ABSTRACT This dataset comprises 38 breast ultrasound scans from patients, encompassing a total of 683 images. The scans were conducted using a Siemens ACUSON S2000TM Ultrasound System from

2022 to 2023. The dataset is specifically created for the purpose of segmenting breast lesions, with the goal of identifying the area and contour of the lesion, as well as classifying it as

either benign or malignant. The images can be classified into three categories based on their findings: 419 are normal, 174 are benign, and 90 are malignant. The ground truth is given as RGB

segmentation masks in individual files, with black indicating normal breast tissue and green and red indicating benign and malignant lesions, respectively. This dataset enables researchers

CURATED BENCHMARK DATASET FOR ULTRASOUND BASED BREAST LESION ANALYSIS Article Open access 31 January 2024 SEMIAUTOMATED SEGMENTATION OF BREAST TUMOR ON AUTOMATIC BREAST ULTRASOUND IMAGE

USING A LARGE-SCALE MODEL WITH CUSTOMIZED MODULES Article Open access 19 May 2025 SEGMENT ANYTHING IN MEDICAL IMAGES Article Open access 22 January 2024 BACKGROUND & SUMMARY While there

are quite a few computer-aided detection (CAD) systems for mammography used in radiology for breast cancer screening, the same cannot be said for CAD systems using breast ultrasound images

(BUS). Mammography CAD systems use a range of techniques, including conventional machine learning approaches1 and deep learning methods2. Implementing a screening system that incorporates

diagnostic tools readily available in most clinical centres, like ultrasound imaging devices, would be a significant breakthrough in combating breast cancer. This system has the potential to

greatly improve breast cancer prognosis and reduce breast mortality due to cancer. Precise detection and segmentation of abnormalities in breast ultrasound images, including both benign and

malignant tumours, is essential for the diagnosis of suspicious masses detected in mammograms and the assessment of dense breasts3. Although there are many computer-aided detection (CAD)

systems for mammography used in radiology for breast cancer screening, CAD systems for breast ultrasound images (BUS) are relatively rare. An exception is the S-Detect™ system offered on

Samsung ultrasound machines. This software analyzes breast lesions and classifies them according to the BI-RADS® ATLAS. This system can improve the accuracy and reliability of breast cancer

detection through ultrasound. Nevertheless, despite the advancements made, numerous challenges must be tackled in order to develop robust machine learning models for breast ultrasound

analysis. One major challenge is the availability of large and well-annotated datasets. High-quality datasets are crucial for the training and validation of machine learning models. In order

to ensure that the models can be applied effectively to real-world situations, that is, to ensure they generalize well to real-world scenarios, it is necessary for them to include a wide

range of examples of breast lesions, encompassing different types and stages of cancer. The dataset introduced herein (BUS-UCLM dataset) aims to provide a comprehensive resource for the

development and evaluation of machine learning algorithms for breast ultrasound image analysis. This dataset comprises a wide range of breast ultrasound images, alongside detailed

annotations provided by expert radiologists. The dataset is designed to support research in a range of tasks, including lesion segmentation, classification, and detection. METHODS IMAGE

ACQUISITION AND ANONYMIZATION Ultrasound images were collected from 2022 to 2023 at Ciudad Real General University Hospital. Images were acquired using the Siemens Acuson S2000 ultrasound

system, with the 18L6 HD probe, and using the standard beamforming method. The pixel resolution varied across the dataset, with the most common resolution being (0.0639205, 0.0639205). Other

resolutions were also present but for a smaller number of images, including (0.0568182, 0.0568182) for 31 images, (0.0710227, 0.0710227) for 51 images, and several other resolutions each

represented by fewer than 20 images. The dimensions of each image were 768 × 1024 pixels. The dataset is derived from authentic clinical studies, without any predefined selection criteria

for patients or images. This approach ensures a realistic representation of clinical scenarios. The study was reviewed and approved by the Ethics Committee of Ciudad Real General University

