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乳房植入物相关间变性大细胞淋巴瘤

Breast Implant-Associated Anaplastic Large Cell Lymphoma.

作者信息

Rastogi P, Deva A K, Prince H Miles

机构信息

Department of Plastic, Reconstructive & Maxillofacial Surgery - Macquarie University, Sydney, New South Wales, Australia.

Medical Oncology and Cancer Immunology, Epworth Healthcare, 140 Clarendon Street, East Melbourne, Victoria, 3002, Australia.

出版信息

Curr Hematol Malig Rep. 2018 Dec;13(6):516-524. doi: 10.1007/s11899-018-0478-2.

Abstract

PURPOSE OF REVIEW

Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) is a recently recognised malignancy of T lymphocytes exclusively associated with textured breast implants. This review aims to evaluate existing theories regarding the epidemiology, pathogenesis, clinical evaluation and management of the disease.

RECENT FINDINGS

The true incidence of BIA-ALCL is difficult to define. Prevailing pathogenic theories recognise the interplay between textured implants, Gram-negative bacteria, host genetics (e.g. JAK/STAT, p53) and time. Patients typically present with a delayed seroma and less commonly with a capsular mass or systemic disease at an average of 8-10 years after implantation. BIA-ALCL staging has evolved from a "liquid tumour" model to a "solid tumour" classification. For localised disease, surgery involving complete capsulectomy and implant removal is the cornerstone of treatment. For more advanced disease, treatment includes surgery followed by chemotherapy (combination anthracycline-based), radiotherapy and the antibody drug conjugate (brentuximab vedotin). The interplay between the Gram-negative biofilm, implant texturing, genetic mutations and time has been implicated in pathogenesis of BIA-ALCL. The identification of a putative infectious cause is not unique to lymphomagenesis. Future research, investigating BIA-ALCL genetic mutations and immunological modulation with Gram-negative biofilm in BIA-ALCL models is warranted.

摘要

综述目的

乳房植入物相关间变性大细胞淋巴瘤(BIA-ALCL)是一种最近才被认识的T淋巴细胞恶性肿瘤,仅与带纹理的乳房植入物有关。本综述旨在评估关于该疾病的流行病学、发病机制、临床评估和管理的现有理论。

最新发现

BIA-ALCL的真实发病率难以确定。流行的致病理论认识到带纹理的植入物、革兰氏阴性菌、宿主遗传学(如JAK/STAT、p53)和时间之间的相互作用。患者通常在植入后平均8至10年出现延迟性血清肿,较少见的是出现包膜肿块或全身性疾病。BIA-ALCL分期已从“液体肿瘤”模型演变为“实体肿瘤”分类。对于局限性疾病,包括完整包膜切除术和植入物取出术的手术是治疗的基石。对于更晚期的疾病,治疗包括手术,随后进行化疗(基于蒽环类药物的联合化疗)、放疗和抗体药物偶联物(维布妥昔单抗)。革兰氏阴性生物膜、植入物纹理、基因突变和时间之间的相互作用与BIA-ALCL的发病机制有关。确定一种假定的感染原因并非淋巴瘤发生所特有。有必要开展未来研究,在BIA-ALCL模型中研究BIA-ALCL基因突变以及革兰氏阴性生物膜对免疫的调节作用。

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