Julie Le
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Julie Le has a total of 23 co-authors. Here are the top co-authors by number of shared publications:
- Sara Grossi
University of California San Diego School of Medicine Department of Surgery, La Jolla, CA, USA
3 shared publications - Ava Hosseini
Department of Surgery, University of California-San Diego, San Diego, USA
2 shared publications - Haydee Ojeda-Fournier
Breast Imaging Division, Department of Radiology, UC San Diego Health, Koman Family Outpatient Pavilion, 9400 Campus Point Dr, La Jolla, CA 92037
2 shared publications - Sarah L. Blair
Department of Surgery, University of California San Diego, San Diego, USA
2 shared publications - Anne M. Wallace
Department of Surgery, University of California San Diego, San Diego, CA 92093, USA
1 shared publication - Cassandra Liu
University of California San Diego School of Medicine Department of Surgery, La Jolla, CA, USA
1 shared publication
Latest Publications
- Open Access
- 10 October 2026
- Published by Elsevier in European Journal of Surgical Oncology
- Vol. 53 (1) , 112183
Preoperative MRI for pleomorphic lobular carcinoma in situ: Implications for surgical management
- 10 October 2026
- Published by Elsevier in European Journal of Surgical Oncology
- Vol. 53 (1) , 112183
Open AccessPreoperative MRI for pleomorphic lobular carcinoma in situ: Implications for surgical management
- 27 May 2026
- Published by Elsevier in Surgical Clinics of North America
- Vol. 106 (4) , 465-479
Genetics, Screening, and Risk-reducing Interventions for Breast Cancer
- 27 May 2026
- Published by Elsevier in Surgical Clinics of North America
- Vol. 106 (4) , 465-479
Genetics, Screening, and Risk-reducing Interventions for Breast Cancer
- Open Access
Distance of Biopsy-Confirmed High-Risk Breast Lesion from Concurrently Identified Breast Malignancy Associated with Risk of Carcinoma at the High-Risk Lesion Site
High-risk breast lesions including incidental intraductal papilloma without atypia (IPA), lobular hyperplasia (LCIS or ALH), flat epithelial atypia (FEA) and complex sclerosing lesion (CSL) are not routinely excised due to low upgrade rates to carcinoma. We aim to identify features of these lesions predictive of upgrade when identified concurrently with invasive disease. Methods: A single-center retrospective cohort study was performed for patients who underwent multi-site lumpectomies with invasive disease at one site and a high-risk lesion at another site between 2006 and 2021. A multinomial logistic regression was performed. Results: Sixty-five patients met the inclusion criteria. Four patients (6.2%) had an upgrade to in situ disease (DCIS) and one (1.5%) to invasive carcinoma. Three upgraded high-risk lesions were ipsilateral to the concurrent carcinoma and two were contralateral. In the multivariate model, a high-risk lesion within 5 cm of an ipsilateral malignancy was associated with increased risk of upgrade. The 3.8% upgrade rate for high-risk lesions located greater than 5 cm from ipsilateral malignancy or in the contralateral breast suggests that omission of excisional biopsy may be considered. Excisional biopsy of lesions within 5 cm of ipsilateral malignancy is recommended given the 25% upgrade risk in our series.
Open AccessDistance of Biopsy-Confirmed High-Risk Breast Lesion from Concurrently Identified Breast Malignancy Associated with Risk of Carcinoma at the High-Risk Lesion Site
High-risk breast lesions including incidental intraductal papilloma without atypia (IPA), lobular hyperplasia (LCIS or ALH), flat epithelial atypia (FEA) and complex sclerosing lesion (CSL) are not routinely excised due to low upgrade rates to carcinoma. We aim to identify features of these lesions predictive of upgrade when identified concurrently with invasive disease. Methods: A single-center retrospective cohort study was performed for patients who underwent multi-site lumpectomies with invasive disease at one site and a high-risk lesion at another site between 2006 and 2021. A multinomial logistic regression was performed. Results: Sixty-five patients met the inclusion criteria. Four patients (6.2%) had an upgrade to in situ disease (DCIS) and one (1.5%) to invasive carcinoma. Three upgraded high-risk lesions were ipsilateral to the concurrent carcinoma and two were contralateral. In the multivariate model, a high-risk lesion within 5 cm of an ipsilateral malignancy was associated with increased risk of upgrade. The 3.8% upgrade rate for high-risk lesions located greater than 5 cm from ipsilateral malignancy or in the contralateral breast suggests that omission of excisional biopsy may be considered. Excisional biopsy of lesions within 5 cm of ipsilateral malignancy is recommended given the 25% upgrade risk in our series.
- Open Access
Omitting axillary staging in selected patients: Rationale of Choosing Wisely in breast cancer treatment
- Open Access
- 16 April 2022
- Published by Springer Nature in Annals of Surgical Oncology
- Vol. 29 (8) , 4727
ASO Visual Abstract: Epigenetic Signatures Predict Pathologic Nodal Stage in Breast Cancer Patients with Estrogen-Receptor-Positive, Clinically Node-Positive Disease
- 16 April 2022
- Published by Springer Nature in Annals of Surgical Oncology
- Vol. 29 (8) , 4727
Open AccessASO Visual Abstract: Epigenetic Signatures Predict Pathologic Nodal Stage in Breast Cancer Patients with Estrogen-Receptor-Positive, Clinically Node-Positive Disease