Hospital as part of project PID2021-127567NB-I00. In addition, informed consent was obtained from all participants to collect and share the data. Participants were assured that their

confidentiality would be maintained. Images were initially stored in DICOM format and subsequently converted to PNG files. To ensure patient privacy and comply with data protection

regulations, folders and DICOM files were renamed using random four-letter sequences, with each sequence uniquely identifying images from the same patient. This approach enables

subject-based cross-validation partitions. Additionally, sensitive data in the DICOM header fields was anonymized, and a YOLOv8-trained CNN was employed for text detection to mask sensitive

information in the DICOM pixel data by overlaying black rectangles4. IMAGE ANNOTATION A diverse dataset comprising both benign and malignant cases was compiled. The malignancy status of each

lesion was verified through biopsy procedures. Expert radiologists then meticulously produced manual annotations. The dataset was labeled with segmentation masks, which made it suitable for

semantic segmentation, instance segmentation or detection tasks. It was noted that in other publicly available datasets, only one lesion per image was labeled, even if more than one lesion

was present. Since having scans with more than one lesion is common, especially when dealing with breast cysts—which represent 25% of all breast masses and often appear in clusters—all

lesions appearing in an image were labeled. One radiologist delineated the lesion contours, which, coupled with diagnostic information, facilitated the creation of precise segmentation

masks. Additionally, another radiologist reviewed and approved the marks, both reaching a consensus on the delineation. For the annotation generation, we employed CVAT, an Open Data

Annotation Platform, to manually generate the ground truth annotations5. All processed images are available in PNG format. Furthermore, scans of normal tissue were included. As it is common

for most of the breast tissue to be normal in an ultrasound session, these samples are important to measure the number of false positives, particularly in the test phase. Some samples with

the segmentation masks overlaid are shown in Fig. 1. Multiple images were collected for each patient, taken from different breast cross-sections to ensure comprehensive coverage of the area

of interest. Therefore, these images are 2D cross-sectional views (Fig. 2). DATA PROTECTION AND COMPLIANCE To ensure compliance with legal and regulatory frameworks for medical data, we

implemented data protection measures in accordance with the General Data Protection Regulation (GDPR) and the Health Insurance Portability and Accountability Act (HIPAA). Specifically, we

adhered to both GDPR Article 9 and HIPAA’s Privacy Rule, which mandate the protection of personal data, by ensuring that all identifiable information was removed from the dataset. This

included both direct identifiers such as names and dates, and indirect identifiers such as unique codes that could be traced back to an individual. These measures ensured that the data could

not be used to identify individuals, either on its own or in combination with other information. These safeguards were applied to the initial DICOM files, ensuring that even the authors do

not retain sensitive data. All anonymized data was handled and stored securely to prevent unauthorized access. Furthermore, only PNG files are publicly shared, which strengthens compliance

with data privacy regulations. The anonymization script, along with other auxiliary code, has been uploaded to a GitHub repository to ensure transparency and reproducibility of our methods

(https://github.com/noeliavallez/BUS-UCLM-Dataset). DATA RECORDS The dataset is available at Mendeley Data6. It is organized into a main folder that includes two subfolders and a CSV file

with image information, including the image name, resolution, label, and whether it was acquired with Doppler, is a combined image, or has masks. One subfolder holds the ultrasound images in

PNG format and the other one the segmentation masks. The images are named using a pattern of four random letters followed by an underscore and a sequence number (e.g., XXXX_YYY.png), where

’XXXX’ represents an anonymized patient identifier and ’YYY’ is the image number within that patient’s study. The segmentation masks utilize a color-coding system in RGB format to indicate

different types of tissue: red (255,0,0) for malignant lesions, green (0,255,0) for benign lesions, and black (0,0,0) for normal breast tissue and other non-lesion areas. A visual

representation of the dataset’s structure is provided in Fig. 3, offering an overview of how the data is organized and labeled. Table 1 contains the number of images per patient. The dataset

is publicly available and free to use for research purposes, fostering collaboration and innovation in the field of breast ultrasound analysis. The dataset is licensed under CC-BY 4.0.

