exceed 0.5. CONCLUSIONS:Internal auditory canal screening MRI protocols can be performed using a 5-fold accelerated T2 SPACE sequence with compressed sensing while preserving diagnostic image quality and acceptable lesion detection rate.
PMID: 30020139
ISSN: 1536-0210
CID: 3200842
Approximating MRI-Based Anatomically Guided PET Reconstruction with a Convolutional Neural Network
Chapter by: Rigie, David; Schramm, Georg; Vahle, Thomas; Shepherd, Timothy; Nuyts, Johan; Boada, Fernando
in: 2018 IEEE Nuclear Science Symposium and Medical Imaging Conference, NSS/MIC 2018 - Proceedings by
[S.l.] : Institute of Electrical and Electronics Engineers Inc., 2018
pp. ?-?
ISBN: 9781538684948
CID: 4164182
White matter microstructure changes in migraine: a diffusional kurtosis imaging study [Meeting Abstract]
Ashina, Sait; Conti, Bettina; Ades-Aron, Benjamin; Lui, Yvonne; Minen, Mia; Novikov, Dmitry; Shepherd, Timothy; Fieremans, Els
ISI:000452730900061
ISSN: 1129-2369
CID: 3587672
Visual detection of regional brain hypometabolism in cognitively impaired patients is independent of positron emission tomography-magnetic resonance attenuation correction method
Franceschi, Ana M; Abballe, Valentino; Raad, Roy A; Nelson, Aaron; Jackson, Kimberly; Babb, James; Vahle, Thomas; Fenchel, Matthias; Zhan, Yiqiang; Valadez, Gerardo Hermosillo; Shepherd, Timothy M; Friedman, Kent P
Fluorodeoxyglucose (FDG) positron emission tomography-magnetic resonance (PET/MR) is useful for the evaluation of cognitively-impaired patients. This study aims to assess two different attenuation correction (AC) methods (Dixon-MR and atlas-based) versus index-standard computed tomography (CT) AC for the visual interpretation of regional hypometabolism in patients with cognitive impairment. Two board-certified nuclear medicine physicians blindly scored brain region FDG hypometabolism as normal versus hypometabolic using two-dimensional (2D) and 3D FDG PET/MR images generated by MIM software. Regions were quantitatively assessed as normal versus mildly, moderately, or severely hypometabolic. Hypometabolism scores obtained using the different methods of AC were compared, and interreader, as well as intra-reader agreement, was assessed. Regional hypometabolism versus normal metabolism was correctly classified in 16 patients on atlas-based and Dixon-based AC map PET reconstructions (vs. CT reference AC) for 94% (90%-96% confidence interval [CI]) and 93% (89%-96% CI) of scored regions, respectively. The averaged sensitivity/specificity for detection of any regional hypometabolism was 95%/94% (P = 0.669) and 90%/91% (P = 0.937) for atlas-based and Dixon-based AC maps. Interreader agreement for detection of regional hypometabolism was high, with similar outcome assessments when using atlas- and Dixon-corrected PET data in 93% (Κ =0.82) and 93% (Κ =0.84) of regions, respectively. Intrareader agreement for detection of regional hypometabolism was high, with concordant outcome assessments when using atlas- and Dixon-corrected data in 93%/92% (Κ =0.79) and 92/93% (Κ =0.78). Despite the quantitative advantages of atlas-based AC in brain PET/MR, routine clinical Dixon AC yields comparable visual ratings of regional hypometabolism in the evaluation of cognitively impaired patients undergoing brain PET/MR and is similar in performance to CT-based AC. Therefore, Dixon AC is acceptable for the routine clinical evaluation of dementia syndromes.
PMCID:6034547
PMID: 30034284
ISSN: 1450-1147
CID: 3215992
A Rare Case of Composite Dural Extranodal Marginal Zone Lymphoma and Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Bustoros, Mark; Liechty, Benjamin; Zagzag, David; Liu, Cynthia; Shepherd, Timothy; Gruber, Deborah; Raphael, Bruce; Placantonakis, Dimitris G
Background/UNASSIGNED:Primary extranodal marginal zone lymphoma (MZL) of the dura is a rare neoplastic entity in the central nervous system (CNS). Methods/UNASSIGNED:We used literature searches to identify previously reported cases of primary dural MZL. We also reviewed clinical, pathologic, and radiographic data of an adult patient with concurrent dural MZL and chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). Results/UNASSIGNED:We identified 104 cases of dural MZL in the literature. None of them presented concurrently with another type of non-Hodgkin lymphoma. This is the first report of composite lymphoma consisting of dural MZL and CLL/SLL in the bone marrow and lymph nodes. Conclusion/UNASSIGNED:Primary dural MZL is a rare, indolent low-grade CNS lymphoma, with a relatively good prognosis. Its treatment is multidisciplinary and often requires surgical intervention due to brain compression, along with low to moderate doses of radiotherapy and/or systemic chemotherapy.
PMCID:5928293
PMID: 29740389
ISSN: 1664-2295
CID: 3085002
Alzheimer's Disease
Chapter by: Franceschi, Ana M; Hoch, Michael J; Shepherd, Timothy M
in: PET/MR Imaging : A Case-Based Approach by Gupta, Rajesh; et al [Ed]
[S.l.] : Springer, 2018
pp. 275-276
ISBN: 978-3-319-65106-4
CID: 5345742
Oligodendroglioma
Chapter by: Hoch, Michael J; Franceschi, Ana M; Shepherd, Timothy M
in: PET/MR Imaging : A Case-Based Approach by Gupta, Rajesh; et al [Ed]
[S.l.] : Springer, 2018
pp. 281-283
ISBN: 978-3-319-65106-4
CID: 5345752
Mesial Temporal Lobe Sclerosis
Chapter by: Franceschi, Ana M; Hoch, Michael J; Shepherd, Timothy M
in: PET/MR Imaging : A Case-Based Approach by Gupta, Rajesh; et al [Ed]
[S.l.] : Springer, 2018
pp. 295-297
ISBN: 978-3-319-65106-4
CID: 5345772