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

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 histologic...

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Veröffentlicht in:Aesthetic surgery journal 2021-04, Vol.41 (5), p.NP214-NP222
Hauptverfasser: Kim, Il-Kug, Hong, Ki Yong, Lee, Choong-Kun, Choi, Bong Gyu, Shin, Hyunjong, Lee, Jun Ho, Kim, Min Kyoung, Gu, Mi Jin, Choi, Jung Eun, Kim, Tae Gon
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container_end_page NP222
container_issue 5
container_start_page NP214
container_title Aesthetic surgery journal
container_volume 41
creator Kim, Il-Kug
Hong, Ki Yong
Lee, Choong-Kun
Choi, Bong Gyu
Shin, Hyunjong
Lee, Jun Ho
Kim, Min Kyoung
Gu, Mi Jin
Choi, Jung Eun
Kim, Tae Gon
description 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.
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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. 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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.</description><subject>Adult</subject><subject>Asia</subject><subject>Breast Implantation - adverse effects</subject><subject>Breast Implants - adverse effects</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - surgery</subject><subject>Breast Surgery</subject><subject>Female</subject><subject>Humans</subject><subject>Lymphoma, Large-Cell, Anaplastic - etiology</subject><subject>Lymphoma, Large-Cell, Anaplastic - genetics</subject><subject>Republic of Korea</subject><issn>1090-820X</issn><issn>1527-330X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU2LFDEQhoMo7rp68i45CtJupZPuTl-EcfBjYURBhb2F6kwyk6G7M6bSwvx7s-y46KWqqHp4q4qXsZcC3gro5TXS4ZoOiLLXj9ilaOqukhJuH5caeqh0DbcX7BnRAaDgrXrKLqSUbdfUcMloNeN4okA8ep73jn-Jo7PLiIl_D7sZ85Lc3eh9ckiZ30zHEedcrYiiDZjdlheB0qMcLN9g2jm-duPIN6fpuI8T8jBznPmKQonfMAc35-fsiceR3ItzvmI_P374sf5cbb5-ulmvNpWVWuRqGJSqddcOHkSjlRtajb0H1w2tQyHR2sYLK1TrW9lLobzyndZbae3QANadvGLv7nWPyzC5rS2rE47mmMKE6WQiBvP_ZA57s4u_jQYFdQNF4PVZIMVfi6NspkC2vIeziwuZWnVSCQ1CF_TNPWpTJErOP6wRYO5sMsUmc7ap0K_-veyB_euL_AMjDpGs</recordid><startdate>20210412</startdate><enddate>20210412</enddate><creator>Kim, Il-Kug</creator><creator>Hong, Ki Yong</creator><creator>Lee, Choong-Kun</creator><creator>Choi, Bong Gyu</creator><creator>Shin, Hyunjong</creator><creator>Lee, Jun Ho</creator><creator>Kim, Min Kyoung</creator><creator>Gu, Mi Jin</creator><creator>Choi, Jung Eun</creator><creator>Kim, Tae Gon</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210412</creationdate><title>Analysis of the Molecular Signature of Breast Implant-Associated Anaplastic Large Cell Lymphoma in an Asian Patient</title><author>Kim, Il-Kug ; 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source MEDLINE; Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection
subjects Adult
Asia
Breast Implantation - adverse effects
Breast Implants - adverse effects
Breast Neoplasms - genetics
Breast Neoplasms - surgery
Breast Surgery
Female
Humans
Lymphoma, Large-Cell, Anaplastic - etiology
Lymphoma, Large-Cell, Anaplastic - genetics
Republic of Korea
title Analysis of the Molecular Signature of Breast Implant-Associated Anaplastic Large Cell Lymphoma in an Asian Patient
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