Analysis of the Molecular Signature of Breast Implant-Associated Anaplastic Large Cell Lymphoma in an Asian Patient

Author:

Kim Il-Kug1,Hong Ki Yong2,Lee Choong-kun3,Choi Bong Gyu1,Shin Hyunjong4,Lee Jun Ho1,Kim Min Kyoung5,Gu Mi Jin6,Choi Jung Eun7,Kim Tae Gon1

Affiliation:

1. Department of Plastic and Reconstructive Surgery, Yeungnam University College of Medicine, Daegu, Korea

2. Department of Plastic and Reconstructive Surgery, Dongguk University Ilsan Hospital, Goyang, Korea

3. Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea

4. Ulsan BB Plastic Surgery Clinic, Ulsan, Korea

5. Division of Hematology-Oncology, Department of Internal Medicine, Yeungnam University College of Medicine, Daegu, Korea

6. Department of Pathology, Yeungnam University College of Medicine, Daegu, Korea

7. Department of Surgery, Yeungnam University College of Medicine, Daegu, Korea

Abstract

Abstract Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL)—a new category of anaplastic large cell lymphoma associated with textured breast implants—has a distinct variation in incidence and is especially rare in Asia. We report the first case of BIA-ALCL in Korea and present its histological and genetic characteristics. A 44-year-old female patient presented with a typical clinical course and symptoms, including breast augmentation with textured breast implants, late-onset peri-implant effusion, and CD30+ALK− histology, followed by bilateral implant removal and total capsulectomy. For histological analysis, we performed immunohistochemistry of the bilateral breast capsules. For transcriptome analysis, we identified highly upregulated gene sets employing RNA-sequencing and characterized the lymphoma immune cell components. In the lymphoma-associated capsule, CD30+ cells infiltrated not only the lymphoma lesion but also the peritumoral lesion. The morphologies of the myofibroblasts and vessels in the peritumoral lesion were similar to those in the tumoral lesion. We observed strong activation of the JAK/STAT3 pathway and expression of programmed death ligand-1 in the lymphoma. Unlike the molecular profiles of BIA-ALCL samples from Caucasian patients—all of which contained activated CD4+ T cells—the Asian patient’s profile was characterized by more abundant CD8+ T cells. This study contributes to a better understanding of the pathogenesis and molecular mechanisms of BIA-ALCL in Asian patients that will ultimately facilitate the development of clinical therapies. Level of Evidence: 5

Funder

National Research Foundation of Korea

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Surgery

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