TECHNICAL VALIDATION The dataset was compiled from ultrasound images acquired at the Ciudad Real General University Hospital between 2022 and 2023. Each image underwent a conversion from

DICOM to PNG format, a process meticulously designed to strip away any identifiable patient information, thereby upholding the strictest standards of privacy and confidentiality. Two expert

radiologists with extensive experience in breast imaging annotated the dataset. Both radiologists reached a consensus on the annotations. This consensus is crucial because it ensures that

the annotations are accurate and reliable, reducing the likelihood of individual bias or error. The malignancy of the lesions was confirmed through biopsy. This direct correlation between

the biopsy results and the annotations ensures that the dataset reflects the highest level of precision and accuracy for lesion classification. The BUS-UCLM includes 683 images collected

from 38 patients, comprising 419 normal, 174 benign, and 90 malignant images. A comparison with other existing public datasets has been made. Generally, the BUS-UCLM dataset is similar to

these datasets but distinguishes itself by including samples without lesions and samples with multiple lesions labelled. A summary of relevant features is presented in Table 3. * The Breast

Ultrasound Images (BUSI) dataset contains 780 images annotated for segmentation, including 437 benign, 210 malignant, and 133 normal images. It is a widely used dataset but has limitations

in the variety of images and the overall size of the dataset, which may not be sufficient for training highly generalizable models. * The UDIAT DatasetB, used in several studies, contains

163 annotated images with 109 benign and 54 malignant cases. This dataset is relatively small and does not include normal tissue images. Furthermore, it is not publicly downloadable, which

limits its accessibility for broader research use, although it can be obtained by contacting the authors. * The RODTOOK dataset includes 144 images with 57 benign and 87 malignant lesions.

Although it is useful for segmentation tasks, its smaller size and lack of normal tissue samples present limitations for comprehensive model training and evaluation. * The Open Access Series

of Breast Ultrasound Data (OASBUD) provides 200 images with an equal split between benign and malignant cases. This dataset is publicly available and has been used in numerous studies.

However, as with other datasets, it does not include normal tissue scans. The image quality of BUS-UCLM is superior to that of other datasets since it was gathered with recent equipment,

more robust to the image noise inherent in ultrasound imaging. Figure 4 shows examples of the 5 datasets with their corresponding segmentation masks. To validate the dataset, a UNet model

was trained using the BUS-UCLM dataset to segment image pixels into background, benign, and malignant categories. Ninety percent of the cases were used for training, and ten percent for

testing, with partitions done at the patient level. The model achieved a Dice score of 0.68, indicating that despite the small size, the dataset is sufficient to develop models with

reasonable performance (Fig. 5). This highlights the great potential of this dataset. When combined with other publicly available BUS segmentation datasets, it may significantly enhance the

reliability and predictive performance of the model across diverse cases. Integrating our dataset with those listed in Table 3 may be particularly beneficial. As a result, despite the modest

sample size, the rich quality of the data and the careful segmentation procedures provide a solid foundation for training and evaluating machine learning models. This approach ensures that

the findings are relevant and meaningful, with the potential for scalability once additional datasets are integrated. Further work will focus on expanding the dataset to include more

examples, which will further improve the model’s performance. IDENTIFICATION OF BIASES The potential sources of bias of the use of the BUS-UCLM dataset have been identified. One of them is

the demographic bias. The dataset was collected exclusively from the General University Hospital of Ciudad Real in Spain. This localized collection process may introduce demographic bias, as

the patient population may not represent broader geographical or ethnic groups. This limitation could impact the applicability of the model to populations with different genetic, ethnic, or

lifestyle factors. Clinical bias is another concern. The dataset primarily includes cases verified through biopsy and annotated by two expert radiologists. While this ensures high-quality

annotations, it may limit variability in the dataset, as diagnoses made by general practitioners or less experienced clinicians are not represented. This could lead to a model that is overly

dependent on expert-level data, reducing its robustness in real-world scenarios where data quality and diagnostic expertise vary. Selection bias may also arise as a result of the limited

dataset size. Despite not having a predefined inclusion criteria, the dataset includes only 38 patients. This small sample size may result in underrepresentation of certain lesion types or

clinical conditions, reducing the diversity of the dataset. Finally, some images in the dataset contain annotations such as arrows, yellow crosses, and bounding boxes that overlap with the

