Automated Classification of Intramedullary Spinal Cord Tumors and Inflammatory Demyelinating Lesions Using Deep Learning
model2026-01-24https://doi.org/10.1148/atlas.1769273116529
30

Overview

Schema Version

https://atlas.rsna.org/schemas/2025-11/model.json

Name

Automated Classification of Intramedullary Spinal Cord Tumors and Inflammatory Demyelinating Lesions Using Deep Learning

Link

https://dx.doi.org/10.1148/ryai.210292

Indexing

Keywords: Spinal Cord MRI, Astrocytoma, Ependymoma, Multiple Sclerosis, Neuromyelitis Optica Spectrum Disorder, Deep Learning
Content: MR, NR
RadLex: RID39467, RID4033, RID4055, RID35105, RID10796

Author(s)

Zhizheng Zhuo
Jie Zhang
Yunyun Duan
Liying Qu
Chenlu Feng
Xufang Huang
Dan Cheng
Xiaolu Xu
Ting Sun
Zhaohui Li
Xiaopeng Guo
Xiaodong Gong
Yongzhi Wang
Wenqing Jia
Decai Tian
Xinghu Zhang
Fudong Shi
Sven Haller
Frederik Barkhof
Chuyang Ye
Yaou Liu

Organization(s)

Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China
Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China
Center for Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China
BioMind, Beijing, China
Department of Medical Imaging Product, Neusoft Group, Shenyang, China
China National Clinical Research Center for Neurologic Diseases, Beijing, China
Department of Neurology and Tianjin Neurologic Institute, Tianjin Medical University General Hospital, Tianjin, China
Department of Imaging and Medical Informatics, University Hospitals of Geneva and Faculty of Medicine of the University of Geneva, Geneva, Switzerland
UCL Institutes of Neurology and Healthcare Engineering, London, England
Department of Radiology and Nuclear Medicine, Amsterdam University Medical Centers, the Netherlands
School of Information and Electronics, Beijing Institute of Technology, Beijing, China

Version

1.0

Contact

Corresponding author: Yaou Liu, email: gro.httjb@uoayuil (as provided in article)

Funding

Supported by the National Science Foundation of China (nos. 81870958 and 81571631), the Beijing Municipal Natural Science Foundation for Distinguished Young Scholars (no. JQ20035), the Special Fund of the Pediatric Medical Coordinated Development Center of Beijing Hospitals Authority (no. XTYB201831), and the ECTRIMS-MAGNMIS Fellowship from ECTRIMS (Y.L.).

Ethical review

Study performed in accordance with the Declaration of Helsinki; approved by the animal and human ethics committee of the local institution; written informed consent obtained from all patients.

Date

Updated: 2022-08-24
Published: 2022-09-07
Created: 2021-11-22

References

[1] Zhuo Z, Zhang J, Duan Y, et al.. "Automated Classification of Intramedullary Spinal Cord Tumors and Inflammatory Demyelinating Lesions Using Deep Learning". Radiology: Artificial Intelligence. 2022 Nov;4(6):e210292.. 2022-09-07. doi:10.1148/ryai.210292. PMID: 36523644. PMCID: PMC9745442.

Model

Architecture

Two-dimensional MultiResUNet for lesion segmentation and DenseNet121 for image-based classification.

Availability

Code publicly available at https://github.com/Leezhaohui/spinalcord_classification

Clinical benefit

Assists accurate radiologic diagnosis by segmenting intramedullary spinal cord lesions and differentiating tumors (astrocytoma, ependymoma) from inflammatory demyelinating lesions (MS, NMOSD) and classifying their subtypes.

Clinical workflow phase

Clinical decision support systems; aids radiologic interpretation and differential diagnosis.

Degree of automation

Semi-automated pipeline: automated segmentation with manual verification/correction for poorly segmented lesions, followed by automated classification.

Indications for use

Differential diagnosis of intramedullary spinal cord lesions in patients with suspected tumors (astrocytoma, ependymoma) or inflammatory demyelinating diseases (MS, NMOSD) using clinically available sagittal T2-weighted MR images in a radiology setting.

Input

Sagittal non-contrast T2-weighted MR images (all sections) of the spinal cord; slices with lesions and corresponding lesion masks are used for classification. Contrast-enhanced T1-weighted images were optionally evaluated and improved MS vs NMOSD classification in sensitivity analysis.

Instructions

First segment lesions on sagittal T2-weighted images using the MultiResUNet model; perform manual verification and correct poorly segmented lesions; then use T2-weighted slices containing lesions and corresponding masks as input into the DenseNet121 classifier for: (1) tumor vs demyelination, (2) astrocytoma vs ependymoma, and (3) MS vs NMOSD.

Limitations

Only T2-weighted images used for primary development/validation; segmentation performance for demyelinating lesions was lower and often required manual review/correction; no external testing beyond the single-center prospective cohort; performance degradation observed in pediatric and male subgroups for astrocytoma vs ependymoma; additional lesion types (e.g., spinal cord infarction) not included.

Output

CDEs: RDE746.3, RDE746.0, RDE1455, RDE1451, RDE746, RDE1452
Description: Lesion segmentation masks and categorical classifications for (1) tumor vs demyelination, (2) astrocytoma vs ependymoma, and (3) MS vs NMOSD.

Recommendation

For differentiating demyelinating lesions (MS vs NMOSD), consider adding contrast-enhanced T1-weighted images to improve classification accuracy.

Use

Intended: Decision support, Image segmentation, Diagnosis, Detection and diagnosis

User

Intended: Radiologist, Subspecialist diagnostic radiologist