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乳腺植入物相关间变性大细胞淋巴瘤:CD30+ 淋巴增殖性疾病谱中的独特实体。

Breast implant-associated ALCL: a unique entity in the spectrum of CD30+ lymphoproliferative disorders.

机构信息

University of Pittsburgh Department of Dermatology, Pittsburgh, Pennsylvania 15213, USA.

出版信息

Oncologist. 2013;18(3):301-7. doi: 10.1634/theoncologist.2012-0238. Epub 2013 Feb 21.

Abstract

CD30(+) lymphoproliferative disorders represent a spectrum of diseases with distinct clinical phenotypes ranging from reactive conditions to aggressive systemic anaplastic lymphoma kinase (ALK)(-) anaplastic large cell lymphoma (ALCL). In January 2011, the U.S. Food and Drug Administration (FDA) announced a possible association between breast implants and ALCL, which was likened to systemic ALCL and treated accordingly. We analyzed existing data to see if implant-associated ALCL (iALCL) may represent a distinct entity, different from aggressive ALCL. We conducted a systematic review of publications regarding ALCL and breast implantation for 1990-2012 and contacted corresponding authors to obtain long-term follow-up where available. We identified 44 unique cases of iALCL, the majority of which were associated with seroma, had an ALK(-) phenotype (97%), and had a good prognosis, different from the expected 40% 5-year survival rate of patients with ALK(-) nodal ALCL (one case remitted spontaneously following implant removal; only two deaths have been reported to the FDA or in the scientific literature since 1990). The majority of these patients received cyclophosphamide, doxorubicin, vincristine, and prednisolone with or without radiation, but radiation alone also resulted in complete clinical responses. It appears that iALCL demonstrates a strong association with breast implants, a waxing and waning course, and an overall good prognosis, with morphology, cytokine profile, and biological behavior similar to those of primary cutaneous ALCL. Taken together, these data are suggestive that iALCL may start as a reactive process with the potential to progress and acquire an aggressive phenotype typical of its systemic counterpart. A larger analysis and prospective evaluation and follow-up of iALCL patients are necessary to definitively resolve the issue of the natural course of the disease and best therapeutic approaches for these patients.

摘要

CD30(+) 淋巴增生性疾病代表了一组具有不同临床表现的疾病,从反应性疾病到侵袭性系统性间变性淋巴瘤激酶(ALK)(-)间变性大细胞淋巴瘤(ALCL)不等。2011 年 1 月,美国食品和药物管理局(FDA)宣布乳房植入物与 ALCL 之间可能存在关联,这种 ALCL 类似于系统性 ALCL,并进行了相应的治疗。我们分析了现有的数据,以确定植入物相关的 ALCL(iALCL)是否可能代表一种不同于侵袭性 ALCL 的独特实体。我们对 1990 年至 2012 年有关 ALCL 和乳房植入物的出版物进行了系统评价,并联系了相应的作者,以获取可用的长期随访数据。我们共发现了 44 例 iALCL 独特病例,其中大多数与血清肿有关,具有 ALK(-)表型(97%),且预后良好,与预期的 40%ALK(-)结外 ALCL 患者 5 年生存率(一例患者在取出植入物后自发缓解;自 1990 年以来,FDA 或科学文献中仅报告了两例死亡)不同。这些患者大多数接受环磷酰胺、多柔比星、长春新碱和泼尼松治疗,联合或不联合放疗,但单独放疗也能使临床完全缓解。iALCL 似乎与乳房植入物强烈相关,具有时起时伏的病程,且总体预后良好,形态学、细胞因子谱和生物学行为与原发性皮肤 ALCL 相似。综上所述,这些数据提示 iALCL 可能首先是一种反应性过程,具有进展并获得其系统性对应物典型侵袭性表型的潜力。需要对 iALCL 患者进行更大规模的分析、前瞻性评估和随访,以明确该疾病的自然病程和最佳治疗方法。

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