mass areas. These marks may influence the outcome of the models, introducing bias. Additionally, some images are Doppler ultrasound images, and others are combined images containing multiple

scans in one. To mitigate these problems, we have provided a CSV file with detailed metadata for each image, including three columns indicating whether the image contains Doppler features,

visual marks, or is a combined image. This allows users to include or exclude specific subsets of images based on their needs. COMBINATION WITH OTHER DATASETS To assess the impact of

combining the BUS-UCLM dataset with other datasets, we integrated all datasets listed in Table 3 and trained five segmentation models (UNet, AttUnet, SK-UNet, DeepLabv3, and Mask R-CNN) with

the five datasets compared in this work, extending the work of Cory _et al_. from binary segmentation to three classes (background, benign, and malignant)7. A 5-fold cross-validation was

employed, ensuring that the folds were the same for all models and that partitions were made at patient level and not at image level to prevent having images from the same patient in more

than one fold. Intersection over union (IoU), accuracy (Acc), Dice score, Precision, and Recall were calculated. The results presented in Table 2 are the averaged results of all folds. From

the five models tested, Mask R-CNN outperformed other networks with the highest average scores across all metrics: IoU=65.46%, Acc=74.38%, Dice=77.09%, Precision=80.29%, and Recall=74.38%.

These results are in line with those presented in the literature7. These results suggest that the dataset does not introduce significant biases that could negatively affect model

performance. However, to enhance the generalizability of diagnostic algorithms, we recommend using this dataset in conjunction with other resources. Although other available datasets are

also small and may share similar biases, integrating multiple datasets can still help create more comprehensive models. This approach captures a broader spectrum of real-world features,

ultimately improving robustness and applicability. CODE AVAILABILITY A source code repository is available on GitHub (https://github.com/noeliavallez/BUS-UCLM-Dataset) with useful scripts to

convert the masks to the COCO annotation format in JSON and overlay the segmented areas onto the original images. REFERENCES * Vallez, N., Bueno, G., Deniz, O., Dorado, J., Seoane, J. A.,

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physics_ 44, 6105–6109 (2017). Article  ADS  PubMed  Google Scholar  Download references ACKNOWLEDGEMENTS This work has been funded by the HANS project (Ref. PID2021-127567NB-I00) supported

by the Spanish Ministry of Science, Innovation, and Universities, and by the European Union NextGenerationEU/PRTR. AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * VISILAB, E.T.S. Ingeniería

Industrial, University of Castilla-La Mancha, Avda. Camilo José Cela s/n, 13005, Ciudad Real, Spain Noelia Vallez, Gloria Bueno & Oscar Deniz * Hospital General Universitario de Ciudad

Real, C/ Obispo Rafael Torija s/n, 13005, Ciudad Real, Spain Miguel Angel Rienda & Carlos Pastor Authors * Noelia Vallez View author publications You can also search for this author

inPubMed Google Scholar * Gloria Bueno View author publications You can also search for this author inPubMed Google Scholar * Oscar Deniz View author publications You can also search for

this author inPubMed Google Scholar * Miguel Angel Rienda View author publications You can also search for this author inPubMed Google Scholar * Carlos Pastor View author publications You

can also search for this author inPubMed Google Scholar CONTRIBUTIONS Noelia Vallez contributed through conceptualization, data curation, software development, and manuscript writing. Gloria

Bueno and Oscar Deniz acquired funding, administered and supervised the project, and contributed in manuscript reviewing and editing. Miguel A. Rienda and Carlos Pastor participated in data

acquisition, labelling and curation. CORRESPONDING AUTHOR Correspondence to Noelia Vallez. ETHICS DECLARATIONS COMPETING INTERESTS The authors declare no competing interests. ADDITIONAL

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licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/. Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Vallez, N., Bueno, G., Deniz, O. _et al._ BUS-UCLM: Breast

ultrasound lesion segmentation dataset. _Sci Data_ 12, 242 (2025). https://doi.org/10.1038/s41597-025-04562-3 Download citation * Received: 21 June 2024 * Accepted: 30 January 2025 *

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