Lukas Heine

Fabian Hörst, Moritz Rempe, Lukas Heine et al.

Nuclei detection and segmentation in hematoxylin and eosin-stained (H&E) tissue images are important clinical tasks and crucial for a wide range of applications. However, it is a challenging task due to nuclei variances in staining and size, overlapping boundaries, and nuclei clustering. While convolutional neural networks have been extensively used for this task, we explore the potential of Transformer-based networks in this domain. Therefore, we introduce a new method for automated instance segmentation of cell nuclei in digitized tissue samples using a deep learning architecture based on Vision Transformer called CellViT. CellViT is trained and evaluated on the PanNuke dataset, which is one of the most challenging nuclei instance segmentation datasets, consisting of nearly 200,000 annotated Nuclei into 5 clinically important classes in 19 tissue types. We demonstrate the superiority of large-scale in-domain and out-of-domain pre-trained Vision Transformers by leveraging the recently published Segment Anything Model and a ViT-encoder pre-trained on 104 million histological image patches - achieving state-of-the-art nuclei detection and instance segmentation performance on the PanNuke dataset with a mean panoptic quality of 0.50 and an F1-detection score of 0.83. The code is publicly available at https://github.com/TIO-IKIM/CellViT

Alexander Jaus, Constantin Seibold, Simon Reiß et al.

Pathological structures in medical images are typically deviations from the expected anatomy of a patient. While clinicians consider this interplay between anatomy and pathology, recent deep learning algorithms specialize in recognizing either one of the two, rarely considering the patient's body from such a joint perspective. In this paper, we develop a generalist segmentation model that combines anatomical and pathological information, aiming to enhance the segmentation accuracy of pathological features. Our Anatomy-Pathology Exchange (APEx) training utilizes a query-based segmentation transformer which decodes a joint feature space into query-representations for human anatomy and interleaves them via a mixing strategy into the pathology-decoder for anatomy-informed pathology predictions. In doing so, we are able to report the best results across the board on FDG-PET-CT and Chest X-Ray pathology segmentation tasks with a margin of up to 3.3% as compared to strong baseline methods. Code and models will be publicly available at github.com/alexanderjaus/APEx.

Lukas Heine, Fabian Hörst, Jana Fragemann et al.

In industries such as healthcare, finance, and manufacturing, analysis of unstructured textual data presents significant challenges for analysis and decision making. Uncovering patterns within large-scale corpora and understanding their semantic impact is critical, but depends on domain experts or resource-intensive manual reviews. In response, we introduce Spacewalker in this system demonstration paper, an interactive tool designed to analyze, explore, and annotate data across multiple modalities. It allows users to extract data representations, visualize them in low-dimensional spaces and traverse large datasets either exploratory or by querying regions of interest. We evaluated Spacewalker through extensive experiments and annotation studies, assessing its efficacy in improving data integrity verification and annotation. We show that Spacewalker reduces time and effort compared to traditional methods. The code of this work is open-source and can be found at: https://github.com/code-lukas/Spacewalker

Fabian Hörst, Moritz Rempe, Helmut Becker et al.

Digital Pathology is a cornerstone in the diagnosis and treatment of diseases. A key task in this field is the identification and segmentation of cells in hematoxylin and eosin-stained images. Existing methods for cell segmentation often require extensive annotated datasets for training and are limited to a predefined cell classification scheme. To overcome these limitations, we propose $\text{CellViT}^{\scriptscriptstyle ++}$, a framework for generalized cell segmentation in digital pathology. $\text{CellViT}^{\scriptscriptstyle ++}$ utilizes Vision Transformers with foundation models as encoders to compute deep cell features and segmentation masks simultaneously. To adapt to unseen cell types, we rely on a computationally efficient approach. It requires minimal data for training and leads to a drastically reduced carbon footprint. We demonstrate excellent performance on seven different datasets, covering a broad spectrum of cell types, organs, and clinical settings. The framework achieves remarkable zero-shot segmentation and data-efficient cell-type classification. Furthermore, we show that $\text{CellViT}^{\scriptscriptstyle ++}$ can leverage immunofluorescence stainings to generate training datasets without the need for pathologist annotations. The automated dataset generation approach surpasses the performance of networks trained on manually labeled data, demonstrating its effectiveness in creating high-quality training datasets without expert annotations. To advance digital pathology, $\text{CellViT}^{\scriptscriptstyle ++}$ is available as an open-source framework featuring a user-friendly, web-based interface for visualization and annotation. The code is available under https://github.com/TIO-IKIM/CellViT-plus-plus.

Moritz Rempe, Lukas Heine, Constantin Seibold et al.

Medical data employed in research frequently comprises sensitive patient health information (PHI), which is subject to rigorous legal frameworks such as the General Data Protection Regulation (GDPR) or the Health Insurance Portability and Accountability Act (HIPAA). Consequently, these types of data must be pseudonymized prior to utilisation, which presents a significant challenge for many researchers. Given the vast array of medical data, it is necessary to employ a variety of de-identification techniques. To facilitate the anonymization process for medical imaging data, we have developed an open-source tool that can be used to de-identify DICOM magnetic resonance images, computer tomography images, whole slide images and magnetic resonance twix raw data. Furthermore, the implementation of a neural network enables the removal of text within the images. The proposed tool automates an elaborate anonymization pipeline for multiple types of inputs, reducing the need for additional tools used for de-identification of imaging data. We make our code publicly available at https://github.com/code-lukas/medical_image_deidentification.

Luc Bouteille, Alexander Jaus, Jens Kleesiek et al.

Traditional loss functions in medical image segmentation, such as Dice, often under-segment small lesions because their small relative volume contributes negligibly to the overall loss. To address this, instance-wise loss functions and metrics have been proposed to evaluate segmentation quality on a per-lesion basis. We introduce CC-DiceCE, a loss function based on the CC-Metrics framework, and compare it with the existing blob loss. Both are benchmarked against a DiceCE baseline within the nnU-Net framework, which provides a robust and standardized setup. We find that CC-DiceCE loss increases detection (recall) with minimal to no degradation in segmentation performance, though with dataset-dependent trade-offs in precision. Furthermore, our multi-dataset study shows that CC-DiceCE generally outperforms blob loss.

Constantin Seibold, Hamza Kalisch, Lukas Heine et al.

In this paper, we tackle the challenge of instance segmentation for foreign objects in chest radiographs, commonly seen in postoperative follow-ups with stents, pacemakers, or ingested objects in children. The diversity of foreign objects complicates dense annotation, as shown in insufficient existing datasets. To address this, we propose the simple generation of synthetic data through (1) insertion of arbitrary shapes (lines, polygons, ellipses) with varying contrasts and opacities, and (2) cut-paste augmentations from a small set of semi-automatically extracted labels. These insertions are guided by anatomy labels to ensure realistic placements, such as stents appearing only in relevant vessels. Our approach enables networks to segment complex structures with minimal manually labeled data. Notably, it achieves performance comparable to fully supervised models while using 93\% fewer manual annotations.